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Duplicity Theory of Vision: From Newton to the Present

Duplicity Theory of Vision: From Newton to the Present

Duplicity Theory of Vision: From Newton to the Present

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98 development <strong>of</strong> <strong>the</strong> duplicity <strong>the</strong>ory from 1930–1966Similarly, a review on change in brightness discrimination withchanges in background intensity showed no clear breaks in <strong>the</strong> extrafovealcurves. The results, <strong>the</strong>refore, were judged <strong>to</strong> indicate overlapping andinteraction <strong>of</strong> <strong>the</strong> brightness functions <strong>of</strong> rods and cones.Fur<strong>the</strong>rmore, evidence presented by Lythgoe (1940) stronglyindicated that rod and cone impulses may also interact <strong>to</strong> determine<strong>the</strong> fusion frequency <strong>of</strong> a flickering light. Measuring <strong>the</strong> fusionfrequency in <strong>the</strong> extrafoveal retina during dark adaptation whilst <strong>the</strong>illumination <strong>of</strong> <strong>the</strong> flickering light was kept constant, he found, inaccord with <strong>the</strong> duplicity <strong>the</strong>ory, that <strong>the</strong> fusion frequency fell or rosedepending on whe<strong>the</strong>r <strong>the</strong> test illumination activated <strong>the</strong> pho<strong>to</strong>picor sco<strong>to</strong>pic mechanism, respectively. However, <strong>the</strong> results displayedno clear-cut change-over from fall <strong>to</strong> rise during <strong>the</strong> dark-adaptationperiod. Instead, <strong>the</strong>y strongly indicated that cones determined <strong>the</strong>critical frequency measurements during <strong>the</strong> first part <strong>of</strong> <strong>the</strong> darkadaptationcurve, both recep<strong>to</strong>r mechanisms during <strong>the</strong> middle partand only rods during <strong>the</strong> last part.Saugstad and Saugstad (1959) also presented evidence thatchallenged <strong>the</strong> basic assumption <strong>of</strong> Schultze (1866) that rods mediatedachromatic vision only. Thus, evidence in support <strong>of</strong> <strong>the</strong> assumptionthat rods may mediate colours <strong>of</strong> short wavelengths was found in <strong>the</strong>results obtained by Hecht, Haig and Chase (1936/1937). Measuring<strong>the</strong> dark-adaptation curve following moderate light adaptation, <strong>the</strong>yshowed that <strong>the</strong> change from coloured <strong>to</strong> colourless perception for aviolet test light in <strong>the</strong> extrafoveal retina could be obtained below <strong>the</strong>cone plateau level.Fur<strong>the</strong>rmore, Kohlrausch (1931) obtained dark-adaptationcurves with only one branch in <strong>the</strong> extrafoveal retina despite <strong>the</strong> factthat colours could be observed at <strong>the</strong> threshold level during <strong>the</strong> firstpart <strong>of</strong> <strong>the</strong> curve. Saugstad and Saugstad (1959) interpreted this result<strong>to</strong> mean that ei<strong>the</strong>r <strong>the</strong> form <strong>of</strong> <strong>the</strong> curves was due <strong>to</strong> interactionbetween rod and cone activities, or, presuming that <strong>the</strong> curves weredetermined by rods alone, that rods mediated <strong>the</strong> colour sensationsobserved.

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