Evidence map›Paper›PMID 39436900›Full record

ArticlePloS one2024

Visual short-term memory for crossed and uncrossed binocular disparities.

Vanda Ágnes Nemes, János Radó, Diána Fülöp, Eszter Mikó-Baráth, Imola Hamvas, Gábor Jandó, Péter Buzás

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Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Vanda Ágnes NemesInstitute of Physiology, Medical School, University of Pécs, Pécs, Hungary.ORCID 0000-0002-7504-2390
János RadóInstitute of Physiology, Medical School, University of Pécs, Pécs, Hungary.
Diána FülöpInstitute of Physiology, Medical School, University of Pécs, Pécs, Hungary.
Eszter Mikó-BaráthInstitute of Physiology, Medical School, University of Pécs, Pécs, Hungary.
Imola HamvasInstitute of Physiology, Medical School, University of Pécs, Pécs, Hungary.
Gábor JandóInstitute of Physiology, Medical School, University of Pécs, Pécs, Hungary.ORCID 0000-0002-3809-890X
Péter BuzásInstitute of Physiology, Medical School, University of Pécs, Pécs, Hungary.ORCID 0000-0002-4390-3360

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Previous work on visual short-term memory (VSTM) has encompassed various stimulus attributes including spatial frequency, color, and contrast, revealing specific time courses and a dependence on stimulus parameters. This study investigates visual short-term memory for binocular depth, using dynamic random dot stereograms (DRDS) featuring disparity planes in front of or behind the plane of fixation. In a delayed match-to-sample paradigm, we employed four distinct reference disparities (17.5', 28.8' either crossed or uncrossed) at two contrast levels (20%, 80%), spanning interstimulus intervals (ISI) of up to 4 s. Test stimuli represented a range of equally spaced values centered around the reference disparity of the ongoing trial. In addition, the impact of a memory masking stimulus was also tested in a separate experiment. Accuracy and point of subjective equality (PSE) served as performance markers. The performance, indicated by the accuracy of responses, was better for smaller reference disparities (±17.5') compared to larger ones (±28'), but both deteriorated as a function of ISI. The PSE demonstrated a consistent shift with increasing ISIs, irrespective of the magnitude of the initial disparity, converging gradually toward the range of 20-22' and deviating from the reference disparity. Notably, the influence of masking stimuli on the PSE was more marked when the mask disparity diverged from the reference value. The findings from our study indicate that the retention of absolute disparity in memory is imprecise, it deteriorates with retention time or due to perturbation by dissimilar masking stimuli. As a result, the memory trace is gradually replaced by a default depth value. This value could potentially signify an optimal point within low-level perceptual memory, however, our results are better explained by perceptual averaging whereby the visual system computationally derives a statistical summary of the presented disparities over time. The latter mechanism would aid in the computation of relative disparity in a dynamically changing environment.

Indexed as

Memory, Short-TermVision DisparityAdultFemaleHumansMalePhotic StimulationVision, BinocularVisual PerceptionYoung Adult

Identifiers

PMID39436900
PMCPMC11495605

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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.