Re: Reproductive Selection

leland.mcin...@xxxxxxxxx wrote:
On Dec 16, 7:33 pm, Treus <treusd...@xxxxxxxxx> wrote:

<snip>

The two allele model does not sufficiently account for the complete
set of traits uniquely necessary to the RC of a population arbitrarily
different from whatever ancestor is taken as the starting point.

Presuming I understand your jargon right, yes, it does. You can
simply apply the two allele model repeatedly at different loci to
generate as large a difference as you like. Equally, once the
reproductive incompatability has been introduced (via, for example,
the two allele model) there's nothing keeping the populations from
diverging drastically by drift, and/or environmental and sexual
selection -- which is to say diverging arbitrarily.

Okay so far, but how are you retaining RC within the respective
populations over time without reproductive selection? Without the
(selection driven) co-evolution of R(Sn,x), where R(Sn,Sn) is at least
equal to R(Sn-1,Sn-1), for every Sn, you have a slow degradation of RC
in each successive generation.

Consider, again, the other model, where "incompatability" at each
generation is small (within the average variation of the population)
but, by progressive increments over many generations, large
incompatbilities can be introduced. This is the "great dane can't
breed with chihuahua" model. Such divergence, with small incremental
steps, doesn't have any clear bounding on it, thus, given enough time
for enough small increments, incompatabilities can be arbitrarily
large. What you really need to demonstrate is some reason why there is
a finite upper bound on how many small increments can accrue. You
haven't done that.

Sure I have, and just did so again in this very post.

.