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| author | YurenHao0426 <Blackhao0426@gmail.com> | 2026-07-23 07:58:09 -0500 |
|---|---|---|
| committer | YurenHao0426 <Blackhao0426@gmail.com> | 2026-07-23 07:58:09 -0500 |
| commit | 670c1399659f31ac79c4b454147417d4f8ddca7d (patch) | |
| tree | aa14a4f1222154631900805c7f2219a13821db77 /ORAL_B_V2.md | |
| parent | ce10335dcc3aa12f4f1e6dd53352d7e71d0cccf7 (diff) | |
protocol: freeze independent oral-B-v2 gates
Diffstat (limited to 'ORAL_B_V2.md')
| -rw-r--r-- | ORAL_B_V2.md | 231 |
1 files changed, 231 insertions, 0 deletions
diff --git a/ORAL_B_V2.md b/ORAL_B_V2.md new file mode 100644 index 0000000..a585b58 --- /dev/null +++ b/ORAL_B_V2.md @@ -0,0 +1,231 @@ +# Oral-B-v2: role-vectorized temporal-difference outcome surprise + +This is a new, independently frozen branch. It does not edit, reopen, or +reinterpret the failed `oral_b_td_confirmation_v1` record in +`results/bci_td_confirmation_gate.json`, and it cannot satisfy the old +oral-A unlock. Its purpose is to answer the strongest reviewer objection to +that branch: the old residual was almost a rank-one role vector multiplied by +instantaneous performance velocity, while a 99.5% evaluation ceiling and the +absence of an explicit reward/timeout phase made balanced outcome decoding +ill-conditioned and structurally disconnected from the implemented +mechanism. + +No oral-B-v2 task endpoint was inspected before this protocol, both runners, +both analyzers, all thresholds, and all seeds were committed. Endpoint-free +mechanics live in `experiments/bci_v2_smoke.py`. + +## Mechanism and claim boundary + +For somatic state `h_t`, a local scalar critic predicts + +```text +V_t = v^T [1, h_t]. +``` + +The environment supplies a dense within-trial performance change and a +terminal rewarded/timeout event, + +```text +rho_t = 0.25 (|e_(t-1)| - |e_t|) + 1{rewarded terminal}, +delta_t = rho_t + gamma (1-terminal_t) V_(t+1) - V_t. +``` + +Sparse antithetic cursor probes estimate each cell's signed causal role +`m_i = dz/dh_i` without reading the synthetic role map. The instructional +apical term is `m_i delta_t`. It is mixed with ordinary soma-predictable +traffic and only the innovation + +```text +r_(i,t) = a_(i,t) - (P_i h_(i,t) + b_i) +``` + +enters the actor update. A local eligibility trace supplies temporal credit: + +```text +E_(ij,t) = 0.8 E_(ij,t-1) + + (1 - h_(i,t)^2) x_(j,t), +Delta W_ij = eta r_(i,t) E_(ij,t). +``` + +The critic, actor, role estimator, and neutral predictor all use explicit +manual local updates under `torch.no_grad()`. There is no task-loss query, +autograd, reverse-mode graph, feedback weight transport, or BP comparison in +this branch. `kappa=0`, so v2 tests innovation-guided plasticity and +outcome-surprise coding, not online apical control. + +The terminal signal is not presented as mysterious evidence: an outcome +bonus directly enters the TD target. The nontrivial tests are that it survives +mixing with ordinary dendritic traffic only after residualization, is +cell-vectorized with the learned causal roles, is modulated by learned +expectedness, drives learning through a local eligibility rule, and replicates +under untouched task-cluster uncertainty. Acute lesions isolate the outcome +and expectedness contributions on identical trained states and trajectories. + +## R0 endpoint-free mechanics gate + +R0 touches no task endpoint. It passes only if all deterministic checks in +`experiments/bci_v2_smoke.py` pass: + +- the simultaneous antithetic role estimate and its local update each have + cosine above 0.99 with an analytic role used only for diagnosis; +- the neutral predictor identifies soma-predictable traffic to numerical + tolerance; +- TD(0), critic, eligibility-trace, and forward updates equal their explicit + local formulas; +- the continuing state's stored value is recomputed after an online critic + update rather than left stale; +- a controlled terminal transition gives positive rewarded surprise and + negative timeout surprise, with exact critic and outcome lesions; +- every episode produces exactly one terminal record under a truncated + horizon, and paired replay is exact; and +- the frozen grouped terminal metrics are finite and preserve pairing. + +Passing R0 changes no score and only permits R1. + +## Frozen task, costs, conditions, and assays + +All runs use 40 cells (`5 P+`, `5 P-`, `30 P0`), 16 context components, 28 +maximum steps per episode, 64 episodes per day, 14 days, target `0.8`, +inertia `0.65`, process noise `0.12`, context AR coefficient `0.8`, neutral +predictor rate `0.2`, role rate `0.03`, perturbation scale `0.03`, one role +probe every four temporal steps, eligibility decay `0.8`, velocity reward +scale `0.25`, terminal reward `1`, and `kappa=0`. + +Every condition first receives 100 instruction-off batches of 64 neutral +states. Every condition consumes the same two scalar cursor observations per +role-probe example; fixed-role and oracle conditions ignore the resulting +target. The oracle reads the analytic role only as a labelled ceiling and is +ineligible for selection. Predictor maximum error must be at most `1e-5`. + +Six paired training conditions share context, process noise, perturbations, +and evaluation trajectories: + +1. intact learned-role actor--critic innovation; +2. fixed random role vector; +3. forward-plasticity lesion; +4. critic training lesion; +5. terminal-outcome training lesion; and +6. exact-role diagnostic oracle. + +Ordinary task performance is evaluated on 256 full-horizon episodes. The +biological signature assay is separate and uses the fixed horizon ladder +`{4, 8, 12, 16, 20, 24, 28}`, with 128 independent episodes at every horizon. +All horizons are pooled; no horizon is selected, reweighted, removed, or +tuned. This deliberately produces rewarded and censored timeout trials +without weakening the trained task or choosing a difficulty after viewing +outcomes. On exactly the same trained intact model and trajectories, the +assay replays intact, acute-critic-lesion, and +acute-terminal-outcome-lesion readouts with all learning disabled. + +Each record reports maximum and actually active state transitions, neutral +examples, role-probe examples, two scalar cursor observations per probe, +terminal observations, evaluation cost, wall time, peak RSS, task-loss +queries, and reverse-mode calls. Early termination is counted rather than +silently charged as a full active trajectory. + +## R1 frozen development selection + +R1 uses fresh development task seeds `20--22` and model seed `0`. It evaluates +the complete Cartesian grid + +```text +forward eta in {0.03, 0.1} +gamma in {0.8, 0.95} +critic eta in {0.01, 0.03} +``` + +for exactly 24 records. Full performance seeds are `400000 + task_seed`. +Horizon-ladder seed for index `k` is `410000 + 1000 task_seed + k`. +Confirmation task seeds `30--35` and model seeds `0--4` remain untouched. + +A candidate is eligible only if every one of its three task seeds passes every +check: + +- intact final success at least 70% and early-to-late gain at least 10 points; +- final success at least 20 points above fixed role and no more than 10 points + below the exact-role oracle; +- the plasticity lesion retains at most half the intact learning gain and the + learned-role cosine is at least 0.80; +- pooled challenge success fraction lies in `[0.15, 0.85]`; +- terminal residual outcome balanced accuracy is at least 65%, role-aligned + rewarded-minus-timeout separation at least `0.03`, and acute outcome lesion + reduces that separation by at least `0.01`; +- mean learned-critic expectedness contribution is at least `0.005` and its + paired contribution correlates at least `0.95` with the stored value + prediction; +- nonterminal mean absolute residual--soma correlation is at most `0.10`, and + raw-minus-residual correlation gap is at least `0.20`; +- preceding surrounding population predicts the sign of a causal cell's + residual with mean balanced accuracy at least 52%, and decoder distance has + residual correlation at least `0.02`; and +- P+/P- performance-change sign inversion is at least `0.01`, with at least + `0.05` absolute CV-correlation advantage for performance velocity over + instantaneous error magnitude. + +Among eligible candidates, selection maximizes worst-task final success, then +worst-task terminal outcome accuracy, then prefers smaller forward rate, +smaller critic rate, and smaller gamma. If no candidate is eligible, v2 +closes. R1 never changes the score. The executable screen and deterministic +analyzer are `experiments/bci_v2_development_screen.sh` and +`experiments/analyze_bci_v2_development.py`. + +## R2 frozen untouched confirmation + +Only a complete eligible R1 gate permits R2. R2 runs the selected candidate +without further selection over task seeds `30--35` and model seeds `0--4`, +exactly 30 paired records. Full performance seeds are +`500000 + task_seed`; ladder seed for index `k` is +`510000 + 1000 task_seed + k`. The task seed is the independent unit: each +metric is first averaged over the five model seeds, then summarized over six +task clusters with a one-sided 95% Student-t bound with five degrees of +freedom. + +Learning and plasticity pass only if: + +- mean intact final success is at least 70%, every task mean and the lower + bound are at least 60%; +- mean learning gain is at least 10 points and its lower bound at least 5; +- mean fixed-role gap is at least 20 points and its lower bound at least 10; +- mean oracle deficit is at most 10 points and its upper bound at most 20; +- the lower bound of `0.5 intact_gain - plasticity_lesion_gain` is + nonnegative; and +- mean role cosine is at least 0.80 and every record is at least 0.70. + +Innovation and network prediction pass only if: + +- mean residual--soma correlation is at most `0.10` with upper bound `0.12`, + and mean raw-minus-residual gap is at least `0.20` with lower bound `0.15`; +- surrounding-event accuracy averages at least 52% with lower bound 50%, and + decoder-distance correlation averages at least `0.05` with nonnegative + lower bound; +- sign inversion is positive in at least 25/30 records and in every + task-cluster mean; and +- velocity advantage averages at least `0.05` with nonnegative lower bound. + +Terminal outcome surprise passes only if: + +- every record's pooled challenge success fraction lies in `[0.10, 0.90]`; +- terminal residual outcome accuracy averages at least 65% with lower bound + 60%; +- role-aligned outcome separation averages at least `0.03` with lower bound + `0.01`; +- acute outcome lesion reduces separation by at least `0.01` on average with + nonnegative lower bound; +- critic expectedness contribution averages at least `0.005` with + nonnegative lower bound; and +- every paired critic contribution/value-prediction correlation is at least + `0.95`. + +The runner and immutable complete-grid analyzer are +`experiments/bci_v2_confirmation.py` and +`experiments/analyze_bci_v2_confirmation.py`. All records bind the protocol, +model, metrics, both analyzers, both runners, D4 gate, preserved failed old R2 +gate, and (for confirmation) R1 gate by SHA-256, require a clean tracked +worktree, reject missing or extra records, and refuse overwrite. + +A complete R2 pass raises the repository's formal milestone score from 7 to 8 +and establishes role-vectorized TD outcome surprise plus innovation-guided +plasticity on this BCI paradigm. It does not establish online apical control, +does not erase the old R2 failure, and does not open the old oral-A panel. It +only permits a separately frozen oral-A-v2 protocol. Any failed R2 is retained +and leaves the formal score at 7. |
