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Hastewell, A. D.

Publications and source records attributed to Hastewell, A. D..

2 recordsLinked to original sources

Takeoff dynamics are stereotyped across jumping spiders

Jumping is a challenging locomotive mode, requiring rapid force generation and precise coordination of multiple limbs. Many animals meet this challenge using elastic mechanisms that store and rapidly release energy. Jumping spiders (Salticidae), however, rely on a semi-hydraulic system that constrains how their legs can generate propulsion. Much about how these spiders reliably generate jumps within these mechanical constraints remains unknown. Here, we analyze 46 individuals spanning 14 genera and significant morphological diversity and show that this physically constrained system is coupled to a remarkably stereotyped coordination strategy. Whole-body kinematics and novel graph-based analyses of inter-limb coordination reveal a stereotyped two-stage takeoff sequence: a "swing" driven by extension of the fourth legs, followed by a rapid "fling" by the third legs that generates propulsion for takeoff. We further demonstrate that this pattern is preserved beyond Amazonian species, persisting in salticids from North America and Australia. Our results suggest that physical and biomechanical constraints may canalize locomotor evolution toward a common dynamical solution.

animal behavior and cognition↗

Embodied behavioural complexity in a ciliated microorganism

Most animals coordinate behaviour using neural computations. Yet, single-celled organisms also exhibit stimulus-responsive, even cognitive, actions. To understand how a single cell can coordinate and drive complex behaviours without any neural encoding, we study an algal protist - a motile cell with four extremely long cilia. The organism displays a surprisingly rich locomotor repertoire, emerging from the intricate dynamics of the cilia, which form a tight bundle when swimming. We leverage high-speed quantitative live imaging to extract the spectrum of possible ciliary beating patterns, and derive a dispersion relation coupling the temporal frequency and spatial wavelength of cilia oscillations. We further reconstruct the attractor manifold embedded in the behavioural space, showing that despite the range and complexity of ciliary beating modes, the underlying behavioural manifold is intrinsically low-dimensional with elaborate topological structure. Dynamic and excitable transitions in motility behaviour are encoded as trajectories in this space.

biophysics↗