Literature DB >> 6875924

The signal-to-noise characteristics of rod-cone interaction.

G M Bauer, T E Frumkes, R W Nygaard.   

Abstract

1. The influence of rods on cone-mediated vision was assessed in eight human observers. To this end, increment threshold functions were obtained by determining thresholds of a cone-detected test flash (25 ms duration, 655 nm wave-length, 13' diameter) as a function of the illuminance of larger, 500 ms duration, rod-detected masking flashes. The type of photoreceptor influenced by each stimulus was carefully checked by means of a series of control procedures involving action spectra and selective rod adaptation.2. When the rod mask was 512 nm in wave-length, 40' in diameter, and less than one scotopic td in illuminance, increment threshold functions show that [Formula: see text], where I(Cth) is cone test threshold, I(R) is rod mask illuminance, and D is a dark noise term similar to that used by Barlow (1956). Further increases in I(R) have no additional influences on cone test threshold until threshold is influenced by the combined action of the mask on both rods and cones. If I(R) is expressed in terms of scotopic flux rather than illuminance, the functional relationship obtained with all rod masks </= 40' diameter and </= 580 nm wave-length is identical.3. Over the range of illuminance where a square-root relationship is obtained, probability of seeing functions show that a signal-to-noise mechanism limits the detectability of the cone test flash. These findings suggests a quantitative model in which cones produce a signal in a detector which is proportional to the illuminance of the cone test flash. Within a neural locus designated E (excitatory spatial summator), a response is produced which over at least a 40' diameter area, is proportional to the scotopic flux of the rod mask. E, however, feeds into a gain box, S, which saturates at illuminance levels at least 3 log(10) units less than usual estimates of rod saturation. Other than saturation, S behaves in a linear fashion.4. As diameter increases beyond 60', rod masks of equal scotopic illuminance have progressively less influence on cone test threshold; rod masks > 2 degrees have negligible influence on cone test threshold. We propose that I (inhibitory spatial summator), a neural locus which responds to scotopic flux provided over a very large area, attenuates the activity of E. The combined action of E and I is designated a rod channel. The response of cones and the rod channel summate at a detector. Within the detector, cone signals are distinguished from rod-related activity and intrinsic dark noise on the basis of signal-to-noise discriminations.5. The neural substrate for this rod channel most probably involves the combined action of several neurones which synapse within the inner plexiform layer of the retina. The relationship of this rod channel to other perceptual phenomena is discussed.

Entities:  

Mesh:

Year:  1983        PMID: 6875924      PMCID: PMC1199097          DOI: 10.1113/jphysiol.1983.sp014614

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


  37 in total

1.  Surround contribution to light adaptation in cat retinal ganglion cells.

Authors:  C Enroth-Cugell; P Lennie; R M Shapley
Journal:  J Physiol       Date:  1975-06       Impact factor: 5.182

2.  Neural theories of simple visual discriminations.

Authors:  H R BLACKWELL
Journal:  J Opt Soc Am       Date:  1963-01

3.  Rod-cone interaction in light adaptation.

Authors:  M Latch; P Lennie
Journal:  J Physiol       Date:  1977-08       Impact factor: 5.182

4.  Cat cones have rod input: a comparison of the response properties of cones and horizontal cell bodies in the retina of the cat.

Authors:  R Nelson
Journal:  J Comp Neurol       Date:  1977-03-01       Impact factor: 3.215

5.  Amacrine cells, bipolar cells and ganglion cells of the cat retina: a Golgi study.

Authors:  H Kolb; R Nelson; A Mariani
Journal:  Vision Res       Date:  1981       Impact factor: 1.886

6.  Rod-cone interaction on large and small backgrounds.

Authors:  S L Buck; W Makous
Journal:  Vision Res       Date:  1981       Impact factor: 1.886

7.  Physiological and pharmacological basis of GABA and glycine action on neurons of mudpuppy retina. III. Amacrine-mediated inhibitory influences on ganglion cell receptive-field organization: a model.

Authors:  T E Frumkes; R F Miller; M Slaughter; R F Dacheux
Journal:  J Neurophysiol       Date:  1981-04       Impact factor: 2.714

8.  Rod threshold: influence of neighboring cones.

Authors:  D W Blick; D I MacLeod
Journal:  Vision Res       Date:  1978       Impact factor: 1.886

9.  Spatial interaction in human cone vision.

Authors:  G Westheimer
Journal:  J Physiol       Date:  1967-05       Impact factor: 5.182

10.  Rod--cone interaction in human scotopic vision--IV. Cones stimulated by contrast flashes influence rod threshold.

Authors:  M C Barris; T E Frumkes
Journal:  Vision Res       Date:  1978       Impact factor: 1.886

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  2 in total

1.  The influence of rod light and dark adaptation upon rod-cone interaction.

Authors:  G M Bauer; T E Frumkes; G R Holstein
Journal:  J Physiol       Date:  1983-04       Impact factor: 5.182

2.  Influence of background size, luminance and eccentricity on different adaptation mechanisms.

Authors:  Alejandro H Gloriani; Beatriz M Matesanz; Pablo A Barrionuevo; Isabel Arranz; Luis Issolio; Santiago Mar; Juan A Aparicio
Journal:  Vision Res       Date:  2016-05-25       Impact factor: 1.886

  2 in total

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