Predicting and controlling nonlinear neuro-mechanical locomotion dynamics

TL;DR

This paper introduces a computational framework that infers predictive neuromechanical models from neural and locomotion data, enabling accurate behavior prediction and control in animals like C. elegans.

Contribution

The authors develop a novel, data-efficient modeling approach combining spectral modes and Bayesian inference for neuromechanical dynamics prediction.

Findings

Accurately describes neural and locomotion dynamics in C. elegans.

Predicts neural activation patterns for controlling locomotion.

Framework is broadly applicable to various species.

Abstract

Neuromechanics aims to understand the link between an animal's neural activity and its physical behaviors. Recent advances in experimental and machine learning techniques enable simultaneous recordings of neural and locomotion dynamics over long time periods and across multiple behavioral transitions in worms, flies, and other organisms. These high-dimensional datasets present the challenge of inferring interpretable low-dimensional dynamical models that quantitatively connect neural activity and behavioral dynamics. However, despite major experimental and theoretical progress, there is currently no end-to-end model for predicting locomotion and other behaviors from neural activity. Here, we present a theoretical and computational framework for inferring multiscale neuromechanical models from state-of-the-art experimental data. Our data-efficient approach combines interpretable spectral mode representations with Helmholtz-Nambu decompositions and Bayesian inference to identify a predictive stochastic model that converts neural activity time series into behavioral locomotion patterns. We first apply this framework to recently published recordings of neural activity and locomotion in the roundworm Caenorhabditis elegans, showing that it accurately describes experimentally observed dynamics. We further demonstrate how the inferred model can be used to predict neural activation patterns for controlling C. elegans locomotion in real time, providing a basis for future optogenetic experiments. Due to its generic formulation, the framework introduced here is broadly applicable to neuromechanical recordings for a wide range of animal species.