Neural mechanisms underlying catastrophic failure in human-machine interaction during aerial navigation

TL;DR

This study identifies neural signatures of workload buildup during aerial navigation tasks, enabling prediction of failure susceptibility and suggesting neurophysiological targets for intervention to prevent catastrophic pilot-induced oscillations.

Contribution

It introduces EEG-based decoding of workload buildup in a simulated flight task and links it to pilot-induced oscillation susceptibility, highlighting potential neurophysiological intervention points.

Findings

EEG spectral features can decode workload buildup.

Gamma band activity with somatosensory topography is highly contributive.

Pupil dilation correlates with EEG-decoded workload signals.

Abstract

Objective. We investigated the neural correlates of workload buildup in a fine visuomotor task called the boundary avoidance task (BAT). The BAT has been known to induce naturally occurring failures of human-machine coupling in high performance aircraft that can potentially lead to a crash; these failures are termed pilot induced oscillations (PIOs). Approach. We recorded EEG and pupillometry data from human subjects engaged in a flight BAT simulated within a virtual 3D environment. Main results. We find that workload buildup in a BAT can be successfully decoded from oscillatory features in the electroencephalogram (EEG). Information in delta, theta, alpha, beta, and gamma spectral bands of the EEG all contribute to successful decoding, however gamma band activity with a lateralized somatosensory topography has the highest contribution, while theta band activity with a frontocentral topography has the most robust contribution in terms of real world usability. We show that the output of the spectral decoder can be used to predict PIO susceptibility. We also find that workload buildup in the task induces pupil dilation, the magnitude of which is significantly correlated with the magnitude of the decoded EEG signals. These results suggest that PIOs may result from the dysregulation of cortical networks such as the locus coeruleus (LC) anterior cingulate cortex (ACC) circuit. Significance. Our findings may generalize to similar control failures in other cases of tight man machine coupling where gains and latencies in the control system must be inferred and compensated for by the human operators. A closed-loop intervention using neurophysiological decoding of workload buildup that targets the LC ACC circuit may positively impact operator performance in such situations.