Wow... You DO know, do you not, that it is possible to actually look back a few pages to see your original claims? Right? Or, one can click on the little arrow in your quote and brings one right to the post you are responding to, right?
Or, one can use the search function to find posts, right?
Ok feel free to provide a model that includes as many neutral mutations as you what
Right after you provide your model with 'non random mutations' playing a major role.
Transposons magically spreading through a population faster than any other mutational event - in 1 generation!
Stawman, all I am saying is that" directed mutations" (like trasposons) are more likely to produce big positive selectable changes, explaining this super fast evolution in the human line
Is that where you will stake your claim, is it?
OK:
The strange case of John Sanford, creationist
"All I am saying is that transposons likely played an important role and are responsible for some of the “evolution”
This mechanism can produce new proteins in just 1 generation so yes under that basis the mechanism is “fast enough “
me:
3. I remind you that a transposon still has to spread through a population like an SNP has to, and ask how this would speed things up. You ignore it.
Yes but transposons can produce new functional and selectable proteins (genes) in 1 generation…….
the RM+NS model would require a gene duplication + thousands of point mutations in order to get something that we would call a “new gene”**
...
"None random mutations are more likely to be positive, more likely to be selected for, more likely to build complex stuff like complete proteins) in a single generation, this is why the would spread faster than random mutations."
And that you consider these:
3. the number of beneficial mutations required to get a human trait from a human ancestor's trait
4. the number of traits that must be accounted for via fixed beneficial mutations
5. what those traits are
6. how were any of the above determined
Irrelevant, shows us all the fact that you cannot grasp the subject matter well enough to understand that without answers to these questions, one CANNOT say or imply or suggest, at all, that whatever number of possible fixed beneficial mutations one calculates are possible is "not enough."
If you do not know how much work is needed to build X, if you do not know what you are even starting from to build X, how can you say you do not have enough time to build X???
Why is this so hard to understand?
Here are pelvis comparisons between
A. afarensis (proposed human ancestor, ~3.2 MYA),
H. erectus (~2 MYA),
H. heidelbergensis (~500K ya), and modern humans:
Please explain to us all with your ReMine/Sanford knowledge and your keen math skills, how many fixed beneficial mutations (of any kind) do you think were required, were evolution true (which you seem to believe) to get a modern human pelvis from a "Lucy"? Please show your work and support it with one or two relevant pieces of supporting evidence.
I said no new random mutations being fixed and dominant in the human population in the Last 30 years
No you didn't:
"Just think about it in the last 30 years (since the genome project started) not a single mutation has been observed to become fixed in the human population, and you are supposed to average 6.6 per year"
Nothing about dominant or beneficial. Not that it matters - you did not demonstrate that all newborns were tested for such mutations (otherwise, how can you write what you did?).
Unless you are one of those dolts that thinks a "mutation" is like a new leg or a wing or something?
Your model predicts 7 mutations per year,.... So if your model is inconsistent to what we observe why are you convinced that your model is true?
You keep forgetting that the 6.6 number came from
YOUR NUMBERS, not 'my model', whatever that is.
Why can't you even keep track of you unsupported claims? I can keep track of your gibberish better than YOU can!!
** - also, why would we need a "new gene" requiring "thousands" of beneficial mutations when all we need to do is tweak a few genes, and alter some regulatory sequence? The more you try to add "problems" for evolution, all you do is show how little you understand genetics!