Specter / Flow Lenia
GARD-inspired Flow Lenia synthesis · 26 Aug 2026

The organism appears first in possibility-space.

Before a coherent body is obvious, the state already has a history-dependent map of what actions can do and which futures remain reachable. Development does not merely reveal a shape. It progressively organizes, interprets, and closes possibility.

prospective direct causal fresh cohorts predeclared secondary
The measured developmental sequence from early causal organization to selective future closure Five measured stages run left to right. At q8 the action-world is already broad. Whole-over-parts prediction rises before visible form. The information compass turns. Visible form is then certified independently. At the structural peak, fine-shape futures narrow while founder composition remains open. EARLY · q8 104.4% of q32 action-world exists BEFORE FORM whole−sum +0.364 predictive whole rises INFORMATION TURN 25% → 75% compass rotates VISIBLE FORM certified later independent detector STRUCTURAL PEAK shape −4.55% one aperture closes FINE SHAPE FUTURES aligned across P6–P12 FOUNDER MIXTURE remains open here
Read left → rightThe organization is visible in forecasts and interventions before it is obvious as a body. Later, only some kinds of future converge.
The instrument, without the fog

Can the whole forecast itself better than its best split?

We take a short history of the current state and ask how much it tells us about the next state. Then we split that state into parts and ask again. The whole-over-parts difference is our Flow Lenia analogue of integrated predictive information.

Only the past chooses the measurement or action. Later morphology stays sealed until the prediction or intervention is fixed.

How whole-over-parts predictive information is measured The same past state is forecast two ways. The whole model keeps all cross-part relationships. The best split model forecasts two groups independently. Subtracting the strongest split forecast from the whole forecast gives whole-over-parts predictive information. SAME PAST STATE Whole forecast all relationships kept I whole − Best split forecast strongest independent groups I split BEST-PARTITION WHOLE−SUM I whole − I split What is left? predictive structure the split cannot keep positive = the coordinated whole carries extra predictive structure
1 · Same evidence.
The whole and split see the identical past. 2 · Hardest comparison.
We freeze the best partition. 3 · Read the remainder.
Positive values mean cross-part organization matters.
Past window onlyfreeze split or actionthen open the future

Two related readings. The diagram shows the frozen best-partition whole−sum primary. The Φ-R MMI companion adds its redundancy correction: +0.364 and +0.171 are not numerically interchangeable.

Integrated predictive information is one partial coordinate and one useful local direction. It is not a scalar magic dial. Its strongest role here is to reveal how the action landscape is organized—and when that organization changes.
What changed our mind

The object kept getting better.

We began by looking for a number that rose before replication. The experiments pushed us toward something richer: the developing system’s counterfactual organization.

01

Fission was too literal.

Reservoir recurrence and committed morphogenesis gave us cleaner Flow Lenia events than silhouette splitting.

02

More Φ was not a universal push.

The information turn replicated prospectively, while Φ-high versus Φ-low changed sign as an actuator.

03

Fans beat endpoints.

Launching matched futures exposed canalization that one final body or one scalar score could not show.

04

The action-world was already there.

At q8, nearly identical visible states carried strongly different causal futures. Spatial scrambling broke their discipline.

05

Commitment has several apertures.

Timing, action semantics, dominant-body allocation, and fine shape do not all close together.

The evidence chain

From prediction to causal closure.

Each step asked a harder question. Does the signal appear? Does it forecast? Can we move it? Does the organism remember? Which dimensions of the future actually close?

Predictive whole

The whole moves before the visible form.

prospectivereplicated precursorspecificity unresolvedcausal atlas

Across a fresh 64-specimen cohort, 54 had complete primary windows: frozen whole−sum predictive organization rose before an independently certified sustained break from the artificial square, while the specificity contrast remained unresolved. Following that same developmental arc with exact local probes showed a second change: the actions favored by integration and by ordinary prediction stopped agreeing.

Fresh pre-form whole−sum+0.364

54 complete primary windows; 95% interval +0.231 to +0.502; 39 positive, with 15 of 16 family means positive.

Developmental atlas−1.75 → −0.32

Whole-over-parts increased by +1.43 from early development to transition; 16 of 16 families rose.

Compass rotation44 → 4

Φ-high and TDMI-high selected the same action in 44 of 64 organisms early, then only 4 at transition. TDMI along Φ flipped +2.16 → −0.73.

What “before the organism” looked like in one held-out trajectoryreal Flow Lenia fields · specimen p01-e046315a
Three grayscale Flow Lenia field frames from the same prospective trajectory. The first is a dense artificial square; by step 42 it has reorganized into an elongated striped form; by step 74 that form persists with further internal rearrangement.
The detector fires lastThe predictive rise is measured before the independently certified sustained departure from the square. These frames show the morphology only; they do not enter the past-only choice.
The system is becoming a coordinated whole before the body detector fires, and the kind of prediction that integration favors is changing as it does.
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ReportResultStatus / claim classCohortCompletion binding
organism-birth-signal-v1/before-the-creature-prospective-result.htmlorganism-birth-signal-v1/prospective-results.jsoncomplete_fresh_prospective_replication
prospective precursor replication without specificity		64 specimens; 16 families; 54 complete primary windows; 63 observed events; 1 right-censoredprospectiveCompletionSHA256 2dbf4f19d65f53490906d111f8262e10502390e5213603199dcea371634e8559
developmental-basin-atlas-v1/before-the-organism-developmental-basin-atlas.htmldevelopmental-basin-atlas-v1/results.jsoncomplete_open_ended_developmental_basin_response_atlas
open-ended causal atlas		64 specimens; 16 families; 5 phases; 1,280 trajectoriesfullCompletionSHA256 4f81f0418fc9a29da4033838c339c320d80ec1ebad38bc72982017ba82dc31e8
Causal compass

The hidden state turns before the form—but Φ is a compass, not an engine.

future-blind clockfresh cohortopen causal atlas

Past-only information geometry tracked actual developmental progress, then reproduced its turn in a disjoint cohort. But pushing the instantaneously Φ-high action did not reliably advance the visible transition. The measurement reads a real developmental coordinate; force along one local axis is not universally the mechanism.

Phase coordinateρ +0.523

Whole-over-parts versus actual progress. Exact countdown did not improve: MAE 39.88 with ordinary controls, 40.46 after adding information geometry.

Fresh turn25% → 75%

Turned-state prevalence from step 24 to 48; 33 organisms crossed into the state and only 1 crossed back.

Actuator testNo fixed sign

Φ-high minus Φ-low timing effects changed sign across four clocks. The order parameter survived; the universal one-shot control claim did not.

The information turn precedes visible formA developmental line moves from an early aligned state through a rotated information state before the visible morphology event. prediction alignedinformation turnvisible formthe compass turns first
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prospective-geometry-clock-v1/the-state-turns-before-the-form.htmlprospective-geometry-clock-v1/results.jsoncomplete_fresh_prospective_geometry_clock
future-blind prospective coordinate		64 specimens; 16 groups; 64 observed eventsfullCompletionSHA256 664cdad167dceff3fc7a880509ea32399187210bd667be862cd44be343e2a88a
geometry-turn-causal-test-v1/geometry-turn-causal-atlas.htmlgeometry-turn-causal-test-v1/results.jsoncomplete_open_causal_susceptibility_atlas
fresh prospective replication plus open causal atlas		64 specimens; 62 untouched observed events; 832 full causal futuresfullCompletionSHA256 3e2106a47f2ae33ea466bde2f6e7dc8695d5207262f0dcbd40287946a4f2e21f
From forecast to intervention

More whole-over-parts predicts a narrower timing future—and an early push can narrow later microscopic possibilities.

prospective forecastdirect causal

Every eligible state received the same full eight-action repertoire. Before visible form, higher whole-over-parts organization forecast a smaller range of transition times beyond ordinary morphology. A separate within-ancestor experiment then changed an early commitment coordinate and found that high-commitment descendants offered the same later action repertoire fewer microscopic outcomes.

Timing repertoire−0.248

Partial rank association, 95% interval [−0.420, −0.045], controlling checkpoint, shape, size, topology, and raw field change.

Same eight actions222 states

All eligible pre-transition states received untouched plus all eight fixed perturbations; 1,840 long futures.

Direct branch effect−0.0078

Mean pairwise final-field repertoire, high minus low commitment; interval [−0.0152, −0.0008].

Two independent ways that possibility-space narrowed The left panel shows the prospective association between higher whole-over-parts prediction and a smaller range of transition times, with partial rank correlation minus 0.248 and its confidence interval. The right panel shows a direct sibling intervention: the same eight later actions produced a narrower final-field fan in high-commitment descendants by minus 0.0078. PROSPECTIVE · BEFORE FORM More organized → less timing spread whole-over-parts organization → timing breadth PARTIAL ρ −0.248 DIRECT CAUSAL · MATCHED SIBLINGS Same actions → narrower field fan low-commitment fan high-commitment fan MEASURED Δ REPERTOIRE −0.0078 forecast on the left · intervention on the right · both point toward contraction
Possibility becomes measurableThe drawn fans explain the measured direction; the coefficients and intervals above are the bound results.
The information coordinate does more than correlate with appearance. It forecasts how redirectable development is, and a sibling intervention changes what later interventions can reach.
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causal-repertoire-contraction-v1/the-future-closes-before-the-organism-appears.htmlcausal-repertoire-contraction-v1/results.jsoncomplete_fresh_full_causal_repertoire_test
fresh future-blind prospective repertoire forecast		64 specimens; 222 eligible states; 9 futures per state; 1,840 long runsfullCompletionSHA256 c04c782477371fb6d504f919467f38ce280680d98157c48dfd52034d391de432
commitment-branching-intervention-v1/one-early-push-narrows-the-later-possibility-space.htmlcommitment-branching-intervention-v1/results.jsoncomplete_fresh_within_ancestor_commitment_intervention_test
direct nested causal intervention		31 fresh ancestors; 30 selected pairs; 18 futures per ancestor; 540 long runsfullCompletionSHA256 4813d53663f893d47f7ba9a992057ab1b372412c6cb063a880a49583dbd00b70
Organized action-world

The future map is already broad at q8. Spatial organization disciplines it.

fixed-age atlasexact spatial ablation

At the earliest measurable two-pulse state, visually close histories already led to strongly separated later futures. Scrambling the exact same cells—while preserving genotype, masses, composition, and world—made formation slower and its action geometry less coherent. Organization did not maximize possibility; it made possibility more structured.

q8 causal world104.4%

q8 already carried 104.4% of the q32 history-conditioned future separation.

Matched futures0.378

q8 history-conditioned future displacement, versus only 0.088 between the corresponding release states.

Scramble delays+12.85 / +22.51 / +30.59

Passages for 8×8 tiles, 4×4 tiles, and cells relative to intact. All 39 states still formed.

The action-world is not generic soup sensitivity. The early organism’s spatial arrangement makes nearby interventions more legible and constrains their distant consequences.
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initial-action-world-v1/plasticity-is-there-from-the-start.htmlinitial-action-world-v1/results.jsoncomplete_fixed_age_q8_to_q32_action_world_curve
fixed-age causal atlas		39 organisms; 156 states; 5,616 causal futures; 312 matched-history pairscompletionSHA256 7de5b00378d093bfa0dfa85fa4f4a2ce4164664436fc88765e0b777c2aa55359
spatial-scale-action-world-v1/organization-disciplines-the-action-world.htmlspatial-scale-action-world-v1/results.jsoncomplete_multiscale_spatial_ablation_of_q8_action_world
direct same-state spatial ablation		39 organisms; 4 exact spatial conditions; 5,616 causal futurescompletionSHA256 c0b1e358be4043343104691412d9709e5b86a2cffbffd9f45a190a7e743c81c4
State-setting and memory

A brief feedback policy holds the causal gate open, then the state carries itself forward.

closed-loop causalselected-future follow-up

The successful controller usually hit hard once and then stopped. Open and closed branches stayed separated after release. In the long follow-up, their field divergence grew even as the special advantage of the originally selected action vanished. The developmental state—not a perpetually privileged input—became the cause.

Post-release memory+0.075

Cumulative open-minus-closed causal-history separation; interval [+0.059, +0.090]. All 16 families positive.

Field divergence0.389 → 0.448

Open versus closed from selection frame to step 256; all 39 organisms remained separated.

Action advantage0.040 → 0.002

Max-selected minus min-selected advantage faded while the state divergence continued to grow.

The pulse ends; the two histories keep becoming differentreal paired futures · specimen s63
A two-by-two grid of real Flow Lenia fields for specimen s63. Columns compare release at step 32 with the later field at step 256. Rows compare the max-selected and min-selected feedback histories. Both histories form structured bodies, but their later morphologies remain visibly distinct.
State, not permanent forcingOne representative paired future. Across all 39 organisms, branch separation persisted after release. This is evidence of developmental memory—not a claim that Φ has one universal actuator sign.
A perturbation can set a developmental condition that outlives the perturbation. Once set, the basin carries the difference.
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commitment-gate-controller-v1/the-gate-stays-open.htmlcommitment-gate-controller-v1/results.jsoncomplete_closed_loop_commitment_gate_control_and_release_test
direct closed-loop control and release		39 organisms; 6,240 candidate probes; 2,496 release readoutscontrollerCompletionSHA256 12009169931a2b3ba330336293f006eb19bf9e9f904935419fc8704583e764fa
commitment-gate-formation-v1/the-hidden-state-becomes-a-body.htmlcommitment-gate-formation-v1/results.jsoncomplete_selected_future_visible_formation_analysis
selected-future long follow-up		39 organisms; 312 trajectories; 79,872 framescompletionSHA256 c0aa1de549c693b060ac885d63bcc63f9e9f7ba1cf2e9d43b5146bdc09500ad9
Embodied decoder

The same visible body can contain a different future.

exact hidden transplantfresh reciprocal cohort

We preserved the visible mass field at every pixel and changed only the hidden channel allocation. That invisible transplant bent later morphology toward the donor’s organism-specific future. A fresh q8↔q12 experiment then isolated a developing hidden direction that actively restrained later body growth.

Visible residualexactly 0.0

All 156 transplant starts preserved channel-summed visible fields bit-for-bit.

Donor-native pull27.9%

Mean movement along the paired donor’s native morphological direction at +128; interval [12.1%, 47.2%].

Hidden counterweight−0.096

q8→q12 hidden displacement on later radius at +96; interval [−0.156, −0.043], about 49% of natural q8→q12 growth.

A visible-field-preserving hidden composition transplant redirects the future Two organisms begin with exactly the same visible field but different hidden allocations across channels. The transplanted hidden allocation moves the later visible morphology 27.9 percent along the donor organism’s native direction, despite a starting visible residual of exactly zero. SAME VISIBLE FIELD recipient allocation SAME OUTLINE · DONOR CHANNELS transplanted allocation +128 later body leans donor-ward STARTING VISIBLE RESIDUAL exactly 0.0 MEAN MOVEMENT ALONG DONOR-NATIVE FUTURE 27.9% · interval 12.1% to 47.2%
Same pixels, different futureThe blobs are a schematic of channel allocation, not specimen screenshots; the residual and donor-ward displacement are exact bound results.
The organism is not exhausted by its visible outline. Hidden composition stores an organism-specific developmental bias, and that bias acquires causal force as the body develops.
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latent-composition-transplant-v1/the-body-stays-the-future-leans.htmllatent-composition-transplant-v1/results.jsoncomplete_hidden_composition_causal_transplant_analysis
direct visible-field-preserving transplant		39 organisms; 16 groups; 156 exact transplants; 1,248 framescompletionSHA256 b3c1354772459d0f7824dcd567c551ca9162789c3c4034dd0c45fc7ea43fe294
developmental-ignition-transplant-v1/the-hidden-future-pushes-back.htmldevelopmental-ignition-transplant-v1/results.jsoncomplete_fresh_reciprocal_hidden_age_transplant_analysis
fresh reciprocal direct intervention		64 organisms; 16 groups; 128 captures; 640 futures; 122,880 framescompletionSHA256 a20346a43025df0b7ef652d73acb1a8f3b934e7e60089959039a2d24bca7a728
Causal grammar

After the information turn, morphology becomes harder to steer and actions acquire more stable meanings.

fixed intervention panelturn fixed upstream

The same four founder interventions lost spatial leverage just after the structural turn while compositional leverage stayed open. In a two-action experiment, the later action’s spatial meaning also became less rewritable by which action came first. The organized whole is starting to impose a grammar on local inputs.

Morphological steerability−13.9%

Turn versus two passages after: +0.00290 leverage before closure, interval [+0.00049, +0.00529].

Action-geometry rewrite−11.1%

Before-minus-after rewrite +0.002935, interval [+0.000493, +0.005409].

Selective closureSpatial first

Founder-composition leverage remained open while later spatial futures became less redirectable and less context-rewritable.

Causal emergence becomes concrete here: the organism-level state increasingly constrains how local founder inputs propagate, without freezing every internal degree of freedom.
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developmental-causal-susceptibility-map-v1/the-future-narrows-here.htmldevelopmental-causal-susceptibility-map-v1/results.jsoncomplete_dense_organism_relative_causal_susceptibility_map
fixed-panel causal commitment map		19 families; 38 schedules; 2,736 futures; 32,832 decoded fieldsmanifestSHA256 45aace45f3fc07b211aa71a1930182205a869e276b38ae31784a8d215770cde8
completionSHA256 e9634826f44cf4e1e74c13bb8af6e31aca7bde21872b662dda7aa3131985ad70
developmental-causal-grammar-v1/the-organism-learns-what-actions-mean.htmldevelopmental-causal-grammar-v1/results.jsoncomplete_two_action_developmental_causal_grammar
future-blind two-action causal grammar		19 families; 38 schedules; 152 complete 4×4 panels; 2,432 trajectoriesmanifestSHA256 dbb2a36d8d77d80d895f07f6f8795f42188aab27a4aaeab8e32dce75590f4dd9
completionSHA256 3753423409b2f86c8df44da7bf4b7942c6049fb514cc2dd63962421d8409db54
Selective future closure

A Φ-directed push narrows different organism-level futures at different developmental moments.

direct causalpost-hoc coarse leadpredeclared fine-shape secondary

A source-bound post-hoc reading of one fixed early-state panel found that Φ-forward made eight unseen futures agree more about which connected body would dominate; the frozen primary in that study was unresolved. In the three-age follow-up, the coarse primary again stayed unresolved—but at each organism’s structural peak, the predeclared fine-morphology panel converged cleanly. The futures did not become identical; one morphological aperture narrowed.

Post-hoc dominant-body lead−0.01358

Φ-forward minus Φ-backward; interval [−0.02509, −0.00181]; 14 of 19 families narrowed.

Fine shape at peak−4.55%

Pairwise shape distance −0.00399, interval [−0.00713, −0.00117]; 13 of 19 families narrowed.

Delayed effectP6–P12

Every fixed passage interval from 6 through 12 pointed toward canalization. Founder mixture and coarse body organization stayed open.

Measured fine-morphology canalization contrast by passageActual family-clustered point estimates and 95 percent intervals for backward minus forward pair distance at passages one through twelve. Positive values mean Phi-forward futures were narrower. Every interval from passage six through twelve is above zero, while the point estimates are visibly non-monotonic. 0.004.008.012 backward − forward pair distancepositive = Φ-forward futures narrower P1P3P6P9P12 P6–P12 · every 95% interval above zero

Actual estimates and family-clustered 95% intervals—not a smoothed developmental trajectory. The effect is directionally consistent from P6 onward, but its magnitude wiggles.

The strongest current reading is multidimensional commitment: development closes specific families of future—not all possibility at once, and not through one universal scalar knob.
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tangent-future-aperture-v1/the-future-chooses-a-main-body.htmltangent-future-aperture-v1/exploration.jsoncomplete_post_hoc_source_bound_exploration
post-hoc direct-intervention lead; frozen primary unresolved		19 families; 38 schedules; 4 treatments; 1,216 trajectories; 8 futures per treatmentmanifestSHA256 f50ead16920b9749a029a728c946459d863cbf172ac1b9ab341a7acfbd60c8b2
completionSHA256 29dad2bbd870ff2eff907f8b31a93e0904b1f31c95d1af602d5008db3588e69f
developmental-commitment-aperture-v1/the-shape-space-closes-late.htmldevelopmental-commitment-aperture-v1/results.jsoncomplete_source_bound_future_blind_analysis
predeclared secondary direct causal result; coarse primary unresolved		19 families; 38 schedules; 3 timings; 4 treatments; 3,648 trajectories; 8 futures per treatmentmanifestSHA256 9d123a6fff24d9675dd0c692c98a214299194b4edef0c15d64339403077eb952
completionSHA256 cc947fc2bf181f4f263312b0c7a7d0710afce04c2a61fd1e66ce84d92d356de1
developmental-commitment-aperture-v1/the-shape-space-closes-late.htmldevelopmental-commitment-aperture-v1/morphology-timing-exploration.jsoncomplete_source_bound_secondary_and_descriptive_analysis
source-bound predeclared secondary and descriptive timing analysis		19 families; fixed P1–P12 morphology panelmanifestSHA256 9d123a6fff24d9675dd0c692c98a214299194b4edef0c15d64339403077eb952
completionSHA256 cc947fc2bf181f4f263312b0c7a7d0710afce04c2a61fd1e66ce84d92d356de1
The synthesis

Commitment is selective closure.

The organism does not arrive in one instant. Different counterfactual freedoms close on different schedules. That is why one scalar sometimes predicts beautifully, sometimes acts weakly, and sometimes points to a very specific causal aperture.

Different dimensions of possibility close on different developmental schedules Five lanes span early development, the information turn, visible formation, structural peak, and later futures. Timing narrows before form. Action meaning stabilizes after the information turn. Dominant-body allocation is tangent-sensitive in a post-hoc result. Fine morphology narrows from passage six to twelve after intervention at the structural peak. Founder mixture remains open in this panel. EARLY INFO TURN VISIBLE FORM PEAK → FUTURE Timing repertoire narrows before form partial ρ −0.248 Action meaning stabilizes after turn context rewrite −11.1% Dominant body tangent-sensitive lead −0.01358 · post-hoc Fine morphology closes late · −4.55% all fixed P6–P12 align Founder mixture remains open in this experiment THE CLAIM IS ASYNCHRONOUS, SELECTIVE CLOSURE — NOT ONE GLOBAL FREEZE
Five apertures, five schedulesHorizontal position shows developmental order. Fan width is explanatory; labels carry the measured effects and evidence class.
One decisive next replication

Freeze the shape claim as the only primary.

This is the experiment that turns the newest signal from a strong predeclared secondary result into a clean headline result.

1

Fresh, unseen cohort

Sample new organic families and new matched future worlds. No reuse of the 19-family outcome panel.

2

Endogenous timing

For each organism, find its structural peak from past-only information geometry and intervene there.

3

Five matched arms

Φ-forward, Φ-backward, orthogonal, score-blind, and untouched—same local dose, same future seeds.

4

One sole primary

Translation-normalized pairwise fine-morphology distance over future passages P6–P12, analyzed by family.

5

One hard question

Does Φ-forward again compress the future shape fan relative to backward, orthogonal, blind, and untouched controls?

No experiment has been launched from this report. The point is to stop here, share the cumulative result honestly, and make the next run maximally decisive.
Open the source-bound evidence ledger · 17 result artifacts

Result SHA-256 values bind the exact JSON read for this synthesis. Completion or manifest SHA-256 values are copied from each bound result artifact.

Experiment / reportResult path · SHA-256Result statusClaim classCompletion / manifest binding
organism-birth-signal-v1/before-the-creature-prospective-result.htmlorganism-birth-signal-v1/prospective-results.json
c6e3c6634d04de86ee89f5d11dec423e936befe81e022240a82dbdbc85daf963		complete_fresh_prospective_replicationprospective precursor replication without specificity · 64 specimens / 16 families; 54 complete primary windowsprospectiveCompletion 2dbf4f19d65f53490906d111f8262e10502390e5213603199dcea371634e8559
developmental-basin-atlas-v1/before-the-organism-developmental-basin-atlas.htmldevelopmental-basin-atlas-v1/results.json
bf1e0f3a082f256747f2d80f054a9d590f34ae9db28a83a6f6b9aa81d2fd2b1a		complete_open_ended_developmental_basin_response_atlasopen-ended causal atlas · 64 specimens / 1,280 trajectoriesfullCompletion 4f81f0418fc9a29da4033838c339c320d80ec1ebad38bc72982017ba82dc31e8
prospective-geometry-clock-v1/the-state-turns-before-the-form.htmlprospective-geometry-clock-v1/results.json
269d280de5e93b8b93882ff900c41fb1f2750a256dfb145e284cbeca2cf4d742		complete_fresh_prospective_geometry_clockfuture-blind prospective coordinate · 64 specimensfullCompletion 664cdad167dceff3fc7a880509ea32399187210bd667be862cd44be343e2a88a
geometry-turn-causal-test-v1/geometry-turn-causal-atlas.htmlgeometry-turn-causal-test-v1/results.json
98a5aa04dba2c35aacd0035fbbb0747c8d792cffc276e7ff480d3f80172a693e		complete_open_causal_susceptibility_atlasfresh replication plus open causal atlas · 64 specimensfullCompletion 3e2106a47f2ae33ea466bde2f6e7dc8695d5207262f0dcbd40287946a4f2e21f
causal-repertoire-contraction-v1/the-future-closes-before-the-organism-appears.htmlcausal-repertoire-contraction-v1/results.json
9fe83df68e0e2cef8ba487673e4bf1005cacc5bb1dbbf84c963b90d8d2602fd4		complete_fresh_full_causal_repertoire_testfuture-blind prospective repertoire forecast · 222 states / 1,840 futuresfullCompletion c04c782477371fb6d504f919467f38ce280680d98157c48dfd52034d391de432
commitment-branching-intervention-v1/one-early-push-narrows-the-later-possibility-space.htmlcommitment-branching-intervention-v1/results.json
2ccd2af0ed14f2f329ca31fc982f0e1e0d314681db43ba9fd2994c2e586dcf64		complete_fresh_within_ancestor_commitment_intervention_testdirect nested causal intervention · 30 sibling pairs / 540 long futuresfullCompletion 4813d53663f893d47f7ba9a992057ab1b372412c6cb063a880a49583dbd00b70
initial-action-world-v1/plasticity-is-there-from-the-start.htmlinitial-action-world-v1/results.json
99727f878bab51518dddfb618cec0cd98c15bb6fe8b3667f515adb6d933e4817		complete_fixed_age_q8_to_q32_action_world_curvefixed-age causal atlas · 39 organisms / 5,616 futurescompletion 7de5b00378d093bfa0dfa85fa4f4a2ce4164664436fc88765e0b777c2aa55359
spatial-scale-action-world-v1/organization-disciplines-the-action-world.htmlspatial-scale-action-world-v1/results.json
6b3a76b4eb347010d9cb14a9bf57d1c70c69f4612a1bf7fee1b41fb57537f186		complete_multiscale_spatial_ablation_of_q8_action_worldexact direct spatial ablation · 39 organisms / 4 statescompletion c0b1e358be4043343104691412d9709e5b86a2cffbffd9f45a190a7e743c81c4
commitment-gate-controller-v1/the-gate-stays-open.htmlcommitment-gate-controller-v1/results.json
7969f195c566d69717b1430095266bab6132472e42d380015e273a46e5b71fc6		complete_closed_loop_commitment_gate_control_and_release_testdirect closed-loop control and release · 39 organismscontrollerCompletion 12009169931a2b3ba330336293f006eb19bf9e9f904935419fc8704583e764fa
commitment-gate-formation-v1/the-hidden-state-becomes-a-body.htmlcommitment-gate-formation-v1/results.json
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latent-composition-transplant-v1/the-body-stays-the-future-leans.htmllatent-composition-transplant-v1/results.json
785e801c2f7c8ad7feba79c25463f195efe55467677f8f04eb78bd28a1b68888		complete_hidden_composition_causal_transplant_analysisdirect exact-field transplant · 39 organisms / 156 runscompletion b3c1354772459d0f7824dcd567c551ca9162789c3c4034dd0c45fc7ea43fe294
developmental-ignition-transplant-v1/the-hidden-future-pushes-back.htmldevelopmental-ignition-transplant-v1/results.json
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developmental-causal-susceptibility-map-v1/the-future-narrows-here.htmldevelopmental-causal-susceptibility-map-v1/results.json
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completion e9634826f44cf4e1e74c13bb8af6e31aca7bde21872b662dda7aa3131985ad70
developmental-causal-grammar-v1/the-organism-learns-what-actions-mean.htmldevelopmental-causal-grammar-v1/results.json
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completion 3753423409b2f86c8df44da7bf4b7942c6049fb514cc2dd63962421d8409db54
tangent-future-aperture-v1/the-future-chooses-a-main-body.htmltangent-future-aperture-v1/exploration.json
aa28dfa388708b7679acce9b7845f48922d9f1886e2bc2a733bef9198d943b23		complete_post_hoc_source_bound_explorationpost-hoc direct-intervention lead; frozen primary unresolved · 19 families / 1,216 trajectoriesmanifest f50ead16920b9749a029a728c946459d863cbf172ac1b9ab341a7acfbd60c8b2
completion 29dad2bbd870ff2eff907f8b31a93e0904b1f31c95d1af602d5008db3588e69f
developmental-commitment-aperture-v1/the-shape-space-closes-late.htmldevelopmental-commitment-aperture-v1/results.json
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completion cc947fc2bf181f4f263312b0c7a7d0710afce04c2a61fd1e66ce84d92d356de1
developmental-commitment-aperture-v1/the-shape-space-closes-late.htmldevelopmental-commitment-aperture-v1/morphology-timing-exploration.json
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completion cc947fc2bf181f4f263312b0c7a7d0710afce04c2a61fd1e66ce84d92d356de1