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Electrophysiological measurements of spectral mechanisms in the retinas of two cervids: white-tailed deer (Odocoileus virginianus) and fallow deer (Dama dama)

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Abstract

Electroretinogram (ERG) flicker photometry was used to study the spectral mechanisms in the retinas of white-tailed deer (Odocoileus virginianus) and fallow deer (Dama dama). In addition to having a rod pigment with maximum sensitivity (λmax) of about 497 nm, both species appear to have two classes of photopic receptors. They share in common a short-wavelength-sensitive cone mechanism having λmax in the region of 450–460 nm. Each also has a cone having peak sensitivity in the middle wavelengths, but these differ slightly for the two species. In white-tailed deer the λmax of this cone is about 537 nm; for the fallow deer the average λmax value for this mechanism was 542 nm. Deer resemble other ungulates and many other types of mammal in having two classes of cone pigment and, thus, the requisite retinal basis for dichromatic color vision.

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Abbreviations

ERG:

electroretinogram

LWS:

long wavelength sensitive

MWS:

middle wavelength sensitive

SWS:

short wavelength sensitive

References

  • Baker RH (1984) Origin, classification and distribution. In: Howells LK (ed) White-tailed deer: Ecology and management. Stackpole Books, Harrisburg Pennsylvania, pp 1–18

    Google Scholar 

  • Baylor DA, Nunn BS, Schnapf JL (1987) Spectral sensitivity of cones of the monkey Macaco fascicularis. J Physiol (Lond) 390:145–160

    Google Scholar 

  • Corbet GB, Hall JE (1991) A world list of mammalian species. 3rd edition. Oxford University Press, Oxford

    Google Scholar 

  • Dalrymple BW (1975) When can your quarry see you? Outdoor Life 156:61–65, 143–144

    Google Scholar 

  • Ebrey RG, Honig B (1977) New wavelength-dependent visual pigment nomograms. Vision Res 17:147–151

    Google Scholar 

  • Hao Y, Soref CM, Geke Jr CG, Wong F (1992) The visual pigment gene family and distribution of photoreceptors in the pig retina. Invest Ophthal Visual Sci 33:1004

    Google Scholar 

  • Jacobs GH (1993) The distribution and nature of colour vision among the mammals. Biol Rev 68:413–471

    Google Scholar 

  • Jacobs GH, Neitz J (1985) Spectral positioning of mammalian cone pigments. J Opt Soc Am A 2:P13

    Google Scholar 

  • Jacobs GH, Neitz J (1987) Inheritance of color vision in a New World monkey (Saimiri sciureus). Proc Natl Acad Sci USA 84:2545–2549

    Google Scholar 

  • Jacobs GH, Neitz J, Deegan II JF (1991) Retinal receptors in rodents maximally sensitive to ultraviolet light. Nature 353:655–656

    Google Scholar 

  • Jacobs GH, Deegan II JF, Crognale MA, Fenwick JA (1993) Photopigments of dogs and foxes and their implications for canid vision. Visual Neurosci 10:173–180

    Google Scholar 

  • Knowles A, Dartnall HJA (1977) The photobiology of vision. In: Davson H (ed) The eye, vol 2B. Academic Press, New York, p 689

    Google Scholar 

  • Marchinton RL, Hirth, DH (1984) Behavior. In: Howells LK (ed) White-tailed deer: Ecology and management. Stackpole Books, Harrisburg Pennsylvania, pp 129–168

    Google Scholar 

  • Mech DL, DelGiudice GD, Keins PD, Seal US (1985) Yohimbine hydrochloride as an antagonist to xylazine hydrochloride-ketamine hydrochloride immobilization of white-tailed deer. J Wildl Disques 21:405–410

    Google Scholar 

  • Neitz J, Jacobs GH (1984) ERG measurements of cone spectral sensitivity in dichromatic monkeys. J Opt Soc Am A 1:1175–1180

    Google Scholar 

  • Neitz J, Jacobs GH (1989) Spectral sensitivity of cones in an ungulate. Visual Neurosci 2:97–100

    Google Scholar 

  • Nowak RM (1991) Walker's mammals of the world. Fifth Edition. The Johns Hopkins University Press, Baltimore

    Google Scholar 

  • Putnam R (1988) The natural history of deer. Comstock Publ Assoc, Ithaca New York

    Google Scholar 

  • Pokorny J, Smith VC, Verriest G, Pinckers AJLG (1979) Congenital and acquired color vision defects. Grune & Stratton, New York

    Google Scholar 

  • Sauer PR (1984) Physical characteristics. In: Howells LK (ed) White-tailed deer: Ecology and management. Stackpole Books, Harrisburg Pennsylvania, pp 73–90

    Google Scholar 

  • Steinberg RH, Reid M, Lacy PL (1973) The distribution of rods and cones in the retina of the cat (Felis domestica). J Comp Neurol 148:229–248

    Google Scholar 

  • Smith BL, Skotko DJ, Owen W, McDaniel RJ (1989) Color vision in white-tailed deer. Psychol Rec 39:195–202

    Google Scholar 

  • Walls GL (1942) The vertebrate eye and its adaptive radiation. The Cranbrook Institute of Science, Bloomfield Hills Michigan

    Google Scholar 

  • Witzel DA, Springer MD, Mollenhauer HH (1978) Cone and rod photoreceptors in the white-tailed deer Odocoileus virginianus. Am J Vet Res 39:699–701

    Google Scholar 

  • Wyszecki G, Stiles WS (1982) Color science. 2nd edition. John Wiley & Sons, New York

    Google Scholar 

  • Zacks JL (1985) Photopic spectral sensitivity of the white-tailed deer, Odocoileus virginianus. Invest Ophthalmol Visual Sci Suppl 26:185

    Google Scholar 

  • Zacks JL, Budde W (1983) Behavioral investigations of color vision in the white-tailed deer, Odocoileus virginianus. Invest Ophthalmol Visual Sci Suppl 24:183

    Google Scholar 

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Authors and Affiliations

  1. Department of Psychology, University of California, 93106, Santa Barbara, CA, USA

    G. H. Jacobs & J. F. Deegan II

  2. Department of Cell Biology and Anatomy, Medical College of Wisconsin, 52226, Milwaukee, WI, USA

    J. Neitz

  3. D. B. Warnell School of Forest Resources, University of Georgia, 30602, Athens, GA, USA

    B. P. Murphy, K. V. Miller & R. L. Marchinton

Authors
  1. G. H. Jacobs
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  2. J. F. Deegan II
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  3. J. Neitz
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  4. B. P. Murphy
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  5. K. V. Miller
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  6. R. L. Marchinton
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Jacobs, G.H., Deegan, J.F., Neitz, J. et al. Electrophysiological measurements of spectral mechanisms in the retinas of two cervids: white-tailed deer (Odocoileus virginianus) and fallow deer (Dama dama). J Comp Physiol A 174, 551–557 (1994). https://doi.org/10.1007/BF00217375

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  • DOI: https://doi.org/10.1007/BF00217375

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