Short-wavelength acuity: blue–yellow and achromatic resolution loss with age

Previous studies have indicated that peripheral resolution for achromatic gratings is sampling limited and directly related to the density of the underlying midget ganglion cell population. Previous studies by the authors have shown that peripheral resolution for blue-cone isolating gratings is also...

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Published inVision research (Oxford) Vol. 43; no. 1; pp. 109 - 115
Main Authors Zlatkova, Margarita B., Coulter, Esther, Anderson, Roger S.
Format Journal Article
LanguageEnglish
Published Oxford Elsevier Ltd 2003
Elsevier Science
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Online AccessGet full text
ISSN0042-6989
1878-5646
DOI10.1016/S0042-6989(02)00411-X

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Abstract Previous studies have indicated that peripheral resolution for achromatic gratings is sampling limited and directly related to the density of the underlying midget ganglion cell population. Previous studies by the authors have shown that peripheral resolution for blue-cone isolating gratings is also sampling limited, is robust to optical defocus and short-wavelength attenuation, and yields estimates of sampling density which correspond closely with the density of small bistratified ganglion cells. We measured peripheral resolution in a group of normal subjects ranging in age from 12 to 72 years, using both achromatic and blue-cone isolating gratings, to determine how performance (and hence ganglion cell density) changed with age for both systems. Resolution was higher for achromatic than blue–yellow gratings and performance was flat for both until the fifth decade. After this, performance declined for both at a rate of ∼14%/decade with no significant difference between the two rates of decline. Individual measurements of lens density were not correlated with short-wavelength sensitive resolution performance in the older subjects, further indicating that the decline in resolution was not attributable to pre-retinal absorption.
AbstractList Previous studies have indicated that peripheral resolution for achromatic gratings is sampling limited and directly related to the density of the underlying midget ganglion cell population. Previous studies by the authors have shown that peripheral resolution for blue-cone isolating gratings is also sampling limited, is robust to optical defocus and short-wavelength attenuation, and yields estimates of sampling density which correspond closely with the density of small bistratified ganglion cells. We measured peripheral resolution in a group of normal subjects ranging in age from 12 to 72 years, using both achromatic and blue-cone isolating gratings, to determine how performance (and hence ganglion cell density) changed with age for both systems. Resolution was higher for achromatic than blue-yellow gratings and performance was flat for both until the fifth decade. After this, performance declined for both at a rate of approximately 14%/decade with no significant difference between the two rates of decline. Individual measurements of lens density were not correlated with short-wavelength sensitive resolution performance in the older subjects, further indicating that the decline in resolution was not attributable to pre-retinal absorption.Previous studies have indicated that peripheral resolution for achromatic gratings is sampling limited and directly related to the density of the underlying midget ganglion cell population. Previous studies by the authors have shown that peripheral resolution for blue-cone isolating gratings is also sampling limited, is robust to optical defocus and short-wavelength attenuation, and yields estimates of sampling density which correspond closely with the density of small bistratified ganglion cells. We measured peripheral resolution in a group of normal subjects ranging in age from 12 to 72 years, using both achromatic and blue-cone isolating gratings, to determine how performance (and hence ganglion cell density) changed with age for both systems. Resolution was higher for achromatic than blue-yellow gratings and performance was flat for both until the fifth decade. After this, performance declined for both at a rate of approximately 14%/decade with no significant difference between the two rates of decline. Individual measurements of lens density were not correlated with short-wavelength sensitive resolution performance in the older subjects, further indicating that the decline in resolution was not attributable to pre-retinal absorption.
Previous studies have indicated that peripheral resolution for achromatic gratings is sampling limited and directly related to the density of the underlying midget ganglion cell population. Previous studies by the authors have shown that peripheral resolution for blue-cone isolating gratings is also sampling limited, is robust to optical defocus and short-wavelength attenuation, and yields estimates of sampling density which correspond closely with the density of small bistratified ganglion cells. We measured peripheral resolution in a group of normal subjects ranging in age from 12 to 72 years, using both achromatic and blue-cone isolating gratings, to determine how performance (and hence ganglion cell density) changed with age for both systems. Resolution was higher for achromatic than blue–yellow gratings and performance was flat for both until the fifth decade. After this, performance declined for both at a rate of ∼14%/decade with no significant difference between the two rates of decline. Individual measurements of lens density were not correlated with short-wavelength sensitive resolution performance in the older subjects, further indicating that the decline in resolution was not attributable to pre-retinal absorption.
Previous studies have indicated that peripheral resolution for achromatic gratings is sampling limited and directly related to the density of the underlying midget ganglion cell population. Previous studies by the authors have shown that peripheral resolution for blue-cone isolating gratings is also sampling limited, is robust to optical defocus and short-wavelength attenuation, and yields estimates of sampling density which correspond closely with the density of small bistratified ganglion cells. We measured peripheral resolution in a group of normal subjects ranging in age from 12 to 72 years, using both achromatic and blue-cone isolating gratings, to determine how performance (and hence ganglion cell density) changed with age for both systems. Resolution was higher for achromatic than blue-yellow gratings and performance was flat for both until the fifth decade. After this, performance declined for both at a rate of approximately 14%/decade with no significant difference between the two rates of decline. Individual measurements of lens density were not correlated with short-wavelength sensitive resolution performance in the older subjects, further indicating that the decline in resolution was not attributable to pre-retinal absorption.
Author Anderson, Roger S.
Zlatkova, Margarita B.
Coulter, Esther
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Issue 1
Keywords Resolution acuity
Short-wavelength sensitive cones
Peripheral vision
Ageing
Eye
Human
Visual system
Senescence
Cone
Photoreceptor
Retina
Visual acuity
Short wave
Language English
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Snippet Previous studies have indicated that peripheral resolution for achromatic gratings is sampling limited and directly related to the density of the underlying...
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SubjectTerms Adolescent
Adult
Aged
Ageing
Aging - physiology
Aging - psychology
Biological and medical sciences
Child
Color Perception - physiology
Contrast Sensitivity - physiology
Eye and associated structures. Visual pathways and centers. Vision
Fundamental and applied biological sciences. Psychology
Humans
Middle Aged
Pattern Recognition, Visual - physiology
Peripheral vision
Photic Stimulation - methods
Psychophysics
Resolution acuity
Retinal Cone Photoreceptor Cells - physiology
Retinal Ganglion Cells - physiology
Short-wavelength sensitive cones
Vertebrates: nervous system and sense organs
Visual Acuity - physiology
Visual Fields - physiology
Title Short-wavelength acuity: blue–yellow and achromatic resolution loss with age
URI https://dx.doi.org/10.1016/S0042-6989(02)00411-X
https://www.ncbi.nlm.nih.gov/pubmed/12505610
https://www.proquest.com/docview/72930989
Volume 43
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