New analytic result for the evolution-of-sex paper: how far can two lineages
diverge before recombination (model merging) stops working? Frames merge failure
as biological reproductive isolation via Bateson-Dobzhansky-Muller
incompatibilities. src/knowledge/speciation.py, kind: speciation, on the E7-E11
genotype machinery (pure seeded NumPy, bitwise-reproducible; no external
simulator whose separate RNG would break that).
- BDM construction (E12.yaml): ancestor + two lineages substituting disjoint loci
(each parent adaptive, incompatibility-free), a fraction rho of cross-lineage
pairs are BDMIs. Sweeping divergence d reproduces the predicted
compatible -> outbreeding depression -> hybrid inviability curve; the isolation
cliff moves to lower d as epistasis density rises (iso at d=20: 0.00/0.03/0.50
for rho 0.1/0.25/0.5); incompatibilities snowball ~ (d/2)^2 (Orr-Turelli).
- NK variant (E12_nk.yaml): parents = hill-climbed local optima; the epistasis
wedge — recombination gain flips 0 -> -0.13 and OD rate 0 -> 0.90 as ruggedness
K rises. At matched divergence, mergeability is governed by epistasis, the axis
no divergence-only ML merge predictor captures.
plot_E12.py (3-panel), +7 tests (138 green), README with honest positioning
(concedes the empirical phenomenon to Pari 2024 / Zhou 2026 + permutation
artefacts to Git Re-Basin; claims the predictive theory + the epistasis wedge).
Wired into make layer1.
Co-Authored-By: Claude Opus 4.8 <noreply@anthropic.com>
The culmination. A finite population of agents (genotypes, L loci) evolves
on a rugged NK landscape that IS reality (knowledge/dynamic_society.py),
composing the four operators the whole study built toward: grounding,
directed recombination (sex), quality-diversity selection, and mutation.
Grounding is made load-bearing via the consensus-conformity (self-
consumption) mechanism (GG decision): selection acts on
g*true_fitness + (1-g)*conformity, where conformity = agreement with the
population's own consensus, so at g=0 the society optimises fitting-the-
crowd rather than reality.
4-arm ablation (12 reps), each breaking distinctly, only the full society
climbing (global_opt ~ 0.79):
- full 0.78 climbs to the optimum, diversity maintained longest
- no_sex 0.77 can't recombine to escape local optima
- no_diversity 0.74 greedy: collapses diversity fastest, worse local optimum
- no_grounding 0.48 self-consumption collapse to an unfit consensus
(trains on the crowd -> confident-but-wrong mean;
conformity-true gap ~ 0.5)
This integrates E1-E6 + the learning kernel + E7-E10 into one system and
shows the Lamarckian society needs ALL of grounding + directed sex +
diversity: on a rugged landscape you need diversity to explore basins, sex
to recombine them, and grounding to select on reality -- remove any one and
you fail differently. Closes the C3 vertical claim analytically; the LLM
rung remains the eventual empirical instantiation.
New: knowledge/dynamic_society.py, configs/layer1/E11.yaml, figures/
plot_E11.py, README, tests/test_dynamic_society.py (+5). kind:
dynamic_society dispatch; make layer1 wired. 122 tests green.
Co-Authored-By: Claude Opus 4.8 <noreply@anthropic.com>
Deepen the sexual-reproduction frame before entering the full society, on
the two facets GG chose: landscape robustness and directed recombination.
Adds a Kauffman NK landscape (genotype.nk_fitness, tunable ruggedness),
finite n-parent crossover (genotype.crossover, per-gap recombination rate),
and hill-climb (parents = local optima = trained models).
E9 (recomb_landscape) -- the "why sex?" test: E8's dramatic super-parent
result used an ADDITIVE landscape. On rugged/epistatic landscapes, blindly
recombining local optima causes OUTBREEDING DEPRESSION -- offspring fall
below the parents, worse with both ruggedness and recombination rate (K=8,
free recomb: ~ -0.23), and the optimal recombination rate shrinks as
ruggedness grows. Design rule: merge freely when skills are complementary/
additive; sparingly (and with selection) when entangled.
E10 (directed_sex) -- directed sex beats biological sex: biology is stuck
with 2 random-mating parents and no offspring preview; an AI can choose
complementary mates, evaluate many recombinant offspring, keep the fittest,
and use unbounded parents (iterated recombine-then-select). Random
("biological") sex craters with ruggedness (0.66->0.51); directed sex
tracks/exceeds the best parent at every ruggedness -- converting the
outbreeding-depression catastrophe into a win. No biological analog.
Complete sexual-transmission picture: dramatic super-parent offspring when
skills are complementary (E8); outbreeding-depression risk when entangled
(E9); directed sex resolves the risk (E10). configs/layer1/{E9,E10}.yaml,
figures/plot_{E9,E10}.py, READMEs, +5 tests (117 green).
Co-Authored-By: Claude Opus 4.8 <noreply@anthropic.com>
Enter the Lamarckian society with a robust theoretical frame. The single-
locus, fixed-p* model can only express recovery toward a ceiling; the
society's load-bearing claim is vertical -- capability that EXCEEDS any
component. Generalize knowledge to a distribution over genotypes (L
biallelic loci, K=2^L, additive fitness = # correct loci), reusing all the
K-mode machinery. The one new operator is recombination: free recombination
sends p -> product of per-locus marginals (linkage equilibrium).
E8 (star, kind: society) -- the vertical claim / Fisher-Muller: decorrelated
PARENTS (specialists, expert on their loci, agnostic elsewhere) are
recombined; sexual merge assembles a genotype fitter than any parent,
climbing to the optimum (12/12, a genotype no parent had) as parent count
grows and rho->0, while the best single parent (~8.7) and the mean-mixture
"model soup" (~11.6) plateau below. Reuses make_retention_matrix (locus
mastery replaces tail-item retention).
E7 (kind: genotype_lineage) -- the advantage of sex: a single population
adapts toward the optimum; the sexual lineage adapts faster than asexual
(clonal interference) by keeping loci in linkage equilibrium (LD->0 vs LD
spike). Honest scope: a speed advantage, not a permanent Muller's-ratchet
gap (subtle to force); E8 carries the headline.
Metaphor shift (per GG): the society is sexual reproduction with UNBOUNDED
parents, not teacher->pupil. Teacher->pupil caps at the ceiling; n-parent
recombination is combinatorial and generative, and unlike biology there is
no two-parent limit. Collapse = asexual degradation; the cure = sex. This
unifies E4 (merge != average) + E6 (irreversibility) under evolution-of-sex
theory and reaches ground Riis's single-locus n-grams cannot.
New: knowledge/{genotype,genotype_lineage,society}.py, configs/layer1/{E7,
E8}.yaml, figures/plot_{E7,E8}.py, READMEs, tests/test_genotype.py (+7).
experiment.py dispatch (kind in {genotype_lineage, society}); make layer1
wired. 112 tests green.
Co-Authored-By: Claude Opus 4.8 <noreply@anthropic.com>
Revisiting Layer 1 against Layer 1.5 (and Riis 2026, arXiv:2604.08554):
neutral Wright-Fisher is a null that BOTH neural architectures deviate
from, in opposite directions. Add a learning kernel to the refit step,
p_{t+1} = T_theta(counts/n), with two population-genetics knobs -- reset u
(mutation toward a prior = smoothing) and temperature tau (sharpening =
mode-competition) -- both identity by default, so the histogram bridge and
all 68 scientific-validation/correctness tests are unchanged.
Result: neutral drift fails both neural models, oppositely.
- VAE regime (n=6000, K=30): neutral drift is inert (no collapse), yet the
real VAE collapsed to one mode. Sharpening tau=0.8 reproduces it -- the
estimator ADDS collapse pressure.
- RNN regime (n=200, K=256): neutral drives H->0, but the real RNN only
partially collapses. Mutation u=0.006 reproduces the H-floor -- the
estimator REMOVES collapse pressure. Honest caveat: uniform-mutation
overshoots the RNN's forward-KL, evidence its smoothing prior is
truth-like, not uniform (future refinement).
This mechanistically explains the architecture-generality result and the
softened neural g*, and develops the estimator axis Riis names as future
work. New: knowledge/kernel.py, configs/layer1/kernel_{sharpen,smooth}.yaml,
figures/plot_kernel.py (overlays analytic arms vs committed neural
endpoints), READMEs, tests/test_kernel.py (+6, 105 total green). Strategic
Riis positioning recorded in CLAUDE.md: concede "collapse=drift" as prior
art; lead with recombination, the kernel axis, and the Lamarckian society.
Co-Authored-By: Claude Opus 4.8 <noreply@anthropic.com>
Finishes the Layer 1 analytical core. All six experiments run with honest,
publication-quality figures; 71 tests green.
- E3 region-matched grounding: `grounding.exercised` knob + per-region tail
survival. Matched holds the exercised region's tail (0.49) where uniform
spreads thin and lets it collapse (0.07).
- E4 multi-teacher recombination: `run_coverage` runner. Union coverage matches
U(K_T,rho,q) exactly. Finding: mean-mixture distillation shows NO surviving
benefit (a conservation law — 1/K_T dilution cancels the union gain); a
union-preserving max-merge (M2N2-style) does. E4 reports both operators.
- E5 QD vs greedy: greedy drives fixation (H~0.01); QD holds H at 0.48-0.88,
rising with the novelty exponent.
- E6 re-mint gate: `arm` multi-override sweep. Re-minting a collapsed lineage
locks in divergence of KL-to-original; gating on diversity prevents it.
- E2 analysis add-ons (from the companion work order, numbers verified): new
analysis.py (reduce_to_stationary, critical_grounding with bootstrap CI ->
g*=0.048, 95% CI [0.047,0.050]); tail_band_metrics + per-band logging; the
E2 figure rebuilt as a 2x2 (defined g*+CI, g=0 flagged as a finite-time
artifact, tail item-vs-mass, per-rarity-band panel). Uses truth-mass-weighted
tail coverage rather than the raw (martingale) tail_mass.
Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
Scaffold plus the Layer 1 analytical core and the first two experiments.
- knowledge/: truth, metrics, teachers (2.7.1 shared-switch construction),
step, lineage, experiment, config, seeding (imported as `knowledge`).
- Validation spine green: neutral decay (Pred 1), fixation (Pred 2), exact
mutation-drift equilibrium (Pred 3), union coverage (Pred 5). 68 tests pass.
- E1 reproduces tail-first collapse. E2 delivers the headline: a grounding
phase boundary g* << 1, with stationary H tracking the exact H_eq closed
form (g=0.005 -> 68% of truth diversity; g=0.05 -> 96%).
- Reproducibility: uv venv from a hash-pinned uv.lock is the source of truth;
every run writes results.parquet + resolved_config.yaml + manifest.json
(lib versions, git commit, sha256). Figures and manifests tracked; the
large regenerable parquet is gitignored.
Co-Authored-By: Claude Opus 4.8 (1M context) <noreply@anthropic.com>
