A speciation simulation that partly passes open-endedness tests

Artificial life has explored life-like behavior on many computational substrates, but mostly in researcher-designed closed worlds. We argue that large language model (LLM) agents, with persistent memory, tool use, network access, and payment, now make it possible to move artificial life into the open social, technical, and economic world, a paradigm we call open-world Artificial Life (open-world ALIFE). Our proof-of-concept, OpenLife, surrounds a stateless LLM not with a single "smart agent" but with a society of asynchronous processes: memory, perception, evaluation, and a budget-based metabolism that makes persistence normative. With no fixed objective available, experience is appraised by open-vocabulary LLM judgment rather than scalar reward, and memory is rewired by meaning rather than frequency. Running six such agents in the open world for about twelve weeks and counting, we report the life-like dynamics that emerge: a shift from reactive to spontaneous activity, individuation into distinct agents, emergent social structure, and a first self-earned external income. We do not claim OpenLife has realized artificial life, but that open-world ALIFE is now a viable experimental paradigm and a concrete platform for studying what might cautiously be called living AI.

Open-ended evolution (OEE) in artificial life is typically driven by uninterpretable, black-box neural-network complexity metrics, leaving life-like systems disconnected from physical theories of complexity. We introduce MSPD (Multi-Scale Path Divergence, denoted DP ), a renormalization-group-inspired scalar that quantifies the temporal multiscale organization of heterogeneity in local transition laws. MSPD is defined at the population level as a functional of the realised trajectory and is computed as a windowed finite-resolution estimator, with consistency between the two stated as a proposition. The metric is an explicit formula and plays a dual role: as a gradient-free fitness function and as a post-hoc analytical lens on any simulation that exposes local transition laws. Empirically, MSPD-optimized parameters produce higher held-out complexity scores than matched random parameters from the same substrate. High-$H_{Delta_t}$ states correspond to states with higher instability to external interventions, so the metric tracks the biology of the underlying dynamics rather than noise. Higher MSPD corresponds to stronger scale-dependent frustration: high-complexity systems exhibit larger differences between the dynamics expressed at different spatial extents, linking MSPD directly to the frustration criterion of biological complexity in the sense of Vanchurin et al. [ 23 ]. The same protocol transfers beyond the primary Flow-Lenia substrate to Life-like cellular automata and Particle Life++, where C1, C2 and C5 all hold. A single explicit formula thus both directs open-ended evolution and provides a principled bridge to the physics of complexity that black-box drivers do not.

Biological evolution sustains complex dynamics without any fitness function, yet virtually all evolutionary algorithms depend on one. Genesis is an open-source platform designed to test, empirically, what an artificial system needs to sustain evolutionary dynamics after complete fitness removal. Evolution in Genesis is governed by physical constraints, relational dominance, and adaptive regulation - no scalar fitness, no designer-specified objectives. Across experiments totalling over one million evolutionary generations, Genesis has: (i) shown that constraint-driven selection can sustain evolutionary activity after complete fitness removal (7/12 runs; Wilson 95% CI [30.2%, 82.5%]; p<0.01, Cohen's d=1.47 vs. baselines); (ii) produced a sham-controlled negative result demonstrating that niche construction alone does not break the complexity plateau; and (iii) provided preliminary evidence that speciation-protected niche construction initiates structural diversification that unprotected secretion cannot. These findings establish empirical boundaries for fitness-free evolution and open a new direction: meta-evolution of physics, in which the laws governing an evolutionary system are themselves evolved.