Ego motion and natural motions in the world generate complex optic flows in the retina. These optic flows, if produced by rigid surface patches, can be decomposed into four components, including rotation and expansion. We showed previously that humans can precisely estimate parameters of these components, such as the angular velocity of a rotational motion and the rate of expansion of a radial motion. However, natural optic flows mostly display motions containing a combination of more than one of these components. Here, we report that when a pure motion (e.g., rotation) is combined with its orthogonal component (e.g., expansion), no bias is found in the estimate of the component parameters. This suggests that the visual system can decompose complex motions. However, this decomposition is such that the presence of the orthogonal component increases the discrimination threshold for the original component. We propose a model for how the brain decomposes the optic flow into its elementary components. The model accounts for how errors in the estimate of local-velocity vectors affect the decomposition, producing the increase of discrimination thresholds.
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http://dx.doi.org/10.1016/j.visres.2005.04.011 | DOI Listing |
Psychon Bull Rev
January 2025
NYU-ECNU Institute of Brain and Cognitive Science, New York University Shanghai, Shanghai, China.
We examined the intricate mechanisms underlying visual processing of complex motion stimuli by measuring the detection sensitivity to contraction and expansion patterns and the discrimination sensitivity to the location of the center of motion (CoM) in various real and unreal optic flow stimuli. We conducted two experiments (N = 20 each) and compared responses to both "real" optic flow stimuli containing information about self-movement in a three-dimensional scene and "unreal" optic flow stimuli lacking such information. We found that detection sensitivity to contraction surpassed that to expansion patterns for unreal optic flow stimuli, whereas this trend was reversed for real optic flow stimuli.
View Article and Find Full Text PDFCornea
January 2025
Department of Ophthalmology, Massachusetts Eye and Ear, Harvard Medical School, Boston, MA.
Purpose: To report on optical coherence tomography angiography (OCTA) in patients with a type 1 Boston keratoprosthesis (KPro) and determine its feasibility through assessment of imaging artifacts.
Methods: KPro and non-KPro subjects were matched for age, gender, and glaucoma diagnosis. OCTA images of the peripapillary optic nerve were obtained, reviewed by 2 readers masked to the diagnosis for artifacts and usability, and used for microvascular measurements.
J Exp Biol
January 2025
Independent researcher, 74 Eccleston Square, London, UK.
The function of zebra stripes has long puzzled biologists: contrasted and conspicuous colours are unusual in mammals. The puzzle appears solved: two lines of evidence indicate that they evolved as a protection against biting flies, the geographical coincidence of stripes and exposure to trypanosomiasis in Africa and field experiments showing flies struggling to navigate near zebras. A logical mechanistic explanation would be that stripes interfere with flies' analysis of the optic flow; however, both spatio-temporal aliasing and the aperture effect seem ruled out following recent experiments showing that randomly checked patterns also interfere with flies' capacity to navigate near zebras.
View Article and Find Full Text PDFPhotodiagnosis Photodyn Ther
January 2025
Istanbul Medeniyet University, Faculty of Medicine, Department of Ophthalmology, Istanbul, Turkey. Electronic address:
Objective: Imaging techniques have demonstrated changes in the choroid and retina in acute central serous chorioretinopathy (CSCR), but the effects on the optic nerve head (ONH) remain unclear. This study investigates ONH structural changes in acute CSCR using enhanced deep imaging optic coherence tomography (EDI-OCT).
Methods: A prospective cohort study included 51 acute CSCR patients and 51 healthy controls aged 18-65 years.
Cell Rep
January 2025
Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Erling Skjalgssons Gate 1, 7491 Trondheim, Norway; Kavli Institute for Systems Neuroscience and Centre for Algorithms in the Cortex, Norwegian University of Science and Technology, Olav Kyrres Gate 9, 7030 Trondheim, Norway. Electronic address:
The brain uses a specialized system to transport cerebrospinal fluid (CSF), consisting of interconnected ventricles lined by motile ciliated ependymal cells. These cells act jointly with CSF secretion and cardiac pressure gradients to regulate CSF dynamics. To date, the link between cilia-mediated CSF flow and brain function is poorly understood.
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