patiodog wrote: ican --
My quibble with the lottery thinking is that, for any given generation, "S" is limited by the previous generation's "I," so to speak, by virtue of the fact that they survive (if I'm understanding the model correctly). Does this make sense?
First, check rosbourne's referenced article and acquiunk's reaction. Then check farmerman's last post. Yours is no quibble -- no quibbles in any these.
Second, I think in our discussion we have finally reached "the core" of the issue.
What must be done to the lottery model to make it completely analogous to the standard evolution model?
Let's start with CA, the genome that was common ancestor to M, the genome of mice, and H, the genome of humans. But let's limit our attention to the evolution of those alleged 300 genes in H that are not found in M
ALLEGATIONS (i.e., from stuff I've read)
1. The evolution of M and H from CA started about 100 million years ago.
2. M evolved about 60 million years ago.
3. H evolved about 0.15 million years ago.
4. In that interval of time, there were three major extinctions: 53%@99 million years ago; 75%@70 million years ago; 35%@40 million years ago.
5. CA and its progeny were edited multiple times over that 100 million year period.
6. An edited GL,
germline ,genome may or may not survive and enconter an opportunity to procreate; even if it does, its progeny may or may not survive to procreate.
7. The 300 gene sequence found in H that is different than M can be represented by a sequence of base-four numbers: 0, 1, 2, 3.
8. This sequence is 300 x 9000 = 2,700,000 base-four numbers long.
ASSUMPTION
None of this sequence existed just before the time CA began to evolve to M and H.
QUESTIONS
1. How many separate edits of CA were required to evolve CA to M and to evolve CA to H.?
2. What was the average rate at which these edits occurred?