Spatial grouping resolves ambiguity to drive temporal recalibration.

Cross-modal temporal recalibration describes a shift in the point of subjective simultaneity (PSS) between 2 events following repeated exposure to asynchronous cross-modal inputs-the adaptors. Previous research suggested that audiovisual recalibration is insensitive to the spatial relationship between the adaptors. Here we show that audiovisual recalibration can be driven by cross-modal spatial grouping. Twelve participants adapted to alternating trains of lights and tones. Spatial position was manipulated, with alternating sequences of a light then a tone, or a tone then a light, presented on either side of fixation (e.g., left tone-left light-right tone-right light, etc.). As the events were evenly spaced in time, in the absence of spatial-based grouping it would be unclear if tones were leading or lagging lights. However, any grouping of spatially colocalized cross-modal events would result in an unambiguous sense of temporal order. We found that adapting to these stimuli caused the PSS between subsequent lights and tones to shift toward the temporal relationship implied by spatial-based grouping. These data therefore show that temporal recalibration is facilitated by spatial grouping. (PsycINFO Database Record (c) 2011 APA, all rights reserved)

Biases in the perceived timing of perisaccadic perceptual and motor events

Subjects typically experience the temporal interval immediately following a saccade as longer than a comparable control interval. One explanation of this effect is that the brain antedates the perceptual onset of a saccade target to around the time of saccade initiation. This could explain the apparent continuity of visual perception across eye movements. Thisantedating account was tested in three experiments in which subjects made saccades of differing extents and then judged either the duration or the temporal order of key events. Postsaccadic stimuli underwent subjective temporal lengthening and had early perceived onsets. A temporally advanced awareness of saccade completion was also found, independently of antedating effects. These results provide convergent evidence supporting antedating and differentiating it from other temporal biases

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

The critical events for motor-sensory temporal recalibration

Determining if we, or another agent, were responsible for a sensory event can require an accurate sense of timing. Our sense of appropriate timing relationships must, however, be malleable as there is a variable delay between the physical timing of an event and when sensory signals concerning that event are encoded in the brain. One dramatic demonstration of such malleability involves having people repeatedly press a button thereby causing a beep. If a delay is inserted between button presses and beeps, when it is subsequently taken away beeps can seem to precede the button presses that caused them. For this to occur it is important that people feel they were responsible for instigating the beeps. In terms of their timing, as yet it is not clear what combination of events is important for motor-sensory temporal recalibration. Here, by introducing ballistic reaches of short or longer extent before a button press, we varied the delay between the intention to act and the sensory consequence of that action. This manipulation failed to modulate recalibration magnitude. By contrast, introducing a similarly lengthened delay between button presses and consequent beeps eliminated recalibration. Thus it would seem that the critical timing relationship for motor-sensory temporal recalibration is between tactile signals relating to the completion of an action and the subsequent auditory percept

Lawn Weeds in Alaska

Many different kinds of plants usually grow in close association with each other in nature. Woodlands, roadsides, mountain slopes, marshlands-almost all places not closely attended by man have their own complex plant associations. A lawn comprised of only one or a few grass species is an unnatural, artificial situation. Accordingly, lawns can be kept attractive only by diligent efforts to eliminate undesirable plants and to prevent the natural invasion of turfs by unwanted plants. This battle must be renewed each year. Knowledge of the habits and weaknesses of weeds enables the lawnkeeper to vanquish these foes in every encounter, usually with little expenditure of effort

Increased motor cortex excitability for concealed visual information

Deceptive behaviour involves complex neural processes involving the primary motor cortex. The dynamics of this motor cortex excitability prior to lying are still not well understood. We sought to examine whether corticospinal excitability can be used to suggest the presence of deliberately concealed information in a modified version of the Guilty Knowledge Test (GKT). Participants pressed keys to either truthfully or deceitfully indicate their familiarity with a series of faces. Motor-evoked-potentials (MEPs) were recorded during response preparation to measure muscle-specific neural excitability. We hypothesised that MEPs would increase during the deceptive condition not only in the lie-telling finger but also in the suppressed truth-telling finger. We report a group-level increase in overall corticospinal excitability 300 ms following stimulus onset during the deceptive condition, without specific activation of the neural representation of the truth-telling finger. We discuss cognitive processes, particularly response conflict and/or automated responses to familiar stimuli, which may drive the observed non-specific increase of motor excitability in deception

Rana aurora

Number of Pages: 4Integrative BiologyGeological Science