Evidence map›Paper›PMID 37967553›Full record

ArticleCurrent biology : CB2023

Melanopsin enhances image persistence.

Tom Woelders, Annette E Allen, Robert J Lucas

Open access · hybridAbstract read
In one paragraph

Article in Current biology : CB, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.7field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Tom WoeldersDivision of Neuroscience and Centre for Biological Timing, School of Biology, Faculty of Biology Medicine and Health, University of Manchester, Upper Brook Street, M13 9PT Manchester, UK. Electronic address: tom.woelders@manchester.ac.uk.
Annette E AllenDivision of Neuroscience and Centre for Biological Timing, School of Biology, Faculty of Biology Medicine and Health, University of Manchester, Upper Brook Street, M13 9PT Manchester, UK.
Robert J LucasDivision of Neuroscience and Centre for Biological Timing, School of Biology, Faculty of Biology Medicine and Health, University of Manchester, Upper Brook Street, M13 9PT Manchester, UK. Electronic address: robert.lucas@manchester.ac.uk.
University of Manchester · GBManchester Academic Health Science Centre · GB

Funding

Wellcome Trust 210684/Z/18/Z
6 · The paper itself

Abstract

Contributions of the inner retinal photopigment melanopsin to human visual perception are incompletely understood. Here, we use a four-primary display to produce stimuli differing in melanopsin versus cone contrast in psychophysical paradigms in eight subjects with normal color vision. We address two predictions from electrophysiological recordings of the melanopsin system in non-human mammals: melanopsin influences color and/or supports image persistence under visual fixation. We first construct chromatic contrast sensitivity contours for stimuli differing in melanopsin excitation presented as a central annulus (10°) or peripheral (22.5°) spot. We find that although including melanopsin contrast produces modest changes in the average chromatic coordinates in both eccentricities, this occurs equally at low (0.5 Hz) and higher (3.75 Hz) temporal frequencies, arguing that it reflects divergence in cone spectral sensitivity in our participants from that captured in standardized cone fundamentals rather than a melanopsin contribution to color. We continue to ask whether the established ability of melanopsin to sustain firing of visual neurons under extended light exposure has a visual correlate, using the optical illusion of Troxler fading in which blurred spots in periphery disappear during visual fixation. We find that introducing additional melanopsin contrast (+28% Michelson contrast) to either bright or dark spots increases fading latency by 35% ± 8.8% and 41% ± 13.6%, respectively. Our data argue that the primary contribution of melanopsin to perception under these conditions is not to provide a color percept but rather to enhance persistence of low spatial frequency patterns during visual fixation.

Indexed as

RetinaRetinal Cone Photoreceptor CellsAnimalsHumansMammalsMelanopsinPhotic StimulationRod OpsinsVision, OcularMelanopsinRod Opsinscolorconesimage persistenceipRGCmelanopsintrichromaticTroxler fading

Identifiers

PMID37967553
PMCPMC7619323
OpenAlexW4388673776

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.