Effects of interval duration on temporal processing in schizophrenia

INTRODUCTION: Temporal processing has received scant attention in the literature pertaining to cognitive deficits in patients with schizophrenia. Previous research suggests that patients with schizophrenia exhibit temporal perception deficits on both auditory and visual stimuli. The current study investigated the effects of interval manipulation to (1) replicate the original findings with a larger sample and an increased number of trials (2) assess the degree to which both patients and controls can differentiate temporal changes in a range of experimental interstimulus intervals, and (3) explore whether different interstimulus interval durations pose different levels of difficulty for the patients with schizophrenia. METHODS: Participants were asked to decide whether temporal intervals were shorter or longer than standard intervals on a computer-based auditory temporal perception task. The standard interval remained the same duration throughout the various tasks. The interstimulus interval separating the standard and experimental intervals varied in the range of 500, 1000, or 3000 ms. Data are presented for a sample of 16 patients with schizophrenia and 15 controls. RESULTS: Data suggest that patients with schizophrenia exhibit deficits in differentiating interval durations across all paradigms compared to their control-group peers on a range of auditory tasks (p<.001). CONCLUSIONS: These results are consistent with a general temporal deficit in schizophrenia. However, the roles of medication and localization are also addressed.     

Time-related processes in time-based prospective memory and in time-interval production

Time-based prospective memory tasks require the retrieval of previously formed plans (e.g., call me on my mobile phone) either at a specified time (e.g., at 3 p.m.) or after a specified period of time has elapsed (e.g., in 3 min). In the present study, we investigated whether the same time-related processes are recruited for a short-duration time-based prospective memory task and for a time-interval production task. In a dual-task paradigm, we required young adult participants to make category-membership decisions, while they were simultaneously engaged either in a time-based prospective memory tasks or in a time-interval production task. Under one set of conditions, participants were instructed to allocate attention equally to the two tasks, whereas in another set of conditions, they allocated attention primarily to the time-relevant task. The findings revealed that time estimates were not affected by the attention allocation manipulation, although it influenced performance on the concurrent category membership decision making task, and as expected time estimates were more accurate on the prospective memory task than on the time-production task. Based on the preponderance of the findings, we suggest that timing is managed by different mechanisms and/or strategies on time-interval production tasks and on short-duration time-based prospective memory tasks.     

Development of time sensitivity: Duration ratios in time bisection

This study investigated the development of children's abilities to discriminate durations as a function of their ratio and examined whether the ability to discriminate durations that differed by a very difficult ratio is related to the development of attention capacities. Children aged 5 and 8 years, as well as adults, performed a series of temporal bisection tasks with a ratio between the short and the long anchor duration that was changed to control the difficulty of the task (5:6, 2:3, and 1:2) in two duration ranges (<1 s and >3 s). In addition, they completed neuropsychological tests in order to assess their short-term memory, working memory, and visual attention abilities. The results showed that, at ratios of 2:3 and 1:2, most participants were able to discriminate the anchor durations in bisection. However, their sensitivity to time improved, whatever the duration range, both as the distance between the anchor durations increased and with increasing age. For the smallest duration ratio (5:6), few of the children were able to discriminate the anchor durations in the bisection task in comparison to adults. Hierarchical regression analyses performed on the neuropsychological tests revealed that, for the 2:3 ratio between anchor durations, the participants' visual attention scores explained a large part of the variance in time sensitivity. The children's lower temporal sensitivity was probably due to their limited visual attention abilities, thus explaining the difficulty they experienced in discriminating very close durations (5:6).     

Alerting attention and time perception in children

This experiment investigated the effect of a signal (i.e., a click) warning of the arrival of a stimulus to be timed on temporal discrimination in children aged 3, 5, and 8 years (N=86), using a bisection task with visual stimuli ranging from 0.5 to 2s or 1 to 4s. In all groups, the psychophysical functions were orderly with the proportion of long responses increasing with the stimulus duration, although the steepness of functions increased with age. Stimulus durations were judged to be longer with than without the click in all age groups. With the click, time sensitivity also improved and more particularly in the younger children. The statistical results suggest, within the framework of the scalar timing theory, that the click reduces the closing latency of the switch that connects the pacemaker to the accumulator in the internal clock and also reduces its trial-by-trial variability.     

Stop using time reproduction tasks in a comparative perspective without further analyses of the role of the motor response: The example of children

The temporal reproduction task is often used to investigate inter-individual differences in the ability to perceive time without any further analyses of the contribution of motor responses to temporal performance. The present study examined the role of motor responses in the reproduction of a 2.5 s and a 4.5 s signal duration in children and adults, with the former producing longer motor responses. The results showed that the 2.5 s duration was overestimated, especially by the younger children, whereas the 4.5 s duration was underestimated in all age groups. Further analyses indicated that the developmental differences related to motor response time explained the age-related difference in temporal reproduction for the shorter duration but not for the longer duration. The modelling of our data suggests that, for the shorter signal duration, the children initiated their responses at the same time as the adults, but that they reproduced longer durations because their motor response took more time to complete. In contrast, for the 4.5 s duration, the children initiated their responses earlier than the adults. However, they reproduced duration values close to the target time because their motor responses took longer. In addition, whatever the duration value to be reproduced, the representation of the sample duration was more variable in the younger children.     

Reward value effects on timing in the peak procedure

Three experiments examined the effect of motivational variables on timing in the peak procedure. In Experiment 1, rats received a 60-s peak procedure that was coupled with long-term, between-phase changes in reinforcer magnitude. Increases in reinforcer magnitude produced a leftward shift in the peak that persisted for 20 sessions of training. In a final phase, the rats received lithium chloride-induced aversion prior to testing and a rightward shift in the peak was observed. Experiment 2 confirmed the rightward shift in the peak under lithium chloride devaluation and induced a comparable shift with satiety devaluation. The degree of rightward shift was neither additive nor multiplicative, suggesting that two processes may have contributed. Experiment 3 examined the effect of extinction on peak responding, revealing a decrease in response rate, but no evidence of any change in the timing of responding. The implications of the results for contemporary timing theories are discussed.     

Temporal perception in closed-skill sports: An experimental study on expert swimmers and runners

The cognitive benefits of closed-skill sports practice have so far been scantily investigated. Here, we thus focused on the potential impact of swimming and running - two sports that highly rely on a precise control of timing - on time processing. To investigate the impact of these closed-skill sports on time perception and estimation, three groups of participants (for a total of eighty-four young adults) took part in the present study: expert swimmers, expert runners, and non-athletes. The ability to process temporal information in the milliseconds and seconds range was assessed through a time reproduction and a finger-tapping tasks, while a motor imagery paradigm was adopted to assess temporal estimation of sport performance in a wider interval range. We also employed the Vividness of Movement Imagery Questionnaire to assess the individual's ability of motor imagery. Results showed that closed-skill sports, specifically time-related disciplines, enhance motor imagery and time perception abilities. Swimmers were more accurate and consistent in perceiving time when compared to runners, probably thanks to the sensory muffled environment that leads these athletes to be more focused on the perception of their internal rhythm.     

Time perception in severe traumatic brain injury patients: A study comparing different methodologies

In this study, we investigated time perception in patients with traumatic brain injury (TBI). Fifteen TBI patients and 15 matched healthy controls participated in the study. Participants were tested with durations above and below 1 s on three different temporal tasks that involved time reproduction, production, and discrimination tasks. Data variables analyzed included amount of errors, relative errors, and coefficient of variation. Both groups completed a neuropsychological battery that included measures of attention, working memory, and executive functions. Results revealed significant differences between groups on the time reproduction and discrimination tasks, whereas groups showed similar performance on the time production task. Correlation analyses showed involvement of attention, working memory and executive functions on the time reproduction and time discrimination tasks, but there was no involvement on the time production task. These findings suggest that TBI does not impact specific temporal function. Rather, impairments in attention, working memory and executive function abilities may explain lower temporal performance in people with TBI.     

Emotional time distortions: The fundamental role of arousal

An emotion-based lengthening effect on the perception of durations of emotional pictures has been assumed to result from an arousal-based mechanism, involving the activation of an internal clock system. The aim of this study was to systematically examine the arousal effect on time perception when different discrete emotions were considered. The participants were asked to verbally estimate the duration of emotional pictures from the International Affective Picture System (IAPS). The pictures varied either in arousal level, i.e., high/low-arousal, for the same discrete emotion (disgust or sadness) or in the depicted emotion, e.g., disgust/fear for pictures matched for arousal (high-arousal). The results systematically revealed a lengthening effect on the perception of the duration of the emotional compared to the neutral pictures and indicated that the magnitude of this effect increased with arousal level. Nevertheless, variations in time perception were observed for one and the same arousal level, with the duration of disgust-inducing pictures (e.g., body mutilation) being judged longer than that of fear-inducing pictures (e.g., snake). These results suggest that arousal is a fundamental mechanism mediating the effect of emotion on time perception. However, the effect cannot be reduced to arousal, since the impact of the content of pictures also plays a critical role.     

时距知觉中的情绪效应

情绪极易影响时距知觉,致使主观时距偏离客观时距。新近研究者们结合日趋成熟的标量计时模型及神经学相关依据,并通过采用标准化情绪诱发材料的实验研究,较为系统地解释了情绪的生理唤醒和注意唤醒两种成分各自对内部计时机制造成的干扰效应。研究发现,两种效应中前者会加长主观时距而后者会使其缩短,且分别有不同的发生特点。该文在介绍国内外关于时距知觉中的情绪效应的新近研究基础上,提出应从探索两种效应的分离方法、考虑记忆效应因素以及增加实验自变量的数目和取值水平三个方面来开展进一步的研究     

Time perception and time perspective differences between adolescents and adults

The present experiment aimed to investigate the differences in time perception and time perspective between subjects representing two developmental stages, namely adolescence and middle adulthood. Twenty Chinese adolescents aged 15–25 and twenty Chinese adults aged 35–55 participated in the study. A time discrimination task and a time reproduction task were implemented to measure the accuracy of their time perception. The Zimbardo Time Perspective Inventory (Short-Form) was adopted to assess their time orientation. It was found that adolescents performed better than adults in both the time discrimination task and the time reproduction task. Adolescents were able to differentiate different time intervals with greater accuracy and reproduce the target duration more precisely. For the time reproduction task, it was also found that adults tended to overestimate the duration of the target stimuli while adolescents were more likely to underestimate it. As regards time perspective, adults were more future-oriented than adolescents, whereas adolescents were more present-oriented than adults. No significant relationship was found between time perspective and time perception.     

Mindfulness meditation and relaxation training increases time sensitivity

Two experiments examined the effect of mindfulness meditation and relaxation on time perception using a temporal bisection task. In Experiment 1, the participants performed a temporal task before and after exercises of mindfulness meditation or relaxation. In Experiment 2, the procedure was similar than that used in Experiment 1, except that the participants were trained to mediate or relax every day over a period of several weeks. The results showed that mindfulness meditation exercises increased sensitivity to time and lengthened perceived time. However, this temporal improvement with meditation exercises was primarily observed in the experienced meditators. Our results also showed the experienced meditators were less anxious than the novice participants, and that the sensitivity to time increased when the level of anxiety decreased. Our results were explained by the practice of mindfulness technique that had developed individuals’ abilities in devoting more attention resources to temporal information processing.     

The emotional body and time perception

We examined the effects of emotional bodily expressions on the perception of time. Participants were shown bodily expressions of fear, happiness and sadness in a temporal bisection task featuring different stimulus duration ranges. Stimulus durations were judged to be longer for bodily expressions of fear than for those of sadness, whereas no significant difference was observed between sad and happy postures. In addition, the magnitude of the lengthening effect of fearful versus sad postures increased with duration range. These results suggest that the perception of fearful bodily expressions increases the level of arousal which, in turn, speeds up the internal clock system underlying the representation of time. The effect of bodily expressions on time perception is thus consistent with findings for other highly arousing emotional stimuli, such as emotional facial expressions.     

The effect of mild depression on time discrimination

Depressed mood states affect subjective perceptions of time but it is not clear whether this is due to changes in the underlying timing mechanisms, such as the speed of the internal clock. In order to study depression effects on time perception, two experiments using time discrimination methods with short (<300 ms) and long (>1,000 ms) durations were conducted. Student participants who were categorized as mildly depressed by their scores on the Beck Depression Inventory were less able than controls to discriminate between two longer durations but were equally able to discriminate shorter intervals. The results suggest that mildly depressed or dysphoric moods do not affect pacemaker speed. It is more likely that depression affects the ability to maintain attention to elapsing duration.     

The effect of Parkinson's disease on time estimation as a function of stimulus duration range and modality

The present research sought to investigate the role of the basal ganglia in timing of sub- and supra-second intervals via an examination of the ability of people with Parkinson's disease (PD) to make temporal judgments in two ranges, 100-500 ms, and 1-5 s. Eighteen non-demented medicated patients with PD were compared with 14 matched controls on a duration-bisection task in which participants were required to discriminate auditory and visual signal durations within each time range. Results showed that patients with PD exhibited more variable duration judgments across both signal modality and duration range than controls, although closer analyses confirmed a timing deficit in the longer duration range only. The findings presented here suggest the bisection procedure may be a useful tool in identifying timing impairments in PD and, more generally, reaffirm the hypothesised role of the basal ganglia in temporal perception at the level of the attentionally mediated internal clock as well as memory retrieval and/or decision-making processes.     

Book review

Wheeldon, L. (Ed.). (2000). Aspects of language production. Hove, UK: Psychology Press. Pp.419. ISBN 0-86377-882-8. Price £3995 (Hbk). ISBN 0-86377-883-6. Price £1995 (Pbk, published 2002).     

The role of timing deviations and target position uncertainty on temporal attending in a serial auditory pitch discrimination task

Listeners were presented with sequences of tones that ascended in semitone intervals. On each trial a single target tone in the sequence was displaced in pitch, and listeners were required to indicate whether the target tone was higher or lower than its normal pitch. Task constraints, specifically target serial position uncertainty and the probabilistic relationship between time deviations and target tones, were varied in order to determine the impact of task constraints on temporal attending strategy. When listeners had no advance knowledge of the serial position of the target, and early and late targets provided information regarding target serial position, performance was better for early and late target trials than for on-time target trials (Experiment 1). When listeners had no advance knowledge of the serial position of the target, and early and late temporal deviations provided no information regarding target serial position, performance for late target trials was superior to that for early and on-time target trials (Experiment 2). Finally, when target serial position uncertainty was eliminated, performance was equivalent across all three levels of target timing (early, on time, late). The results indicate that performance profiles based on stimulus timing properties are affected by various task constraints as well as by stimulus properties.     

Effects of signaling on temporal control of behavior in response‐initiated fixed intervals

Behavior and events distributed in time can serve as markers that signal delays to future events. The majority of timing research has focused on how behavior changes as the time to some event, usually food availability, decreases. The primary objective of the two experiments presented here was to assess how behavior changes as time passes between two time markers when the first time marker was manipulated but the second, food delivery, was held constant. Pigeons were exposed to fixed‐interval, response‐initiated fixed‐interval, and signaled response‐initiated fixed‐interval 15‐ and 30‐s schedules of reinforcement. In Experiment 1, first‐response latencies were systematically shorter in the signaled response‐initiated schedules than response‐initiated schedules, suggesting that the first response was a more effective time marker when it was signaled. In Experiment 2, responding in no‐food (i.e. “peak”) trials indicated that timing accuracy was equivalent in the three schedule types. Compared to fixed interval schedules, timing precision was reduced in the signaled response‐initiated schedules and was lowest in response‐initiated schedules. Results from Experiments 1 and 2 coupled with previous research suggest that the overall “informativeness” of a time marker relative to other events and behaviors in the environment may determine its efficacy.