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Dealing with Illumination in Visual Scenes: Effects of Ageing and Alzheimer's Disease
Various visual functions decline in ageing and even more so in patients with Alzheimer's disease (AD). Here we investigated whether the complex visual processes involved in ignoring illumination-related variability (specifically, cast shadows) in visual scenes may also be compromised. Participa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3454404/ https://www.ncbi.nlm.nih.gov/pubmed/23028786 http://dx.doi.org/10.1371/journal.pone.0045104 |
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author | Porter, Gillian Leonards, Ute Troscianko, Tom Haworth, Judy Bayer, Antony Tales, Andrea |
author_facet | Porter, Gillian Leonards, Ute Troscianko, Tom Haworth, Judy Bayer, Antony Tales, Andrea |
author_sort | Porter, Gillian |
collection | PubMed |
description | Various visual functions decline in ageing and even more so in patients with Alzheimer's disease (AD). Here we investigated whether the complex visual processes involved in ignoring illumination-related variability (specifically, cast shadows) in visual scenes may also be compromised. Participants searched for a discrepant target among items which appeared as posts with shadows cast by light-from-above when upright, but as angled objects when inverted. As in earlier reports, young participants gave slower responses with upright than inverted displays when the shadow-like part was dark but not white (control condition). This is consistent with visual processing mechanisms making shadows difficult to perceive, presumably to assist object recognition under varied illumination. Contrary to predictions, this interaction of “shadow” colour with item orientation was maintained in healthy older and AD groups. Thus, the processing mechanisms which assist complex light-independent object identification appear to be robust to the effects of both ageing and AD. Importantly, this means that the complexity of a function does not necessarily determine its vulnerability to age- or AD-related decline. We also report slower responses to dark than light “shadows” of either orientation in both ageing and AD, in keeping with increasing light scatter in the ageing eye. Rather curiously, AD patients showed further slowed responses to “shadows” of either colour at the bottom than the top of items as if they applied shadow-specific rules to non-shadow conditions. This suggests that in AD, shadow-processing mechanisms, while preserved, might be applied in a less selective way. |
format | Online Article Text |
id | pubmed-3454404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34544042012-10-01 Dealing with Illumination in Visual Scenes: Effects of Ageing and Alzheimer's Disease Porter, Gillian Leonards, Ute Troscianko, Tom Haworth, Judy Bayer, Antony Tales, Andrea PLoS One Research Article Various visual functions decline in ageing and even more so in patients with Alzheimer's disease (AD). Here we investigated whether the complex visual processes involved in ignoring illumination-related variability (specifically, cast shadows) in visual scenes may also be compromised. Participants searched for a discrepant target among items which appeared as posts with shadows cast by light-from-above when upright, but as angled objects when inverted. As in earlier reports, young participants gave slower responses with upright than inverted displays when the shadow-like part was dark but not white (control condition). This is consistent with visual processing mechanisms making shadows difficult to perceive, presumably to assist object recognition under varied illumination. Contrary to predictions, this interaction of “shadow” colour with item orientation was maintained in healthy older and AD groups. Thus, the processing mechanisms which assist complex light-independent object identification appear to be robust to the effects of both ageing and AD. Importantly, this means that the complexity of a function does not necessarily determine its vulnerability to age- or AD-related decline. We also report slower responses to dark than light “shadows” of either orientation in both ageing and AD, in keeping with increasing light scatter in the ageing eye. Rather curiously, AD patients showed further slowed responses to “shadows” of either colour at the bottom than the top of items as if they applied shadow-specific rules to non-shadow conditions. This suggests that in AD, shadow-processing mechanisms, while preserved, might be applied in a less selective way. Public Library of Science 2012-09-24 /pmc/articles/PMC3454404/ /pubmed/23028786 http://dx.doi.org/10.1371/journal.pone.0045104 Text en © 2012 Porter et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Porter, Gillian Leonards, Ute Troscianko, Tom Haworth, Judy Bayer, Antony Tales, Andrea Dealing with Illumination in Visual Scenes: Effects of Ageing and Alzheimer's Disease |
title | Dealing with Illumination in Visual Scenes: Effects of Ageing and Alzheimer's Disease |
title_full | Dealing with Illumination in Visual Scenes: Effects of Ageing and Alzheimer's Disease |
title_fullStr | Dealing with Illumination in Visual Scenes: Effects of Ageing and Alzheimer's Disease |
title_full_unstemmed | Dealing with Illumination in Visual Scenes: Effects of Ageing and Alzheimer's Disease |
title_short | Dealing with Illumination in Visual Scenes: Effects of Ageing and Alzheimer's Disease |
title_sort | dealing with illumination in visual scenes: effects of ageing and alzheimer's disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3454404/ https://www.ncbi.nlm.nih.gov/pubmed/23028786 http://dx.doi.org/10.1371/journal.pone.0045104 |
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