ArticleProceedings of the National Academy of Sciences of the United States of America2024
What can the eye see with melanopsin?
Article in Proceedings of the National Academy of Sciences of the United States of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
What it found
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Who cites it
9 citing papers in PubMed.
- Photoreceptor-specific scene statistics reveal melanopic structure in natural environments.iScience · 2026Article
- The Diverse Role of ipRGCs in Visual Perception Beyond Non-Image-Forming Functions.The European journal of neuroscience · 2026Review
- Filling-in of the foveal rod scotoma and confidence preference for central vision under mesopic viewing conditions.Vision research · 2026Article
- ISCEV extended protocol for the photoreceptor directed ERG using full-field silent substitution stimuli.Documenta ophthalmologica. Advances in ophthalmology · 2026Review
- Rapid test for detecting red-green color vision deficiencies using a neural network-assisted color-naming task.Scientific reports · 2026Article
- A method for setting the melanopsin and rhodopsin content in commercial LED sources to investigate the effects of ambient light on behavior.Behavior research methods · 2025Article
- IMI: The Role of Light in Refractive Development and Myopia: Evidence from Animal and Human Studies.Investigative ophthalmology & visual science · 2025Review
- Melanopsin-mediated image statistics from natural and human-made environments.Scientific reports · 2025Article
- Intrinsically photosensitive retinal ganglion cells and visual processing: ipRGCs beyond non-image-forming functions.Frontiers in neuroscience · 2025Review
Corrections and comments
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Authors and funding
2 authors.
Funding
Abstract
A subpopulation of human retinal ganglion cells contains the melanopsin photopigment, allowing them to act as a fifth photoreceptor class. These ganglion cells project to the visual cortex, but to reveal its intrinsic contribution to conscious vision is technically challenging as it requires melanopsin to be separated from the responses originating in the rods and three cone classes. Using a display engineered to isolate the melanopic visual response, we show that it detects lowpass spatial (≤0.35 cycles per degree) and temporal image content (≤1 Hz) but cannot reconstruct the stimulus form necessary for object recognition. We demonstrate that a model of the spatially diffuse intrinsically-photosensitive retinal ganglion cells' sampling structure is predictive of the measured image reconstruction limits of melanopic spatial vision. Separately, we find that under five-photoreceptor silent substitution conditions, rod pathways alone can support form vision in bright lighting when typically thought to be in saturation. Form vision that is absent from melanopsin can be only perceived in mixtures of both melanopsin and rod signals because it is the rod pathway that sees the form. Our findings show that melanopsin's unique tuning to the diffuse and slow-changing elements in the world provides a stabilized reference point for vision.
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Registered trials
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.