vp_frontal — the second brain simulation

vp_frontal is the second long-term simulation of the brain project and the companion of the Felt Cognition paper. Simulation 1 — the frozen 12-node ephaptic mind engine — left the cortex as a single undifferentiated node and omitted the second physical coupling channel. Simulation 2 is an additive program that fills those gaps without changing the frozen kernel: every addition sits behind a node of the byte-frozen engine, so the M9 anchor R = 0.38961455156044245 keeps reproducing bit-for-bit. The chain has five gaps; four are fillable and each survived a stress test designed to break it, and the fifth — felt quality — is kept as an explicit open blank.

Status: Sim 2 COMPLETE — the project is CLOSED. The integration pass (Chunk E) re-derived every committed digest from the artifacts on disk: all seven build and stress-test artifacts reproduce bit-for-bit (broke_on = []), the frozen engine is byte-unchanged, the firewall held on every gap (consciousness_claim = 0, hard_problem_open = 1), and the new tuned constants summed over the whole chain is 0sim2_complete = True, project_closes = True.

What the second simulation adds

Simulation 1 is the heavy, successful run: a physics-grounded engine that emerges brain organs from measured 4D-DNA master genes, builds θ/γ brainwaves, memory, inter-organ coordination, the embodied loop, and a 28-module clinical atlas — under strict no-tuning discipline, with its honest negatives preserved and the consciousness firewall held. It is frozen and read-only.

Simulation 2 does three additive things on top of it. It gives the cortex the internal microstructure Sim 1 left as one node (Hard Limit 1). It adds the second physical coupling channel — the axonal connectome — that Sim 1, being ephaptic/proximity-only, omitted. And it operationalizes the cognition / consciousness-access / body framework as a faithful, non-circular set of probes. The precedent that makes this possible without breaking the kernel is the hippocampus: a 120-cell internal model already sits behind a single node of the frozen 12-organ engine without changing it.

The five gaps (the v2 atlas)

The mechanism chain — gene → cell → rhythm → coordination → memory → stream → selection → body, looping back — is complete at the mechanism level. Five gaps remain. Each fillable gap below entered a hypothesis and was then stress-tested to destruction; the grade is the one the module itself emitted. Each gap has its own page with the full build, the stress test, the data tables, and the preserved honest residuals.

#GapOutcome
1EM-field causal efficacyin-silico [L] — survived ST-1 (causal window sign-stable across 36 cells; peak ~3× above measured stays [O])
2Cortical microstructurein-silico [L] — survived ST-2 (additive micro-model sufficient; kernel fork not triggered; gene-blind [O])
3Axonal connectome (O×W axes)in-silico [L] — survived ST-3 (two separable axes; relative-selectivity / gene-blind [O])
4Access window (consciousness)in-silico [L] for the conscious/unconscious split — survived ST-4; [O] within-unconscious ordering (recorded honest negative)
5Felt quality (the hard problem)OPEN by principle — the explicit firewall blank; the chain closes with this blank, never by erasing it

The discipline that holds it together

The core long-term rule is the Stress Principle: every hypothesis is stress-tested to destruction, and if it collapses, the collapse is recorded and accepted and the affected line restarts with the collapse built in. Refinement means surviving the stress, never avoiding it — the same way Sim 1 preserved its honest negatives rather than tuning them away. The methodology page sets out the six governing principles inherited verbatim from Sim 1, the additive discipline, and the correction that opened Sim 2.

How the project closed

An integration pass has exactly one thing that can break: a recorded survivor that no longer reproduces. So the closing stress test was an end-to-end digest audit — recompute every committed digest from the artifacts and require that the recomputed value equals the stored value equals the independently committed expected-SHA, for all seven artifacts, with the engine byte-unchanged and the firewall held. It survived. The integration and closure page carries the audit table, the end condition, and the v2 atlas figure; the reproduction and provenance page carries the engine, the modules, the digests, and the citations.

Firewall (Axis-A). Every quantity on this page is a structural quantity of an in-silico model — a sign, a margin, an ordering — and is not a felt state, an experienced quality, or a level of consciousness (consciousness_claim = 0; the hard problem stays open, hard_problem_open = 1). These are model results, not validated neuroscience and not clinical guidance. efficacy = 0; not medical advice.

Scope — what the two simulations cover, and where the boundary is

At the organ level the brain is covered by a saturated 12-region atlas — exactly the major regions that possess an unambiguous single canonical developmental master gene: neocortex, hippocampus, thalamus, striatum, cerebellum, hypothalamus, midbrain, brainstem, pallidum, the forebrain GABAergic interneurons, the basal-forebrain cholinergic system, and the olfactory bulb. Three regions are excluded for a principled biological reason — no single non-redundant master — and kept open rather than forced: the amygdala, the septum, and the preoptic area. The atlas grows only as measured, unambiguous masters become available; the boundary is set by the biology, not by a target region count.

At the function level, thought is decomposed into fourteen faculties. Ten are built and bit-reproducible — perception, attention, the serial stream (working memory), memory, learning, the affect mechanism, arousal/sleep, dreaming, large-scale binding, and pathology — and four are honestly owed with their external inputs named: language, volition, social cognition, and metacognition. The clinical atlas spans roughly nine disorders (autism, ADHD, schizophrenia, epilepsy, depression, bipolar disorder, addiction, OCD, and Alzheimer's), with region-specific applications for focal epilepsy, stroke and diaschisis, and targeted neuromodulation.

What is not in scope: subnuclei granularity (a different atlas), and a complete anatomical or physiological map of every structure. This is a cognition / affect / consciousness dynamics model — fine motor microcircuitry, glia and vasculature, and the peripheral and autonomic systems beyond what the hypothalamus and brainstem carry are outside its stated frame. Within that frame it covers the large majority of the brain's major regions and cognitive faculties; outside it, the boundaries are stated, not hidden.

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