Mobile defects born from an energy cascade shape the locomotive behavior of a headless animal

TL;DR

This paper investigates how an active-elastic energy cascade in a simple animal model shapes its locomotive behavior, revealing emergent low-dimensional dynamics driven by physical mechanisms rather than neural control.

Contribution

It introduces a physical model of organism locomotion based on an active-elastic sheet and demonstrates how energy cascades produce stable locomotive modes without neural input.

Findings

Energy cascades transfer power from small to large scales.

Defects in the ciliary field generate stable locomotive modes.

The model links physical defects to organism movement patterns.

Abstract

The physics of behavior seeks simple descriptions of animal behavior. The field has advanced rapidly by using techniques in low dimensional dynamics distilled from computer vision. Yet, we still do not generally understand the rules which shape these emergent behavioral manifolds in the face of complicated neuro-construction -- even in the simplest of animals. In this work, we introduce a non-neuromuscular model system which is complex enough to teach us something new but also simple enough for us to understand. In this simple animal, the manifolds underlying the governing dynamics are shaped and stabilized by a physical mechanism: an active-elastic, inverse-energy cascade. Building upon pioneering work in the field, we explore the formulation of the governing dynamics of a polarized active elastic sheet in terms of the normal modes of an elastic structure decorated by a polarized activity at every node. By incorporating a torque mediated coupling physics, we show that power is pumped from the shortest length scale up to longer length scale modes via a combination of direct mode coupling and preferential dissipation. We use this result to motivate the study of organismal locomotion as an emergent simplicity governing organism-scale behavior. To master the low dimensional dynamics on this manifold, we present a zero-transients limit study of the dynamics of +1 or vortex-like defects in the ciliary field. We show, experimentally, numerically and analytically that these defects arise from this energy cascade to generate long-lived, stable modes of locomotive behavior. Using a geometric model, we can link defects to organism locomotion. We extend this framework to study larger organisms with non-circular shape and introduce local activity modulation for defect steering. We expect this work to inform the foundations of organismal control of distributed actuation without muscles or neurons.