Evidence map›Paper›PMID 31209058›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Asymmetries between achromatic and chromatic extraction of 3D motion signals.

Milena Kaestner, Ryan T Maloney, Kirstie H Wailes-Newson, Marina Bloj, Julie M Harris, Antony B Morland, Alex R Wade

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

7 authors at 3 institutions in 1 country.

Milena KaestnerDepartment of Psychology, University of York, YO10 5DD York, United Kingdom; milenak@stanford.edu.ORCID 0000-0003-1202-7772
Ryan T MaloneyDepartment of Psychology, University of York, YO10 5DD York, United Kingdom.
Kirstie H Wailes-NewsonDepartment of Psychology, University of York, YO10 5DD York, United Kingdom.
Marina BlojSchool of Optometry and Vision Sciences, University of Bradford, BD7 1DP Bradford, United Kingdom.
Julie M HarrisSchool of Psychology and Neuroscience, University of St. Andrews, KY16 9JP St. Andrews, United Kingdom.
Antony B MorlandDepartment of Psychology, University of York, YO10 5DD York, United Kingdom.
Alex R WadeDepartment of Psychology, University of York, YO10 5DD York, United Kingdom.ORCID 0000-0003-0656-2664
University of York · GBUniversity of Bradford · GBUniversity of St Andrews · GB

Funding

Biotechnology and Biological Sciences Research Council BB/M001210/1Biotechnology and Biological Sciences Research Council BB/M001660/1Biotechnology and Biological Sciences Research Council BB/M002543/1
6 · The paper itself

Abstract

Motion in depth (MID) can be cued by high-resolution changes in binocular disparity over time (CD), and low-resolution interocular velocity differences (IOVD). Computational differences between these two mechanisms suggest that they may be implemented in visual pathways with different spatial and temporal resolutions. Here, we used fMRI to examine how achromatic and S-cone signals contribute to human MID perception. Both CD and IOVD stimuli evoked responses in a widespread network that included early visual areas, parts of the dorsal and ventral streams, and motion-selective area hMT+. Crucially, however, we measured an interaction between MID type and chromaticity. fMRI CD responses were largely driven by achromatic stimuli, but IOVD responses were better driven by isoluminant S-cone inputs. In our psychophysical experiments, when S-cone and achromatic stimuli were matched for perceived contrast, participants were equally sensitive to the MID in achromatic and S-cone IOVD stimuli. In comparison, they were relatively insensitive to S-cone CD. These findings provide evidence that MID mechanisms asymmetrically draw on information in precortical pathways. An early opponent motion signal optimally conveyed by the S-cone pathway may provide a substantial contribution to the IOVD mechanism.

Indexed as

3D motionbinocular visioncolor

Identifiers

PMID31209058
PMCPMC6612918
OpenAlexW2953103068

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.