Novel time-stamped pixel structure for high-speed 2D CMOS visual motion sensor

Author(s):  
Guangbin Zhang ◽  
Jin Liu
2015 ◽  
Vol 9 (2) ◽  
pp. 207-216 ◽  
Author(s):  
Shih-Chii Liu ◽  
MinHao Yang ◽  
Andreas Steiner ◽  
Rico Moeckel ◽  
Tobi Delbruck

2009 ◽  
Vol 277 (1685) ◽  
pp. 1209-1217 ◽  
Author(s):  
Norbert Boeddeker ◽  
Jan M. Hemmi

As animals travel through the environment, powerful reflexes help stabilize their gaze by actively maintaining head and eyes in a level orientation. Gaze stabilization reduces motion blur and prevents image rotations. It also assists in depth perception based on translational optic flow. Here we describe side-to-side flight manoeuvres in honeybees and investigate how the bees’ gaze is stabilized against rotations during these movements. We used high-speed video equipment to record flight paths and head movements in honeybees visiting a feeder. We show that during their approach, bees generate lateral movements with a median amplitude of about 20 mm. These movements occur with a frequency of up to 7 Hz and are generated by periodic roll movements of the thorax with amplitudes of up to ±60°. During such thorax roll oscillations, the head is held close to horizontal, thereby minimizing rotational optic flow. By having bees fly through an oscillating, patterned drum, we show that head stabilization is based mainly on visual motion cues. Bees exposed to a continuously rotating drum, however, hold their head fixed at an oblique angle. This result shows that although gaze stabilization is driven by visual motion cues, it is limited by other mechanisms, such as the dorsal light response or gravity reception.


2012 ◽  
Vol 20 (6) ◽  
pp. 1450-1460 ◽  
Author(s):  
Jeroen de Best ◽  
René van de Molengraft ◽  
Maarten Steinbuch

Symmetry ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 749
Author(s):  
Tihomir Taskov ◽  
Juliana Dushanova

A universal signature of developmental dyslexia is literacy acquisition impairments. Besides, dyslexia may be related to deficits in selective spatial attention, in the sensitivity to global visual motion, speed processing, oculomotor coordination, and integration of auditory and visual information. Whether motion-sensitive brain areas of children with dyslexia can recognize different speeds of expanded optic flow and segregate the slow-speed from high-speed contrast of motion was a main question of the study. A combined event-related EEG experiment with optic flow visual stimulation and functional frequency-based graph approach (small-world propensity ϕ) were applied to research the responsiveness of areas, which are sensitive to motion, and also distinguish slow/fast -motion conditions on three groups of children: controls, untrained (pre-D) and trained dyslexics (post-D) with visual intervention programs. Lower ϕ at θ, α, γ1-frequencies (low-speed contrast) for controls than other groups represent that the networks rewire, expressed at β frequencies (both speed contrasts) in the post-D, whose network was most segregated. Functional connectivity nodes have not existed in pre-D at dorsal medial temporal area MT+/V5 (middle, superior temporal gyri), left-hemispheric middle occipital gyrus/visual V2, ventral occipitotemporal (fusiform gyrus/visual V4), ventral intraparietal (supramarginal, angular gyri), derived from θ-frequency network for both conditions. After visual training, compensatory mechanisms appeared to implicate/regain these brain areas in the left hemisphere through plasticity across extended brain networks. Specifically, for high-speed contrast, the nodes were observed in pre-D (θ-frequency) and post-D (β2-frequency) relative to controls in hyperactivity of the right dorsolateral prefrontal cortex, which might account for the attentional network and oculomotor control impairments in developmental dyslexia.


2013 ◽  
Vol 13 (3) ◽  
pp. 1025-1035 ◽  
Author(s):  
Frédéric L. Roubieu ◽  
Fabien Expert ◽  
Guillaume Sabiron ◽  
Franck Ruffier
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