Evidence map›Paper›PMID 42270430›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2026

Spatiotemporal Divergence Between Intrinsic And Evoked Cortical Activity Predicts Visual Detection.

Dylan Jensen, Zachary W Davis

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 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

2 authors.

Dylan JensenDepartment of Ophthalmology and Visual Sciences, University of Utah.
Zachary W DavisDepartment of Ophthalmology and Visual Sciences, University of Utah.

Funding

University of Utah, Core Vision Research GrantP30EY014800 · NEI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Bryan William Jones · 2005 to 2026
$14.6M
Vision Research Training Grant at the University of UtahT32EY024234 · NEI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI DAVID KRIZAJ, Monica L Vetter · 2014 to 2026
$2.3M
NEI NIH HHS P30 EY014800NEI NIH HHS T32 EY024234
6 · The paper itself

Abstract

The threshold for sensory detection varies with fluctuations in intrinsic cortical activity. When stimulus-encoding cortical populations are more excitable, stimuli elicit stronger neural responses that are more likely to be detected. However, the detection of a stimulus is also more likely when cortical populations are less excitable because there is less background "noise". Therefore, it is unclear how the variable states of cortical activity interact to impact sensory detection. We hypothesize the answer depends on the spatiotemporal structure of intrinsic activity states across stimulus encoding and non-encoding populations. To test this, we examined intrinsic and target-evoked population activity across cortical Area MT in common marmosets (Callithrix jacchus; one male and one female) while they performed a threshold visual detection task. We compared detection performance based on target-evoked responses and the state of intrinsic activity in the larger surrounding population. We find that the intrinsic activity in the surrounding, non-encoding population predicted trial-by-trial detection performance better than the population encoding the target-evoked response. Furthermore, we find that the detection performance of the monkey was best predicted by the divergence in activity between the encoding and surrounding non-encoding population. These findings suggest that, rather than a source of noise or irrelevant to sensory processing, the distributed spatiotemporal state of intrinsic activity directly influences how sensory signals are represented in cortical populations and can influence perceptual thresholds in visual detection.

Identifiers

PMID42270430
PMCPMC13336573

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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.