Eyes on the prize: a neural basis of perceptual choking under pressure

McDonnell, M. E.; Chandrasekaran, A. N.; Ki, C. S.; Smoulder, A. L.; Miyata, H.; Yu, B.; Batista, A. P.; Smith, M. A.; Chase, S. M.

doi:10.64898/2026.09.30.755534

bioRxiv · 10.64898/2026.09.30.755534

Eyes on the prize: a neural basis of perceptual choking under pressure

McDonnell, M. E.·Chandrasekaran, A. N.·Ki, C. S.·Smoulder, A. L.·Miyata, H.·Yu, B.·Batista, A. P.·Smith, M. A.·Chase, S. M.

View original source ↗Export metadata ↓

Abstract

Even professional athletes sometimes fail to perform when it matters most. This phenomenon, known as choking under pressure, has been observed in a variety of motor and cognitive tasks. Can inordinately large rewards influence even sensory processing, and if so, what might be its neural basis? To probe this, we studied rhesus monkeys performing a challenging color change detection task and recorded from populations of neurons in visual area V4. We found that monkeys underperformed when offered rare "jackpot" rewards and uncovered associated detrimental alterations in V4 population activity. These findings were consistent with misallocated spatial attention, providing a potential neural basis for perceptual choking under pressure.

Explore related subjects

neuroscience Preprint

Keep this discovery

Explore connections, maps & timelines

BibTeX RIS

McDonnell, M. E., Chandrasekaran, A. N., Ki, C. S., Smoulder, A. L., Miyata, H., Yu, B., Batista, A. P., Smith, M. A., Chase, S. M.. 2026-10-08. Eyes on the prize: a neural basis of perceptual choking under pressure. https://doi.org/10.64898/2026.09.30.755534

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

bioRxiv2026

Human iEEG recordings during audiovisual speech violations support and extend predictive routing models

Rather than constantly reconstructing the world solely through sensory input, predictive processing theories posit that the brain utilizes predictions maintained as internal representations to guide sensory processing. An emerging model, predictive routing, proposes that an interplay between neuronal gamma (40-150 Hz) and alpha-beta (10-30 Hz) rhythms implements a dynamic mechanism for predictive processing. Namely, predictions enhance alpha-beta oscillations that suppress gamma activity during the processing of predicted inputs. While this model is supported by animal studies, its validity has not been fully explored within the human brain. The present study addresses this by leveraging human intracranial EEG (iEEG) recordings across superior temporal and prefrontal/premotor areas of seven presurgical epilepsy patients during an audiovisual speech paradigm. We calculated iEEG power in the theta, alpha-beta, and high gamma bands during simple auditory deviance, multisensory integration, and a condition where an incongruent visual cue (lip movements) clashed with an auditory stimulus (a syllable), creating audiovisual incongruence that can elicit the McGurk illusion. Results revealed increased high-gamma and decreased alpha-beta power in the superior temporal cortex in response to auditory deviance and the McGurk condition, while frontal areas, despite reflecting a similar decrease in alpha-beta power, did not present this high gamma prediction error signal. Instead, the theta band revealed a strong prediction error signal in the McGurk condition, consistent with theories on the role of theta in reorganizing cortical networks. These results both support and extend existing predictive routing models for human-specific forms of predictive processing.

neuroscience↗

bioRxiv2026

A Unified World Model in Human Posterior Parietal Cortex

How does the brain understand the physical world, predict future events, and plan actions? Are these problems solved by a unified world model, as hypothesized by cognitive scientists and artificial intelligence researchers? Posterior parietal cortex has been implicated in all these functions, but whether the same neurons support each of them is unknown. We recorded from the superior parietal lobule (SPL) of two tetraplegic participants implanted with microelectrode arrays. SPL units preferentially engaged by intuitive physics, judging block-tower stability and viewing naturalistic physical events, also predicted whether moving objects would collide hundreds of milliseconds before contact, generalizing between different physical scenarios. These populations also encoded which hand action the participant intended to perform. These findings identify SPL as a substrate for physical world modeling.

neuroscience↗

bioRxiv2026

Cortical long-range dynamics track excitation-inhibition balance across cognitive states and organizational principles

A fundamental question in systems neuroscience is how the brain's excitation-inhibition (E/I) balance shapes the temporal structure of neural activity and whether we can non-invasively recover this relationship from neural scaling properties. We show that MRS-derived E/I balance is expressed in long-range temporal dynamics and constrained by cytoarchitecture. The laminar organisation of inhibitory circuits, spanning agranular to granular cortex, determines how faithfully regional dynamics reflect E/I balance. This neurochemical signature is state-dependent: its relationship with cortical dynamics reverses during task engagement, consistent with traversal of dynamical regimes around a critical point. It extends beyond fMRI to arousal-linked dynamics, indexed by pupil diameter and microsaccades, indicating a global mode of cortical state rather than a regionally isolated property. The imprint of E/I balance on long-range dynamics follows the sensory-association axis at rest, and is reconfigured during task engagement. These findings establish E/I balance as a neurochemical quantity with structured, scalable signatures across the temporal and spatial organization of the human cortex.

neuroscience↗