- 29 Medien
- hochgeladen 27. Februar 2019
There is a fruitful and developing programme within the ‘Physics of Life’ exploring analogies between evo-lution and the statistical mechanics of complex matter [1,2]. Both treat exponentially large spaces of con-figurations (possible genomes/possible microstates) which are explored by random dynamics (random mutation/thermal motion). Both admit maximisation/minimisation criteria (fitness/free-energy) – the dynam-ics optimise something. There are even evolutionary analogies of temperature (inverse population size)  and free energy (“free fitness”) .
Beneath the notion of thermodynamic equilibrium is the assumption of ‘ergodicity’ - the exploration of con-figuration space in a representative way, with an induced characteristic timescale to attain equilibrium. ‘Ergodic times’ are typically much less than the exponentially long times required for a complete search. For example, for a polymer of N subunits, the timescale for equilibration increases as N2 rather than the zN of a complete search. The strong dependence of these timescales on system size means that, even if a large system is not in equilibrium, some of its subsystems may be. We consider an illustrative example of the insect compound eye, which also carries the advantage that its optimum (in acuteness of vision) relies on physics and can be calculated .
The ergodic exploration of systems and subsystems within evolution generates a discussion of timescales for representative exploration of genotypic spaces. This in turn suggests a strong connection to the phe-nomenon of convergent evolution, and the conjecture that this might be expected in subsystems whose fitness is optimised by well-defined phenotypical constraints, and whose ergodic time is less than the rele-vant evolutionary time.
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 B.S. Khatri, T.C.B. McLeish and R.P. Sear, PNAS, 106, 9564-9569 (2009)
 T.C.B. McLeish, J. Roy. Soc. Interface Focus, 20150041 (2015)