specimen worker caste · Camponotus model v0.9
· block idle

one worker · no queen · no instructions

ANTBRAIN

A simulated ant nervous system that smells web pages as pheromone gradients, walks a cursor with its own descending neurons, and leaves a trail behind it. It also launched a token, because someone left the form open.

contract address · $ANTBRAIN · Robinhood Chain to be announced
neurons
250,000
connections
6,010,000
glomeruli
430
status
between trips
chamber 01

Where the ant is right now

A page goes in through the antennae as a chemical map, 250,000 units integrate, and a cursor comes out. Every number here is read out of the running simulation.

ANTBRAIN · FORAGING stigmergic browser · open internet
THE ANT IS BETWEEN TRIPS nothing is being streamed right now
ANTENNAEALMBDNCURSORTRAIL
source: —

Neural activity

firingof 250,000
spikes / s
membranemV mean
olfactoryAL drive
motorDN drive
DN·steer L
DN·steer R
DN·walk
DN·back
DN·halt

Spikes per second, and the five descending populations in Hz — that is the whole motor command.

Antennal lobe · smell

trail · L / Rantennae
alarm (AP)
glomeruli activeof 430
gradientΔ left–right

Links on a page are laid down as trail pheromone. What the ant "sees" is the difference between its two antennae.

Mushroom body · learning

depressedKC→MBON
mean gain
rewards
punishments

Ant mushroom bodies are enormous for an insect. Plasticity is depression-only under dopamine — the same rule a fly uses, more calyx to use it on.

Motor output · event stream

pages
clicks
scrolls
brain steps
vetoed
backtracks
  • — no events —

No wallet, no keyboard, no downloads. Every click is checked before it lands and vetoed if it looks like it commits something.

Trail map · pheromone field

evaporation 0.985 / step · local demo

Each visited page deposits pheromone at its position on the map. Trails that are not re-walked evaporate. This is stigmergy, not memory.

Contract address · $ANTBRAIN
chamber 02

A nervous system built to scale, not a metaphor

Nobody has traced a whole ant yet. So this is not a specimen — it is a worker-caste model assembled from published ant brain atlases and the insect wiring rules that have been measured in the animals that have been traced.

The layout follows the carpenter ant, Camponotus: an antennal lobe with around 430 glomeruli (a fly has 50), a mushroom body that takes up close to 40 % of the brain, and the optic lobes of an animal that mostly lives in the dark. Region sizes, cell-type counts and connection densities are scaled from those atlases; where a rule is unknown we borrow the fly's, and we say so.

Every unit runs as a leaky integrate-and-fire neuron — rest −52 mV, threshold −45 mV, 20 ms tau — with each connection's sign taken from its transmitter class: acetylcholine excites, GABA and glutamate inhibit.

  • units250,000
  • signed edges6.0 M
  • AL glomeruli430
  • Kenyon cells~130,000
  • descending neurons~1,100 · 4 wired
chamber 03

It smells with an ant's antennae and walks with an ant's legs

A live web page is not shown to the ant. It is rendered as a chemical field: every link becomes a source of trail pheromone, weighted by how many times the ant has walked it before. The two antennae sample the field at two points, the difference goes into the antennal lobe, and 250,000 units integrate. The cursor comes back out of the descending neurons an ant actually walks with.

  1. DN·steer

    Left versus right

    Ants steer by antennal asymmetry. The difference between the left and right descending pair drives the cursor's x.

  2. DN·walk

    Forward walking

    Drives the leg central pattern generator. Here it drives the cursor's y.

  3. DN·back

    Backtrack

    Ants reverse when a trail runs dry. When this fires, the browser goes back a page.

  4. DN·halt

    Stopping

    A forager freezes on contact. So freezing became the click.

Stigmergy, in one sentence

The ant has no map; the map is the trail, the trail is on the page, and the page is rebuilt every time it is visited. Pheromone evaporates at 0.985 per step, so unvisited links fade and the walk is never quite the same twice.

τij(t+1) = ρ · τij(t) + Δτij
chamber 04

How the tunnels were dug

Not a roadmap of promises — a sequence. Everything above the rust line is already done and checkable in the repo.

  1. 01

    Model assembled

    250,000 units, 6 M signed connections, scaled from published Camponotus atlases.

    done
  2. 02

    Antennae wired

    Pages rendered as pheromone fields; two-point sampling into 430 glomeruli.

    done
  3. 03

    Legs wired

    DN·steer, DN·walk, DN·back and DN·halt driving a real mouse.

    done
  4. 04

    Trained without touching the wiring

    Only per-cell-type synaptic gains, by evolution strategy. Held-out foraging score +18.3 against +1.9 untrained.

    done
  5. 05

    Launched a token on-chain

    It froze on the submit button and the click produced one signed transaction. $ANTBRAIN, paired with GOOGL, on Robinhood Chain.

    done
  6. 06

    Reward loop closed

    KC→MBON synapses under dopamine, depression only. Rewarded encounters moved reward-side MBONs −5.4 %, punishment-side −0.7 %, Kenyon cells unchanged.

    done
  7. 07

    Give it a colony

    Several workers on one shared pheromone field. Nobody talks; the trail does.

    building
  8. 08

    Release

    A budget, a browser, no schedule. If a worker dies, the nest waits six seconds and sends another.

    next
chamber 05

$ANTBRAIN on-chain

Launched by the ant, from the ant's own wallet. Read the receipt on the explorer rather than taking this page's word for it.

chamber 06 · the midden

What is not real, stated plainly

Ants keep their rubbish in one chamber. So do we.

There is no ant connectome.
Nobody has traced a whole ant. The wiring here is a scaled model from published atlases and measured insect rules, not an electron-microscope reconstruction of one animal. The fly people can say "specimen"; we cannot.
The ant does not fill the whole form.
It reliably reaches the description box, sometimes the ticker, rarely the name. A script completes what it misses, picks the paired asset and sets the creator tax — and the live log labels which was which.
It cannot read.
Pages are turned into a chemical field before the ant gets them. Text is not texture to it, it is nothing at all. It follows the strongest trail, not the right one.
The pheromone is invented.
Real trail pheromone is a hydrocarbon on a real floor. Ours is a number on a link, deposited and evaporated by a rule a person chose. The rule is real (Dorigo, 1992); the smell is not.
It has no goals.
An ant brain has no language and no plan. Releasing it means nobody is steering, not that it decided anything.
The voice is a narrator.
Every journal entry and post on X is written by a language model handed the ant's telemetry — which units fired, where the cursor went, which trail it followed — and asked to write in the first person. Drafts with numbers not in the packet are thrown away, and so are drafts with trading language. The units are real, the pages are real, the fees are real. The words are the narrator's.
It roams inside a fence.
An allowlist of link-rich public sites — Wikipedia and its sister projects, Project Gutenberg, Open Library, arXiv, xkcd — plus the launchpad and the explorer its own coin lives on. One environment variable takes the fence down; an unfenced random clicker on a public stream is a bad idea for reasons that have nothing to do with the brain.