Update 2026-06-29-tripartite-synapse_v17.md
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# Tripartite Synapse — Pseudocode v17
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> Companion: `tripartite_synapse_v17_biology.md` · principle: `logic_principles_v5`.
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@@ -134,7 +130,7 @@ its structure rebuilt) OR energy is spent (overloaded — unspent tags carry to
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## Conventions
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```
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SCOPE = {DAY, NIGHT} CONTEXT = {AP, NOT_AP, NOT_SPIKE_TRAIN, bAP, NOT_bAP, CONTINUOUS}
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SCOPE = {DAY, NIGHT} DAY CONTEXT = {AP, REFRACTORY⊂NOT_AP, NOT_AP, NOT_SPIKE_TRAIN, CONTINUOUS} NIGHT CONTEXT = {NON_REM_1, NON_REM_2, REM}
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THE THREE CATEGORIES (see logic_principles "The Ring"): (ACTION ⇄ RECOVERY) × many, then PREPARATION
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ACTION the component's defining deed; deposits the fast trace. ALWAYS LOCAL to the acting
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@@ -157,7 +153,23 @@ CONTEXT LICENSES PHASE (context = the imposed condition; phase = the work it per
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NOT_SPIKE_TRAIN no spike AND no train ⊂ NOT_AP → adds PREPARATION (runs on top of NOT_AP)
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A process runs in the SHORTEST quiet its timescale fits: fast-trace decay and partial pool refill
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in NOT_AP (they ride the train and set short-term depression); tag formation, full refill, and
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occupancy read-out in NOT_SPIKE_TRAIN. (Components without trains use bAP / NOT_bAP, or continuous.)
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occupancy read-out in NOT_SPIKE_TRAIN. (Components without trains use continuous flow.)
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WHO EMITS THE CONTEXT (a context is a signal from ABOVE, not self-generated):
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AP, REFRACTORY emitted by SOMA — its own firing state (AP = it fired; REFRACTORY = the recovery
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window after, when it cannot fire again yet). What was "NOT_AP" is REFRACTORY.
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NOT_SPIKE_TRAIN emitted by the NEURON — sustained absence of soma spikes can only be tracked from
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ABOVE the soma (a component cannot easily know "I have not fired for a while");
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the neuron keeps count of the gap and broadcasts it down.
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NON_REM_1/2, REM emitted top-down within the NIGHT context (see DAY/NIGHT switch) — the night's
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sub-phases: NON_REM_1 → ACTION (build⇄release), NON_REM_2 → RECOVERY
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(import+free), REM → PREPARATION (replay+measure+prime).
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POST INVERTS THE DAY MAP. For the postsynapse the deed is RECEIVING, which happens whenever no
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descending spike is arriving, so: NOT_AP → ACTION (open AMPA/NMDA, respond), AP → RECOVERY (the
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brief descending spike, driven from above, restore + boost traces), NOT_SPIKE_TRAIN → PREPARATION.
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POST's ACTION continues through the soma's REFRACTORY (refractory is the soma's state, not POST's;
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from POST it is NOT_AP), which is how the spine charges up to ready the next spike.
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VARIABLE TIERS (timescale = meaning; see logic_principles "The Timescale Ladder")
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FAST (ms–s) immediate response fast_trace
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@@ -459,63 +471,67 @@ The postsynaptic spine is the synapse's primary memory locus: it detects coincid
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runs the calcium dynamics that decide potentiation versus depression, and requires the most
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validation (three coincidences) before committing.
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**POST's ACTION is the synaptic event (context NOT_bAP).** Integration is graded and ongoing
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rather than spike-punctate, so POST's action-context is "glutamate present, no bAP": three calcium
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sources feed the fast trace — AMPA current (small Ca, begins ejecting the NMDA Mg block) and NMDA
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(large Ca, only on the local coincidence of depolarization + astrocyte D-serine + glutamate). The
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action deposits the calcium trace and emits the two retrograde messages. Because POST's receptors
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are physical coincidence detectors, two of its three tag-coincidences (astro D-serine, and the bAP
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below) are detected *in the action*; only the organism's dopamine coincidence is left to evaluation.
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**POST's ACTION is the synaptic response (context NOT_AP).** Integration is graded and ongoing
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rather than spike-punctate, so POST's action-context is "no descending AP arriving": it opens its
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channels and responds to whatever glutamate has arrived. Three calcium sources feed the fast trace —
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AMPA current (small Ca, begins ejecting the NMDA Mg block) and NMDA (large Ca, scaled by the local
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coincidence of depolarization + astrocyte D-serine + glutamate). The action deposits the calcium
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trace and emits the two retrograde messages. Crucially POST's ACTION **continues through the soma's
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refractory period**: the refractory belongs to the soma, not to POST — from POST it is simply NOT_AP,
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so the spine keeps responding and integrating, charging up so the neuron is ready to fire again once
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its refractory ends.
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**bAP is a second, vertical action-context.** The soma's back-propagating spike arrives, adds
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depolarization and calcium, and supralinearly amplifies an existing candidate — the soma's
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confirmation that it fired, detected in the action-moment (instantaneous coincidence).
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**POST's RECOVERY is the descending AP (context AP) — a brief event.** When the soma's spike arrives
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it adds depolarization and calcium, supralinearly boosts an existing candidate (the soma's
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confirmation that it fired), and resets the spine: calcium extrudes, the NMDA Mg-block re-establishes
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as Vm falls, and the trace relaxes — restoring the ability to respond again. This is the *alter-ego*
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of the response, and it is short (the spike event), not the whole refractory window.
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**EVALUATION FOLDS INTO PREPARATION.** POST runs the same three categories as every component.
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ACTION is the synaptic response (integrate glutamate, detect the instantaneous coincidences, emit
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the retrogrades). RECOVERY restores the ability to respond again — calcium extrusion and NMDA
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Mg-block re-establishment, the fast alter-ego of the response. PREPARATION shapes what comes next:
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fills AMPA surface toward the slot ceiling from accumulated calcium (short-term potentiation, no
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**EVALUATION FOLDS INTO PREPARATION (context NOT_SPIKE_TRAIN).** PREPARATION shapes what comes next:
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it fills AMPA surface toward the slot ceiling from accumulated calcium (short-term potentiation, no
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dopamine — for the next response), climbs the tag on the dopamine coincidence (for the night),
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refills budget, and settles. A fuel shortfall while calcium was climbing toward a tag is endurance
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evidence (a preparation deposit made during action); a surface already at its ceiling is a
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structural limit, not endurance.
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**During NIGHT — the same three categories, turned inward.** RECOVERY imports material/energy and
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primes AMPA responsiveness from the standing tag. PREPARATION replays: POST responds to the
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re-evoked glutamate exactly as it responds by day (same AMPA/NMDA machinery, same endurance
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deposit into the same trace), reading the response as participation rather than transmitting — no
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dopamine. ACTION is the structural change: general homeostatic lowering, then rebuild where the tag
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stands and participation was confirmed, consuming the tag. Both ceilings draw the same finite pool
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and compete; unmaintained ceilings drift down.
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**During NIGHT — the same three categories, turned inward, in sleep-stage contexts.** NON_REM_2
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(RECOVERY) imports material/energy and primes AMPA responsiveness from the standing tag. REM
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(PREPARATION) replays: POST responds to the re-evoked glutamate exactly as it responds by day (same
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AMPA/NMDA machinery, same endurance deposit into the same trace), reading the response as
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participation rather than transmitting — no dopamine. NON_REM_1 (ACTION) is the structural change:
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rebuild where the tag stands and participation was confirmed (consuming the tag) ⇄ release where
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participation was low. Both ceilings draw the same finite pool and compete; unmaintained ceilings
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drift down.
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```
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// PARAMETERS K_AMPA · AMPA_Ca · AMPA_cost · NMDA_cost · bAP_cost · pka_cost · traffic_cost
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// PARAMETERS K_AMPA · AMPA_Ca · AMPA_cost · NMDA_cost · AP_cost · pka_cost · traffic_cost
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// req_cost · Mg_eject · K_Ds · Ca_STP · Ca_TAG · eCB_thr · drift · baseline
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// NO_synth_cost · eCB_synth_cost
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// INTERFACE
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// EMIT retro_NO (+), retro_eCB (−) → PRE
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// RECEIVE (signals) glutamate ← PRE ; astro_Dserine ← ASTRO ; bAP ← DEND/SOMA ; dopamine
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// READ glutamate ; astro_Dserine (GAIN, not gate) ; bAP (dend_structure.bAP_fidelity) ; dopamine
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// RECEIVE (signals) glutamate ← PRE ; astro_Dserine ← ASTRO ; AP (descending) ← DEND/SOMA ; dopamine
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// READ glutamate ; astro_Dserine (GAIN, not gate) ; AP via dend_structure.bAP_fidelity ; dopamine
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// OWN post_structure{slot_ceiling, spine_volume, reserve_ceiling} ; post_budget_ceiling
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// SUPPLY astro_lactate[syn] ← ASTRO ; dend_ship_post ← DEND ; post_material ← DEND(NIGHT) ; post_energy ← SOMA(NIGHT)
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// EMERGENCY shockwave_lockdown ← ASTRO
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// NOTE POST endurance is own-state only (own Ca climbing); no arrived feedback term.
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// coincidences sort by timescale: D-serine/bAP detected IN ACTION (instantaneous); dopamine in PREPARATION.
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// THE THREE CATEGORIES (same at DAY and NIGHT; here DAY, subject = arrived glutamate / bAP):
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// ACTION respond: integrate glutamate, detect instantaneous coincidences, emit retro (NOT_bAP);
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// bAP is a second, vertical action-context (soma's spike confirms)
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// RECOVERY restore the ability to respond: Ca extrusion + NMDA Mg-block re-establish
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// PREPARATION shape what comes next: AMPA fill (next response) + tag climb (NIGHT) + refill + settle
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// Coincidences sort by timescale: D-serine/bAP detected IN ACTION (instantaneous); dopamine in PREPARATION.
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// THE THREE CATEGORIES (same at DAY and NIGHT; here DAY, subject = arrived glutamate / AP):
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// ACTION (NOT_AP) respond: open AMPA/NMDA channels, integrate glutamate, detect the
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// instantaneous coincidence, emit retro. This is POST's defining deed and it happens
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// ALWAYS EXCEPT during an arriving AP — INCLUDING through the soma's refractory period:
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// refractory is the SOMA's state, not POST's; from POST it is simply NOT_AP, so POST
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// keeps responding and integrating, charging the spine so the neuron is ready to fire
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// again once refractory ends.
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// RECOVERY (AP) the BRIEF descending-spike arrival (ms): POST is driven from above, restores its
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// ability to respond (Ca extrusion, Mg-block re-establishes as Vm falls), and deposits/
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// boosts traces. Short event, not a long window.
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// PREPARATION (NOT_SPIKE_TRAIN) shape what comes next: AMPA fill (next response) + tag climb (NIGHT)
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// + refill + settle.
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// Coincidences sort by timescale: D-serine detected IN ACTION (instantaneous); dopamine in PREPARATION.
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// ===== ACTION =====
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DAY | bAP: // second action-context (vertical): soma confirms
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Vm += bAP_depol × dend_structure.bAP_fidelity; post_budget -= bAP_cost
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if post_possible_tag > Ca_TAG: post_fast_trace += bAP_Ca_boost() // amplify only if candidate present
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DAY | NOT_bAP: // respond to arrived input (the defining deed)
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// ===== ACTION (NOT_AP: open channels, respond — continues through the soma's refractory) =====
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DAY | NOT_AP: // respond to arrived input (the defining deed)
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a = sat(glutamate, K_AMPA)
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AMPA_current = a × AMPA_surface; Vm += AMPA_current; post_budget -= AMPA_cost // SOURCE 1 AMPA
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post_fast_trace += AMPA_Ca·AMPA_current // @cut affords: channel-opening frequency, response magnitude (quantity of response) [ms]
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@@ -526,13 +542,15 @@ DAY | NOT_bAP: // respond to arrived
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if Vm > eCB_thr:
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retro_eCB += eCB_emit(Vm); post_budget -= eCB_synth_cost // EMIT − brake
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// ===== RECOVERY (restore the ability to respond; alter-ego of the response) =====
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DAY | NOT_bAP · recovered: // Ca extrusion + Mg-block re-establish
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post_fast_trace *= decay(ms) // FAST — Ca extruded, trace relaxes
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// ===== RECOVERY (AP: brief descending-spike arrival — restore + boost traces) =====
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DAY | AP: // soma's spike arrives (ms event), driven from above
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Vm += AP_depol × dend_structure.bAP_fidelity; post_budget -= AP_cost
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if post_possible_tag > Ca_TAG: post_fast_trace += AP_Ca_boost() // boost only if a candidate is present
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post_fast_trace *= decay(ms) // Ca extruded, trace relaxes — ready to respond again
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// (NMDA Mg-block re-establishes as Vm falls — implicit in the Vm>Mg_eject gate next response)
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// ===== PREPARATION (shape the next response AND the NIGHT) =====
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DAY | quiet: // sustained quiet
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// ===== PREPARATION (NOT_SPIKE_TRAIN: shape the next response AND the NIGHT) =====
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DAY | NOT_SPIKE_TRAIN: // sustained quiet (emitted by NEURON — above SOMA)
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// for NIGHT: climb the tag; dopamine is the integrable coincidence (#3)
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if post_fast_trace > Ca_TAG: post_possible_tag += post_fast_trace; post_budget -= pka_cost // @cut affords: participation / consistency of co-activity (running average) [min]
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if dopamine > dop_thr and post_possible_tag > tag_thr:
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@@ -557,7 +575,7 @@ DAY | quiet: // sustained quiet
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// ACTION (same AMPA/NMDA machinery, same endurance trace), read for participation not significance.
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// ===== ACTION (build ⇄ release; participation gates direction; tag funds build, persists across cycles) =====
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NIGHT | build or release:
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NIGHT | NON_REM_1:
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if rest_permission and post_tag > tag_expiry and post_participation ≥ MEDIUM: // BUILD (slice)
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Δ = min(slot_batch, post_material, post_energy·f_cap, post_tag) × post_participation
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post_structure += Δ; post_material -= Δ; post_energy -= Δ·assembly_cost
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@@ -573,7 +591,7 @@ NIGHT | build or release:
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// else: HOLD — tag waits for its pattern
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// ===== RECOVERY (acquire material/energy in CONTENTION with other components; receive freed material) =====
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NIGHT | import + free:
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NIGHT | NON_REM_2:
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post_material += transit(post_material_ship, τ_transport_spine) // import (contested pool)
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post_energy += transit(post_energy_ship, τ_transport_spine)
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post_material += post_freed_material; post_freed_material = 0 // reclaim what release freed
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@@ -584,7 +602,7 @@ NIGHT | import + free:
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post_structure += min(post_maint, maint_cost) // hold up what is used
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// ===== PREPARATION (REPLAY the response — SAME machinery as day ACTION; multi-timescale) =====
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NIGHT | replay + measure + prime:
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NIGHT | REM:
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// FAST: replay the response to the re-evoked input (probe)
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if arrived_glutamate_replay or arrived_replay_AP:
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a = sat(glutamate, K_AMPA)
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