Evidence map›Paper›PMID 38496618›Full record

ArticlebioRxiv : the preprint server for biology2025

FOUNDATIONS OF VISUAL FORM SELECTIVITY IN MACAQUE AREAS V1 AND V2.

Timothy D Oleskiw, Justin D Lieber, Eero P Simoncelli, J Anthony Movshon

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In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

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

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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

4 authors.

Timothy D OleskiwCenter for Neural Science, New York University.ORCID 0000-0003-2631-4406
Justin D LieberCenter for Neural Science, New York University.ORCID 0000-0001-8221-7008
Eero P SimoncelliCenter for Computational Neuroscience, Flatiron Institute.ORCID 0000-0002-1206-527X
J Anthony MovshonCenter for Neural Science, New York University.ORCID 0000-0002-0274-9213

Funding

Visual pattern representation in the extrastriate cortexR01EY022428 · NEI · NEW YORK UNIVERSITY · PI J ANTHONY MOVSHON, Eero Peter Simoncelli · 2013 to 2026
$5.2M
NEI NIH HHS R01 EY022428
6 · The paper itself

Abstract

Neurons early in the primate visual cortical pathway generate responses by combining signals from other neurons: some from downstream areas, some from within the same area, and others from areas upstream. Here we develop a model that selectively combines afferents derived from a population model of V1 cells. We use this model to account for responses we recorded of both V1 and V2 neurons in awake fixating macaque monkeys to stimuli composed of a sparse collection of locally oriented features ("droplets") designed to drive subsets of V1 neurons. The first stage computes the rectified responses of a fixed population of oriented filters at different scales that cover the visual field. The second stage computes a weighted combination of these first-stage responses, followed by a final nonlinearity, with parameters optimized to fit data from physiological recordings and constrained to encourage sparsity and locality. The fitted model accounts for the responses of both V1 and V2 neurons, capturing an average of 43% of the explainable variance for V1 and 38% for V2. The models fitted to droplet recordings predict responses to classical stimuli, such as gratings of different orientations and spatial frequencies, as well as to textures of different spectral content, which are known to be especially effective in driving V2. The models are less effective, however, at capturing the selectivity of responses to textures that include naturalistic image statistics. The pattern of afferents - defined by their weights over the 4 dimensions of spatial position, orientation, and spatial frequency - provides a common and interpretable characterization of the origin of many neuronal response properties in the early visual cortex.

Identifiers

PMID38496618
PMCPMC10942284

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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.