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. 1975 Oct;15(10):1013–1031. doi: 10.1016/S0006-3495(75)85880-2

White noise analysis of Phycomyces light growth response system. II. Extended intensity ranges.

E D Lipson
PMCID: PMC1334769  PMID: 1203439

Abstract

By means of white gaussian noise stimulation, the Wiener kernels are derived for the Phycomyces light growth response for a variety of intensity conditions. In one experiment the intensity I, rather than log I, is used as the input variable. Under the very limited dynamic range of that experiment, the response is fairly linear. To examine the dependence of the kernels on dynamic range, a series of experiments were performed in which the range of log I was halved and doubled relative to normal. The amplitude of the kernels, but not the time course, is affected strongly by the choice of dynamic range, and the dependence reveals large-scale nonlinearities not evident in the kernels themselves. In addition kernels are evaluated for experiments at a number of absolute intensity levels ranging from 10(-12) to 10(-3) W/cm2. The kernel amplitudes are maximal at about 10(-6) W/cm2. At 10(-12) W/cm2, just above the absolute threshold, the respond is very small. The falloff at high intensity, attributable to inactivation of the photoreceptor, is analyzed in the framework of a first-order pigment kinetics model, yielding estimates for the partial extinction coefficient for inactivation epsilonI455 = (1.5 +/- 0.2) X 10(4) liter/mol-cm and a regeneration time constant of tau = (2.7 +/- 0.6) min. A model is introduced which associates the processes of adaptation and photoreceptor inactivation. The model predicts that the time constants for adaptation and pigment should be identical. This prediction is consistent with values in this and the preceding paper. The effects of pigment inactivation are simulated by a linear electronic analog circuit element, which may be cascaded with the linear simulator circuit in the preceding paper.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Alpern M. Rhodopsin kinetics in the human eye. J Physiol. 1971 Sep;217(2):447–471. doi: 10.1113/jphysiol.1971.sp009580. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. DOWLING J. E. NEURAL AND PHOTOCHEMICAL MECHANISMS OF VISUAL ADAPTATION IN THE RAT. J Gen Physiol. 1963 Jul;46:1287–1301. doi: 10.1085/jgp.46.6.1287. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Delbrück M., Shropshire W. Action and Transmission Spectra of Phycomyces. Plant Physiol. 1960 Mar;35(2):194–204. doi: 10.1104/pp.35.2.194. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Foster K. W., Lipson E. D. The light growth response of Phycomyces. J Gen Physiol. 1973 Nov;62(5):590–617. doi: 10.1085/jgp.62.5.590. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Norren D. V., Padmos P. Dark adaptation of separate cone systems studied with psychophysics and electroretinography. Vision Res. 1974 Aug;14(8):677–686. doi: 10.1016/0042-6989(74)90064-9. [DOI] [PubMed] [Google Scholar]
  6. Poff K. L., Butler W. L. Absorbance changes induced by blue light in Phycomyces blakesleeanus and Dictyostelium discoideum. Nature. 1974 Apr 26;248(5451):799–801. doi: 10.1038/248799a0. [DOI] [PubMed] [Google Scholar]
  7. RUSHTON W. A. Kinetics of cone pigments measured objectively on the living human fovea. Ann N Y Acad Sci. 1959 Nov 12;74(2):291–304. doi: 10.1111/j.1749-6632.1958.tb39552.x. [DOI] [PubMed] [Google Scholar]
  8. RUSHTON W. A. VISUAL ADAPTATION. Proc R Soc Lond B Biol Sci. 1965 Mar 16;162:20–46. doi: 10.1098/rspb.1965.0024. [DOI] [PubMed] [Google Scholar]
  9. Robinson G. W. Rhodopsin cooperativity in visual response. Vision Res. 1975 Jan;15(1):35–48. doi: 10.1016/0042-6989(75)90057-7. [DOI] [PubMed] [Google Scholar]
  10. Rushton W. A., Henry G. H. Bleaching and regeneration of cone pigments in man. Vision Res. 1968 Jun;8(6):617–631. doi: 10.1016/0042-6989(68)90040-0. [DOI] [PubMed] [Google Scholar]
  11. WALD G., BROWN P. K. The molar extinction of rhodopsin. J Gen Physiol. 1953 Nov 20;37(2):189–200. doi: 10.1085/jgp.37.2.189. [DOI] [PMC free article] [PubMed] [Google Scholar]

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