Abstract
VISUAL ACUITY in falconiform birds has been shown to be higher than man. For instance, vultures with eyes similar in size to those of man have a grating detectability of about twice the spatial frequency of man1. This is consistent with measured image quality in an eagle eye similar in size to the human eye2. Recently a falcon (Falco sparverius) has been shown to have a grating detectability 2.6 greater than that of man3. Although the image quality of these falconiform eyes is at least twice as good as man, their minimum intercone spacing is only slightly less than in the human retina. Unless the ratio of focal length to the axial eye length of these birds greatly exceeds that in man, falconiform eyes, unlike man, would be unable to resolve their best retinal image quality. We show here that the presence of a spherical depression in the deep fovea of falconiforms may act like the negative lens component in a telephoto lens system or opera glass. The focal length of the birds' dioptrics can then in theory exceed the axial length of the eye, thus providing the relatively large images necessary for more complete image reconstruction (high resolving power) in a localised region of the retina.
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References
Fischer, A. B. Zool. Jb. Syst. Bd. 96, 81 (1969).
Shlaer, R. Science 176, 922 (1972).
Fox, R., Lehmkuhle, S. W. & Westendorf, D. H. Science 192, 263 (1976).
Miller, W. H. & Snyder, A. W. (in preparation).
Westheimer, G. in The Handbook of Sensory Physiology, Vol. VII/2 (ed. by Fuortes, M. G. F.)(Springer, New York, 1972).
Pumphrey, R. J. in Biology and Comparative Physiology of Birds (ed. Marshall, A. J.) (Academic, New York, 1961).
Hughes, A. in The Handbook of Sensory Physiology Vol. VII/5, Part A (ed. Crescetelli, F.) (Springer, New York, 1977).
Walls, G. L. The Vertebrate Eye (Cranbrook Institute of Science, Bloomfield Hills, Michigan, 1942).
Fite, K. V. Brain, Behav. Evol. 12, 97 (1975).
Pumphrey, R. J. J. exp. Biol. 25, 299 (1948).
Levi, L. Applied Optics (Wiley, New York, 1968).
Maurice, D. M. in The Eye Vol. 1 (ed. Davson, H.) 523 (Academic, New York, 1969).
Sidman, R. L. J. Biophys. Biochem. Cytol. 3, 15 (1957).
Wood, C. A. The Fundus Occuli of Birds plate XXXIII (Lakeside Press, Chicago, 1917).
Harkness, L. & Bennet-Clark, H. C. Nature 272, 814 (1978).
Snyder, A. W. J. opt. Soc. Am. 62, 1267 (1972).
Campbell, F. W. & Gubisch, R. W. J. Physiol., Lond. 186, 555 (1966).
Donner, K. O. Acta zool. fennica 66, 2 (1951).
Miller, W. H. & Snyder, A. W. Invest. Ophthal. Vis. Sci. Suppl. 105 (1977).
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SNYDER, A., MILLER, W. Telephoto lens system of falconiform eyes. Nature 275, 127–129 (1978). https://doi.org/10.1038/275127a0
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DOI: https://doi.org/10.1038/275127a0
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