A neural theory of human lightness computation is described and computer-simulated. The theory proposes that lightness is derived from transient ON and OFF cell responses in the early visual pathways that have different characteristic neural gains and that are generated by fixational eye movements (FEMs) as the eyes transit luminance edges in the image. The ON and OFF responses are combined with corollary discharge signals that encode the eye movement direction to create directionally selective ON and OFF responses. Cortical neurons with large-scale receptive fields independently integrate the outputs of all of the directional ON or OFF responses whose associated eye movement directions point towards their receptive field centers, with a spatial weighting determined by the receptive field profile. Lightness is computed by subtracting the spatially integrated OFF activity from spatially integrated ON activity and normalizing the difference signal so that the maximum response in the spatial lightness map at any given time equals a fixed activation level corresponding to the percept of white. Two different mechanisms for ON and OFF cells responses are considered and simulated, and both are shown to produce an overall lightness model that explains a host of quantitative and qualitative lightness phenomena, including the Staircase Gelb and related illusions, failures of lightness constancy in the simultaneous contrast illusion, Chevreul's illusion, lightness filling-in, and perceptual fading of stabilized images. The neural plausibility of the two variants of the theory, as well as its implication for lightness constancy and failures of lightness constancy are discussed.
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http://dx.doi.org/10.1016/j.visres.2024.108517 | DOI Listing |
Vision Res
January 2025
Department of Psychology, University of Nevada, Reno, NV 89557, United States.
A neural theory of human lightness computation is described and computer-simulated. The theory proposes that lightness is derived from transient ON and OFF cell responses in the early visual pathways that have different characteristic neural gains and that are generated by fixational eye movements (FEMs) as the eyes transit luminance edges in the image. The ON and OFF responses are combined with corollary discharge signals that encode the eye movement direction to create directionally selective ON and OFF responses.
View Article and Find Full Text PDFAm J Psychoanal
December 2024
Adult and Child Psychoanalyst, British Psychoanalytical Society, 25 Drylands Rd, N89HN, London, United Kingdom.
This paper revisits D. W. Winnicott's famous account of his patient Piggle to examine the profound nature of her response to the birth of her baby sister in the light of the concepts of object constancy and absence.
View Article and Find Full Text PDFJ Imaging
October 2024
Center for Coastal and Ocean Mapping, University of New Hampshire, Durham, NH 03824, USA.
Color is an important cue in object recognition and classification problems. In underwater imagery, colors undergo strong distortion due to light propagation through an absorbing and scattering medium. Distortions depend on a number of complex phenomena, the most important being wavelength-dependent absorption and the sensitivity of sensors in trichromatic cameras.
View Article and Find Full Text PDFJ Vis
October 2024
Air Force Research Laboratory, 711th Human Performance Wing, Bioeffects Division, JBSA Fort Sam Houston, TX, USA.
The visual system adapts dynamically to stabilize perception over widely varying illuminations. Such adaptation allows the colors of objects to appear constant despite changes in spectral illumination. Similarly, the wearing of colored filters also alters spectral content, but this alteration can be more extreme than typically encountered in nature, presenting a unique challenge to color constancy mechanisms.
View Article and Find Full Text PDFJ Morphol
October 2024
Department of Invertebrate Systematics and Ecology, Institute of Environmental Biology, Wroclaw University of Environmental and Life Sciences, Wrocław, Poland.
Species of mites (Chelicerata: Arachnida) show a great variety of structures of the female gonads. In both evolutionary lines, Acariformes and Parasitiformes, the panoistic ovary, in which all germline cysts differentiate into oocytes, and the meroistic ovary, in which the oocytes grow supported by the nurse cells, have been documented. A less pronounced variation in the gonad structure could be expected at lower systematic levels, hence, we ask about the degree of differences within the family that is subordinate to Acariformes and represents the cohort Parasitengona.
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