The future comes first.
At q8 the action-world is already as separated as at q32, and a whole-over-parts signal rises before sustained visible structure.
Flow Lenia is a continuous, multichannel field that can reorganize into organic-looking bodies. We asked when its future first becomes constrained as an individual, and how that constraint changes what interventions can do. We compared prospective forecasting, exact future fans, closed-loop controls, releases, and hidden-composition transplants. Across them, the organism appears in possibility space before silhouette; development then makes it harder to rewrite without forcing siblings toward one shape.
At q8 the action-world is already as separated as at q32, and a whole-over-parts signal rises before sustained visible structure.
A specimen-or-genotype-specific response is re-identifiable across the earliest interval tested, q12→24. Its onset is left-censored.
Timing and spatial leverage harden while sibling shape spread widens. Rigidity is not convergence.
Flow Lenia is a continuous, multichannel field. We ask whether its present state constrains its future as a coordinated whole, how interventions reshape that future, and whether the response later becomes individually recognizable.
The whole-over-parts instrument compares how well the full state forecasts its next state with the strongest tested separable split. A positive change means the whole is catching up with that split. It is not IIT Φ, and in the prospective precursor the absolute whole-minus-sum level remains negative: the best split still forecasts better at every phase.
The campaign therefore does not rest on a single score. It triangulates information, direct interventions, held-out releases, exact visible-state controls, and hidden-composition transplants.
Run matched interventions or noise futures from the same checkpoint and measure how far their outcomes spread.
The visible field sums channels. Different channel mixtures can be exactly invisible in that sum while changing later response.
Frozen tests answer predeclared questions. Post-hoc panels are valuable for mechanism and next experiments, but do not inherit that status.
Two early facts arrive by different routes: the fresh prospective whole-over-parts relation rises, while a fixed-age descriptive assay finds alternative-action futures already richly separated at q8.
95% interval +0.231 to +0.502; 39/54 eligible windows and 15/16 family means positive. This is catch-up, about 4% of the whole-state ~8.76 nats—not whole-state dominance.
Controls move from 0.8089 to 0.8093 when whole−sum is added. Specific event prediction is unresolved.
Whole−sum predicts a narrower future timing range after checkpoint, shape, topology, size, and raw-change controls; interval −0.420 to −0.045.
Future-history separation at q8 is 104.4% of q32 across 39 organisms and 5,616 futures.
Past-only geometry tracked developmental progress—39 of 62 trajectories were strictly monotone—but adding it did not improve held-out countdown error (39.88 steps with ordinary controls, 40.46 with geometry). Direct Φ-high versus Φ-low intervention effects also changed sign with phase.
The information geometry was useful as a coordinate. It was not a universal button that advanced development.
The system loses particular degrees of freedom on different schedules: timing futures contract, spatial interventions lose leverage, and action meanings become less context-sensitive. Other degrees remain open.
Higher prospective whole−sum predicts less timing spread across nine matched futures. Fresh, future-blind cohort.
Cumulative open-minus-closed causal-history distance after release; interval +0.059 to +0.090, 16/16 family directions.
Turn minus two passages later; interval +0.00049 to +0.00529. The predeclared four-passage persistence rule failed.
Before-turn minus after-turn context rewrite; interval +0.000493 to +0.005409 across 19 families.
The strongest prospective relation is to timing-range contraction. A direct nested branching primary on timing itself was null; a predeclared fine-field secondary shifted by roughly 2.3%.
Scrambling the same cells while preserving genotype, mass, composition, and world slows formation by 12.85, 22.51, and 30.59 passages at successively finer scrambling scales.
The six-edge geometry of second-action outcomes changes less across first-action contexts after the turn.
Initialization-perturbed width grows from 0.032 at age 60 to 0.079 at age 900. “Commitment” is individuation plus rigidity, not convergence.
Across 156 transplant starts, visible fields were bit-for-bit identical while hidden channel composition differed. The frozen donor-axis primary was null, +0.050 [−0.258,+0.370], and hybrids were farther from donor than host in all 16 families. Yet a predeclared secondary followed 27.9% of the donor’s natural growth direction [12.1%,47.2%], 14/16 families, with strong directional asymmetry.
A fresh older-composition ignition test did not shift the developmental clock. A separate post-hoc counterweight found hidden displacement restrained later radius, −0.096 [−0.156,−0.043]. Together: hidden composition changes futures, but not as a simple donor identity or older-state clock. frozen posthoc
Four sibling tests turned one narrow “fine-shape closure” story into a richer one: push susceptibility falls with age, but siblings do not converge and a fresh confirmation cannot resolve the original tiny shape effect.
The earlier −0.00399 fine-shape result was one predeclared secondary contrast, but its structural-peak timing arm was selected post-hoc and only 5 of 78 predeclared contrasts resolved. The fresh 12-family experiment made that shape contrast its sole primary and returned an interval crossing zero.
Interval −0.0076 to +0.0038; six families each direction; no arm contrast separates from zero. The earlier −0.0040 remains within what 12 families could miss.
Pre-turn pushes move later futures more than post-turn pushes; interval +0.00185 to +0.00545, 15/16 families. Push divergence falls about 69% with age.
The frozen prediction expected positive early-minus-late width. Every family goes the other way.
Matched-present future-distance ratio does not rise cleanly. A separate pre-named lookalike count collapses 6,144→1,665 with ρ −0.988.
Across 64 organisms, 16 groups, 19 ages, and 7,296 futures, fixed writes retain the same affected-matter fraction yet lose downstream leverage. This is development-wide damping, not an information-turn-locked transition.
Late minus early difference; interval −0.002155 to −0.001579, all 16 families.
Realized matter L1 falls 56.94→34.18, but D4 per physical write still falls to factor 0.0799 [0.0661,0.0969].
Only 1,880 of 3,648 selected matches lie within 25% of target; early dose-floor fallback was used in 401/768.
On common support, D120 and D240 damping remain −0.00461 and −0.00889, all 16 families.
The corrected frozen comparator includes sham, replay, and the strongest local controller per instance. Under that protocol, active whole-state achievement survives; whole-over-best advantage and developmental gain do not.
The frozen plan included sham=0 in the maximum comparator. The original analysis omitted it. Corrected result SHA 4b30ab79… replaces the original result SHA 25e2802b… for every joint-decision claim.
Interval +3.4167 to +5.0271; 16/16 family directions. Active achievement survives correction.
Interval -0.6762 to +1.2916; strongest per-instance sham/replay/local comparator. Null.
Interval -0.5633 to +1.6612. Null.
Interval -11.2502 to -2.7983; 12/16 families negative. The advantage reverses after release.
A response fingerprint can re-identify the source specimen across development after removing the linear component of 17 predefined passive summaries. Because each specimen has a unique genotype, the safe claim is specimen-or-genotype-specific.
Top-1 retrieval versus frozen 99% permutation threshold 7/72; residual margin +0.23063 [0.18599,0.27062].
Within same source quartet, margin +0.19440. The signal is not merely broad group separation. Post-hoc.
Hidden-composition fingerprint is strong; strict-quartet retrieval reaches 63/72. Post-hoc.
t8 and t32 fail; field response passes while scalar-only response does not. This maps where the address lives. Post-hoc.
These panels replay existing receipts only. They are explicitly post-hoc and identify the next frozen discriminators; they do not change the frozen passport decision.
An independent source-bound implementation recovered the primary passport and transplant quantities without numerical drift.
q12→q24 residual margin against only the other three members of each frozen quartet; interval [0.143, 0.245], 17/18 groups positive. Within-quartet top-1 is 59.7% against 25% chance.
Visible-field features pass the frozen gate; 384 scalar features alone do not. The scalar margin interval [-0.008, 0.082] crosses zero.
Each bar is the q12→q24 residual same-specimen margin. Isolated t8 and t32 slices do not pass the frozen gate; t128 does.
Native and orthogonal probes, and positive and negative signs, each pass when isolated. Their similar margins point to a distributed reaction structure.
All four anchors retain positive mean margins; A03 alone misses its own permutation gate. The signature is broad, but not spatially uniform.
Across 432 hidden-response features, q12→q24 top-1 is 45.8% and within-quartet top-1 is 87.5%. This still cannot separate specimen identity from genotype because every specimen has a unique genotype.
Pooled visible top-1 falls below its 8.3% null bound, yet the strict within-quartet margin is 0.236, within-quartet top-1 is 56.9%, and hidden top-1 remains 36.1%. This is pooled-visible address reorganization and crowding, not loss of individuality.
Aligned-near minus phase-scrambled donor-axis projection at q24 and q48. Both intervals cross zero. Near-donor host-response distance exceeds self re-encode by 40.23 at q24 and 21.64 at q48, showing disruption without donor-passport specificity.
The combined evidence supports a developmental causal individual—not a unique final morphology, a magic Φ lever, or an autonomous replicator.
A pre-form state already supports a structured action-world and a prospective whole-over-parts rise. The informative object is the space of possible continuations, not only the current image.
Timing, spatial leverage, and action-context rewrite harden. Sibling basins widen, so commitment is selective closure within plural morphology.
Feedback moves target scores during the active window. It gains no corrected unique whole-state advantage, and the comparative whole-policy advantage reverses after release.
By the earliest tested interval, a distributed causal response predicts specimen-or-genotype across time beyond 17 linear passive summaries.
These are developmental organisms and exact intervention assays, not a demonstration of endogenous replication.
Specimen and genotype are confounded; the transplant fails a donor-specific transfer contrast.
Information, morphology, impedance, action grammar, and retrieval have related but non-identical clocks.
The next experiments should discriminate mechanisms that the present corpus has made separable—not just rerun the same tiny contrasts with more seeds.
The campaign contains 98 experiment folders, consequential nulls, wrong-way results, sealed aborts, and one material protocol correction. They are part of the result.
| Experiment | Outcome | What changed |
|---|---|---|
| reservoir-causal-steering-v1 | primary chain not met | 1,920 trajectories; onset reward and Φ-specific steering failed. The campaign moved from universal steering to developmental coordinates. |
| geometry-turn / countdown | null as lever / null countdown gain | Geometry tracks progress; it does not universally advance the transition or improve held-out countdown. |
| tangent-induced causal grammar | primary unresolved; secondary wrong way | The first-action memory secondary moved opposite the proposed grammar stabilization direction. |
| developmental causal plasticity window | null | Structural peaks did not generalize into broad fanout windows. |
| fresh organic q40 replication | null | Spearman ρ +0.093, interval −0.178 to +0.352. |
| causal compass peak | null | Primary +0.0023, interval −0.0028 to +0.0073. |
| commitment branching | timing primary null | A predeclared fine-field secondary suggested a small contraction, motivating direct confirmation. |
| latent / ignition transplant | frozen primaries null | Hidden composition affects future direction, but primary donor-axis and older-clock transfer claims failed. |
| fine-shape confirmation | unresolved | The original small secondary remains possible but unconfirmed; shape closure is no longer the central conclusion. |
| basin-width init variation | wrong direction | Siblings widen across age. Rigidity and convergence are different axes. |
| whole-control tournament | corrected joint primary null | Original pass superseded after restoring sham to the frozen comparator; active achievement remains real. |
| causal passport transplant | donor-specific contrast null | Aligned transplant does not beat phase-scrambled. Generic disruption is not portable identity. |
| five sealed aborts | stopped | goal-state bite calibration; goal-state matched-wound recovery; perturbation-recovery engineering v1/v2; reservoir-cycle emergence census. |
| three mechanical stops | no verdict | goal-state tomography 0/8 valid; preinjury predictor feature unavailable; orthogonal pulse release declaration never bound after qualification abort. |
| Role | Bound source | SHA-256 |
|---|---|---|
| audited synthesis-v4 canonical predecessor and embedded native montages | evidence-source/gard-compositional-causal-emergence-v1/synthesis-v4/the-organism-appears-first-in-possibility-space.html | 69107dac3f182d4876e3bafe167f33a711c693c68f6f15e1c9a65fc7873af0fd |
| cold-reader vocabulary and onboarding design reference; not a claim source | evidence-source/gard-compositional-causal-emergence-v1/synthesis-v4/jana-shareable-flow-lenia-causal-emergence.html | b20cf14e68213fc6a06bb2e7f7c449622604008b7f95042b71bdc91558eaa88b |
| fully audited synthesis-v5 predecessor | evidence-source/gard-compositional-causal-emergence-v1/synthesis-v5/the-body-learns-its-own-response.html | a9539ecc2dfddc963bd9476b126e369ca28f0ed0eaa0cdeaedec6c8c97a360a5 |
| fully audited synthesis-v5 provenance manifest | evidence-source/gard-compositional-causal-emergence-v1/synthesis-v5/source-manifest.json | 60f34545ebae16a529a93c864f7e16f242557e5bc08d8c3c4de7b7e73be1dff5 |
| fully audited synthesis-v5 chart and image renderer | evidence-source/gard-compositional-causal-emergence-v1/synthesis-v5/build_report.py | 419d60eb54b703f5eafbdd8c1d4f5579a5b97a0db9187d458f928a89a4e19407 |
| shared Specter paper-sheet style | evidence-source/gard-compositional-causal-emergence-v1/_report-style/specter-report.css | a28376706e9e68b08ed3d8e07cbe97c7b63be4817de94e0bf55c67a1184c09ce |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/organism-birth-signal-v1/prospective-results.json | c6e3c6634d04de86ee89f5d11dec423e936befe81e022240a82dbdbc85daf963 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/developmental-basin-atlas-v1/results.json | bf1e0f3a082f256747f2d80f054a9d590f34ae9db28a83a6f6b9aa81d2fd2b1a |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/prospective-geometry-clock-v1/results.json | 269d280de5e93b8b93882ff900c41fb1f2750a256dfb145e284cbeca2cf4d742 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/geometry-turn-causal-test-v1/results.json | 98a5aa04dba2c35aacd0035fbbb0747c8d792cffc276e7ff480d3f80172a693e |
| post-hoc geometry-turn discovery map | evidence-source/gard-compositional-causal-emergence-v1/geometry-turn-causal-test-v1/open-discovery.json | 2074c1bd5abcfef399d5070f1d0b2f1c551ab8ec138d6d36e69bd58272a29753 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/causal-repertoire-contraction-v1/results.json | 9fe83df68e0e2cef8ba487673e4bf1005cacc5bb1dbbf84c963b90d8d2602fd4 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/commitment-branching-intervention-v1/results.json | 2ccd2af0ed14f2f329ca31fc982f0e1e0d314681db43ba9fd2994c2e586dcf64 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/initial-action-world-v1/results.json | 99727f878bab51518dddfb618cec0cd98c15bb6fe8b3667f515adb6d933e4817 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/spatial-scale-action-world-v1/results.json | 6b3a76b4eb347010d9cb14a9bf57d1c70c69f4612a1bf7fee1b41fb57537f186 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/commitment-gate-controller-v1/results.json | 7969f195c566d69717b1430095266bab6132472e42d380015e273a46e5b71fc6 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/commitment-gate-formation-v1/results.json | b7fc337afa1f605e7de16a59c9e9797804b5039b29fa45f600529dd930d6aac3 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/latent-composition-transplant-v1/results.json | 785e801c2f7c8ad7feba79c25463f195efe55467677f8f04eb78bd28a1b68888 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/developmental-ignition-transplant-v1/results.json | f6d6078b264fb0285a1dd8982fe9bd3a749f01a0ace89f766a8735297f822e40 |
| post-hoc hidden-composition counterweight | evidence-source/gard-compositional-causal-emergence-v1/developmental-ignition-transplant-v1/counterweight-results.json | 086729c395b6d6c06b79969a0eacb7fb615f8ec0a3ac7a333efb28bcbbfc2f33 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/developmental-causal-susceptibility-map-v1/results.json | ef00428ea459e805f786f32fc7f399528c3cb589f1991ed6f39b0a9f20d37a00 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/developmental-causal-grammar-v1/results.json | 200e1c14daef2d965fff12ccb167ca70b7ecaad410393ab2a7d445401d920e17 |
| post-hoc tangent aperture exploration | evidence-source/gard-compositional-causal-emergence-v1/tangent-future-aperture-v1/exploration.json | aa28dfa388708b7679acce9b7845f48922d9f1886e2bc2a733bef9198d943b23 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/developmental-commitment-aperture-v1/results.json | abd5bbe063064cc4b1d1c55d331a51b4970d764412ab776bcd79010c236c948d |
| source-bound morphology timing exploration | evidence-source/gard-compositional-causal-emergence-v1/developmental-commitment-aperture-v1/morphology-timing-exploration.json | e31b5f34e1dfc8f5573c8433c0ff6d05777f7fc52fe116a71cbbc140f47fec21 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/fresh-cohort-fine-shape-confirmation-v1/results.json | 5318aa930cd789d446372828dd0fc1bcf55edbeafc7b07d7868feb76d5bc77d4 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/steerability-age-profile-v1/results.json | 7f88560f446752adb31483f8f9e5f851a67069e97050d40393ab26784f98f949 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/basin-width-init-variation-v1/results.json | f71fd77f180cd081ea9011970ac2e109ec7b25179b5b7982f467a8f40deed91e |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/history-disambiguation-curve-v1/results.json | 6cb3e4a06fa6244bc2347d11543d0a54484105edb7fbd346c0e9202380bf68f1 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/reservoir-causal-steering-v1/prospective-results-v1b/prospective-analysis-report-v1b.json | eab15f3c894edf4c8865f8ebc22f7ee84a9052b630d1376c593ae29967ca1815 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/tangent-induced-causal-grammar-v1/results.json | 3ff7652b91f2670201364275e46dc11bb806c0316f574cff79847f889971436e |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/developmental-causal-plasticity-window-v1/results.json | 18eed6194ce1125f77e12ca0966b3104b8388d89b09fdce13678d5faf43d3ac6 |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/fresh-organic-q40-replication-v1/results.json | a321b7922195f0a8cf3198d6961f2159ed4c6065b8cef69a3b9e616d21f7bc2e |
| claim-bearing result | evidence-source/gard-compositional-causal-emergence-v1/causal-compass-peak-v1/results.json | 779277c93261976e9d95eacb2812cbc4f69e03005e9af3063d7329f4a30fb8f3 |
| frozen impedance result | evidence-source/gard-compositional-causal-emergence-v1/developmental-causal-impedance-v1/results.json | c1ed7f40cfe27c71101bdded5786905e718ba2b12bb48aa6ced7a5b824377b81 |
| post-hoc source-bound impedance exploration | evidence-source/gard-compositional-causal-emergence-v1/developmental-causal-impedance-v1/exploration.json | c33c34b4e60a742ca3f0b390aacc48c0216a67bf460a47e2c7d654d671375ca7 |
| frozen impedance protocol material | evidence-source/gard-compositional-causal-emergence-v1/developmental-causal-impedance-v1/plan.json | 15ddf2289ad599582e3bae62314a55c8f696670364b351069e501e215af6ee98 |
| impedance freeze receipt | evidence-source/gard-compositional-causal-emergence-v1/developmental-causal-impedance-v1/freeze.json | 750a3ebb726e2515ee32ce46914b7b2dcfc6a2fd3e34c3780daecc38b1bf9f3b |
| protocol-conformant corrected tournament result | evidence-source/gard-compositional-causal-emergence-v1/developmental-whole-control-tournament-v1/corrected-results.json | 4b30ab79f8df950d34d506b9727760681bd74d4380a1adefed8fe0ac8605eeeb |
| superseded original tournament result; non-authoritative joint decision | evidence-source/gard-compositional-causal-emergence-v1/developmental-whole-control-tournament-v1/results.json | 25e2802b7a73e4117466b5226e6e52aa3def11140fff866f2ac6fe8bb6a5e9fb |
| source-bound controller sequence material; post-hoc architecture diagnostic | evidence-source/gard-compositional-causal-emergence-v1/developmental-whole-control-tournament-v1/sequences.json | 2487686622838460878ab9ec43654f88913932103a2071e8bfe834b8f3881b58 |
| frozen tournament protocol material | evidence-source/gard-compositional-causal-emergence-v1/developmental-whole-control-tournament-v1/plan.json | a8919863c8bddf7c02c8d9309b9164068b77643f419b1cc678940d8f1e25bb23 |
| frozen causal-passport result | evidence-source/gard-compositional-causal-emergence-v1/birth-of-causal-individuality-v1/results.json | 1d9ff7e65115ea4ac80a0e2e4d1171625b556e1497401eb067ddea3e8d1e17c3 |
| post-hoc source-bound passport exploration and exact replay | evidence-source/gard-compositional-causal-emergence-v1/birth-of-causal-individuality-v1/exploration.json | 30936fc81d2527c7458de1f0095f2fd828badfe820389369fe7ac8f421c1eb88 |
| frozen causal-passport protocol material | evidence-source/gard-compositional-causal-emergence-v1/birth-of-causal-individuality-v1/plan.json | 9c4e4face3df57b152d10fc764ca4cf27675d317cf35b622138ba57ea44c8a1e |
| causal-passport freeze receipt | evidence-source/gard-compositional-causal-emergence-v1/birth-of-causal-individuality-v1/freeze.json | b055e6a19eb38e551f05db07bbdb8c8b36614d9468f7c59a4b2f8c7b73488b42 |
| Role | Bound image or state source | SHA-256 |
|---|---|---|
| byte-extracted native prospective developmental trajectory montage | evidence-source/gard-compositional-causal-emergence-v1/synthesis-v4/the-organism-appears-first-in-possibility-space.html | 3e5670c3ad3ab7d2beab36cdb529eb2d66f42816cfbc9ccbbd80027dbe2d1d4c |
| byte-extracted native feedback release comparison montage | evidence-source/gard-compositional-causal-emergence-v1/synthesis-v4/the-organism-appears-first-in-possibility-space.html | a6e9572da0d7d71a4104284ea0f06da81f34d9af0ccdff358ec5154e6a5263bb |
| native developmental frame at age 60 | evidence-source/visuals/gard-compositional-causal-emergence-v1/developmental-causal-impedance-v1/capture/s01-a780/frames/frame_000060.png | 7a1c39cb454d6c022c706d87d417d0a4b14fb1fa6c647a55a254382854847a9d |
| native developmental frame at age 180 | evidence-source/visuals/gard-compositional-causal-emergence-v1/developmental-causal-impedance-v1/capture/s01-a780/frames/frame_000180.png | c56cf492b396830a881833a8c82d6869a4e8cce48863cb460602a3e7e412e7db |
| native developmental frame at age 380 | evidence-source/visuals/gard-compositional-causal-emergence-v1/developmental-causal-impedance-v1/capture/s01-a780/frames/frame_000380.png | fa119a60abc8e3ff224d7172761f9c66c0a091d59383afd0d6df210798025972 |
| native developmental frame at age 580 | evidence-source/visuals/gard-compositional-causal-emergence-v1/developmental-causal-impedance-v1/capture/s01-a780/frames/frame_000580.png | 7a1093501672d8b50fb34435cbb7344c2ae31c4f96d8d18e8026f6aaee955d1f |
| native developmental frame at age 780 | evidence-source/visuals/gard-compositional-causal-emergence-v1/developmental-causal-impedance-v1/capture/s01-a780/frames/frame_000780.png | ed28a6850c663844e4d72cf08b6e5f96c964313235346f3cbe3711cb34005338 |
| native tournament exemplar Active · whole | evidence-source/visuals/gard-compositional-causal-emergence-v1/developmental-whole-control-tournament-v1/candidates/s18-a780-expansive-skeletal-elongated-whole-r04-c05/frames/frame_000016.png | cc724f622f78c40a9171eebb5d2194199c80f428b12da113519f6290e38f1af4 |
| native tournament exemplar Active · best local | evidence-source/visuals/gard-compositional-causal-emergence-v1/developmental-whole-control-tournament-v1/candidates/s18-a780-expansive-skeletal-elongated-bestLocal-r04-c06/frames/frame_000016.png | aad362c0e100004e3bf2c8436bb2b6bcce756a9788b98c7e1c44158a29693ec6 |
| native tournament exemplar Active · replay | evidence-source/visuals/gard-compositional-causal-emergence-v1/developmental-whole-control-tournament-v1/replay/s18-a780-expansive-skeletal-elongated-replay-r04/frames/frame_000016.png | 1c7d63537fa9cbc3aaeda55947d50db175b104245783f084a69c1a8b8088ed35 |
| native tournament exemplar Active · sham | evidence-source/visuals/gard-compositional-causal-emergence-v1/developmental-whole-control-tournament-v1/sham/s18-a780-sham-r04/frames/frame_000016.png | 3947254526a4326db4efbd8d150a7fa884cf2a81cc9a0c392795551ef06255e5 |
| native tournament exemplar +128 · whole | evidence-source/visuals/gard-compositional-causal-emergence-v1/developmental-whole-control-tournament-v1/release/s18-a780-expansive-skeletal-elongated-whole-release/frames/frame_000128.png | 959d277763b6c7ebcdfc2be0f3b1ee34c4aa9b575dd1bdc89ecfecb68bd32e0b |
| native tournament exemplar +128 · best local | evidence-source/visuals/gard-compositional-causal-emergence-v1/developmental-whole-control-tournament-v1/release/s18-a780-expansive-skeletal-elongated-bestLocal-release/frames/frame_000128.png | d6cd010127373694c8892494c1e323bf7348dcde5a80d6779f3762f3ae182f11 |
| native tournament exemplar +128 · replay | evidence-source/visuals/gard-compositional-causal-emergence-v1/developmental-whole-control-tournament-v1/release/s18-a780-expansive-skeletal-elongated-replay-release/frames/frame_000128.png | ba06a3425f6cf4edca537ff2a3613a59ce2d82b048daba4ff702c69d2cdb2be8 |
| native tournament exemplar +128 · sham | evidence-source/visuals/gard-compositional-causal-emergence-v1/developmental-whole-control-tournament-v1/release/s18-a780-untargeted-sham-release/frames/frame_000128.png | c2686e7804629f4779dbe1ec9cf84111ea5e832b04d14ffbf26f68ed6a3cfea2 |
| derived visible/hidden q48 render for self_reencode | evidence-source/visuals/gard-compositional-causal-emergence-v1/birth-of-causal-individuality-v1/frozen-states/s001-q048-self_reencode.state-patch.json | aad030fc4e254401c3e2e3bc353ad84b8d1a4c1e4b3536460e12662fceff9813 |
| derived visible/hidden q48 render for near_donor | evidence-source/visuals/gard-compositional-causal-emergence-v1/birth-of-causal-individuality-v1/frozen-states/s001-q048-near_donor.state-patch.json | 9c0d888446c9aba66f232d2c4d0fa3eca8a1c69bbc55ee93851fa71e7875aa8a |
| derived visible/hidden q48 render for far_donor | evidence-source/visuals/gard-compositional-causal-emergence-v1/birth-of-causal-individuality-v1/frozen-states/s001-q048-far_donor.state-patch.json | 59c66e2a14dcf96cc417f8a6ebfb8a354aa5b019fec6267b16dfa642b9a982ad |
| derived visible/hidden q48 render for near_scrambled | evidence-source/visuals/gard-compositional-causal-emergence-v1/birth-of-causal-individuality-v1/frozen-states/s001-q048-near_scrambled.state-patch.json | 40b1248b51715f4147a9194c54d266edbfeb5067aec0fd8587f51e5f0f9ea686 |
| Canonical synthesis-v4 | 69107dac3f182d4876e3bafe167f33a711c693c68f6f15e1c9a65fc7873af0fd |
|---|---|
| Final audited synthesis-v5 | a9539ecc2dfddc963bd9476b126e369ca28f0ed0eaa0cdeaedec6c8c97a360a5 |
| v5 manifest | 60f34545ebae16a529a93c864f7e16f242557e5bc08d8c3c4de7b7e73be1dff5 |
| v5 generator | 419d60eb54b703f5eafbdd8c1d4f5579a5b97a0db9187d458f928a89a4e19407 |
| Corrected tournament result | 4b30ab79f8df950d34d506b9727760681bd74d4380a1adefed8fe0ac8605eeeb |
| Superseded tournament result | 25e2802b7a73e4117466b5226e6e52aa3def11140fff866f2ac6fe8bb6a5e9fb |
| Passport frozen result | 1d9ff7e65115ea4ac80a0e2e4d1171625b556e1497401eb067ddea3e8d1e17c3 |
| Passport audit replay | maximum absolute difference 0; exploration SHA 30936fc81d2527c7458de1f0095f2fd828badfe820389369fe7ac8f421c1eb88 |