Digital Drosophila Archive
92 lines
5.2 KiB
Markdown
92 lines
5.2 KiB
Markdown
# Normal olfactory acquisition: independent D18 branch
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This phase does not modify MaleCNS reference/runtime, Phase 1–4AQ data, the
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base graph, the 14,232 candidate edges, eligibility-v2, APL gain, cell thresholds,
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transmitter signs or any previously sealed failure. An engineering interface
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PASS is not evidence of learning.
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## Fixed science
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The original AO file (SHA-256
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`a7bda850ee87df4d9f647994e1a1a4074dfea5793184edb1822ab3d8c02e8216`)
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supplies master 20260930, all semantic seeds, ordered cues and control schedules.
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The old frozen evaluation policy supplies completed-epoch snapshot boundaries.
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There are 40 normal blocks: physiological/matched-energy × PAM15/PPL103 ×
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reciprocal reinforced odor × five training replicates. A is 4-ethylphenol, B is
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3-hexanone. Evaluation uses 80 independently registered input streams.
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All seven arms are real: paired, D=0, frozen, random reward, unpaired, CS-only
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and DAN-only. 30,000 complete fresh training/control epochs and 3,920 real
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fresh A/B probes are required. Even identical baselines are executed, not
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relabelled copies. Snapshots 0/1/2/5/10/20/50 never authorize outcome selection.
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Only the 50-pairing terminal outcome determines acquisition. Every arm finishes
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its entire original schedule, including trailing neutral or blank epochs.
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Epochs are 120 ms, CS is [0,100) ms, scheduled artificial US is at 90 ms.
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PAM15 and PPL103 use only their existing confirmed compartment-specific DAN
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identities. The positive/negative behavioral predictions are explicit model
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hypotheses, not a claim that every PAM/PPL neuron has that function. Scheduled
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D is an artificial dimensionless interface, not measured dopamine concentration
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or the number of accepted DAN spikes. US attempts/rejections and actual events
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remain in the original runtime artifacts. No resampling compensates for a
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rejected pulse.
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Fresh neural state is reset each epoch; only the separately authenticated
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plastic delta carries forward. Original E/U compute the end-of-epoch update,
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then a separate CPU process recomputes it from sealed actual KC events. Probes
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have no US, no E/update and no feedback. Brain math is untouched.
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## Readout and gates
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The frozen AQ `learning_gates.py` and original `metrics.py` are pinned before
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sampling. All six controls, raw signed MBON balance, functional count/latency
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change, MBON separation and both downstream readouts remain mandatory. The
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same replicate must satisfy the conjunction; at least three of five pass in
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each of the eight cells. PAM/PPL or input modes are never pooled to rescue a
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failure. Original H mean-control rules are reported separately for each DAN
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control source, both required. Delta change alone cannot imply learning.
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Readout populations are anatomical, never inferred from active/plastic subsets.
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The original H actual MBON downstream edge table defines legacyDownstream;
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nonMBONDownstream is its exact set difference with the full MBON population.
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Missing identity or an altered frozen source stops preparation.
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## Execution, resources and integrity
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Use only the registered 4090 UUID and serial execution. ComfyUI admission must
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be empty; never stop or evict a service. Source code is committed before
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registration. Static tables invoke the original L PN-rate transform, preserving
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all original PN columns for both modes. Shared CS aliases reuse saved input
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bytes only. The full 63-bit CUDA sampler, full matrix draw and CS window are
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unchanged; there is no CPU-RNG replacement.
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The engineering ceiling is 256 GiB of new outputs, at least 100 GiB disk reserve,
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1,800 seconds per child and an absolute 21-day registration deadline. The AQ
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linear estimate is only planning arithmetic from limited warm measurements,
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not a measured forecast across all conditions. Exceeding a limit means an
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incomplete preserved experiment, not shortened trials or changed parameters.
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Each child has an exclusive start record, actual parent-observed exit,
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dependency hashes and immutable output inventory. A stopped or uncommitted
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child is never silently retried. A persistent incremental ledger avoids
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rehashing every historical trial on every iteration; each invocation still
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rehashes its actual consumed dependencies. Full audits read every unique file
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and reject missing, extra, changed, linked or incomplete output. They are not
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claimed to be atomic filesystem snapshots. Mutable compiler cache is accounted
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separately. CPU/source tests are not described as GPU numerical regression.
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A detached supervisor keeps the serial controller alive across SSH disconnects.
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Administrative logs live in `/data/digital-drosophila/logs/phase4ar-normal-conditioning/`,
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outside the immutable per-trial ledger. The final outer auditor must retain
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these logs and its actual exit receipt. A launch PID alone proves no completion.
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All original event/state/queue/update artifacts are retained; no dense wholebrain
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time-by-neuron output is added. Complete historical sealed integrity is checked
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at the boundaries. The five historical reference trials are preserved evidence,
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not claimed as newly rerun here.
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Normal acquisition is the only authorized scientific scope of this registration.
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No delayed/reversal/retention assay starts automatically, and no candidate is
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issued from normal acquisition alone. There is no game, action decoder, RL,
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visual input, training of base weights, web service or 3D interface.
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