Synthetic and biological living polymers are self-assembling chains whose
chain length distributions (CLDs) are dynamic. We show these dynamics are
ultrasensitive: even a small perturbation (e.g. temperature jump) non-linearly
distorts the CLD, eliminating or massively augmenting short chains. The origin
is fast relaxation of mass variables (mean chain length, monomer concentration)
which perturbs CLD shape variables before these can relax via slow chain growth
rate fluctuations. Viscosity relaxation predictions agree with experiments on
the best-studied synthetic system, alpha-methylstyrene.Comment: 4 pages, submitted to Phys. Rev. Let