Originally Posted by
Croakmore
> John, let me try to answer you this way and explain to you why
> your statistical model is not a good idea.
> These are the known causes of evolution:
> 1. Random genetic drift, caused by a critical decrease in
> population size, which can lead to either the “bottleneck effect”
> (e.g., excessive hunting of California elephant seals) or the
> “founder effect” (e.g., Asian migration into Western hemisphere
> following Ice Ages). Neither are considered “selective” in the
> neo-Darwinian sense.
> 2. Gene flow, caused by the trans-species migration of genes, as
> they are well known to “jump” around (e.g., tsetse fly genes are
> known to have “jumped” into the human gene pool…Kersplash!)
> 3. Random mutations of genes, caused by some kind of reshuffling
> of the DNA or RNA sequence that somehow finds genetic durability;
> maybe just a single substitution of a nucleotide in a codon,
> leading to a slightly different genetic expression (e.g., UV light
> can force enough energy into a DNA molecule to randomly alter its
> sequence).
> 4. Disproportionate mating in a population, cause by preferential
> factors that influence mating options (e.g., some guys are luckier
> than others), which are nevertheless non-selective in a Darwinian
> sense.
> 5. Natural selection, caused by disproportionate success in
> reproduction. This is the only cause that biologists regard as
> “selective,” because nature makes the rules that all biological
> systems must measure up to. (When the pioneers went West, they had
> a proverb: “Root, hog, or die.” Those who could either root or hog
> were “selected” by virtue of the fact that they were the only ones
> left to advance their genes.
> Notice that evolution usually is a combination of these five
> factors, and so there may be many permutations, and each with a
> different emphasis here or there.
> Confusing this even further is that jumping-gene business. It
> occurs in all forms of life (e.g., it’s going on right now in your
> intestines, wherein many of your resident E. coli are conjugating
> like crazy to keep their genes in the game). The most confounding
> thing that amazes me is this business of “crossing over,”
> occurring in the gamete production process known as meiosis. In
> the first prophase some genes actually jump from one paired
> chromosome to the other; it appears to be random and with no
> predictive model possible. The end result of crossing over is
> huge, because the gamete (sperm or egg) is the ONLY part of any
> individual of any species that moves on in time or otherwise
> survives. This is called “homology,” and it certainly does make
> evolution appear to be mostly a genetic gambit. But the field of
> biology is still mulling over the idea that giraffes got their
> long necks the old Lamarckian way – by way of something that
> somehow eludes the rule of homology.
> All of this is to say, John, that the blithering complication of
> factors and multi-conditional bifurcations leave nothing but
> confusion for the biologist who seeks to build a model of
> biological evolution, especially a statistical one. I know of two
> biologist who managed to observe evolution in a fruit-fly
> population (Drosophila) by actually watching the appearance of a
> new species. They concluded that drift and selection shared almost
> equally in explaining the cause of this speciation. Furthermore,
> they concluded after a rigorous study that this speciation had
> very little influence from genetic mutation per se.
> From my POV, I can’t see any reasonable way to build a statistical
> model of evolution that will account for your giraffe’s long neck.
> Others will disagree with me, especially those who do not prefer
> the neo-Darwinian approach. They want to sell me a different kind
> of vacuum cleaner; I’ll listen to their pitch, but I don’t let
> them in the door.