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Visual acuity of the midland banded water snake estimated from evoked telencephalic potentials

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Abstract

The visual acuity of seven midland banded water snakes was measured by recording evoked responses from telencephalon to temporally modulated square wave grating patterns. Using conventional electrophysiological techniques and signal averaging, high contrast square wave gratings of different spatial frequencies were presented. Acuity was estimated by extrapolating relative response amplitude/log10 spatial frequency functions which yielded an average acuity of 4.25 cycles/degree. Refractive state was also estimated by recording evoked potentials to intermediate spatial frequencies with different lenses in front of the eye. Polynomial fits indicated that under the experimental conditions the snakes were around 6.4 diopters hyperopic suggesting a corrected acuity of 4.89 cycles/degree. Reduction of grating luminance resulted in a reduction in evoked potential acuity measurements. These results indicate that the spatial resolution of midland banded water snakes is the equal of cat; about 20/120 in human clinical terms.

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References

  • Apesteguia S, Hussam Z (2006) A Cretaceous terrestrial snake with robust hindlimbs and a sacrum. Nature 440:1037–1040

    Article  PubMed  CAS  Google Scholar 

  • Bartol SM, Musick JA, Ochs AL (2001) Visual acuity thresholds of juvenile loggerhead sea turtles (Caretta caretta): an electrophysiological approach. J Comp Physiol A 187:953–960

    Article  Google Scholar 

  • Bellairs Ad’ A, Underwood G (1951) The origins of snakes. Biol Rev 26:193–237

    Google Scholar 

  • Berkley MA, Watkins DW (1973) Grating resolution and refraction in the cat estimated from evoked cerebral potentials. Vis Res 13:403–415

    Article  PubMed  CAS  Google Scholar 

  • Campbell FW, Maffei L (1970) Electrophysiological evidence for the existence of orientation and size detectors in the human visual system. J Physiol 207:635–652

    PubMed  CAS  Google Scholar 

  • Drummond H (1985) The role of vision in the predatory behavior of natricine snakes. Anim Behav 33:206–215

    Article  Google Scholar 

  • Dudziak J (1955) Ostrość widzenia u zolwia blotnego (Emys orbicularis L.) przy patrzeniu w środowisku powietrznym i wodntm. Fol Biol 3:205–228

    Google Scholar 

  • Glickstein M, Millodot M (1970) Retinoscopy and eye size. Science 168:605–606

    Article  PubMed  CAS  Google Scholar 

  • Goris RC, Atobe Y, Nakano M, Hisajima T, Funakoshi K, Kadota (2003) The microvasculature of python pit organs: morphology and blood flow microkinetics. Microvasc Res 65:179–185

    Article  PubMed  Google Scholar 

  • Hartikainen K, Rorarius MGK (1999) Cortical responses to auditory stimuli during isoflurane burst suppression anaesthesis. Anaesthesia 54:210–214

    Article  PubMed  CAS  Google Scholar 

  • Jacobs GH, Fenwick JA, Crognale MA, Deegan JF (1992) The all-cone retina of the garter snake: spectral mechanisms and photopigment. J Comp Physiol A 170:701–707

    Article  Google Scholar 

  • Moon C, Terashima S (2002) Responses of the infrared receptors of a crotaline snake to ethanol. Neurosci Lett 334:29–32

    Article  PubMed  CAS  Google Scholar 

  • Murphy CJ, Mutti DO, Zadnik K, Ver Hoeve K (1997) Effect of optical defocus on the visual acuity in dogs. Am J Vet Res 58:414–418

    PubMed  CAS  Google Scholar 

  • Northcutt RG, Butler AB (1974) Retinal projections in the northern water snake Natrix sipedon sipedon (L). J Morphol 142:117–136

    Article  PubMed  CAS  Google Scholar 

  • Northmore DPM, Granda AM (1991) Refractive state, contrast sensitivity, and resolution in the freshwater turtle, Pseudemys scripta elegans, determined by tectal visual-evoked potentials. Vis Neurosci 7:619–625

    Article  PubMed  CAS  Google Scholar 

  • Pasternak T, Merigan WH (1981) The luminance dependence of spatial vision in the cat. Vis Res 21:1333–1339

    Article  PubMed  CAS  Google Scholar 

  • Prusky GT, West PWR, Douglas RM (2000) Behavioral assessment of visual acuity in mice and rats. Vis Res 40:2201–2209

    Article  PubMed  CAS  Google Scholar 

  • Repérant J, Rio J-P, Ward R, Hergueta S, Miceli D, Lemire M (1992) Comparative analysis of the primary visual system of reptiles. In: Gans C, Ulinski PS (eds) Biology of the Reptilia. vol 17 University of Chicago Press, Chicago, pp 175–240

    Google Scholar 

  • Rojas MJ, Navas JA, Rector DM (2006) Evoked response potential markers for anesthetic and behavioral states. Am J Physiol Regulatory Integrative Comp Physiol 292:189–196

    Article  CAS  Google Scholar 

  • Schaeffel F (1991) Underwater vision in semi-aquatic European snakes. Naturwissenschaften 78:373–375

    Article  Google Scholar 

  • Schaeffel F, De Queiroz A (1990) Alternative mechanisms of enhanced underwater vision in the garter snake Thamnophis melanogaster and T. couchii Copeia (1):50–58

  • Shlaer S (1937) The relation between visual acuity and illumination. J Gen Physiol 21:165–188

    Article  Google Scholar 

  • Sillman AJ, Govardovskii VI, Röhlich, Southard JA, Loew ER (1997) The photoreceptors and visual pigments of the garter snake (Thamnophis sirtalis): a microspectrophotometric, scanning electron microscope and immunocytochemical study. J Comp Physiol A 181:89–101

    Article  PubMed  CAS  Google Scholar 

  • Sivak JG (1977) The role of the spectacle in the visual optics of the snake eye. Vis Res 17:293–298

    Article  PubMed  CAS  Google Scholar 

  • Walls G (1942) The vertebrate eye and its adaptive radiation. Bull Cranbrook Inst Sci 19:1–785

    Google Scholar 

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Acknowledgments

This work was supported by NIH Grant P30/EY03039 through the assistance of Mr. Jerry Millican. SP was an NSF SPIN (DBI-0453429) summer student. The experiments comply with the “Principles of Animal Care” (NIH publication No.86–23, revised 1985) and were approved by the UAB Institutional Animal Care and Use Committee. We thank Adam Gordon for his shared insights regarding equivalent power of snake eyes.

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Correspondence to Michael S. Loop.

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Baker, R.A., Gawne, T.J., Loop, M.S. et al. Visual acuity of the midland banded water snake estimated from evoked telencephalic potentials. J Comp Physiol A 193, 865–870 (2007). https://doi.org/10.1007/s00359-007-0240-z

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  • DOI: https://doi.org/10.1007/s00359-007-0240-z

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