Biomedical subjects

Gordon D Logan

Publications and source records attributed to Gordon D Logan.

At least 19 recordsLinked to original sources

PubMed2006

Influence of history on saccade countermanding performance in humans and macaque monkeys.

The stop-signal or countermanding task probes the ability to control action by requiring subjects to withhold a planned movement in response to an infrequent stop signal which they do with variable success depending on the delay of the stop signal. We investigated whether performance of humans and macaque monkeys in a saccade countermanding task was influenced by stimulus and performance history. In spite of idiosyncrasies across subjects several trends were evident in both humans and monkeys. Response time decreased after successive trials with no stop signal. Response time increased after successive trials with a stop signal. However, post-error slowing was not observed. Increased response time was observed mainly or only after cancelled (signal inhibit) trials and not after noncancelled (signal respond) trials. These global trends were based on rapid adjustments of response time in response to momentary fluctuations in the fraction of stop signal trials. The effects of trial sequence on the probability of responding were weaker and more idiosyncratic across subjects when stop signal fraction was fixed. However, both response time and probability of responding were influenced strongly by variations in the fraction of stop signal trials. These results indicate that the race model of countermanding performance requires extension to account for these sequential dependencies and provide a basis for physiological studies of executive control of countermanding saccade performance.

Animals↗

PubMed2006

Hierarchical control of cognitive processes: switching tasks in sequences.

Hierarchical control of cognitive processes was studied by examining the relationship between sequence- and task-level processing in the performance of explicit, memorized task sequences. In 4 experiments, switch costs in task-switching performance were perturbed by sequence initiation times that varied with sequence complexity, preparation time, and type of sequence transition (repetition or switch). Hierarchical control was inferred from these sequence initiation time effects and the recurrent finding of no switch cost at the first serial position across sequences, the point at which sequence-level processes are likely active in maintaining or instantiating a hierarchical control structure in working memory. These findings resonate with past research on motor programs and serial memory and provide new insights into the concepts of task set and control.

Attention↗

PubMed2006

Interpreting instructional cues in task switching procedures: the role of mediator retrieval.

In 3 experiments the role of mediators in task switching with transparent and nontransparent cues was examined. Subjects switched between magnitude (greater or less than 5) and parity (odd or even) judgments of single digits. A cue-target congruency effect indicated mediator use: subjects responded faster to congruent cue-target combinations (e.g., ODD-3) than to incongruent cue-target combinations (e.g., ODD-4). Experiment 1 revealed significant congruency effects with transparent word cues (ODD, EVEN, HIGH, and LOW) and with relatively transparent letter cues (O, E, H, and L) but not with nontransparent letter cues (D, V, G, and W). Experiment 2 revealed significant congruency effects after subjects who were trained with nontransparent letter cues were informed of the relations between cues and word mediators halfway through the experiment. Experiment 3 showed that congruency effects with relatively transparent letter cues diminished over 10 sessions of practice, suggesting that subjects used mediators less as practice progressed. The results are discussed in terms of the role of mediators in interpreting instructional cues.

Analysis of Variance↗

PubMed2006

Priming or executive control? Associative priming of cue encoding increases "switch costs" in the explicit task-cuing procedure.

The explicit task-cuing procedure involves presenting a cue that indicates which task to perform on a target. Responses are typically faster when tasks repeat than when they alternate, and this difference is often interpreted as a measure of the time required for executive control processes to change task set. This article suggests that the difference reflects priming of cue encoding when successive cues are identical or associatively related. Subjects responded to task repetitions more quickly when the cue on the current trial was associatively related to the cue on the previous trial (e.g., day --> night) than when the cues were unrelated (e.g., verb --> night). Models applied to the time course function--generated by manipulating the interval between the onsets of the cue and the target--showed that the facilitation was due to cue encoding, a process that does not require online executive control.

Attention↗

PubMed2006

Parallel response selection in dual-task situations.

Semantic priming and response priming were studied in a dual-task procedure. In two experiments, reaction times to the first and second stimuli were faster when the finger required for the Task 1 response was the same as the finger required for the Task 2 response. Such priming suggests that Task 2 response information was generated prior to the completion of Task 1 response selection. These data pose a potential challenge to the response-selection bottleneck (RSB) theory of dual-task performance, since they may indicate a violation of the discrete-stage processing assumption on which the underlying locus-of-slack logic depends. Accommodating these data while preserving the essential bottleneck character of RSB theory may be possible but may also alter the very nature of the bottleneck itself.

Choice Behavior↗

PubMed2006

Out with the old, in with the new: more valid measures of switch cost and retrieval time in the task span procedure.

Two experiments provided new measures of switch cost and retrieval time in the task span procedure. In Experiment 1, subjects were given lists of six task names to remember, followed by six targets on which to perform the tasks named in the list. The lists contained alternations and repetitions, and switch costs were estimated by comparing reaction time (RT) on alternation and repetition trials. The experiment also included memory span and single task conditions, so switch costs could be estimated by subtracting the sum of the RT in those conditions from the task span RT, as in the original report (Logan, 2004). The data suggested that the original measure of switch cost was invalid and that the new measure was preferable. In Experiment 2, subjects performed each task on the list twice. Retrieval was required on the first but not on the second trial in each pair. Retrieval time was estimated by comparing the RT on trials that required retrieval with trials that did not require retrieval. This measure was more valid than the RT in the memory span condition of Experiment 1, which was used in the original report.

Attention↗

PubMed2006

Priming cue encoding by manipulating transition frequency in explicitly cued task switching.

Explicitly cued task switching with multiple cues per task permits three types of transitions: cue repetitions (cue and task repeat), task repetitions (cue changes but task repeats), and task alternations (cue and task change). The difference between task alternations and task repetitions can be interpreted as a switch cost, but its magnitude varies substantially across experiments. We investigated how switch cost is affected by transition frequency (how often subjects repeat and switch tasks) with an experiment in which each transition had a frequency of .70 in separate sessions. Switch cost was smallest when task alternations were frequent and largest when task repetitions were frequent. Mathematical modeling of the data indicated that the different "switch costs" reflected priming of cue encoding for frequent transitions. Interpretations of our findings based on automatic priming from memory retrieval of past transitions and strategic priming from transition expectancies are discussed.

Attention↗

PubMed2005

Modeling task switching without switching tasks: a short-term priming account of explicitly cued performance.

Switch costs in task switching are commonly attributed to an executive control process of task-set reconfiguration, particularly in studies involving the explicit task-cuing procedure. The authors propose an alternative account of explicitly cued performance that is based on 2 mechanisms: priming of cue encoding from residual activation of cues in short-term memory and compound cue retrieval of responses from long-term memory. Their short-term priming account explains the repeated cue encoding benefit, switch cost, reduction in switch cost with preparation time, and other effects. The authors develop a mathematical model of their priming account and fit it to data from 3 experiments, demonstrating that a set of basic psychological processes can produce several effects--including putative switch costs--without switching tasks.

Attention↗

PubMed2005

Voluntary task switching: chasing the elusive homunculus.

In the voluntary task switching procedure, subjects choose the task to perform on a series of bivalent stimuli, requiring top-down control of task switching. Experiments 1-3 contrasted voluntary task switching and explicit task cuing. Choice behavior showed small, inconsistent effects of external stimulus characteristics, supporting the assumption of top-down control of task choice. Switch costs were smaller when subjects chose to switch tasks than when instructed by an external cue. Experiments 4-6 separated choice costs from switch costs. These findings support models of task switching that incorporate top-down processes in accounts of switch costs. The degree to which task switching procedures capture top-down versus bottom-up processes may depend on the extent of environmental support provided by the procedure.

Attention↗

PubMed2005

A memory-based account of automatic numerosity processing.

We investigated the mechanisms responsible for the automatic processing of the numerosities represented by digits in the size congruity effect (Henik & Tzelgov, 1982). The algorithmic model assumes that relational comparisons of digit magnitudes (e.g., larger than {8,2}) create this effect. If so, congruity effects ought to require two digits. Memory-based models assume that associations between individual digits and the attributes "small" and "large" create this effect. If so, congruity effects ought only to require one digit. Contrary to the algorithmic model and consistent with memory-based models, congruity effects were just as large when subjects judged the relative physical sizes of small digits paired with letters as when they judged the relative physical sizes of two digits. This finding suggests that size congruity effects can be produced without comparison algorithms.

Automatism↗

PubMed2005

The time it takes to switch attention.

An experiment is reported that measured the time it takes to switch attention from one set of locations to another in response to a cue that indicates the relevant locations. The experiment compared sequences of trials in which the same locations were cued in succession with sequences in which different locations were cued in succession in order to separate cue-encoding time from attention-switching time. Same-location sequences require cue encoding but not attention switching. They were substantially faster than different-location sequences, which require both cue encoding and attention switching. Formal models were fitted to time-course functions generated by presenting the cues 0, 100, 200, 300, or 400 msec before the target displays. The model fits suggest that cue encoding took 67-74 msec and attention switching took 76-101 msec.

Attention↗

PubMed2004

Evidence for an error monitoring deficit in attention deficit hyperactivity disorder.

We studied error monitoring in ADHD and control children in a task requiring inhibition of a motor response. The extent of slowing following successful (stopped) and failed (nonstopped) inhibition was compared across groups. We also measured the time required to inhibit a response (stop signal reaction time, SSRT). Compared to controls, ADHD participants slowed less following nonstopped responses. Slowing did not vary with comorbid reading, oppositional, conduct or anxiety disorder, sex or ADHD subtype. Slowing after nonstopped responses was marginally, although significantly correlated with total ADHD symptoms and with age. ADHD participants had significantly longer SSRT than controls, but SSRT was not significantly correlated with slowing. The apparent deficit in error monitoring in ADHD and its independence from the inhibition deficit observed in ADHD has implications for executive control models of ADHD, performance problems associated with the disorder and for component theories of executive control.

Adolescent↗

PubMed2004

Working memory, task switching, and executive control in the task span procedure.

Four experiments explored the task span procedure: Subjects received lists of 1-10 task names to remember and then lists of 1-10 stimuli on which to perform the tasks. Task span is the number of tasks performed in order perfectly. Experiment 1 compared the task span with the traditional memory span in 6 practiced subjects and found little difference. Experiment 2 compared the task span and the memory span in 64 unpracticed subjects and also found little difference. Experiment 3 compared practice with consistent and varied lists to address retrieval from long-term memory. Experiment 4 manipulated the number of task switches and found that it had little effect on task spans. The results suggest there is no trade-off between storage and task switching, which supports some theories of executive control and challenges others.

Adult↗

PubMed2004

The cost of a voluntary task switch.

Task-switching paradigms are widely used to study executive control. However, standard paradigms may not require active control to switch tasks. We examined voluntary task switching by having subjects choose which task to perform on a series of bivalent stimuli. Subjects performed parity or magnitude judgments on single digits. Instructions were to perform the two tasks equally often and in a random order. The response-to-stimulus interval (RSI) was either 100 or 1,000 ms, manipulated between blocks. Task alternations were slower than task repetitions, and this switch cost was greater at the short RSI than at the long RSI (310 and 94 ms, respectively). Additionally, subjects produced more task repetitions than expected if the tasks were performed in a random sequence. These results show costs associated with a voluntary task switch, when subjects must actively control the choice of the task to be performed.

Cognition↗

PubMed2004

Cumulative progress in formal theories of attention.

Formal theories of attention based on similarity-choice theory and signal-detection theory are reviewed to document cumulative progress in theoretical understanding of attention from the 1950s to the present. Theories based on these models have been developed to account for a wide variety of attentional phenomena, including attention to dimensions, attention to objects, and executive control. The review describes the classical similarity-choice and signal-detection theories and relates them to current theories of categorization, Garner tasks, visual search, cuing procedures, task switching, and strategy choice.

Attention↗

PubMed2004

Very clever homunculus: compound stimulus strategies for the explicit task-cuing procedure.

In two experiments, subjects were given arbitrary letter cues or meaningful word cues that specified the task to be performed on a subsequent target stimulus. Letter and word cues were presented in separate blocks. There were two cues of each type for each task. Three kinds of transitions separated tasks: cue repetitions, in which both the cue and the task repeated; task repetitions, in which the cue changed but the task repeated; and task alternations, in which both the cue and the task changed. Responses were faster for cue than for task repetitions for both cue types. With word cues, task repetitions were not reliably faster than task alternations. With letter cues, task repetitions were reliably faster than task alternations in the first block but not in the second block. The results suggest that subjects responded to the compound of the cue and the target rather than switching task set between trials.

Cognition↗

PubMed2004

Episodic and semantic components of the compound-stimulus strategy in the explicit task-cuing procedure.

The explicit task-cuing procedure is commonly used to study executive control processes involved in set switching, but performance in this task-switching procedure may be accomplished without switching tasks. Subjects may perform both tasks by using a compound-stimulus strategy, in which subjects encode the cue, encode the target, and use the combination as a compound retrieval cue to choose the appropriate response. We manipulated the number of targets (8, 16,32, or 640) that subjects experienced in a four-cue/two-task procedure to separate episodic and semantic memory retrieval components of the compound-stimulus strategy. Cue repetitions were faster than task repetitions, and task repetitions were only slightly faster than task alternations, suggesting that cue repetition effects account for the bulk of the difference between repetitions and alternations. We found the same effects with all target set sizes. The results are consistent with use of a semantic compound-stimulus strategy.

Cues↗

PubMed2003

Horse-race model simulations of the stop-signal procedure.

In the stop-signal paradigm, subjects perform a standard two-choice reaction task in which, occasionally and unpredictably, a stop-signal is presented requiring the inhibition of the response to the choice signal. The stop-signal paradigm has been successfully applied to assess the ability to inhibit under a wide range of experimental conditions and in various populations. The current study presents a set of evidence-based guidelines for using the stop-signal paradigm. The evidence was derived from a series of simulations aimed at (a) examining the effects of experimental design features on inhibition indices, and (b) testing the assumptions of the horse-race model that underlies the stop-signal paradigm. The simulations indicate that, under most conditions, the latency, but not variability, of response inhibition can be reliably estimated.

Animals↗