TY - JOUR
T1 - Noise correlations and neuronal diversity may limit the utility of winner-take-all readout in a pop out visual search task
AU - Hendler, Ori
AU - Segev, Ronen
AU - Shamir, Maoz
N1 - Publisher Copyright:
Copyright: © 2025 Hendler et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2025/5/1
Y1 - 2025/5/1
N2 - Visual search involves active scanning of the environment to locate objects of interest against a background of irrelevant distractors. One widely accepted theory posits that pop out visual search is computed by a winner-take-all (WTA) competitio between contextually modulated cells that form a saliency map. However, previous studies have shown that the ability of WTA mechanisms to accumulate information from large populations of neurons is limited, thus raising the question of whether WTA can underlie pop out visual search. To address this question, we conducted a modeling study to investigate how accurately the WTA mechanism can detect the deviant stimulus in a pop out task. We analyzed two types of WTA readout mechanisms: single-best-cell WTA, where the decision is made based on a single winning cell, and a generalized population-based WTA, where the decision is based on the winning population of similarly tuned cells. Our results show that neither WTA mechanism can account for the high accuracy found in behavioral experiments. The inherent neuronal heterogeneity prevents the single-best-cell WTA from accumulating information even from large populations, whereas the accuracy of the generalized population-based WTA algorithm is negatively affected by the widely reported noise correlations. These findings underscore the need to revisit the key assumptions explored in our theoretical analysis, particularly concerning the decoding mechanism and the statistical properties of neuronal population responses to pop out stimuli. The analysis identifies specific response statistics that require further empirical characterization to accurately predict WTA performance in biologically plausible models of visual pop out detection.
AB - Visual search involves active scanning of the environment to locate objects of interest against a background of irrelevant distractors. One widely accepted theory posits that pop out visual search is computed by a winner-take-all (WTA) competitio between contextually modulated cells that form a saliency map. However, previous studies have shown that the ability of WTA mechanisms to accumulate information from large populations of neurons is limited, thus raising the question of whether WTA can underlie pop out visual search. To address this question, we conducted a modeling study to investigate how accurately the WTA mechanism can detect the deviant stimulus in a pop out task. We analyzed two types of WTA readout mechanisms: single-best-cell WTA, where the decision is made based on a single winning cell, and a generalized population-based WTA, where the decision is based on the winning population of similarly tuned cells. Our results show that neither WTA mechanism can account for the high accuracy found in behavioral experiments. The inherent neuronal heterogeneity prevents the single-best-cell WTA from accumulating information even from large populations, whereas the accuracy of the generalized population-based WTA algorithm is negatively affected by the widely reported noise correlations. These findings underscore the need to revisit the key assumptions explored in our theoretical analysis, particularly concerning the decoding mechanism and the statistical properties of neuronal population responses to pop out stimuli. The analysis identifies specific response statistics that require further empirical characterization to accurately predict WTA performance in biologically plausible models of visual pop out detection.
UR - http://www.scopus.com/inward/record.url?scp=105004724067&partnerID=8YFLogxK
U2 - 10.1371/journal.pcbi.1013092
DO - 10.1371/journal.pcbi.1013092
M3 - Article
C2 - 40334249
AN - SCOPUS:105004724067
SN - 1553-734X
VL - 21
JO - PLoS Computational Biology
JF - PLoS Computational Biology
IS - 5 May
M1 - e1013092
ER -