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Zeki, S.

Publications and source records attributed to Zeki, S..

4 recordsLinked to original sources

The Biological Basis of Mathematical Beauty

Through our past studies of the neurobiology of beauty, we have come to divide aesthetic experiences into two broad categories: biological and artifactual. The aesthetic experience of biological beauty is dictated by inherited brain concepts, which are resistant to change even in spite of extensive experience. The experience of artifactual beauty on the other hand is determined by post-natally acquired concepts, which are modifiable throughout life by exposure to different experiences (Zeki, 2009). Hence, in terms of aesthetic rating, biological beauty (in which we include the experience of beautiful faces or human bodies) is characterized by less variability between individuals belonging to different ethnic origins and cultural backgrounds or the same individual at different times. Artifactual beauty (in which we include the aesthetic experience of human artifacts such as buildings and cars) is characterized by greater variability between individuals belonging to different ethnic and cultural groupings and by the same individual at different times. In this paper, we present results to show that the experience of mathematical beauty (Zeki et al 2014), even though it constitutes an extreme example of beauty that is dependent upon (mathematical) culture and learning, belongs to the biological category and obeys one of its characteristics, namely a lesser variability in terms of the aesthetic ratings given to mathematical formulae experienced as beautiful.

neuroscience

Very Early Responses to Colour Stimuli Detected in Prestriate Visual Cortex by Magnetoencephalography (MEG)

Previous studies with the visual motion and form systems show that visual stimuli belonging to these categories trigger much earlier latency responses from the visual cortex than previously supposed and that the source of the earliest signals can be located in either the prestriate cortex or in both the striate (V1) and prestriate cortex. This is consistent with the known anatomical connections since, in addition to the classical retino-geniculo-striate cortex input, there are direct anatomical inputs from both the lateral geniculate nucleus and the pulvinar that reach the prestriate visual cortex without passing through V1. In pursuing our studies, we thought it especially interesting to study another cardinal visual attribute, namely colour, to learn whether colour stimuli also provoke very early responses, at less than 50 ms, from visual cortex. To address the question, we asked participants to view stimuli that changed in colour and used magneto-encephalography to detect very early responses (< 50 ms) in the occipital visual cortex. Our results show that coloured stimuli also provoke an early cortical response (M30), with an average peak time at 30.8 ms, thus bringing the colour system into line with the visual motion and form systems. We conclude that colour signals reach visual cortex, including prestriate visual cortex, earlier than previously supposed.\n\nKey points summaryO_LIWe measured visual evoked responses to colour stimuli using magnetoencephalography.\nC_LIO_LIAn early response was identified, at around 30 ms after stimulation.\nC_LIO_LIThe sources of the response were estimated to be in prestriate cortex.\nC_LIO_LIColour signals thus appear to evoke very early cortical responses, just like form and motion signals.\nC_LI\n\nAbbreviations list

neuroscience

The Constancy of Colored After-Images

We undertook psychophysical experiments to determine whether the color of the after-image produced by viewing a colored patch which is part of a complex multi-colored scene depends on the wavelength-energy composition of the light reflected from that patch. Our results show that, just as the color of a patch which is part of a complex scene is independent of the wavelength-energy composition of the light coming from it alone, but depends as well on the wavelength-energy composition of the light coming from its surrounds, so is the color of its after-image. Hence, traditional accounts of after-images as being the result of retinal adaptation or the perceptual result of physiological opponency, are inadequate. We propose instead that the color of after-images is generated after colors themselves are generated in the visual brain.

neuroscience

The Bayesian-Laplacian Brain

We outline what we believe could be an improvement in future discussions of the brain acting as a Bayesian-Laplacian system. We do so by distinguishing between two broad classes of priors on which the brains inferential systems operate: in one category are biological priors ({beta} priors) and in the other artifactual ones ( priors). We argue that {beta} priors, of which colour categories and faces are good examples, are inherited or acquired very rapidly after birth, are highly or relatively resistant to change through experience, and are common to all humans. The consequence is that the probability of posteriors generated from {beta} priors having universal assent and agreement is high. By contrast, priors, of which man-made objects are examples, are acquired post-natally and modified at various stages throughout post-natal life; they are much more accommodating of, and hospitable to, new experiences. Consequently, posteriors generated from them are less likely to find universal assent. Taken together, in addition to the more limited capacity of experiment and experience to alter the {beta} priors compared to priors, another cardinal distinction between the two is that the probability of posteriors generated from {beta} priors having universal agreement is greater than that for priors. The two categories are not, however, always totally distinct and can merge into one another to varying extents, resulting in posteriors that draw upon both categories.

neuroscience