Cargando…
Numerosity tuning in human association cortices and local image contrast representations in early visual cortex
Human early visual cortex response amplitudes monotonically increase with numerosity (object number), regardless of object size and spacing. However, numerosity is typically considered a high-level visual or cognitive feature, while early visual responses follow image contrast in the spatial frequen...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924234/ https://www.ncbi.nlm.nih.gov/pubmed/35292648 http://dx.doi.org/10.1038/s41467-022-29030-z |
_version_ | 1784669807013003264 |
---|---|
author | Paul, Jacob M. van Ackooij, Martijn ten Cate, Tuomas C. Harvey, Ben M. |
author_facet | Paul, Jacob M. van Ackooij, Martijn ten Cate, Tuomas C. Harvey, Ben M. |
author_sort | Paul, Jacob M. |
collection | PubMed |
description | Human early visual cortex response amplitudes monotonically increase with numerosity (object number), regardless of object size and spacing. However, numerosity is typically considered a high-level visual or cognitive feature, while early visual responses follow image contrast in the spatial frequency domain. We find that, at fixed contrast, aggregate Fourier power (at all orientations and spatial frequencies) follows numerosity closely but nonlinearly with little effect of object size, spacing or shape. This would allow straightforward numerosity estimation from spatial frequency domain image representations. Using 7T fMRI, we show monotonic responses originate in primary visual cortex (V1) at the stimulus’s retinotopic location. Responses here and in neural network models follow aggregate Fourier power more closely than numerosity. Truly numerosity tuned responses emerge after lateral occipital cortex and are independent of retinotopic location. We propose numerosity’s straightforward perception and neural responses may result from the pervasive spatial frequency analyses of early visual processing. |
format | Online Article Text |
id | pubmed-8924234 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89242342022-04-01 Numerosity tuning in human association cortices and local image contrast representations in early visual cortex Paul, Jacob M. van Ackooij, Martijn ten Cate, Tuomas C. Harvey, Ben M. Nat Commun Article Human early visual cortex response amplitudes monotonically increase with numerosity (object number), regardless of object size and spacing. However, numerosity is typically considered a high-level visual or cognitive feature, while early visual responses follow image contrast in the spatial frequency domain. We find that, at fixed contrast, aggregate Fourier power (at all orientations and spatial frequencies) follows numerosity closely but nonlinearly with little effect of object size, spacing or shape. This would allow straightforward numerosity estimation from spatial frequency domain image representations. Using 7T fMRI, we show monotonic responses originate in primary visual cortex (V1) at the stimulus’s retinotopic location. Responses here and in neural network models follow aggregate Fourier power more closely than numerosity. Truly numerosity tuned responses emerge after lateral occipital cortex and are independent of retinotopic location. We propose numerosity’s straightforward perception and neural responses may result from the pervasive spatial frequency analyses of early visual processing. Nature Publishing Group UK 2022-03-15 /pmc/articles/PMC8924234/ /pubmed/35292648 http://dx.doi.org/10.1038/s41467-022-29030-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Paul, Jacob M. van Ackooij, Martijn ten Cate, Tuomas C. Harvey, Ben M. Numerosity tuning in human association cortices and local image contrast representations in early visual cortex |
title | Numerosity tuning in human association cortices and local image contrast representations in early visual cortex |
title_full | Numerosity tuning in human association cortices and local image contrast representations in early visual cortex |
title_fullStr | Numerosity tuning in human association cortices and local image contrast representations in early visual cortex |
title_full_unstemmed | Numerosity tuning in human association cortices and local image contrast representations in early visual cortex |
title_short | Numerosity tuning in human association cortices and local image contrast representations in early visual cortex |
title_sort | numerosity tuning in human association cortices and local image contrast representations in early visual cortex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8924234/ https://www.ncbi.nlm.nih.gov/pubmed/35292648 http://dx.doi.org/10.1038/s41467-022-29030-z |
work_keys_str_mv | AT pauljacobm numerositytuninginhumanassociationcorticesandlocalimagecontrastrepresentationsinearlyvisualcortex AT vanackooijmartijn numerositytuninginhumanassociationcorticesandlocalimagecontrastrepresentationsinearlyvisualcortex AT tencatetuomasc numerositytuninginhumanassociationcorticesandlocalimagecontrastrepresentationsinearlyvisualcortex AT harveybenm numerositytuninginhumanassociationcorticesandlocalimagecontrastrepresentationsinearlyvisualcortex |