SMH....
YOU presented the claim, with NO support whatsoever. Asking me to then refute the mere assertion you made (copied from Don Batten) is disingenuous and lame.
So can you provide rationale and evidence FOR? it was, after all, your claim.
See, it doesn't work the way you want it to - you cannot just toss out an assertion then demand others refute it. Your way is the child's way. Are you a child?
What is your evidence for your yet-again repeated claim about neutral mutations?
Thanks. Now how about providing some actual SUPPORT for your Batten/ReMine paraphrases?
Like about neutral mutations? Like about how all the mutational differences between humans and chimps are beneficial? Like ignoring the Grant and Flake papers and the Ewans' quote? Like your repeated unsupported claims about 50,000 mutations being 'too few'?
Let me help you out, as you are clearly in over your head -
Haldane's model was about FIXED, BENEFICIAL MUTATIONS.
NOT total number of mutations. NOT NOT NOT total number of mutations.
Get it?
Well, we can start by your favorably referring to the Batten essay, wherein he implies that Haldane's model was about 'building' genomes. Then we have you bringing up neutral mutations.
Anything else?
You referred to neutral mutations and total mutations in a discussion on Haldane's model, which is only about fixing beneficial mutations.
If you knew all about that, why did you even mention neutral mutations?
As a dodge? As a distraction?
Why?
You referred to neutral mutations and total mutations in a discussion on Haldane's model, which is only about fixing beneficial mutations.
If you knew all about that, why did you even mention neutral mutations?
As a dodge? As a distraction?
Why?
I never mentioned neutral mutations - YOU DID.
So tell me why YOU brought up neutral mutations in the first place.
Have you read ReMine's book? It seems not, for even the great electrical engineer creationist ReMine allowed for some tens of thousands of fixed neutral mutations on top of his calculated 1667 fixed beneficial ones. He said they were too few, of course - but like you and Batten, he never even tried to explain why he drew that conclusion.
By the way - yes, neutral mutant alleles can affect phenotype, but by definition, the changes are do not affect fitness.
The fact that you brought up neutral mutations.
Can you SUPPORT it with evidence or not? Can you even provide a logical rationale for asserting that it is too few?
It seems the answer is no, and you expect me to "refute" a made-up assertion.
Unlike you - or Batten, or ReMine - I, at least, provided a rationale and some supporting evidence. Odd that you decided to totally ignore it.
Um....
Yes, I can refute your claim that the article you linked indicates that "3,000,000 mutations where cruzial [sic] in developing important stuff that differentiate us from chimps" is at all relevant to your initial claims (which you are now, of course, changing upon realizing that you screwed up royally) -
"Most of these differences lie in what is believed to be DNA of little or no function. However, as many as 3 million of the differences may lie in crucial protein-coding genes or other functional areas of the genome."
No mention of "fixed beneficial mutations", which is what your original claims ala Batten/ReMine were about. Just "differences".
Remember? CONGRATS! You just DEMOLISHED ReMine's and Batten's Haldane's Dilemma argument!
LOL!!!
And the very next sentence:
"As the sequences of other mammals and primates emerge in the next couple of years, we will be able to determine what DNA sequence changes are specific to the human lineage. The genetic changes that distinguish humans from chimps will likely be a very small fraction of this set,"
The word "beneficial" occurs nowhere in the article.
FAIL.
Please provide evidence that 50,000 FIXED BENEFICIAL mutations are "too few" to account for human evolution from an apelike ancestor.
No more dodging and obfuscation and goal post shifting.
As I have already outlined (and you either did not understand or ignored for "plausible deniability" purposes), I do not think some gigantic number of mutations (beneficial or otherwise) are "required" to explain human traits evolved from an ape-like ancestor for the following reasons:
1. There really no 'brand new' traits that humans possess that chimps do not, indicating that our common ancestor also that the same basic traits
2. Therefore, we only need to "tweak" existing traits, and tweaking an existing trait does NOT require some large number of beneficial mutations
3. Support for this - point mutation in the FGFR-3 gene causing achondroplasia - altered limb-to-trunk proportion, altered facial characteristics, reduced joints, etc. All from one mutation. Reminder - I am NOT presenting this as a beneficial mutation, just the reality that MULTIPLE phenotypic traits can be altered, in this case, by a single mutation.
I predict that it will be possible, at some point, to map out specific mutations that resulted in specific phenotypes. We are not there now. But at least I have a foundationally-supported position with an example.
You have mere assertions premised on someone else's mere assertions based on someone else's mere assertions, who premised those assertions on personal incredulity, ignorance, and a desire to sway the under-informed to a creationist viewpoint by arguing with numbers.
Now YOU provide the evidence-based rationale for YOUR position, that "50,000 mutations do not even explain a small portion of the differences between chimps and humans" - and to be specific, this has to be 'fixed, beneficial mutations', because THAT is what Haldane's model and the creationist argument based on that is actually about.
In order for you to make your position valid, you must, at least:
1. Pick a trait that you think is so special in us
2. Identify the ancestral version of it
3. explain how many fixed beneficial mutations would have been required for that transition
4. explain how you know this, with at least a real-life "model" as I presented
OR
You could just admit that you were taken in by Don Batten's distorted misrepresentation of Haldane's model (it is NOT about 'building' a genome!) and ran with it without understanding the premise.
Your move.