Literature DB >> 5498457

The attenuation of rod signals by backgrounds.

M Alpern, W A Rushton, S Torii.   

Abstract

1. The paper which precedes this investigated the nerve interaction between two flashes, lambda at centre (Fig. 1a) and varphi on the surround region (but not on the centre). The size of the inhibitory nerve signal V generated by varphi is given by V = varphi(varphi + sigma), where sigma is the semi-saturation constant.2. A former paper (Alpern & Rushton, 1967) had shown that when the flash varphi falls upon a steady background theta, V suffers attenuation in the G-box (Fig. 1b) down to the fraction theta(D)/(theta(D) + theta) where theta(D) is the eigengrau or receptor noise. Thus, in general, the nerve signal N is given by [Formula: see text].3. This formula had only been established for a moderate range of values. In this paper we use extreme values to explore the limits of its validity. We find the equation to be true over the entire intensity range where N is measurable.4. Six different types of experiment have been performed to test various features of the equation. For instance, if log N is plotted against log varphi for various fixed values of theta, the curve is always the same with simply a vertical shift. And the shift is equal to log(1 + theta/theta(D)) for all values both of theta and of varphi.5. The most interesting curve is the plot of log varphi against log theta for fixed N. This is similar to the Weber-Fechner increment threshold but the criterion is not that varphi be strong enough to be detected, but strong enough to generate an N signal just sufficient to inhibit some fixed lambda flash. These curves (below the onset of saturation) are all the same except for vertical separation, and prove that the condition for flash detection is that a fixed signal, N(0), is generated of size 10(-5) of the maximum signal obtainable (i.e. with varphi large and theta zero).6. With strong backgrounds the curves of (5) above exhibit a marked saturation of the Aguilar & Stiles' type (1954). The family of curves each with a fixed N value shows a remarkable symmetry (Fig. 8) which in fact follows from the equation in (2) above. It has nothing to do with bleached pigment, but follows from the equation in (1) above. V there cannot exceed unity, thus when scaled by the G-box below the criterion level, further increase in varphi will not bring improvement.

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Year:  1970        PMID: 5498457      PMCID: PMC1348596          DOI: 10.1113/jphysiol.1970.sp009007

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  8 in total

1.  ROD-CONE INDEPENDENCE IN THE AFTER-FLASH EFFECT.

Authors:  M ALPERN
Journal:  J Physiol       Date:  1965-02       Impact factor: 5.182

2.  Rhodopsin measurement and dark-adaptation in a subject deficient in cone vision.

Authors:  W A RUSHTON
Journal:  J Physiol       Date:  1961-04       Impact factor: 5.182

3.  Increment thresholds at low intensities considered as signal/noise discriminations.

Authors:  H B BARLOW
Journal:  J Physiol       Date:  1957-05-23       Impact factor: 5.182

4.  The nature of rise in threshold produced by contrast-flashes.

Authors:  M Alpern; W A Rushton
Journal:  J Physiol       Date:  1967-04       Impact factor: 5.182

5.  The size of rod signals.

Authors:  M Alpern; W A Rushton; S Torii
Journal:  J Physiol       Date:  1970-01       Impact factor: 5.182

6.  Computer assisted analysis of S-potentials.

Authors:  K I Naka
Journal:  Biophys J       Date:  1969-06       Impact factor: 4.033

7.  The rod increment threshold during dark adaptation in normal and rod monochromat.

Authors:  C B Blakemore; W A Rushton
Journal:  J Physiol       Date:  1965-12       Impact factor: 5.182

8.  S-potentials from luminosity units in the retina of fish (Cyprinidae).

Authors:  K I Naka; W A Rushton
Journal:  J Physiol       Date:  1966-08       Impact factor: 5.182

  8 in total
  19 in total

1.  Proceedings Correlation between ultrastructure and histochemistry of mammalian intrafusal muscle fibres.

Authors:  R W Banks; D Barker; D W Harker; M J Stacey
Journal:  J Physiol       Date:  1975-11       Impact factor: 5.182

2.  The effects of maintained light stimulation on S-potentials recorded from the retina of a teleost fish.

Authors:  K H Ruddock; G Svaetichin
Journal:  J Physiol       Date:  1975-01       Impact factor: 5.182

3.  On the analysis of nerve signals deduced from metacontrast experiments with human observers.

Authors:  B A Wandell
Journal:  J Physiol       Date:  1976-12       Impact factor: 5.182

4.  The nature of the pi1 colour mechanism of W.S. Stiles.

Authors:  E N Pugh
Journal:  J Physiol       Date:  1976-06       Impact factor: 5.182

5.  Background adaptation in the rods of the frog's retina.

Authors:  S Hemilä
Journal:  J Physiol       Date:  1977-03       Impact factor: 5.182

6.  Interpreting trans-retinal recordings of spectral sensitivity.

Authors:  T H Goldsmith
Journal:  J Comp Physiol A       Date:  1986-10       Impact factor: 1.836

7.  Responses of crayfish photoreceptor cells following intense light adaptation.

Authors:  D R Cummins; T H Goldsmith
Journal:  J Comp Physiol A       Date:  1986-01       Impact factor: 1.836

Review 8.  Pigments and signals in colour vision.

Authors:  W A Rushton
Journal:  J Physiol       Date:  1972-02       Impact factor: 5.182

Review 9.  Toward a general theory of visual adaptation.

Authors:  R M Glantz
Journal:  Doc Ophthalmol       Date:  1971-09-12       Impact factor: 2.379

10.  Determining consequences of retinal membrane guanylyl cyclase (RetGC1) deficiency in human Leber congenital amaurosis en route to therapy: residual cone-photoreceptor vision correlates with biochemical properties of the mutants.

Authors:  Samuel G Jacobson; Artur V Cideciyan; Igor V Peshenko; Alexander Sumaroka; Elena V Olshevskaya; Lihui Cao; Sharon B Schwartz; Alejandro J Roman; Melani B Olivares; Sam Sadigh; King-Wai Yau; Elise Heon; Edwin M Stone; Alexander M Dizhoor
Journal:  Hum Mol Genet       Date:  2012-10-03       Impact factor: 6.150

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