Evidence map›Paper›PMID 42818580›Full record

ArticlebioRxiv : the preprint server for biology2026

Neural subpopulations in marmoset area MT/MTC detect and discount saccade-related retinal motion.

Amy Bucklaew, Shanna H Coop, Jude F Mitchell

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Amy BucklaewNeuroscience Graduate Program, University of Rochester.ORCID 0000-0002-2964-6345
Shanna H CoopBrain and Cognitive Sciences, University of Rochester.ORCID 0000-0002-8189-2359
Jude F MitchellNeuroscience Graduate Program, University of Rochester.ORCID 0000-0003-0197-7545

Funding

VISUAL SCIENCET32EY007125 · NEI · UNIVERSITY OF ROCHESTER · PI Krystel R Huxlin, Duje Tadin · 1990 to 2026
$7.1M
Neural basis of trans-saccadic perceptionR01EY030998 · NEI · UNIVERSITY OF ROCHESTER · PI MITCHELL, JUDE F · 2020 to 2024
$1.9M
NEI NIH HHS R01 EY030998NEI NIH HHS T32 EY007125
6 · The paper itself

Abstract

Primates rely on eye movements made 2-3 times every second to scan their visual environment. Each eye movement induces substantial retinal motion, yet observers readily suppress it to stitch together the percept of a stable world. Neurons in the middle temporal (MT) and medial superior temporal (MST) areas respond to motion, but also suppress that response during eye movements (Bremmer et al., 2009; Leopold & Logothetis, 1998; Thiele et al., 2002). This saccadic suppression could reflect the influence of corollary feedback from eye movement related brain structures (Berman et al., 2017). However, visual signals that detect wide-field motion characteristic of a saccade could also contribute to suppression, akin to visual masking (Idrees et al., 2020). We sought to disentangle the relative contributions of visual signals and corollary discharge in driving saccadic suppression in areas MT and MTC in marmoset monkeys. Marmosets freely viewed natural images, blank backgrounds, or externally moving images that simulated saccades, and also made saccades in complete darkness. We found a diversity of saccadic modulation across the population. Some neurons showed short latency excitatory responses to saccades while others showed suppression. Still others showed a bi-phasic response that began with suppression followed by an excitatory rebound. Neurons with early responses were frequently tuned for the direction of saccades on natural images and retained that same tuning for saccades on blank screens or in complete darkness, thus supporting a role for corollary feedback. However, these neurons also responded with similar directional tuning for retinal motion created by simulating saccades while the eyes were fixed, and thus also appear to integrate visual cues for saccadic motion. More so, these units were biased towards having narrow spike waveforms consistent with putative inhibitory cells, which drive suppression observed in the rest of the population. We also found a subset of neurons that responded robustly to simulated saccadic motion but had negligible response to motion from real saccades, such that they discounted saccade induced motion. Those neurons were biased to have broader spike waveforms, consistent with being putative excitatory projection neurons and could support our percept of stability during eye movements.

Identifiers

PMID42818580
PMCPMC13622534

What Socratic holds

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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 Socratic graph.