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