CRN Dynamics on Basal Ganglia Pathways
Interactive GKSL open-system transport on DTI-derived connectome subgraphs. Explore the inverted-U selectivity window predicted by CRN theory across two functionally distinct neural pathways.
T2 / T3 Dissociation
Both ports show the inverted-U transport profile (ENAQT), but respond differently to weight perturbation. In T2 (gating), shuffling edge weights destroys selectivity (G > 0) โ the specific DTI weight pattern matters. In T3 (relay), surrogates perform equally well (G โ 0) โ topology alone suffices. This double dissociation is a core prediction of CRN.
Connectome โ Live GKSL Dynamics
Rโ(t) โ Selectivity Dynamics
Inverted-U โ Rโ(Tend) vs ฮบ
PT(t) โ Target Absorption
PD(t) โ Distractor Leakage
T3 โ Motor Relay Pathway
T3 shows an inverted-U transport profile (ENAQT exists), but unlike T2, weight-shuffled surrogates perform equally well โ graph geometry alone drives transport. CRN theory predicts this: gating circuits (T2) require weight-tuned interference, relay circuits (T3) broadcast via structure.
โ T3 trajectory data not loaded. Run: python crn_dump_trajectories.py --port T3 --outfile trajectories_100206_T3.json
CRN framework: Dolgikh (2026). doi:10.5281/zenodo.18249250
GKSL solver: RK2, dt=0.05, Tend=10, ฮณT=1.0, ฮณL=5ร10โปโด, ฮต=2.0