Neural mechanisms of timing

A crucial step in timing research is to isolate clock components from other sources of temporal variability. Significant progress has been made both behaviorally and neurologically, using elaborate experimental designs that separate timing mechanisms from motoric sensory and mnemonic processes. Marked similarities between the temporal characteristics of the clock in perception and production tasks implicate a common timing system. Similar conclusions can be reached from clinical studies, indeed individuals with neocerebellar damage are impaired at discriminating and reproducing short intervals. However, other patient populations, especially those with disorders affecting the basal ganglia, also exhibit deficits in timing tasks. It therefore appears that temporal computation may be distributed throughout the brain with specific roles for different neural structures.     

Overproduction timing errors in expert dancers

The authors investigated how expert dancers achieve accurate timing under various conditions. They designed the conditions to interfere with the dancers' attention to time and to test the explanation of the interference effect provided in the attentional model of time processing. Participants were 17 expert contemporary dancers who performed a freely chosen duration while walking and executing a bilateral cyclic arm movement over a given distance. The dancers reproduced that duration in different situations of interference. The process yielded temporal overproductions, validating the attentional model and extending its application to expert populations engaged in complex motor situations. The finding that the greatest overproduction occurred in the transfer-with-improvisation condition suggests that improvisation within a time deadline requires specific training.     

Developmental course of the temporal relationship between gaze direction and vocal production in typical and Down's syndrome infants

This study was aimed at examining the temporal relationship between gaze and vocal production behaviour among typically developing infants, infants with Down's syndrome, and their mothers. If gaze–voice timing behaviour is an organizing principle of communicative interaction in typical population, then studying it should provide insight into how children with Down's syndrome and their mothers use this temporal relationship to structure their exchanges. Forty-four mother–infant dyads (22 dyads with a Down's syndrome child and 22 with a typical child) were observed. The developmental course of timing pattern was not different between DS and typically developing infants from 4 to 19 months (DA). Insofar as the timing patterns differed between DS and typical infants at 20 months, this could be explained by their differing level of language acquisition. With the use of language, the timing patterns will reappear equal in the both populations. Results suggest that (i) the children's behaviours could be partially explained by the behaviours of their mothers. The mother–child dyad would be the mould that shapes the child's future sociolinguistic skills, and (ii) for the two populations, the timing-pattern changes could be explained by the emergence of language.     

The effects of spatial stimulus-response compatibility on choice time production accuracy and variability

Five experiments examined the relations between timing and attention using a choice time production task in which the latency of a spatial choice response is matched to a target interval (3 or 5 s). Experiments 1 and 2 indicated that spatial stimulus-response incompatibility increased nonscalar timing variability without affecting timing accuracy and that choice reaction time practice reduced choice time production variability. These data support a "temporal discounting" model in which response choice and timing occur in series, but the interval timed is shortened to account for nontemporal processing. In Experiment 3, feedback and anticipation task demands improved choice time production accuracy. In Experiments 4 and 5, the delay between the start-timing and choice-decision signals interacted with choice difficulty to affect choice time production accuracy and variability when timing a 3- but not a 5-s interval, suggesting that attention mediates timing before and after an interruption in timing.     

时间复制任务中的计时中断效应

以计时中断范式和时间复制任务相结合,考察了时间复制任务中是否存在计时中断效应。结果表明：（1）计时中断范式中1700ms和2300ms时距复制均出现高估现象,说明两种时距均低于相邻的高低估现象的转换点;（2）计时中断范式中1700ms和2300ms的时距复制任务没有支持计时标量特性;（3）计时中断范式中1700ms和2300ms的时间复制任务出现了计时中断效应。     

Scalar Timing in Animals and Humans

John Gibbon's lifetime work provided a deep understanding of the mechanisms whereby the time sense indexes the passage of time (its accumulation) and records, that is, stores, relevant time intervals in memory, enabling behavior to occur at the right time. The Scalar Expectancy Theory (SET; Gibbon, 1977) remains the most prominent of the theoretical accounts of animal and human timing. SET deals with the three principle psychophysical properties of timing data: flexible accuracy, multiplicative variance, and ratio comparisons. It differs from many other timing theories in its emphasis on scalar variability, a term that refers to the linear increase in the standard deviation of timing errors as a task's criterion time increases. Recently, research based on the conceptual framework and analytic tools of SET in John Gibbon's lab was expanded from a decades-long focus on nonhuman species to an assessment of timing performance in “normal” and brain-diseased human subjects, aimed at understanding the functional and neural mechanisms underlying interval timing in humans. This review is aimed at showing that animal and human data obtained with a variety of timing paradigms are both amenable to analyses of accuracy and scalar variability under the SET framework. In the second part of this report we discuss advances made in our understanding of neurobiological mechanisms underlying interval timing by taking advantage of the SET framework. Issues awaiting new theoretical developments in modeling time production and perception, as revealed by psychophysical findings of recent clinical research that are still not well understood (i.e., sources of nonscalar variability), are raised at the end.     

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.     

Testing the co-existence of two timing strategies for motor control in a unique task: The synchronisation spatial-tapping task

The control of rhythmic action sequences may involve two distinct timing strategies, i.e., event-based and emergent timing, which are usually revealed through finger-tapping and circle-drawing tasks, respectively. There is a lively debate concerning the possibility of coexistence of the two modes of timing for the execution of a single task. If one considers emergent timing as simply an absence of explicit representation of a time interval, then by definition, the two modes of timing cannot coexist. However, if one considers that emergent timing engages control of another motor parameter, e.g., a control of movement through space rather than time, then the possibility of coexistence needs to be reassessed. In the present study, we designed a hybrid of finger-tapping and circle-drawing tasks for which the demands for space and time control were present at the same time in order to reassess the coexistence hypothesis. Seventy-eight participants performed a spatial-tapping task in which finger taps were to be produced in synchrony with a regular metronome to 6 visual targets presented around a virtual circle. The metronome set ten distinct tempi (1100–300 ms). Using autocorrelation analyses on timing variables, we show that motor timing was event-based at slow tempi and emergent at faster tempi. Through an analysis of the trajectory, we confirm that an increase in the spatial control of movement took place congruently with a switch from event-based to emergent timing modes. At these fast tempi, timing and spatial errors were correlated but only at the specific target location for which a dynamical anchor point was revealed. Hence, we conclude that the coding of emergent timing has a spatial nature from which emerge timing regularities. This spatio-temporal strategy insures the performance of sequential motor actions when cognitive effort is too high for the use of pure event-based timing strategies.     

The role of practice and automaticity in temporal and nontemporal dual-task performance

Research on time and attention shows that a nontemporal task may interfere with a concurrent timing task by making time judgments shorter, more variable, and/or more inaccurate compared to timing-only conditions. Brown (1998, Psychological Research, 61, 71-81) counteracted the interference effect by giving subjects automaticity training on a nontemporal task to reduce the amount of processing resources the task required. Such practice attenuated interference in timing. Two new experiments were designed to replicate and extend the previous findings. Subjects generated a series of 5-s temporal productions under single-task (timing only) and dual-task (timing plus nontemporal task) conditions. The nontemporal tasks were pursuit rotor tracking (Experiment 1), and mirror-reversed reading (Experiment 2). We employed a pretest-practice-posttest paradigm, with the practice sessions devoted to performance of the nontemporal task. Pretest-posttest comparisons showed that practice reduced interference in timing in both experiments. Dual-task probe trials were given during the practice sessions to trace the time course of the improvement in timing. The results showed that interference in timing was reduced with even small amounts of practice. The findings support the idea that timing is very sensitive to changes in the allocation of attentional resources.     

Two-Timing: Politics and Response Latencies in a Bilingual Survey

Through the recording of response times in a national four-wave bilingual panel survey, this study reports improvements in the prediction of vote choice up to 1 year in advance of a federal election. These results were achieved with conventional computer-assisted telephone interviewing (CATI) software, indicating that the immediate use of response time measures isboth practical and attractive for commercial as well as academic survey units. Even so, response latencies were found to be sensitive to political circumstance, such that timings should be analyzed separately for minority and majority populations. Moreover, a broad analytic focus, beyond timing only vote intention and partisan commitment, is recommended because latency data on core questions of identity and allegiance reveal a great deal about the contours ofpolitical context.     

Evaluation of quantitative theories of timing

Scalar timing theory is a clear, complete, modular, and precise theory of timing that explains much of the data from many timing procedures, but not all of the data from all of the procedures. The multiple-time-scale theory of timing provides an alternative representation of time that has not yet been tested with respect to its fit to timing data.     

Population clocks: motor timing with neural dynamics

An understanding of sensory and motor processing will require elucidation of the mechanisms by which the brain tells time. Open questions relate to whether timing relies on dedicated or intrinsic mechanisms and whether distinct mechanisms underlie timing across scales and modalities. Although experimental and theoretical studies support the notion that neural circuits are intrinsically capable of sensory timing on short scales, few general models of motor timing have been proposed. For one class of models, population clocks, it is proposed that time is encoded in the time-varying patterns of activity of a population of neurons. We argue that population clocks emerge from the internal dynamics of recurrently connected networks, are biologically realistic and account for many aspects of motor timing.     

Analysis of timing variability in human movements by aligning parameter curves in time

The analysis of timing in human movements requires a reference with which timing can be quantified. In reactive movements this reference is given by the stimulus. However, many movements do not respond to such an external event. In throwing, for instance, the hand opening for release has to be timed to an acceleration of the throwing arm. A common approach to analyzing release-timing variability is to choose a landmark in the movement that is supposed to have a fixed temporal relation to the release. Such distinct landmarks, however, are not always well definable. Therefore, the present article describes an alternative approach analyzing timing variability on the basis of the alignment of different trials relative to their kinematic shape, by shifting the trials in the time domain. The basic assumption behind this approach is that single throwing movements are one instance of an acquired movement template, and thus show a considerable similarity. In contrast, the location of the temporal moment of release varies from trial to trial, generating imprecision regarding the release timing. In trials synchronized with respect to the release, this variability can be assessed by shifting the kinematic profiles of the throwing movements in time such that they superimpose as closely as possible. As a result, the corresponding time shifts for all trials represent a measure of the release time deviations across trials, and the standard deviation of these deviations represents the timing variability. Aside from timing analyses in such movements as throwing, the approach can be applied to very different tasks with timing demands—for example, to neurophysiological signals.     

The distinction between tapping and circle drawing with and without tactile feedback: An examination of the sources of timing variance

An internal clock-like process has been implicated in the control of rhythmic movements performed for short (250–2,000 ms) time scales. However, in the past decade, it has been claimed that a clock-like central timing mechanism is not required for smooth cyclical movements. The distinguishing characteristic delineating clock-like (event) from non-clock-like (emergent) timing is thought to be the kinematic differences between tapping (discrete-like) and circle drawing (smooth). In the archetypal event-timed task (tapping), presence of perceptual events is confounded with the discrete kinematics of movement (table contact). Recently, it has been suggested that discrete perceptual events help participants synchronize with a metronome. However, whether discrete tactile events directly elicit event timing has yet to be determined. In the present study, we examined whether a tactile event inserted into the circle drawing timing task could elicit event timing in a self-paced (continuation) timing task. For a majority of participants, inserting an event into the circle drawing task elicited timing behaviour consistent with the idea that an internal timekeeper was employed (a correlation of circle drawing with tapping). Additionally, some participants exhibited characteristics of event timing in the typically emergently timed circle drawing task. We conclude that the use of event timing can be influenced by the insertion of perceptual events, and it also exhibits persistence over time and over tasks within certain individuals.     

The distinction between tapping and circle drawing with and without tactile feedback: an examination of the sources of timing variance

An internal clock-like process has been implicated in the control of rhythmic movements performed for short (250-2,000 ms) time scales. However, in the past decade, it has been claimed that a clock-like central timing mechanism is not required for smooth cyclical movements. The distinguishing characteristic delineating clock-like (event) from non-clock-like (emergent) timing is thought to be the kinematic differences between tapping (discrete-like) and circle drawing (smooth). In the archetypal event-timed task (tapping), presence of perceptual events is confounded with the discrete kinematics of movement (table contact). Recently, it has been suggested that discrete perceptual events help participants synchronize with a metronome. However, whether discrete tactile events directly elicit event timing has yet to be determined. In the present study, we examined whether a tactile event inserted into the circle drawing timing task could elicit event timing in a self-paced (continuation) timing task. For a majority of participants, inserting an event into the circle drawing task elicited timing behaviour consistent with the idea that an internal timekeeper was employed (a correlation of circle drawing with tapping). Additionally, some participants exhibited characteristics of event timing in the typically emergently timed circle drawing task. We conclude that the use of event timing can be influenced by the insertion of perceptual events, and it also exhibits persistence over time and over tasks within certain individuals.     

Multiple roles for time in short-term memory: evidence from serial recall of order and timing

Three experiments are reported that examine the relationship between short-term memory for time and order information, and the more specific claim that order memory is driven by a timing signal. Participants were presented with digits spaced irregularly in time and postcued (Experiments 1 and 2) or precued (Experiment 3) to recall the order or timing of the digits. The primary results of interest were as follows: (a) Instructing participants to group lists had similar effects on serial and timing recall in inducing a pause in recall between suggested groups; (b) the timing of recall was predicted by the timing of the input lists in both serial recall and timing recall; and (c) when the recall task was precued, there was a tendency for temporally isolated items to be more accurately recalled than temporally crowded items. The results place constraints on models of serial recall that assume a timing signal generates positional representations and suggest an additional role for information about individual durations in short-term memory.     

Timing accuracy under Microsoft Windows revealed through external chronometry

Recent studies by Myors (1998, 1999) have concluded that the Microsoft Windows operating system is unable to support sufficient timing precision and resolution for use in psychological research. In the present study, we reexamined the timing accuracy of Windows 95/98, using (1) external chronometry, (2) methods to maximize the system priority of timing software, and (3) timing functions with a theoretical resolution of 1 msec or better. The suitability of various peripheral response devices and the relative timing accuracy of computers with microprocessors with different speeds were also explored. The results indicate that if software is properly controlled, submillisecond timing resolution is achievable under Windows with both old and new computers alike. Of the computer input devices tested, the standard parallel port was revealed as the most precise, and the serial mouse also exhibited sufficient timing precision for use in single-interval reaction time experiments.     

Response timing variability: coherence of kinematic and EMG parameters

A detailed kinematic and electromyographic (EMG) analysis of single degree of freedom timing responses is reported to (a) determine the coherence of kinematic and EMG variability to the reduced timing error variability exhibited with amplitude increments within a given criterion movement time and (b) understand the temporal organization of various movement parameters in simple responses. The data reveal that the variability of kinematic (time to peak acceleration, duration of acceleration phase, time to peak deceleration) and EMG (duration of agonist burst, duration of antagonist burst, time to antagonist burst) timing parameters decreased with increments of average velocity in a manner consistent with the variable timing error. In addition, the coefficient of variation for peak acceleration, peak deceleration, and integrated EMG of the agonist burst followed the same trend. Increasing average movement velocity also led to decreases in premotor and motor reaction times. Overall, the findings suggest a strong coherence between the variability of response outcome, kinematic, and EMG parameters.     

Response Timing Variability

A detailed kinematic and electromyographic (EMG) analysis of single degree of freedom timing responses is reported to (a) determine the coherence of kinematic and EMG variability to the reduced timing error variability exhibited with amplitude increments within a given criterion movement time and (b) understand the temporal organization of various movement parameters in simple responses. The data reveal that the variability of kinematic (time to peak acceleration, duration of acceleration phase, time to peak deceleration) and EMG (duration of agonist burst, duration of antagonist burst, time to antagonist burst) timing parameters decreased with increments of average velocity in a manner consistent with the variable timing error. In addition, the coefficient of variation for peak acceleration, peak deceleration, and integrated EMG of the agonist burst followed the same trend. Increasing average movement velocity also led to decreases in premotor and motor reaction times. Overall, the findings suggest a strong coherence between the variability of response outcome, kinematic, and EMG parameters.     

Millisecond interval timer and auditory reaction time programs for the IBM PC

Many types of behavioral research require the determination of elapsed time, for example to establish interstimulus intervals and to measure reaction time. The use of an IBM PC for on-line control of such applications is limited by the poor timing resolution ordinarily available. The IBM BIOS time information that is used for the BASIC TIMER function can result in interval timing errors as great as 110 msec. A machine language subroutine is described that can provide 1-msec accuracy. A BASIC program is also described that employs this subroutine to measure auditory reaction time.