Slowing down an internal clock: implications for accounts of performance on four timing tasks

An experiment investigated the potential effects of lowering arousal on performance on time perception tasks. Four participant groups received different tasks: Normal and episodic temporal generalization, bisection, and verbal estimation, all involving judgements of the duration of visual stimuli. Self-rated arousal during the experimental session was lowered by spacing experimental trials approximately 10 s apart. Between the early and late blocks of the experiment, performance changed on normal temporal generalization and verbal estimation, but not on episodic temporal generalization and bisection. The changes were consistent with the idea that the pacemaker of the participant's internal clock had been slowed down by the slow trial spacing. Results suggested that bisection was based on a criterion that adjusted during the experiment, whereas verbal estimation was based on preexisting standards, or those established early in the experiment.     

Slowing down an internal clock: Implications for accounts of performance on four timing tasks

An experiment investigated the potential effects of lowering arousal on performance on time perception tasks. Four participant groups received different tasks: Normal and episodic temporal generalization, bisection, and verbal estimation, all involving judgements of the duration of visual stimuli. Self-rated arousal during the experimental session was lowered by spacing experimental trials approximately 10 s apart. Between the early and late blocks of the experiment, performance changed on normal temporal generalization and verbal estimation, but not on episodic temporal generalization and bisection. The changes were consistent with the idea that the pacemaker of the participant's internal clock had been slowed down by the slow trial spacing. Results suggested that bisection was based on a criterion that adjusted during the experiment, whereas verbal estimation was based on preexisting standards, or those established early in the experiment.     

Subjective time: Cognitive and physical secondary tasks affect timing differently

Humans were trained on a temporal discrimination to make one response when the stimulus duration was short (2 s) and a different response when the stimulus duration was long (8 s). They were then tested with stimulus durations in between to determine the bisection point. In Experiment 1, we examined the effect of a secondary cognitive task (counting backwards by threes) on the bisection point when participants were trained without a cognitive load and were tested with a cognitive load or the reverse (relative to appropriate controls). When the cognitive load increased from training, the psychophysical function plotting long responses against the increase in stimulus duration shifted to the right (as if the internal clock slowed down), and when the cognitive load decreased from training the psychophysical function shifted to the left (as if the internal clock speeded up). In Experiment 2, when the secondary task consisted of exerting continuous force on a transducer (a physically effortful task), it had the opposite effect. When the required force increased from training, the psychophysical function shifted to the left (as if the internal clock speeded up), and when the required force decreased from training, the psychophysical function shifted to the right (as if the internal clock slowed down). The results support an attentional view of the subjective passage of time. A cognitive secondary task appears to decrease attention to temporal cues, resulting in the underestimation of the passage of time, whereas a force requirement appears to increase attention to temporal cues, resulting in the overestimation of the passage of time.     

Subjective time: cognitive and physical secondary tasks affect timing differently

Humans were trained on a temporal discrimination to make one response when the stimulus duration was short (2 s) and a different response when the stimulus duration was long (8 s). They were then tested with stimulus durations in between to determine the bisection point. In Experiment 1, we examined the effect of a secondary cognitive task (counting backwards by threes) on the bisection point when participants were trained without a cognitive load and were tested with a cognitive load or the reverse (relative to appropriate controls). When the cognitive load increased from training, the psychophysical function plotting long responses against the increase in stimulus duration shifted to the right (as if the internal clock slowed down), and when the cognitive load decreased from training the psychophysical function shifted to the left (as if the internal clock speeded up). In Experiment 2, when the secondary task consisted of exerting continuous force on a transducer (a physically effortful task), it had the opposite effect. When the required force increased from training, the psychophysical function shifted to the left (as if the internal clock speeded up), and when the required force decreased from training, the psychophysical function shifted to the right (as if the internal clock slowed down). The results support an attentional view of the subjective passage of time. A cognitive secondary task appears to decrease attention to temporal cues, resulting in the underestimation of the passage of time, whereas a force requirement appears to increase attention to temporal cues, resulting in the overestimation of the passage of time.     

Why 'Sounds Are Judged Longer Than Lights': Application of a Model of the Internal Clock in Humans

Three experiments, using temporal generalization and verbal estimation methods, studied judgements of duration of auditory (500-Hz tone) and visual (14-cm blue square) stimuli. With both methods, auditory stimuli were judged longer, and less variable, than visual ones. The verbal estimation experiments used stimuli from 77 to 1183 msec in length, and the slope of the function relating mean estimate to real length differed between modalities (but the intercept did not), consistent with the idea that a pacemaker generating duration representations ran faster for auditory than for visual stimuli. The different variability of auditory and visual stimuli was attributed to differential variability in the operation of a switch of a pacemaker-accumulator clock, and experimental datasuggested that such switch effects were separable from changes in pacemaker speed. Overall, the work showed how a clock model consistent with scalar timing theory, the leading account of animal timing, can address an issue derived from the classical literature on human time perception.     

Dissecting the clock: understanding the mechanisms of timing across tasks and temporal intervals

Currently, it is unclear what model of timing best describes temporal processing across millisecond and second timescales in tasks with different response requirements. In the present set of experiments, we assessed whether the popular dedicated scalar model of timing accounts for performance across a restricted timescale surrounding the 1-second duration for different tasks. The first two experiments evaluate whether temporal variability scales proportionally with the timed duration within temporal reproduction. The third experiment compares timing across millisecond and second timescales using temporal reproduction and discrimination tasks designed with parallel structures. The data exhibit violations of the assumptions of a single scalar timekeeper across millisecond and second timescales within temporal reproduction; these violations are less apparent for temporal discrimination. The finding of differences across tasks suggests that task demands influence the mechanisms that are engaged for keeping time.     

The role of executive functions in human prospective interval timing

Human timing is thought to be based on the output of an internal clock. Whilst the functioning of this clock is well documented, it is unclear which other cognitive resources may moderate timing. Brown (2006) and Rattat (2010) suggest that the central executive of working memory may be recruited during timing. However it seems likely that the fractionated executive component processes identified by Miyake et al. (2000) and Fisk and Sharp (2004) may differentially contribute to timing performance; further exploration of this was the aim of the present study. An interference paradigm was employed in which participants completed an interval production task, and tasks which have been shown to tap the four key executive component processes (shifting, inhibition, updating and access) under single and dual-task conditions. Comparison of single and dual-task performance indicated that timing always became more variable when concurrently performing a second task. Bidirectional interference only occurred between the interval production task and the memory updating task, implying that both tasks are competing for the same executive resource of updating. There was no evidence in the current study to suggest that switching, inhibition or access was involved in timing, however they may be recruited under more difficult task conditions.     

"Time flies in the presence of angry faces"… depending on the temporal task used!

A number of studies have reported that the perception of an arousing emotional stimulus, such as an angry face, results in temporal overestimations which are probably due to the speeding up of a clock-like system. The aim of the present study was to examine whether this emotional effect can be generalized to all temporal tasks irrespective of the underlying cognitive processes involved in each task. Five different temporal tasks involving the presentation of neutral and angry faces were therefore tested: bisection, generalization, verbal estimation, production and reproduction. Our results showed an overestimation of time for the angry compared to the neutral faces in the temporal bisection, verbal estimation and production tasks but not in the temporal generalization and reproduction tasks. Moreover, the results obtained in the temporal verbal estimation and production tasks suggest that this temporal overestimation of the angry faces was associated with relatively more accurate estimates. The involvement of both arousal and attention mechanisms in the effect of emotional facial expressions on time perception is discussed in the light of the differences in the impact of the same emotional stimulus as a function of the temporal task considered.     

Good vibrations: Human interval timing in the vibrotactile modality

This article reports a detailed examination of timing in the vibrotactile modality and comparison with that of visual and auditory modalities. Three experiments investigated human timing in the vibrotactile modality. In Experiment 1, a staircase threshold procedure with a standard duration of 1,000 ms revealed a difference threshold of 160.35 ms for vibrotactile stimuli, which was significantly higher than that for auditory stimuli (103.25 ms) but not significantly lower than that obtained for visual stimuli (196.76 ms). In Experiment 2, verbal estimation revealed a significant slope difference between vibrotactile and auditory timing, but not between vibrotactile and visual timing. That is, both vibrations and lights were judged as shorter than sounds, and this comparative difference was greater at longer durations than at shorter ones. In Experiment 3, performance on a temporal generalization task showed characteristics consistent with the predications of scalar expectancy theory (SET: Gibbon, 1977) with both mean accuracy and scalar variance exhibited. The results were modelled using the modified Church and Gibbon model (MCG; derived by Wearden, 1992, from Church & Gibbon 1982). The model was found to give an excellent fit to the data, and the parameter values obtained were compared with those for visual and auditory temporal generalization. The pattern of results suggest that timing in the vibrotactile modality conforms to SET and that the internal clock speed for vibrotactile stimuli is significantly slower than that for auditory stimuli, which is logically consistent with the significant differences in difference threshold that were obtained.     

Attention and interference in prospective and retrospective timing.

Subjects listened to a series of musical selections and then judged the duration of each selection. Some subjects were informed beforehand that timing was involved (prospective timing) whereas others were informed afterwards (retrospective timing). Half the groups performed a concurrent proofreading task during stimulus presentation. The results showed a trade-off between temporal and nontemporal task performance: prospective-timing groups were more accurate in judging time and were worse at proofreading, whereas retrospective-timing groups were relatively poor at judging time but better at proofreading. This pattern is consistent with Michon's notion of an essential equivalence between temporal and nontemporal processing, and supports the predictions of an attentional allocation model of timing. The proofreading task interfered both with prospective and with retrospective timing, and both types of time judgments were influenced in the same way by effects of stimulus context. These results imply that similar timing processes operate under prospective and retrospective conditions.     

Stimulus timing by people with Parkinson's disease

Previous literature suggests that Parkinson’s disease is marked by deficits in timed behaviour. However, the majority of studies of central timing mechanisms in patients with Parkinson’s disease have used timing tasks with a motor component. Since the motor abnormalities are a defining feature of the condition, the status of timing in Parkinson’s disease remains uncertain. Data are reported from patients with mild to moderate Parkinson’s disease (both on and off medication) and age- and IQ-matched controls on a range of stimulus timing tasks without counting. Tasks used were temporal generalization, bisection, threshold determination, verbal estimation, and a memory for duration task. Performance of patients was generally “normal” on all tasks, but significant differences from performance of controls were found on the memory for duration task. Among the “normal” effects noted were arithmetic mean bisection, asymmetric temporal generalization gradients, and subjective shortening on the memory for duration task. The results suggest (a) that some previous reports of timing “deficits” in Parkinson’s patients were possibly due to the use of tasks requiring a timed manual response and (b) small differences between patients and controls may be found on tasks where two stimuli are presented on each trial, whether patients are on medication or off it.     

Children's time production for concurrent nontemporal motor tasks

An internal clock model has often been used to explain disruptions in timing production that occur when temporal and nontemporal tasks are performed simultaneously. In this study, participants' ability to walk 8 m in 8 sec. while executing various secondary concurrent nontemporal tasks was assessed for 16 children enrolled in sports at school. Children participated in six trials under five randomized task conditions involving different coordinative and cognitive workloads. The duration of timing production increased as the attention requirements or cognitive demands placed upon the completion of the task increased. However, participants also showed learning of timing over the six trials. Significant differences were found between the timing task and the concurrent nontemporal tasks depending on the difficulty and cognitive load of the secondary tasks. Results are discussed using attention models of time estimation and production.     

Attention allocation policy influences prospective timing

The role of attention allocation policy control in prospective duration judgments was tested in two experiments. In the first experiment, it was demonstrated that prospective duration judgments of same clock durations are longer when timing is treated as a primary task than when it is treated as a secondary task, regardless of the difficulty of the nontemporal task filling the to-be-judged interval. In the second experiment, this finding was replicated. Additionally, it was demonstrated that when prospective timing is not preassigned a specific priority, duration judgments are longer than those obtained under secondary-task conditions, but shorter than those obtained under primary-task conditions. It was also revealed that when attention is distracted from timing, prospective duration judgments become shorter than when attention is not distracted. These findings support the notion that prospective timing creates a dual-task condition in which magnitude of duration judgments reflects the amount of attentional resources allocated for temporal information processing.     

Ketamine "unlocks" the reduced clock-speed effects of cocaine following extended training: evidence for dopamine--glutamate interactions in timing and time perception

The present study examined the clock-speed modulating effects of acute cocaine administration in groups of male rats that received different amounts of baseline training on a 36-s peak-interval procedure prior to initial drug injection. After injection of cocaine (10, 15, or 20mg/kg, ip), rats that had received a minimal amount of training (e.g., or=180 sessions) prior to cocaine (15 mg/kg, ip) administration did not produce this "classic" curve-shift effect, but instead displayed a general disruption of temporal control following drug administration. Importantly, when co-administered with a behaviorally ineffective dose of ketamine (10mg/kg, ip) the ability of cocaine to modulate clock speed in rats receiving extended training was restored. A glutamate "lock/unlock" hypothesis is used to explain the observed dopamine-glutamate interactions as a function of timing behaviors becoming learned habits.     

Interval timing as an emergent learning property

Interval timing in operant conditioning is the learned covariation of a temporal dependent measure such as wait time with a temporal independent variable such as fixed-interval duration. The dominant theories of interval timing all incorporate an explicit internal clock, or "pacemaker," despite its lack of independent evidence. The authors propose an alternative, pacemaker-free view that demonstrates that temporal discrimination can be explained by using only 2 assumptions: (a) variation and selection of responses through competition between reinforced behavior and all other, elicited, behaviors and (b) modulation of the strength of response competition by the memory for recent reinforcement. The model departs radically from existing timing models: It shows that temporal learning can emerge from a simple dynamic process that lacks a periodic time reference such as a pacemaker.     

Is the interference between memory processing and timing specific to the use of verbal material?

Increasing load in a memory task performed simultaneously with a timing task shortens perceived time, an effect that has been observed previously with memory tasks using verbal material. The present experiments examine whether two similar memory tasks, one in which verbal material is used and another one in which nonverbal material is used, would produce similar interference effects on concurrent time reproduction. In Experiment 1, the number of nonverbal stimuli (pseudo‐random dot patterns) was manipulated in a memory task performed while a temporal interval to be reproduced was encoded. Reproductions shortened proportionally to the duration of memory processing executed during time estimation. Verbal stimuli (consonants) were used in Experiment 2 in otherwise identical experimental conditions. Effects observed in Experiment 2 were comparable to those obtained in Experiment 1. Taken together, these results support the notion that interference from memory tasks on concurrent time estimation is not determined by the specific type of material processed in memory, but instead by the duration of memory processing.     

Is the interference between memory processing and timing specific to the use of verbal material?

Increasing load in a memory task performed simultaneously with a timing task shortens perceived time, an effect that has been observed previously with memory tasks using verbal material. The present experiments examine whether two similar memory tasks, one in which verbal material is used and another one in which nonverbal material is used, would produce similar interference effects on concurrent time reproduction. In Experiment 1, the number of nonverbal stimuli (pseudo-random dot patterns) was manipulated in a memory task performed while a temporal interval to be reproduced was encoded. Reproductions shortened proportionally to the duration of memory processing executed during time estimation. Verbal stimuli (consonants) were used in Experiment 2 in otherwise identical experimental conditions. Effects observed in Experiment 2 were comparable to those obtained in Experiment 1. Taken together, these results support the notion that interference from memory tasks on concurrent time estimation is not determined by the specific type of material processed in memory, but instead by the duration of memory processing.     

Action, arousal, and subjective time

Saccadic chronostasis refers to the subjective temporal lengthening of the first visual stimulus perceived after an eye movement. It has been quantified using a duration discrimination task. Most models of human duration discrimination hypothesise an internal clock. These models could explain chronostasis as a transient increase in internal clock speed due to arousal following a saccade, leading to temporal overestimation. Two experiments are described which addressed this hypothesis by parametrically varying the duration of the stimuli that are being judged. Changes in internal clock speed predict chronostasis effects proportional to stimulus duration. No evidence for proportionality was found. Two further experiments assessed the appropriateness of the control conditions employed. Results indicated that the chronostasis effect is constant across a wide range of stimulus durations and does not reflect the pattern of visual stimulation experienced during a saccade, suggesting that arousal is not critical. Instead, alternative processes, such as one affecting the onset of timing (i.e., the time of internal clock switch closure) are implicated. Further research is required to select between these alternatives.     

Interval timing predicts impulsivity in intertemporal choice: combined behavioral and drift-diffusion model evidence

ABSTRACT

This study investigated the relationship between interval timing and impulsivity in intertemporal choice in a healthy population. A duration production task was used to assess interval timing. Choice impulsivity was assessed using a hypothetical money choice task. Results from 134 participants indicated that faster internal clock significantly predicted lower choice impulsivity. A subsequent drift-diffusion model analysis of the behavioural data revealed that in the sub-group of relatively farsighted participants, faster internal clock predicted consideration of more information before making a choice, which in turn was associated with lower choice impulsivity. In the sub-group of relatively impatient participants too, faster internal clock predicted consideration of more information, but which in turn was associated with higher choice impulsivity. It is concluded that among relatively farsighted individuals in a normal population, faster internal clock favours a more deliberate processing of the options at hand, thus eliciting less impulsive choices.     

When do auditory/visual differences in duration judgements occur?

Four experiments examined judgements of the duration of auditory and visual stimuli. Two used a bisection method, and two used verbal estimation. Auditory/visual differences were found when durations of auditory and visual stimuli were explicitly compared and when durations from both modalities were mixed in partition bisection. Differences in verbal estimation were also found both when people received a single modality and when they received both. In all cases, the auditory stimuli appeared longer than the visual stimuli, and the effect was greater at longer stimulus durations, consistent with a “pacemaker speed” interpretation of the effect. Results suggested that Penney, Gibbon, and Meck's (2000) “memory mixing” account of auditory/visual differences in duration judgements, while correct in some circumstances, was incomplete, and that in some cases people were basing their judgements on some preexisting temporal standard.