8,928 q48 frames · every direction age · every zero-net history

The mature body frays
before it divides.

The q48 component signal is real—but it is not full fission. Hidden order changes the connectivity of tiny, mid-density peripheral structures while leaving macroscopic daughter incidence almost unchanged. We found a density-specific topological susceptibility.

+0.345direction-specific microcomponents at the original 13/255 body threshold
-0.278same response in the dense 51/255 core—the sign reverses
+0.20%detached mass-share shift; interval crosses zero
+1.7 ppchange in incidence of a ≥5%-mass secondary body
01 / Follow the components

More blobs did not mean more daughters.

The native order creates +0.339 extra thresholded components across the q48 future, and the direction-specific contrast is +0.329. But almost all of that signal disappears when each component must carry even 0.25% of the body’s field mass.

+0.00+0.25+0.50all componentsmicro <0.25% mass≥0.25% mass

All thresholded components

+0.329 [+0.069, +0.654]

The original topology panel is reproducible across the whole future.

Microcomponents

+0.345 [+0.151, +0.560]

Seven of eight family groups carry the effect.

Meaningful-mass components

-0.016 [-0.134, +0.110]

The added count is not macroscopic daughter production.

q48 cancel first grayscale body
cancel first
raw field
q48 cancel first component map at 13 of 255
cancel first
13/255 topology
q48 cancel first component map at 51 of 255
cancel first
51/255 dense core
q48 amplify first grayscale body
amplify first
raw field
q48 amplify first component map at 13 of 255
amplify first
13/255 topology
q48 amplify first component map at 51 of 255
amplify first
51/255 dense core

Mechanically selected source 14, q48 direction, release +4: its full-future native component-order effect is closest to the cohort mean. Component map: cream = largest body; cyan = detached component carrying at least 0.25% of total field mass; orange = microcomponent below 0.25%.

02 / The topology has a depth

The causal effect lives in one density shell.

At 5/255, the diffuse halo remains connected and the order effect is small. At 13/255, the peripheral structure splits into extra islands. By 51/255, the microcomponent response has inverted. Hidden order is changing the stratification of connectivity through the body, not merely adding noise.

-0.50+0.00+0.505/25513/25526/25551/25577/255density threshold defining the body’s connected topology
all component-count specificitymicrocomponent specificity

13/255 surface band

+0.345 [+0.151, +0.560]

More mid-density peripheral islands under native cancel-first order.

Density-shell inversion

+0.624 [+0.212, +1.053]

13/255 minus 51/255 microcomponent specificity. The response genuinely changes sign through the body.

The mature organism behaves like a stratified material near a connectivity transition. A hidden information direction changes which density shell percolates into one body.

03 / What it does—and does not—move

Surface topology changes before mass partitioning.

Detached mass share changes by only +0.20 percentage points, and the second component’s mean mass share changes by +0.11 points. Neither is cleanly separated from zero.

Detached mass

+0.00198 [-0.00299, +0.00695]

Connectivity changes without a comparable redistribution of total matter.

≥5% daughter incidence

+0.017 [-0.028, +0.062]

Cancel-first does not make large daughter events more common at this dose.

≥5% spell duration

+0.535 [+0.191, +0.917]

When large separations happen, cancel-first tends to prolong them by about half a sampled frame—an intriguing lead, not yet a direction-specific result.

This is not a failed fission experiment. It identifies a causal precursor layer: the body’s surface connectivity moves before daughter mass does.

04 / The next direct swing

Push the surface transition until it becomes a daughter.

Dose

Scale the same q48 direction across a wide dose range and map when microfraying becomes a macroscopic second body.

Duration

Hold the drive for different pulse lengths and ask whether the connectivity shell develops memory or hysteresis.

Lineage

Track mass, separation, survival, and independent motion continuously—no single component threshold decides the answer.

The bold hypothesis is now concrete: information geometry may control a topological phase transition in the mature Flow Lenia body. The current dose reaches surface fraying. The next experiment asks where full fission begins.