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This special visual ability for biological motion perception has been found to involve the posterior superior temporal sulcus (STSp).
The modulatory effect of auditory information on visual motion perception has been also reported.
With regard to audiovisual interaction in motion perception, the effect of visual motion information on auditory motion perception has been mainly reported.
Color-blindness in edge detection and motion perception has also been observed in honeybees [16], which possess excellent trichromatic color vision comprising UV, blue and green photoreceptors.
When considering the temporal dynamics of perception, the superiority of motion discrimination capability over subjective motion perception has an interesting consequence: awareness and discrimination become dissociated in time, i.e., perceptual awareness lags discrimination, in the sense that it takes longer to reach the same performance level and to stabilize.
Other research on haptic motion perception has focused on apparent motion (e.g., Harrar, Winter, & Harris, 2008; Kirman, 1983).
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Existing studies of biological motion perception have required a number of different types of judgment to be made about the stimuli, ranging from detection of the presence of a human walker in a PLD [18], to making an assessment about the perceived PLD, such as the perceived emotional state [15], [16].The type of response required may be a source of variability in this field.
Problems with motion perception have been reported in many studies.
In particular, attempts to define and quantify self-motion perception have been prominent when investigating humans' abilities to use particular sensory cues in isolation.
One explanation for this double-failure is that our motion perception system has its own stopwatch, recording how fast things are moving across our vision – and when this is disrupted by brain injury, the world stands still.
The focus in the research on biological motion perception traditionally has been restricted to the visual modality.
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