Evidence map›Paper›PMID 35834376›Full record

ArticleJournal of vision2022

Fixational eye movements enable robust edge detection.

Lynn Schmittwilken, Marianne Maertens

Abstract read
In one paragraph

Article in Journal of vision, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. 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

2 authors.

Lynn SchmittwilkenScience of Intelligence and Computational Psychology, Faculty of Electrical Engineering and Computer Science, Technische Universität Berlin, Berlin, Germany.
Marianne MaertensScience of Intelligence and Computational Psychology, Faculty of Electrical Engineering and Computer Science, Technische Universität Berlin, Berlin, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human vision relies on mechanisms that respond to luminance edges in space and time. Most edge models use orientation-selective mechanisms on multiple spatial scales and operate on static inputs assuming that edge processing occurs within a single fixational instance. Recent studies, however, demonstrate functionally relevant temporal modulations of the sensory input due to fixational eye movements. Here we propose a spatiotemporal model of human edge detection that combines elements of spatial and active vision. The model augments a spatial vision model by temporal filtering and shifts the input images over time, mimicking an active sampling scheme via fixational eye movements. The first model test was White's illusion, a lightness effect that has been shown to depend on edges. The model reproduced the spatial-frequency-specific interference with the edges by superimposing narrowband noise (1-5 cpd), similar to the psychophysical interference observed in White's effect. Second, we compare the model's edge detection performance in natural images in the presence and absence of Gaussian white noise with human-labeled contours for the same (noise-free) images. Notably, the model detects edges robustly against noise in both test cases without relying on orientation-selective processes. Eliminating model components, we demonstrate the relevance of multiscale spatiotemporal filtering and scale-specific normalization for edge detection. The proposed model facilitates efficient edge detection in (artificial) vision systems and challenges the notion that orientation-selective mechanisms are required for edge detection.

Indexed as

Eye MovementsForm PerceptionHumansNoiseVision, Ocular

Identifiers

PMID35834376
PMCPMC9290315

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.