Living beings are not devoid of axles and wheels; rather, they are entirely composed of them, at scales and in forms compatible with biology.

At every relevant level, life relies on rotating and cyclic structures coupled through continuous material exchange. The objection to wheels in animals assumes that axles and wheels must be rigid, permanently isolated parts. Biology does not work this way. Instead of discrete components joined once and preserved unchanged, living systems implement rotation through structures that are simultaneously connected, repaired, and replaced.

Cells are full of rotary and quasi-rotary machinery. Flagella are true rotating motors with stators, rotors, bearings, and torque generation via ion gradients. ATP synthase is literally a wheel-and-axle device, converting rotational motion into chemical energy and back again. The fact that these devices operate at molecular scale does not make them conceptually different from macroscopic axles; it shows that evolution favors rotation precisely where continuous repair and material flow are required.

At larger scales, joints function as constrained rotational interfaces. Hips, shoulders, knees, and vertebrae are axles embedded in living bearings, lubricated, rebuilt, and reshaped throughout life. Bone remodeling, cartilage regeneration, and synovial fluid circulation solve the very problem claimed to prohibit wheels: permanent connection combined with continuous maintenance. The difference from artificial machines is not the absence of rotation, but the absence of rigid separability.

Even limbs themselves behave as compound wheels. Gait cycles convert linear muscle contraction into rotational motion around joints, then back into translation. Tendons wrap around bones as belts around pulleys. Muscles do not rotate indefinitely, but unlimited rotation is not a requirement for a wheel; it is a requirement imposed by certain human machines. Biological wheels rotate as much as function demands, then reverse, exactly as many engineered systems do.

The claim that active wheels require exotic motors overlooks that biology already uses fields and flows. Ionic gradients are electric fields. Blood pressure, osmotic pressure, and gas expansion are fluid-based actuators. Electric fish demonstrate macroscopic bioelectric control, and insect flight shows that indirect actuation can drive cyclic motion far from the muscle itself. The distinction between electromagnetic motors and biological motors is one of implementation, not principle.

What evolution did not produce is a detachable, externally replaceable wheel, because life does not outsource maintenance. Instead, it internalizes repair, redundancy, and gradual replacement. From this perspective, an animal is not a wheeled vehicle lacking wheels; it is a dense hierarchy of axles and wheels whose boundaries are soft, whose materials are alive, and whose motion is inseparable from their growth and repair.

Life did not fail to invent wheels. It dissolved them into itself.

They are not. Turbine engines require much higher quality manufacturing and tolerances and operate at much higher speeds and pressures. There is more to it than the perceived number of moving parts.