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Neural circuit dynamics underlying accumulation of time-varying evidence during perceptual decision-making
Open accessAbstract
How do neurons in a decision circuit integrate time-varying signals, in favor of or against alternative choice options? To address this question, we used a recurrent neural circuit model to simulate an experiment in which monkeys performed a direction-discrimination task on a visual motion stimulus. In a recent study, it was found that brief pulses of motion perturbed neural activity in the lateral intraparietal area (LIP), and exerted corresponding effects on the monkey's choices and response times. Our model reproduces the behavioral observations and replicates LIP activity which, depending on whether the direction of the pulse is the same or opposite to that of a preferred motion stimulus, increases or decreases persistently over a few hundred milliseconds. Furthermore, our model accounts for the observation that the pulse exerts a weaker influence on LIP neuronal responses when the pulse is late relative to motion stimulus onset. We show that this violation of time-shift invariance (TSI) is consistent with a recurrent circuit mechanism of time integration. We further examine time integration using two consecutive pulses of the same or opposite motion directions. The induced changes in the performance are not additive, and the second of the paired pulses is less effective than its standalone impact, a prediction that is experimentally testable. Taken together, these findings lend further support for an attractor network model of time integration in perceptual decision making.
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In the citing paper
“Within each pyramidal neural group, strong recurrent excitatory connections can sustain persistent activity triggered by a transient preferred stimulus.”
From Decision Making in Recurrent Neuronal Circuits (2008) · cites this paper as Wong et al., 2007
In the citing paper
“The two neural groups compete through feedback inhibition from interneurons.”
From Decision Making in Recurrent Neuronal Circuits (2008) · cites this paper as Wong et al., 2007
In the citing paper
“In a two-pool version of the model, subpopulations of spiking neurons are selective for two-choice alternatives (e.g., A = left motion, B = right motion).”
From Decision Making in Recurrent Neuronal Circuits (2008) · cites this paper as Wong et al., 2007
In the citing paper
“This prediction is also confirmed by the monkey experiment, which showed that the impact of a brief motion pulse in addition to the random-dot stimulus was greater with an earlier onset time (Huk and Shadlen, 2005; Wong et al., 2007).”
From Decision Making in Recurrent Neuronal Circuits (2008) · cites this paper as Wong et al., 2007
In the citing paper
“In fact, in contrast to the recurrent circuit model, the LCA model actually predicts that later, not earlier, signals influence more the ultimate decision, because an earlier pulse is gradually “forgotten” due to the leak and does not affect significantly the decision that occurs much later (Wong et al., 2007).”
From Decision Making in Recurrent Neuronal Circuits (2008) · cites this paper as Wong et al., 2007
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Cites
Nonlinear Dynamics and Chaos: With Applications to Physics, Biology, Chemistry, and Engineering
Strogatz, S. H., Friedman, M. J., Mallinckrodt, A. J., & McKay, S. R. (1994) · Computers in Physics · doi:10.1063/1.4823332 · Cited by 4,654
The Neural Basis of Decision Making
Gold, J. I., & Shadlen, M. N. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.29.051605.113038 · Cited by 3,764
Nonlinear Dynamics and Chaos: With Applications to Physics, Biology, Chemistry and Engineering
Strogatz, S. H., & Fox, R. F. (1995) · Physics Today · doi:10.1063/1.2807947 · Cited by 2,584
The time course of perceptual choice: The leaky, competing accumulator model.
Usher, M., & McClelland, J. L. (2001) · Psychological Review · doi:10.1037/0033-295x.108.3.550 · Cited by 2,152
(1986) · Cited by 2,022
Bogacz, R., Brown, E., Moehlis, J., Holmes, P. J., & Cohen, J. D. (2006) · Psychological Review · doi:10.1037/0033-295x.113.4.700 · Cited by 1,945
Neural Basis of a Perceptual Decision in the Parietal Cortex (Area LIP) of the Rhesus Monkey
Shadlen, M. N., & Newsome, W. T. (2001) · Journal of Neurophysiology · doi:10.1152/jn.2001.86.4.1916 · Cited by 1,755
Roitman, J. D., & Shadlen, M. N. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-21-09475.2002 · Cited by 1,589 · cited 8×
“We designed our model to replicate a dip of neural firing at the onset of the motion stimulus, as observed in LIP neurons (Huk and Shadlen, 2005; Roitman and Shadlen, 2002).”
BackgroundMethodResultInfluentialModeling Response Times for Two-Choice Decisions
Ratcliff, R., & Rouder, J. N. (1998) · Psychological Science · doi:10.1111/1467-9280.00067 · Cited by 1,478
A Comparison of Sequential Sampling Models for Two-Choice Reaction Time.
Ratcliff, R., & Smith, P. L. (2004) · Psychological Review · doi:10.1037/0033-295x.111.2.333 · Cited by 1,288
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Research works printed but not linked: 1
- Shadlen M. N. Gold J. I. (2004). The neurophysiology of decision-making as a window on cognition. In The Cognitive Neurosciences, 3rd edn, Gazzaniga M. S., ed. (Cambridge, MA, MIT).
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Schoemann, M., & Scherbaum, S. (2020) · Cognitive Processing · doi:10.1007/s10339-020-00953-z · Cited by 8
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Feng, S. F. (2012) · Cited by 1
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Kim, W., & Yoo, Y. (2020) · Neural Computation · doi:10.1162/neco_a_01326 · Cited by 1
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(2022) · Wiley Interdisciplinary Reviews Cognitive Science · doi:10.1002/wcs.1601 · Cited by 2
Disinhibition as a canonical neural mechanism for flexible behavior
Standage, D., Paré, M., & Blohm, G. (2018) · Conference on Cognitive Computational Neuroscience (CCN) · doi:10.32470/ccn.2018.1165-0 · Cited by 1
Cavanagh, S. E., Lam, N. H., Murray, J. D., Hunt, L. T., & Kennerley, S. W. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/826214 · Cited by 1
Liu, B., Lo, C., & Wu, K.-A. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.05.463257 · Cited by 1
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Neural stochastic dynamics of perceptual decision making
Ortega, D. (2008) · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas)
Piu, P., Fargnoli, F., Innocenti, A., & Rufa, A. (2014) · Computational Intelligence and Neuroscience · doi:10.1155/2014/383790
Competition between visual stimuli in the monkey parietal cortex
Falkner, A. L. (2012) · doi:10.7916/d8794bpx
A theoretical and experimental dissociation of two models of decision‐making
Carland, M. A. (2014) · doi:10.71781/27734
Statistical physics approaches to neuronal network dynamics.
Cai, D., & Tao, L. (2011) · PubMed
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Caballero, J. A., Humphries, M. D., & Gurney, K. N. (2016) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/036277
Qiu, S. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.15.426814
程振波, 邓志东, & 杨博 (2009) · Science in China Series C-Life Sciences (in Chinese) · doi:10.1360/zc2009-39-8-783
Cecchini, G., DePass, M., Baspinar, E., Andujar, M., Ramawat, S., Pani, P., Ferraina, S., Alain Destexhe, A., Moreno‐Bote, R., & Cos, I. (2023) · Research Square · doi:10.21203/rs.3.rs-3241114/v1
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Inner Speech, Self-regulation and the Modular-with-Feedback-Theory of Free WillPreprint
Lugten, P., & Morin, A. (2025) · Qeios · doi:10.32388/7xgjtm
Crosstalk between delayed and immediate subjective evaluation tasks
Niu, G., & Lauwereyns, J. (2025) · Scientific Reports · doi:10.1038/s41598-025-04828-1
Nonlinear feedback modulation contributes to the optimization of flexible decision-makingPreprint
Wu, X., & Zhou, Y. (2025) · eLife · doi:10.7554/elife.96402.2
Minimal mean-field gated parietal circuit model for flexible perceptual decisionsPreprint
Lenfesty, B., Azimi, A., Bhattacharyya, S., Shushruth, S., & Wong‐Lin, K. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.09.675139
Information integration in perceptual and value-based decisions
Tsetsos, K. (2012) · UCL Discovery (University College London)
Probabilistic models for studying variability in single-neuron and neuronal ensemble activity
Ponce‐Alvarez, A. (2010) · theses.fr (ABES) · doi:10.70675/22be3a6aze6ebz4160z9c02z98d7a5e5e8c5
From neural coding to decision-making
Berlemont, K. (2020) · theses.fr (ABES) · doi:10.70675/98ad90cazb967z4ef3zb51az8213de1b171f
Βases cérébrales du compromis coûts/bénéfices
Clairis, N. (2020) · theses.fr (ABES) · doi:10.70675/5e0e9c10z2c72z4ed2zb4caz900659cedbc0
Recurrent Neural Networks models : inference, representations, and the role of regularization
Fanthomme, A. (2021) · theses.fr (ABES) · doi:10.70675/afd73818z7545z4451zb9a3zd32aa98cd0f6
Internal state dynamically gates task-specific attractor dynamics in prefrontal cortexPreprint
Osako, Y., Buschman, T. J., & Sur, M. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.05.20.726585
Cerebellar microcircuits enable robust evidence-based decisions through cortico–cerebellar coupling
Bao, Y., Yu, L., Lu, L., Yang, Z., & Zang, Y. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2616911123 · Cited by 1
Metadata
- Authors
- Wong, K.-F.
- Venue
- Frontiers in Computational Neuroscience
- Publisher
- Frontiers Media SA
- Published
- 2007
- Volume
- 1
- Pages
- 6-6
- ISSN
- 1662-5188 (ISSN-L)
- PMC
- PMC2525934
- OpenAlex
- W1993762087
- Cited by
- 204
- References
- 32
- Citations by year
- 2026: 3 · 2025: 11 · 2024: 7 · 2023: 7 · 2022: 7 · 2021: 15 · 2020: 15 · 2019: 9 · 2018: 13 · 2017: 6 · 2016: 16 · 2015: 9 · 2014: 10 · 2013: 15 · 2012: 21
- FWCI
- 4.84
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- cc-by
- Locations
- Frontiers in Computational Neuroscience (publishedVersion, cc-by)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Ulster University Research Portal (Ulster University) (submittedVersion, other-oa)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- Brandeis University
- University of Texas at Austin
- National Institutes of Health
- National Institute of Mental Health (R01MH062349)
- National Institute on Drug Abuse (R01DA016455)
- National Eye Institute (R01EY011378)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Keywords
- perceptual decision making, time integration, recurrent neural circuits, attractor networks, lateral intraparietal area, motion direction discrimination, time shift invariance
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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