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.
Most of what you have said is not different from what I have said.
All the rotating parts bigger than some tens of micrometers have only a limited rotation angle, where the limits are enforced by the solid connections between the 2 mobile parts, e.g. tendons, nerves and blood vessels.
The bacterial flagella and the rotating enzymes, which are powered by ionic currents, cannot be scaled to greater sizes. Already the flagella of nucleated cells (eukaryotes) are no longer based on rotating motors, but on contractile proteins, which must be attached at both ends on the mobile parts, limiting the relative movement.
Unlimited rotation is an absolutely necessary condition for a wheel that is used in locomotion, otherwise it is no longer a wheel.
A wheel used in locomotion that would have limited rotation would be just a leg that happens to have the shape of a wheel, because like a leg it would have to be raised from the ground for the forward motion, eliminating the exact advantage in efficiency that wheeled vehicles and tracked vehicles have over legs (i.e. that backward and forward movement are simultaneous and not separated in time during a step cycle, and no energy is wasted with a vertical oscillation of the leg).
The distinction between electromagnetic motors and biological motors is definitely one of principle and not an implementation detail. The only resemblance is that both are motors.
It is true that you can claim that when analyzing both chemical reactions and the interactions between the mobile parts of an electromagnetic motor they can be eventually reduced to electromagnetic interactions. Nevertheless such an assertion is completely useless, because most things that matter to us in the surrounding world can be reduced to electromagnetic interactions. Knowing this is not helpful at all for classifying them and understanding the differences between them.
The contraction of a protein caused by a chemical transformation and the magnetic forces that appear either between electrical currents through conductors or between electrical currents and ferromagnetic materials are very different phenomena and knowing that both of them have as primary cause electromagnetic interactions is of absolutely no help for understanding how they work or for designing either kind of motors.
Electromagnetic motors that are not extremely small need ferromagnetic materials. The only ferromagnetic material that is known to be synthesized by living beings is magnetite. Magnetite crystals can be good enough for sensing the magnetic field of the Earth, but they would be a very poor material for motors.
An easier to evolve rotating biological motor would be a rotating hydraulic motor, e.g. powered by pumped blood or lymph. This could work if the wheel would become non-living after being grown, to no longer need nerves and blood vessels. However it would be very difficult for a living being to seal the space between an axis and the rotating wheel in such a way so that blood or lymph would not spill out through the interstice.
MetaARPA tier membership (quarterly fee) is required to have HTTPS on your personal website - personal sites hosted on the main BSD cluster don’t have it.
Well I'm a dumbass! LOL!
In my defense , I've never seen those cars in real life before. I saw all the Flock cameras everywhere and just assumed they were something the police were using.
Thanks for pointing this out. I'll go ahead and give myself 10 minutes in the corner of shame.
> By default, copilot utilizes Claude Sonnet 4. We also support GPT-5 via an environment variable. Run COPILOT_MODEL=gpt-5 copilot to launch in GPT-5 mode. Or on Windows, run set COPILOT_MODEL=gpt-5 before running copilot.
> Today, when you share your Bridge’s connection with Sidewalk, total monthly data used by Sidewalk, per account, is capped at 500MB, which is equivalent to streaming about 10 minutes of high definition video.
This definitely isn't just a Scotland thing... I grew up in Alabama and this was common there, and honestly I've seen this all over rural America. It's very common for farm stands during the harvesting season.
Still, cool website, I enjoyed a few articles there even if this one was very short.
When I was a preteen kid many years ago in Massachusetts enjoying the rural summer life, we used to go around to the local farms and beg produce off the farmers. We'd then set up a card table and a cash box at the side of the road somewhere and then go off to play for the day. While we were gone, the kindly wives of the farmers we'd gotten the produce from would come and buy back the produce from us for whatever minimal price we'd set on it. So as the afternoon wore on, we'd head back and excitedly collect our change and then head to the local general store to buy penny candy.
We didn't know at the time that it was the wives buying the produced back. We just thought we were amazingly successful shop keepers.
Yes, I've seen this in rural America. Purchased some firewood at a random stand on the highway. Pick some up, leave $5 in the box. Really nice to see this sort of thing in action.
It’s more common than you think - because in many areas transporting firewood into parks, etc from more than 5/10/15 miles away is prohibited- to prevent the spread of tree pests.
Firewood is one of those things that should always be local.
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.
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