MORPH: Self-Organising Multi-Robot Task Allocation via Neuroplasticity-Inspired Adaptive Topology
Organizations: Department of Information Technology, Uppsala University, 751 05 Uppsala, Sweden
Abstract
Multi-robot task allocation (MRTA) in dynamic environments faces a fundamental tension: effective coordination requires learned structure, but that structure must adapt when conditions change. Existing methods resolve this by assuming prior task knowledge, a utility function, a cost matrix, or a trained policy making them brittle when deployed without such knowledge or when task distributions shift. We present MORPH(Multi-agent Online Rewiring through Plasticity-guided Hierarchy), a training-free MRTA framework where global allocation quality emerges from 4 local plasticity rules (synaptic, homeostatic, structural, and metaplasticity) applied to a directed pairwise preference matrix updated from runtime co-occurrence and task-completion feedback. MORPH requires no task model, no bid computation, and no offline training; response decisions use learned AGV-to-Picker preferences rather than a fixed proximity rule. Within the Gerkey-Mataric MRTA taxonomy, MORPH is the first method in the single-task, single-robot, instantaneous-assignment class to learn directed pairwise allocation preferences online. Evaluated on the TA-RWARE warehouse benchmark (8-24 agents, 4 maps, 800 steps per episode, 5 seeds), MORPH achieves 110% of all-to-all throughput at N=24 while using only 21% of possible coordination links as an efficiency advantage that grows monotonically with fleet size. Under spatial task distribution shift, MORPH degrades 3x less than proximity-based methods while its learned preferences remain uncorrelated with Manhattan distance. Systematic ablation confirms all four plasticity rules contribute measurably. Two allocation properties emerge without programming: cross-type preference dominance and progressive preference sparsification, mirroring the developmental refinement of biological neural circuits. Learned preferences are driven by task co-occurrence history, not spatial proximity.
Figures & tables
| Rule | Plasticity form | Biological basis | Failure prevented |
|---|---|---|---|
| R1 | Synaptic | Hebbian LTP + dopamine gating [ 13 , 5 ] | Stale preferences persist |
| R2 | Homeostatic | Synaptic scaling [ 33 ] | Isolation / hub collapse |
| R3 | Structural | Synaptogenesis + pruning [ 15 ] | Cold start; slow rewiring |
| R4 | Metaplasticity | BCM-inspired dynamic thresholds [ 1 , 7 , 36 ] | Saturation; shift inertia |
| Parameter | Symbol | Value |
|---|---|---|
| Synaptic learning rate | 0.18 | |
| Base decay rate | 0.98 | |
| Homeostatic rate | 0.04 | |
| Formation threshold (start/end) | 0.75 / 0.45 | |
| Pruning threshold | 0.008 | |
| Target degree fraction | 0.35 |
| Scale ( ) | Method | Deliveries | %AP | Links (%max) |
|---|---|---|---|---|
| Tiny (8) | Proximity | 108% | 22.2 (79%) | |
| TSG | 96% | 2.6 (9%) | ||
| MORPH | 108% | 27.0 (97%) | ||
| Full Graph | 100% | 28.0 (100%) | ||
| Small (12) | Proximity | 117% | 36.2 (55%) | |
| TSG | 111% | 3.7 (6%) |
| Condition | P1 | P2 | P3 | P4 | P5 | P6 | r3 | r4 | r5 | r6 | |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Proximity | 51.1 | 48.2 | 45.7 | 41.8 | 37.9 | 34.1 | 45.0 | 57.9 | 96.0 | 83.5 | |
| TSG | 49.9 | 46.0 | 44.6 | 41.4 | 38.8 | 38.1 | 40.8 | 54.6 | 39.8 | 50.0 | |
| MORPH | 50.0 | 49.1 | 47.5 | 46.1 | 45.2 | 44.0 | 36.9 | 23.1 | 35.7 | 17.7 | |
| MORPH (reset at shift) | 50.0 | 48.9 | 48.2 | 46.5 | 43.9 | 40.8 | 31.4 | 17.1 | 49.5 | 18.1 |