Evidence map›Paper›PMID 40531345›Full record

ArticleBiological cybernetics2025

Relationships between the degrees of freedom in the affine Gaussian derivative model for visual receptive fields and 2-D affine image transformations with application to covariance properties of simple cells in the primary visual cortex.

Tony Lindeberg

Abstract read
In one paragraph

Article in Biological cybernetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

1 author.

Tony LindebergComputational Brain Science Lab, Division of Computational Science and Technology, KTH Royal Institute of Technology, SE-100 44, Stockholm, Sweden. tony@kth.se.ORCID 0000-0002-9081-2170

Funding

Vetenskapsrådet 2022-02969
6 · The paper itself

Abstract

When observing the surface patterns of objects delimited by smooth surfaces, the projections of the surface patterns to the image domain will be subject to substantial variabilities, as induced by variabilities in the geometric viewing conditions, and as generated by either monocular or binocular imaging conditions, or by relative motions between the object and the observer over time. To first order of approximation, the image deformations of such projected surface patterns can be modelled as local linearizations in terms of local 2-D spatial affine transformations. This paper presents a theoretical analysis of relationships between the degrees of freedom in 2-D spatial affine image transformations and the degrees of freedom in the affine Gaussian derivative model for visual receptive fields. For this purpose, we first describe a canonical decomposition of 2-D affine transformations on a product form, closely related to a singular value decomposition, while in closed form, and which reveals the degrees of freedom in terms of (i) uniform scaling transformations, (ii) an overall amount of global rotation, (iii) a complementary non-uniform scaling transformation and (iv) a relative normalization to a preferred symmetry orientation in the image domain. Then, we show how these degrees of freedom relate to the degrees of freedom in the affine Gaussian derivative model. Finally, we use these theoretical results to consider whether we could regard the biological receptive fields in the primary visual cortex of higher mammals as being able to span the degrees of freedom of 2-D spatial affine transformations, based on interpretations of existing neurophysiological experimental results.

Indexed as

Models, NeurologicalNeuronsPrimary Visual CortexVisual CortexVisual FieldsAnimalsHumansNormal DistributionPhotic StimulationAffineCovarianceGaussian derivativeImage transformationsReceptive fieldSimple cell

Identifiers

PMID40531345
PMCPMC12176974

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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 OpenQuestion graph.