- aext recalibrated to 0.275 against ATUS and social-media time-use data; baseline attention headroom now ~0.49 instead of rising to 0.65 - T03/T04 stages stay reproducible (t03_params, t04_params; verified) - organism_grid.py: factorial analysis; lineage ownership is the strongest organism lever, then membrane control, then attention protection (which acts on A, not on power); lineage x membrane complementary at baseline; organism governance without attention protection raises attention draw Co-Authored-By: Claude Opus 5.5 <noreply@anthropic.com> Assistant: claude-code Assistant-Model: opus Assistant-Process: 1494246@bnt-lap001 Assistant-Session: caf6de6f-f9e4-47ce-a584-49baa271fa4b
14 KiB
Generative Assembly Dynamics Model — GADM-0.2
Status: exploratory hypothesis generator. Not calibrated to any real economy. All numbers are in normalized, unitless model space.
GADM-0.2 extends GADM-0.1 (GenerativeAssemblyDynamicsModel.md) in three
ways:
- It specifies every flow with signs (see
GADM-CLD.md). - It adds the information-organism extensions selected below.
- It is implemented as a runnable toy simulation.
1. Decision: which organism extensions enter GADM-0.2 (T03)
Candidates from InformationOrganismsInGADM.md § 4:
| Candidate | Decision | Rationale |
|---|---|---|
| Split K into K_phys + K_Ω | in | Learning with use (R7) and lineage control (R8) are the main new loops. Without the split, they cannot be expressed. |
| Attention headroom A | in | Reference scarce resource of the program. Needed to test whether VFAC without A misses attention harm. |
| Organism selection channel O | in | Cheap to add. Needed to examine hypothesis M3 (O's quality and its contribution to P share a cause). |
| Membrane control and lineage concentration in Ṗ | in, as levers m and L |
Main institutional levers of the organism lens. |
| Participation claims C_p | in, as lever cp |
Lets scenarios test a post-work claim channel. It is treated as a share of capital return, which is a simplification (see § 6). |
| Compute C as its own stock | deferred to 0.3 | Represented for now as a direct draw of K_Ω on E (e2). A separate stock only pays off once energy classes are modeled (GADM-0.4). |
| Age cohorts | deferred to 0.3 | See GADM-0.3-Candidates.md. |
2. State
Twelve stocks, all in [0, 1]:
| Symbol | Code | Stock | New in 0.2 |
|---|---|---|---|
| H | H |
Human capability | |
| X | X |
Assembly commons | |
| K_phys | Kp |
Physical / conventional productive capacity | split |
| K_Ω | Ko |
Information-organism capability | ✓ |
| F | F |
Risk capacity | |
| G | G |
Effective agency | |
| N | N |
Diversity & composability | |
| Q | Q |
Epistemic capacity | |
| P | P |
Domination concentration | |
| E | E |
Ecological headroom | |
| S | S |
Social cohesion | now a stock relaxing to a target |
| A | A |
Attention headroom: unclaimed, self-directed attention | ✓ |
Bounding convention. Every stock follows
\dot x = \text{inflow}\cdot(1-x) - \text{outflow}\cdot x, so stocks stay in
[0, 1] without clipping. Clipping is applied only as a numerical guard.
Institutional levers (scenario axes, all in [0, 1]):
| Lever | Meaning |
|---|---|
m |
membrane control held by users and communities rather than operators |
L |
lineage diffusion: 0 = concentrated, 1 = diffuse ownership of organism lineages |
lin_open |
share of lineages that are openly inheritable (commons rather than enclosure) |
std |
open standards and interoperability |
disc |
discovery concentration |
expl |
explainability and provenance enforcement |
x_att |
attention regime: 0 = protected, 1 = extraction-funded |
auto, dshare, cp, od |
automation intensity, social dividend share, participation claims share, ownership diffusion of private returns |
3. Equations
3.1 Auxiliaries
[ K = 1-(1-K_{phys})(1-K_\Omega), \qquad Y^* = K\sqrt{E} ]
Claims (GADM-0.1 § 9, extended with C_p):
[ w_L = w_{L0}(1-auto\cdot K_\Omega),\quad c = 1-w_L,\quad \Pi_p = c,(1-dshare-cp) ] [ B = w_L + c,(dshare+cp) + \Pi_p\cdot od ]
B is the breadth of claims: the share of output reaching the broad
population as wages, dividends, participation claims or diffused ownership.
Demand factor: dem = (0.4+0.6B)(0.6+0.4S).
Experimentation (GADM-0.1 § 5, plus a Q-gated organism term, hypothesis M2):
[ V = \min!\left(1,; v_0 H^{.5}X^{.5}F^{.3}G^{.4}N^{.3}Q^{.3}(1-P)^{.5} + v_o K_\Omega Q\right) ]
Selection (GADM-0.1 § 6, plus organism channel O weighted by prevalence):
[ M=\sqrt{A\cdot dem},\quad O = Q(1-disc) ] [ \sigma = \frac{w_m M + w_s Q + w_c N(1-P) + w_p S + w_o K_\Omega O}{w_m+w_s+w_c+w_p+w_o K_\Omega}, \qquad V_{sel} = V\sigma ]
Reuse: \rho = \min(1, \rho_0 + \rho_O K_\Omega\, lin\_open).
3.2 Stocks
[ \begin{aligned} \dot X &= (a_X\rho V_{sel} + I_X)(1-X) - (\delta_X + l_X P + l_{Xo}K_\Omega(1-lin_open))X\ \dot K_{phys} &= a_K V_{sel},dem,(1-K_{phys}) - \delta_K K_{phys}\ \dot K_\Omega &= (a_O V_{sel},dem + \ell K_\Omega,dem,Q + o_{seed})(1-K_\Omega) - \delta_O K_\Omega\ \dot H &= (h_0(\tfrac{S+B}{2}) + h_A A + h_T X)(1-H) - (\delta_H + desk\cdot K_\Omega(1-m))H\ \dot F &= (f_0 + f_Y Y^* B)(1-F) - \delta_F F\ \dot G &= (g_1B + g_2X(1-P) + g_3F + g_4K_\Omega m)(1-G) - (\delta_G + b_1P + b_2K_\Omega(1-m))G\ \dot N &= (n_1V(1-P) + n_2X,std)(1-N) - (\delta_N + n_3P + n_4K_\Omega(1-L))N\ \dot Q &= (q_0 + q_1X + q_oK_\Omega,expl)(1-Q) - (\delta_Q + q_2P + q_xK_\Omega(1-expl) + q_3\max(0,V-Q))Q\ \dot P &= (p_1V_{sel}(1-B) + p_2,disc + p_3K_\Omega(1-m) + p_4K_\Omega(1-L))(1-P) - (p_5QS + p_6X,std + p_7B)P\ \dot E &= e_{reg}(1-E) - (e_1K_{phys},dem,thr + e_2K_\Omega)E\ \dot S &= s_{rate}\left(G^{.4}(1-P)^{.3}B^{.2}A^{.1} - S\right)\ \dot A &= a_{rec}(0.4+0.6B)(1-A) - a_{ext},x_att,(0.2+K_\Omega)A \end{aligned} ]
Parameter values are in simulations/gadm02/gadm02.py (PARAMS, INIT).
3.3 Diagnostics
[ VFAC = \left(H,X,G,N,Q,S,E,(1-P),A\right)^{1/9},\qquad VFAC_{0.1} = \left(H,X,G,N,Q,S,E,(1-P)\right)^{1/8} ]
These use equal exponents. VFAC is 0 if any factor is 0. As in GADM-0.1, VFAC is a research instrument, not a welfare function.
Constitutional floors, checked separately: G \ge 0.2,\; E \ge 0.2,\; P \le 0.7,\; A \ge 0.2.
3.4 Calibration
Time unit: one period = one year (ASSEMBLY-WP-0005-T01), so all rates are
per year and the horizon is 100 years. The implied timescales are mostly
plausible: commons obsolescence about 25 years (dX), physical capital about
20 years (dK), cohesion adjustment about 5 years (srate). Organism
capability, at about 17 years (dO), is the main exception (§ 5.1).
There is no empirical calibration. Three coefficients were adjusted so that the baseline stays near its initial state, instead of trivially collapsing or saturating:
v0= 2.5: the seven-factor product is about 0.14 at initial values.aK= 0.35 andn1= 0.30: otherwise K_phys and N decay to about 0.12.
Everything else is a first guess, chosen so that rates fall roughly in 0.03–0.3 per period.
4. Scenario results (T05)
Full table: simulations/gadm02/results/summary.md. Scenario definitions:
scenarios/. Final values at t = 100:
| Scenario | VFAC | VFAC_0.1 | P | G | A | B | Notes |
|---|---|---|---|---|---|---|---|
| Baseline | 0.46 | 0.44 | 0.52 | 0.44 | 0.65 | 0.59 | slow erosion of X and N, rising P |
| Automated capitalism | 0.32 | 0.29 | 0.73 | 0.28 | 0.58 | 0.33 | P ceiling breached in 69 % of periods; demand and cohesion fall |
| Dividend abundance | 0.45 | 0.43 | 0.54 | 0.45 | 0.62 | 0.69 | demand stabilized, but VFAC ≈ baseline |
| Universal venture access | 0.49 | 0.47 | 0.52 | 0.57 | 0.64 | 0.58 | agency up via restartability |
| Commons-rich | 0.54 | 0.54 | 0.48 | 0.47 | 0.62 | 0.57 | X 0.27 → 0.66; second best overall |
| Attention oligopoly | 0.37 | 0.36 | 0.69 | 0.38 | 0.55 | 0.61 | P approaches the ceiling; N collapses to 0.17 |
| Generative regime | 0.65 | 0.64 | 0.31 | 0.64 | 0.78 | 0.70 | stable; lowest ecological headroom (E 0.48) |
| — with concentrated lineages | 0.53 | 0.50 | 0.50 | 0.46 | 0.79 | 0.71 | loses about two thirds of the gain over baseline |
| — with attention extraction | 0.58 | 0.59 | 0.41 | 0.60 | 0.45 | 0.71 | VFAC_0.1 understates the loss |
Readings
These describe the model's behavior under its assumed signs. They are candidate hypotheses, not claims about economies.
- Abundance without breadth fails (automated capitalism). Output Y* is close to the baseline (0.50 vs. 0.53), but domination crosses its ceiling and claims breadth B drops from 0.59 to 0.33. This reproduces GADM-0.1's primary question in model form.
- Dividends stabilize demand, not agency. Dividend abundance raises B from 0.59 to 0.69, but G, P and VFAC barely move. In this model, claims alone do not counter domination or commons erosion.
- Reuse matters through large shifts, not interaction. The
commons-rich regime is the strongest single-lever regime, but
rho0alone is not a top driver (rank 20 of 80 one-at-a-time). The original reading, "reuse works as a bundle", was refuted by the global analysis (§ 5.1): the bundle shows almost no interaction. The scenario's effect comes from moving I_X, ρ_0 andlin_openby 100–200 %, far outside local sensitivity ranges. - Organism governance dominates the generative regime. Concentrating
lineages (
L,lin_open,mlow) costs about two thirds of the generative regime's VFAC gain over baseline (0.65 → 0.53, baseline 0.46). An extraction-funded attention regime costs about 40 % (0.65 → 0.575). - VFAC without attention understates attention harm. Moving from the
generative regime to its attention-extraction variant, VFAC falls by 0.075,
but VFAC_0.1 falls by only 0.042 (0.636 → 0.594). In the extraction
variant, VFAC_0.1 even ranks above VFAC, the reverse of every other
scenario. This supports including A, and also the Goodhart warning in
InformationOrganismsInGADM.md§ 4.1. - The generative regime has an ecological cost. It has the lowest E of
all regimes. It stays above the floor, but
eregranks third in its sensitivity. Abundance needs throughput decoupling (GADM-0.1 § 14) to stay generative.
5. Sensitivity (T06)
Full tables: simulations/gadm02/results/sensitivity.md
(one-at-a-time, ±20 %, effect on final VFAC).
| Rank | Baseline | Generative regime |
|---|---|---|
| 1 | dO organism depreciation (+) |
m membrane control (+) |
| 2 | ell organism learning (−) |
L lineage diffusion (+) |
| 3 | p7 claims breadth checking P (+) |
ereg ecological regeneration (+) |
| 4 | wL0 labor share (+) |
expl explainability (+) |
| 5 | IX commons investment (+) |
v0 experimentation (+20 % → −) |
Readings:
- Under baseline governance, faster organism learning lowers VFAC. Higher
elland lowerdOboth reduce VFAC: K_Ω grows under operator-controlled membranes (m= 0.3) and concentrated lineages, and this feeds P, lock-in and deskilling. In the generative regime, the same organism growth is beneficial, and the governance leversmandLbecome the top drivers. This is the model form of hypothesis M3. Caveat: it follows directly from the assumed moderation of links #39–#41 bymandL. The model shows that these assumptions matter most, not that they are true. - More experimentation can hurt in the generative regime (+20 %
v0→ lower VFAC). This happens through the epistemic brake B3 (link #33, a contested link). - One-at-a-time analysis cannot detect interactions. The global analysis in § 5.1 checks for them.
5.1 Global sensitivity (ASSEMBLY-WP-0005-T01)
Full tables: simulations/gadm02/results/gsa.md. Method: Morris screening
over all 80 parameters (20 trajectories), then Sobol indices for the top 10
plus the reuse bundle. Parameters vary ±50 %, N = 256, with bootstrap 95 %
intervals. S1 uses the Saltelli (2010) estimator with centred outputs; ST
uses the Jansen estimator. The uncentred S1 estimators were tried first and
were unusable (VFAC's mean is large relative to its spread).
| Baseline | Generative regime | |
|---|---|---|
| Top ST | dO 0.34, p7 0.13, ell 0.10, wL0 0.07, IX 0.07 |
m 0.27, L 0.13, ereg 0.13, p7 0.07, expl 0.06 |
| ΣS1 (analysed set) | 1.04 | 1.06 |
| Reuse bundle ΣS1 / ΣST | 0.09 / 0.11 | 0.08 / 0.09 |
Readings:
- The model is nearly additive within ±50 %. ST ≈ S1 for every analysed parameter, and ΣS1 ≈ 1. Interactions are small, so the one-at-a-time rankings in § 5 are confirmed.
- The "reuse as a bundle" reading is refuted. The bundle explains about 10 % of variance, with negligible interaction (ΣST − ΣS1 ≈ 0.01–0.02). Reading 3 in § 4 has been corrected.
- Organism governance remains the dominant lever in the generative
regime. Membrane control
malone explains roughly 27–32 % of variance, and lineage diffusionLa further 13–16 %. Reading 4 in § 4 holds globally. - Calibration priority:
dO. Organism-capability depreciation explains about a third of baseline variance. At 0.06 per year it implies a 17-year lifetime, which is plausibly too long for AI systems. It should be calibrated first.
6. Known limitations
- No units, no calibration. Comparisons between scenarios are meaningful; absolute values are not.
- Every structural sign comes from
GADM-CLD.md. The contested links (#33, #40, #41, #46, #49) drive several readings. - Participation claims
cpare a fixed share of capital return. A real mechanism would tie them to contributions (attention, judgment, governance), which is WS-14 work. - A single population with no cohorts, sectors or regions.
- Attention dynamics are weak: in the attention oligopoly, A falls only to
0.55.
aextmay be underestimated. Resolved in GADM-0.3 (GADM-0.3.md§ 4.1:aextrecalibrated to 0.275 against time-use evidence). - Euler integration, dt = 0.1. No stiffness issues were observed at these rates.
7. Reproduce
python3 -m unittest discover -s simulations/gadm02
cd simulations/gadm02 && python3 run_scenarios.py && python3 sensitivity.py
cd simulations/gadm02 && python3 gsa.py # ~5 min; --quick for a smoke run