... the only difference in mechanisms is that the "tendency towards stasis" no longer operates once a population has divided.
Not exactly -- that's more of a result than a mechanism. To me it is a subtle little difference but important enough to consider.
After a speciation separation, each population now has a new {stasis equilibrium} point that it will try to "center" (chose mates) around, and there is no mixing of genes between the divided populations so those {stasis equilibrium} points can diverge.
But there are other population dynamics that are involved both before and after that are different. Take pelycodus:
(Image copied to mirror site to save bandwidth originally from A Smooth Fossil Transition: Pelycodus)
Where you see a general (normal) trend toward larger individuals as time passes, and then a speciation event with subsequest divergence between two populations. The right branch continues with the linear increase in size, however the left branch dives back to re-occupy the original {size\niche\function}. This would be forced by competition between the two groups, a selection pressure that doesn't happen while they are one population. Once they have diverged sufficiently that such competition does not threaten survival of one population, then each are free to take whatever evolutionary paths they want, but they will not be the same path - that bridge is burned.
Note that the reduction in size is faster than the general increase in size. This is the effect of being de-linked.
Note also that the population variation is restricted to the same general width rather than getting broader at each time level. This is the effect of the trendency towards stasis.
Stasis doesn't have to be a result, btw, it can be {static relative to a continued trend} as above; it is just a tendency inherent in sexual selection (imho) towards average individuals in a population -- ie sexual selection could be a two-edged sword, allowing greater (liberal) mixing of genes along with quick (conservative) selection to omit extreme divergence.
I tried to find the post where I had come to this conclusion last night and couldn't (silly ol search system + tired brain + impatience), but you can think of all the selection pressures that operate within a population and all the selection pressures that operate between populations as being the essential difference in the shape of the evolution that is observed.
Wait, I finally found the post
Message 267
"micro"evolution is the individual changes in species over time (and space), each change is a separate "micro"evolutionary event. This represents short term trends and fluctuations (larger beaks or smaller beaks etc), the change that occurs before speciation takes place.
"macro"evolution is the accumulation of changes over long periods of time, thus "macro"evolution is not the {change in species over time due to mutation and natural selection} but the {accumulation of changes incorporated into species by "micro"evolution ... and natural selection}. This represents long term trends - the change that continues (by continued "micro" changes) to occur once speciation has been achieved.
Which is further refined in
Message 278
The more I think about it, the more it seems to me that it's more than that, it's also the difference between application at different levels:
(1) the individual level -- each individual is conceived with it's basic kit of mutations and the fitness of the individual is tested to survive to live and breed, those with non-lethal mutations live, those without disabling mutations survive and grow, those without disadvantageous mutations - and maybe a bit of luck - breed. This is where continued mutation and adaptation occur.
(2) the population level -- the population is made up of individuals with a wide variety of mutations, adaptations and abilities, and the dynamics of interactions of the members of the population in reaction to the environmental pressures is where change versus stasis tendencies are selected, this is where the dynamics of the different adaptations and abilities come into play, whether for survival or for breeding. It can only act on the basis of the net accumulation of mutations that are available.
You could also say that "micro" changes are not fixed in the population, as the population as a whole can revert under changed selection pressures (the way the beak size can revert). Whether the {features\alleles\variations} can become part of the defining characteristics of the species is debatable, as this gets into what distinguishes one species from another (especially on a timeline).
Once a speciation has occurred those changes have become part of the {defining genome} of the species and so do become fixed (as part of the previous amount of variation is discarded in the divide), albeit still subject to "micro" changes around that {center\node\nexus}.
Speciation is the dividing line then between "micro" and "macro" -- and once
two speciation events occur in succession the fact that "macro"evolution (by this definition) has occurred cannot be denied either: that is all that is needed to show that evolutionary branches occur and that the result is a nested hierarchy, which is the basis of all upper level taxonomy divisions.
You could also use the genetic differences between the species in these subsequent speciations and of their ancestors to validate the genetic tree derivations. I would think this has been done and that there would be ongoing work on it to refine the marker systems used (anybody know of papers on this?).
You can't have "macro" without "micro" -- the basic mechanism of change is still the same -- but you could have "micro" without "macro" ... hence evidence of such effect is different than evidence of (species) change over time.
Hope that helps.
Enjoy.
Edited by RAZD, : added (species) at end
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