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Regional specialization in the eye of the sphingid moth Manduca sexta: Blue sensitivity of the ventral retina

Published online by Cambridge University Press:  02 June 2009

Ruth R. Bennett ,
Richard H. White  and
Jeffery Meadows
Ruth R. Bennett
Affiliation:
Department of Biology, University of Massachusetts at Boston, Boston
Richard H. White
Affiliation:
Department of Biology, University of Massachusetts at Boston, Boston
Jeffery Meadows
Affiliation:
Department of Biology, University of Massachusetts at Boston, Boston
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Abstract

The compound eye of the tobacco hornworm moth Manduca sexta contains green-, blue-, and ultraviolet-sensitive photoreceptors. Electroretinogram spectral-sensitivity measurements were recorded from different regions of the retina in order to broadly map the distribution of the three receptor types. The relative contribution of the three receptors to spectral-sensitivity curves was estimated by fitting theoretical curves based on the absorption spectra of the three rhodopsins. This analysis indicated that the dorsal retina is green and ultraviolet dichromatic, with green-sensitive cells greatly predominating. The ventral retina is trichromatic with a substantial population of blue- and ultraviolet-sensitive receptors. We previously showed that flower visitation for nectar feeding is mediated mainly by blue-sensitive cells. Their localization in the ventral retina seems an appropriate adaptation of the receptor mosaic, since the moths hover above flowers as they feed.

Keywords

Manduca sextaRetinaBlue-sensitive photoreceptorsFeeding behavior
Type
Research Articles
Information
Visual Neuroscience , Volume 14 , Issue 3 , May 1997 , pp. 523 - 526
Copyright
Copyright © Cambridge University Press 1997

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References

REFERENCES

Arikawa, K., Inokuma, K. & Eguchi, E. (1987). Pentachromatic visual system in a butterfly. Naturwissenschaften 74, 297–298.CrossRefGoogle Scholar
Bennett, R.R. (1983). Circadian rhythm of visual sensitivity in Manduca sexta and its development from an ultradian rhythm. Journal of Comparative Physiology A 150, 165–174.CrossRefGoogle Scholar
Bennett, R.R. & Brown, P.K. (1985). Properties of the visual pigments of the moth Manduca sexta and the effects of two detergents, digitonin and CHAPS. Vision Research 25, 1771–1781.CrossRefGoogle ScholarPubMed
Bennett, R.R. & White, R.H. (1989). Influence of carotenoid deficiency on visual sensitivity, visual pigment and P-face particles of photoreceptor membrane in the moth Manduca sexta. Journal of Comparative Physiology A 164, 321–331.CrossRefGoogle Scholar
Bennett, R.R. & White, R.H. (1991). 11-cis retinal restores visual function in vitamin A-deficient Manduca. Visual Neuroscience 6, 473–479.CrossRefGoogle ScholarPubMed
Bernard, G.D. & Remington, C.L. (1991). Color vision in Lycaena butterflies: Spectral tuning of receptor arrays in relation to behavioral ecology. Proceedings of the National Academy of Sciences of the U.S.A. 88, 2783–2787.CrossRefGoogle ScholarPubMed
Chase, M.R., Bennett, R.R. & White, R.H. (1996). Expression of opsin mRNA in normal and vitamin A-deficient retinas of the sphingid moth Manduca sexta. Visual Neuroscience 13, 353–358.CrossRefGoogle ScholarPubMed
Cutler, D.E., Bennett, R.R., Stevenson, R.D. & White, R.H. (1995). Feeding behavior in the nocturnal moth Manduca sexta is mediated mainly by blue receptors, but where are they located in the retina? Journal of Experimental Biology 198, 1909–1917.CrossRefGoogle ScholarPubMed
Dafni, A. & Kevan, P.G. (1995). Hypothesis on adaptive features of the compound eye of bees: Flower-specific specializations. Evolutionary Ecology 9, 236–241.CrossRefGoogle Scholar
Ephrussi, B. & Beadle, G.W. (1936). A technique of transplantation for Drosophila. American Naturalist 70, 218–225.CrossRefGoogle Scholar
Hardie, R.C. (1986). The photoreceptor array of the dipteran retina. Trends in Neurosciences 9, 419–423.CrossRefGoogle Scholar
Hardie, R.C., Franceschini, N., Ribi, W. & Kirschfeld, K. (1981). Distribution and properties of sex-specific photoreceptors in the fly Musca domestica. Journal of Comparative Physiology A 145, 139–152.CrossRefGoogle Scholar
Hausen, K. & Strausfeld, N.J. (1980). Sexually dimorphic interneuron arrangements in the fly visual system. Proceedings of the Royal Society B (London) 208, 57–71.Google Scholar
Ichikawa, T. & Tateda, H. (1982). Distribution of color receptors in the larval eyes of four species of Lepidoptera. Journal of Comparative Physiology A 149, 317–324.CrossRefGoogle Scholar
Kelber, A. & Varjú, D. (1995). Flower size and flower patterns: Preferences and learning in Macroglossum stellatarum (Lepidoptera, Sphingidae). In Learning and Memory. Proceedings of the 23rd Göttingen Neurobiology Conference, Vol. 1, ed. Elsner, N. & Menzel, R., p. 50. Stuttgart: G. Thieme Verlag.Google Scholar
Labhart, T. (1996). How polarization-sensitive interneurones of crickets perform at low degrees of polarization. Journal of Experimental Biology 199, 1467–1475.CrossRefGoogle ScholarPubMed
Marshall, N.J., Land, M.F., King, C.A. & Cronin, T.W. (1991). The compound eyes of mantis shrimps (Crustacea, Hoplocarida, Stomatopoda). II. Colour pigments in the eyes of stomatopod crustaceans: Polychromatic vision by serial and lateral filtering. Philosophical Transactions of the Royal Society B (London) 334, 57–84.Google Scholar
Menzel, J., Wunderer, H. & Stavenga, D.G. (1991). Functional morphology of the divided compound eye of the honeybee drone (Apismèllifera). Tissue and Cell 23, 525–535.CrossRefGoogle Scholar
Scherer, C. & Kolb, G. (1987 a). Behavioral experiments on the visual processing of color stimuli in Pieris brassicae L. (Lepidoptera). Journal of Comparative Physiology A 160, 645–656.CrossRefGoogle Scholar
Scherer, C. & Kolb, G. (1987 b). The influence of color stimuli on visually controlled behavior in Aglais urticae L. and Pararge aegeria L. (Lepidoptera). Journal of Comparative Physiology A 161, 891–898.CrossRefGoogle Scholar
Snyder, A.W., Menzel, R. & Laughlin, S.B. (1973). Structure and function of the fused rhabdom. Journal of Comparative Physiology 87, 99–135.CrossRefGoogle Scholar
Stavenga, D.G. (1992). Eye regionalization and spectral tuning of retinal pigments in insects. Trends in Neurosciences 15, 213–218.CrossRefGoogle ScholarPubMed
Wehrhahn, C. (1979). Sex-specific differences in the chasing behaviour of houseflies (Musca). Biological Cybernetics 32, 239–241.CrossRefGoogle Scholar
White, R.H., Brown, P.K., Hurley, A.K. & Bennett, R.R. (1983). Rhodopsins, retinula cell ultrastructure and receptor potentials in the developing pupal eye of the moth Manduca sexta. Journal of Comparative Physiology A 150, 153–163.CrossRefGoogle Scholar
White, R.H., Stevenson, R.D., Bennett, R.R., Cutler, D.E. & Haber, W.A. (1994). Wavelength discrimination and the role of ultraviolet vision in the feeding behavior of hawkmoths. Biotropica 26, 427–435.CrossRefGoogle Scholar