The future map comes first.
Development begins with causal multiplicity.
This is not an early hint that later becomes a causal landscape. At the first window we measured, the landscape is already mature.
The action world starts high and stays high.
Each point is the distance between futures reached through different histories while final Φ‑R is held approximately fixed. The curve is flat from 28.5 passages before formation through the crossing itself.
None of the first two eight-passage transitions changes the future displacement detectably. The only clear adjacent change is a small decline approaching the near-event state: -0.007, 95% interval -0.012 to -0.001.
Morphology progressively folds around that map.
The same matched-history distance measured directly in the release state grows at every developmental step. From earliest state to crossing it rises by 21.0%.
Future map
Already mature at the earliest measurement.
State geometry
Deepens steadily as formation approaches.
Interpretation
Development writes an existing causal multiplicity into increasingly distinct bodies.
The early system has more freedom over when it forms.
At the earliest window, four information-directed histories spread the same later morphology event across almost six passages. By the crossing state that range has fallen to about three—a 50% contraction.
The route direction is not universally “faster” or “slower”; it depends on organism, ending level, and local state. The stable phenomenon is broader timing leverage early and narrower leverage near commitment.
The visible change is gradual.
This organism's certified transition is q56. The five images span the exact interval analyzed. Nothing in the first image announces that its intervention-response map is already as separated as it will be near q56.
Four near-matched presents.
At q24—32 passages before this organism's certified event—the four history-conditioned states are hard to distinguish by eye. The median matching gap across the cohort is only 1.64% of the local Φ‑R range.
Four visibly different futures.
Apply the same c04 intervention after release and follow each state to q900. The small-looking early differences reorganize the later form. Across the cohort, the history displacement is roughly one full local repertoire width.
Commitment is a transfer of structure.
later: stable future map + deeper body fold + narrower timing freedom
The system does not acquire a future map when it becomes visibly organized. It begins with multiple history-dependent futures, then progressively converts that hidden organization into morphology while losing freedom over the timing of formation.
A useful name for this is causal-first development: causal response structure leads; visible form consolidates it.
Was the future map inherited—or self-assembled?
We still have not found its beginning. The earliest relative window was already too late. The next experiment goes to fixed absolute ages: the first possible two-pulse sheet, then q8, q16, q24, and q32. That will tell us whether the action world is present almost immediately after initialization or rises during the ecology's earliest self-organization.
If it is immediate, we compare against scrambled/spatially rearranged founder controls. If it rises, we intervene at the rise and ask whether redirecting it changes which form later consolidates.