Evidence map›Paper›PMID 30679564›Full record

ArticleScientific reports2019

Speed-Selectivity in Retinal Ganglion Cells is Sharpened by Broad Spatial Frequency, Naturalistic Stimuli.

César R Ravello, Laurent U Perrinet, María-José Escobar, Adrián G Palacios

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

11 citing papers in PubMed.

  1. Review
  2. Article
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  4. Article
  5. Attention maps reveal stimulus-dependent retinal population codes.Frontiers in computational neuroscience · 2026
    Article
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  7. Article
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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

4 authors.

César R RavelloCentro Interdisciplinario de Neurociencia de Valparaíso, Universidad de Valparaiso, Valparaiso, Chile. cesar.ravello@cinv.cl.ORCID 0000-0002-5513-1222
Laurent U PerrinetInstitut de Neurosciences de la Timone, Aix Marseille Université/CNRS, Marseille, France.ORCID 0000-0002-9536-010X
María-José EscobarUniversidad Técnica Federico Santa María, Departamento de Electrónica, Valparaíso, Chile. mariajose.escobar@usm.cl.ORCID 0000-0003-1563-624X
Adrián G PalaciosCentro Interdisciplinario de Neurociencia de Valparaíso, Universidad de Valparaiso, Valparaiso, Chile. adrian.palacios@uv.cl.ORCID 0000-0003-1532-7527

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motion detection represents one of the critical tasks of the visual system and has motivated a large body of research. However, it remains unclear precisely why the response of retinal ganglion cells (RGCs) to simple artificial stimuli does not predict their response to complex, naturalistic stimuli. To explore this topic, we use Motion Clouds (MC), which are synthetic textures that preserve properties of natural images and are merely parameterized, in particular by modulating the spatiotemporal spectrum complexity of the stimulus by adjusting the frequency bandwidths. By stimulating the retina of the diurnal rodent, Octodon degus with MC we show that the RGCs respond to increasingly complex stimuli by narrowing their adjustment curves in response to movement. At the level of the population, complex stimuli produce a sparser code while preserving movement information; therefore, the stimuli are encoded more efficiently. Interestingly, these properties were observed throughout different populations of RGCs. Thus, our results reveal that the response at the level of RGCs is modulated by the naturalness of the stimulus - in particular for motion - which suggests that the tuning to the statistics of natural images already emerges at the level of the retina.

Indexed as

MotionAlgorithmsAnimalsCircadian RhythmInhibitory Postsynaptic PotentialsModels, NeurologicalMotion PerceptionMovementNerve NetOctodonPhotic StimulationRetinaRetinal Ganglion CellsSynaptic Transmission

Identifiers

PMID30679564
PMCPMC6345785

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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.