Neural mechanism for coding depth from motion parallax in area MT: gain modulation or tuning shifts?

2021 ◽  
pp. JN-RM-1240-21
Author(s):  
Zhe-Xin Xu ◽  
Gregory C. DeAngelis
2017 ◽  
Vol 37 (34) ◽  
pp. 8180-8197 ◽  
Author(s):  
HyungGoo R. Kim ◽  
Dora E. Angelaki ◽  
Gregory C. DeAngelis

2013 ◽  
Vol 33 (35) ◽  
pp. 14061-14074 ◽  
Author(s):  
J. W. Nadler ◽  
D. Barbash ◽  
H. R. Kim ◽  
S. Shimpi ◽  
D. E. Angelaki ◽  
...  

2021 ◽  
Author(s):  
HyungGoo Kim ◽  
Dora Angelaki ◽  
Gregory DeAngelis

Detecting objects that move in a scene is a fundamental computation performed by the visual system. This computation is greatly complicated by observer motion, which causes most objects to move across the retinal image. How the visual system detects scene-relative object motion during self-motion is poorly understood. Human behavioral studies suggest that the visual system may identify local conflicts between motion parallax and binocular disparity cues to depth, and may use these signals to detect moving objects. We describe a novel mechanism for performing this computation based on neurons in macaque area MT with incongruent depth tuning for binocular disparity and motion parallax cues. Neurons with incongruent tuning respond selectively to scene-relative object motion and their responses are predictive of perceptual decisions when animals are trained to detect a moving object during selfmotion. This finding establishes a novel functional role for neurons with incongruent tuning for multiple depth cues.


2012 ◽  
Vol 12 (14) ◽  
pp. 16-16
Author(s):  
H.-G. R. Kim ◽  
D. E. Angelaki ◽  
G. C. DeAngelis

2007 ◽  
Vol 97 (4) ◽  
pp. 2780-2789 ◽  
Author(s):  
Wu Zhou ◽  
Youguo Xu ◽  
Ivra Simpson ◽  
Yidao Cai

Multiplicative computation is a basic operation that is crucial for neural information processing, but examples of multiplication by neural pathways that perform well-defined sensorimotor transformations are scarce. Here in behaving monkeys, we identified a multiplication of vestibular and eye position signals in the vestibulo-ocular reflex (VOR). Monkeys were trained to maintain fixation on visual targets at different horizontal locations and received brief unilateral acoustic clicks (1 ms, rarefaction, 85∼110 db NHL) that were delivered into one of their external ear canals. We found that both the click-evoked horizontal eye movement responses and the click-evoked neuronal responses of the abducens neurons exhibited linear dependencies on horizontal conjugate eye position, indicating that the interaction of vestibular and horizontal conjugate eye position was multiplicative. Latency analysis further indicated that the site of the multiplication was within the direct VOR pathways. Based on these results, we propose a novel neural mechanism that implements the VOR gain modulation by fixation distance and gaze eccentricity. In this mechanism, the vestibular signal from a single labyrinth interacts multiplicatively with the position signals of each eye (Principle of Multiplication). These effects, however, interact additively with the other labyrinth (Principle of Addition). Our analysis suggests that the new mechanism can implement the VOR gain modulation by fixation distance and gaze eccentricity within the direct VOR pathways.


2012 ◽  
Vol 108 (5) ◽  
pp. 1228-1243 ◽  
Author(s):  
Amol Gharat ◽  
Curtis L. Baker

From our daily experience, it is very clear that relative motion cues can contribute to correctly identifying object boundaries and perceiving depth. Motion-defined contours are not only generated by the motion of objects in a scene but also by the movement of an observer's head and body (motion parallax). However, the neural mechanism involved in detecting these contours is still unknown. To explore this mechanism, we extracellularly recorded visual responses of area 18 neurons in anesthetized and paralyzed cats. The goal of this study was to determine if motion-defined contours could be detected by neurons that have been previously shown to detect luminance-, texture-, and contrast-defined contours cue invariantly. Motion-defined contour stimuli were generated by modulating the velocity of high spatial frequency sinusoidal luminance gratings (carrier gratings) by a moving squarewave envelope. The carrier gratings were outside the luminance passband of a neuron, such that presence of the carrier alone within the receptive field did not elicit a response. Most neurons that responded to contrast-defined contours also responded to motion-defined contours. The orientation and direction selectivity of these neurons for motion-defined contours was similar to that of luminance gratings. A given neuron also exhibited similar selectivity for the spatial frequency of the carrier gratings of contrast- and motion-defined contours. These results suggest that different second-order contours are detected in a form-cue invariant manner, through a common neural mechanism in area 18.


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