Ostriches are the fastest bipedal runners alive (up to ~70 km/h) because of a real spring-mass leg: the gastrocnemius–Achilles tendon complex stretches and recoils like a spring, storing and returning elastic strain energy each stride instead of paying for it all with muscle. This lab runs two mechanically distinct models of a single effective stance leg, switched automatically by the walk→run transition:
Walk (v < v_t): compass-gait inverted pendulum
θ'' = (g/L)·sinθ (rigid strut, continuous contact)
ω+ = ω-·cos(2α)·η (heel-strike collision loss)
Run (v ≥ v_t): damped spring-leg (SLIP)
F_leg = k·(L0−ℓ) − c·ℓ' (stance, ℓ = leg length)
x'' = 0, y'' = −g (flight, aerial phase)
v_t = √(Fr_c·g·L0), Fr_c ≈ 0.5
Touchdown angle is set each step by a proportional speed controller (α adjusts toward the target speed slider — the same strategy hopping robots and running animals use to regulate stride without a fixed gait plan). The tendon-efficiency slider (η) scales the velocity that survives heel-strike in the walk and the internal damping coefficient (c) in the run; "measured energy return" compares actual mechanical energy just after push-off to just before touchdown, so it reflects what the dynamics really did, not just the slider value.
- Ground reaction force — vertical stance force in multiples of body weight; running shows a single bell-shaped peak per step, walking a flatter double-hump.
- Froude number — v²/(g·L), the dimensionless speed used across biomechanics to predict the walk-run transition independent of body size.