Time perception

About: Time perception is a research topic. Over the lifetime, 1918 publications have been published within this topic receiving 87020 citations.

Temporoparietal encoding of space and time during vestibular-guided orientation

Abstract: When we walk in our environment, we readily determine our travelled distance and location using visual cues. In the dark, estimating travelled distance uses a combination of somatosensory and vestibular (i.e., inertial) cues. The observed inability of patients with complete peripheral vestibular failure to update their angular travelled distance during active or passive turns in the dark implies a privileged role for vestibular cues during human angular orientation. As vestibular signals only provide inertial cues of self-motion (e.g., velocity, °/s), the brain must convert motion information to distance information (a process called 'path integration') to maintain our spatial orientation during self-motion in the dark. It is unknown, however, what brain areas are involved in converting vestibular-motion signals to those that enable such vestibular-spatial orientation. Hence, using voxel-based lesion-symptom mapping techniques, we explored the effect of acute right hemisphere lesions in 18 patients on perceived angular position, velocity and motion duration during whole-body angular rotations in the dark. First, compared to healthy controls' spatial orientation performance, we found that of the 18 acute stroke patients tested, only the four patients with damage to the temporoparietal junction showed impaired spatial orientation performance for leftward (contralesional) compared to rightward (ipsilesional) rotations. Second, only patients with temporoparietal junction damage showed a congruent underestimation in both their travelled distance (perceived as shorter) and motion duration (perceived as briefer) for leftward compared to rightward rotations. All 18 lesion patients tested showed normal self-motion perception. These data suggest that the cerebral cortical regions mediating vestibular-motion ('am I moving?') and vestibular-spatial perception ('where am I?') are distinct. Furthermore, the congruent contralesional deficit in time (motion duration) and position perception, seen only in temporoparietal junction patients, may reflect a common neural substrate in the temporoparietal junction that mediates the encoding of motion duration and travelled distance during vestibular-guided navigation. Alternatively, the deficits in timing and spatial orientation with temporoparietal junction lesions could be functionally linked, implying that the temporoparietal junction may act as a cortical temporal integrator, combining estimates of self-motion velocity over time to derive an estimate of travelled distance. This intriguing possibility predicts that timing abnormalities could lead to spatial disorientation.

Sex Differences in Time Perception

Abstract: In an experiment on discrimination of duration of auditory stimuli in the range of milliseconds 16 men and 16 women were tested. Men scored better than women in discrimination of duration as well as in required session time. These results were discussed in terms of the assumption of a neurotransmitter-related internal clock and with respect to sex differences in reaction time.

About the (non)scalar property for time perception.

Abstract: Approaching sensation scientifically is relatively straightforward. There are physical attributes for stimulating the central nervous system, and there are specific receptors for each sense for translating the physical signals into codes that brain will recognize. When studying time though, it is far from obvious that there are any specific receptors or specific stimuli. Consequently, it becomes important to determine whether internal time obeys some laws or principles usually reported when other senses are studied. In addition to reviewing some classical methods for studying time perception, the present chapter focusses on one of these laws, Weber law, also referred to as the scalar property in the field of time perception. Therefore, the question addressed here is the following: does variability increase linearly as a function of the magnitude of the duration under investigation? The main empirical facts relative to this question are reviewed, along with a report of the theoretical impact of these facts on the hypotheses about the nature of the internal mechanisms responsible for estimating time.

Brief subjective durations contract with repetition.

Abstract: Neural responses to a repeated stimulus typically diminish, an effect known as repetition suppression. We here demonstrate what appear to be parallel effects of repetition on subjective duration, even when stimuli are presented too rapidly for explicit temporal judgments. When a brief visual stimulus (e.g., a letter, word, object, or face) was serially flashed in different locations, several stimuli appeared to be present simultaneously due to persistence of visionVwe term this the Proliferation Effect. Critically, fewer stimuli were perceived to be simultaneously present when the same stimulus was flashed repeatedly than when a different stimulus was used for each flash, indicating that persistence of vision (and hence subjective duration) shrinks for predictable stimuli. These short-timescale experiments demonstrate that subjective durations are computed at a preconscious and implicit level of processing, thereby changing the temporal interpretation of visual scenes. Further, these findings suggest a new, instant diagnostic test for deficits in repetition suppression, such as those found in schizophrenia.