Stern Cardinale: Response to Price, Carter, and Sanford on Genetic Entropy

What puerile nonsense. This from someone who lectures published text authors that they are oversimplifying. A variation in regulation is nothing like a divide by zero crash or overflow or anything to do with a Turing machine.

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Could we have @Joe_Felsenstein explain his analogy and what his terms meant? Or even if he can say he agrees with you that would be helpful. I would actually like to know how he views this, and I’d like to learn something.

The constant discussion of what terms mean in biology and when they’re used is frustrating.

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The quote you’re referring to was from Sanford himself. So yes, he agrees with himself. But he never said that Dr Felsenstein was not an expert in “population genetics”.

Yet, they are not experts on the specific topic at hand. They have not spent the last twenty years studying the problem of mutation accumulation.

My sense of Sanford’s meaning here is that these particular scientists being addressed are not known to be experts in the specific niche topic of mutation accumulation, in the way we would think of names such as Kondrashov, Keightley, Lynch, and Eyre-Walker. I don’t believe he meant it as an insult, just a clarifying remark about the nature of their comments.

I did get myself in trouble the way I used “substitution”. I meant it in the sense of the mutation event followed by the gene frequency changes that get it to fixation. That works in a smallish population. In a bigger one, it may not get all the way to fixation, so things are more complicated.

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Literally half my thesis. One chapter was even on inducing error catastrophe in ssDNA bacteriophage populations. Take 5 minutes to google me? Apparently not. Easier to just assume I don’t know what I’m talking about, I guess.

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Have you and Carter spent the last the last twenty years studying the problem of mutation accumulation? What research has Sanford done or published on the topic in the last twenty years?

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How, exactly, does one become an authority on population genetics and variation without consideration of mutation accumulation?

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Absolutely. I’m also well aware that mutations are produced by chemical reactions, most often transitions caused by keto-enol tautomerizations. Are those not chemical reactions in your expert opinion?

Why would you describe me as a molecular biologist before trying to rebut the points I made about virology, given that my graduate work was in virology?

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Can you remind me what the context of this question is? Where am I supposed to have said something that you’re responding to with this?

I believe I just defaulted to the description you’ve got here. I don’t know your full history or anything.

We’re also talking about nature itself, in the form of the frequent misrepresentations of data that are true without any interpretation or speculation. The idea that we are interpreting the same data differently is absurd, because you are ignoring most of the data.

So why are you making grandiose claims about expertise when you can’t be bothered to do a simple PubMed search? And we already clearly established that I was a virologist in a previous conversation. Remember when you tried to claim that none of the data mattered to your claim that H1N1 is extinct, and you were correct because a CDC chart had a little red arrow that you had misinterpreted?

But Sanford isn’t an expert either. He literally doesn’t know that virologists clone viral isolates. In case you don’t get it, that has a lot to do with mutation accumulation. John Holland, whose paper Sanford cites and misunderstands, was a mentor of mine.

Have you figured out what the “H” and “N” mean in influenza subtype names yet?

Can you explain why Carter’s having done the alignment means that he would therefore be capable of distinguishing changes caused by point mutations from those caused by reassortments? That makes absolutely no sense.

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It’s not hidden, and it’s not unquestioned, it’s simply that the evidence for deep time is overwhelming and includes a lot of data that is completely independent of genetics.

So if GE really does say we’d all be dead by now, then the argument is very simple:

  1. If GE is true, then deep time is false.
  2. Deep time is true.
  3. Therefore GE is false.

QED.

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Still repeating blatantly false claims, I see. This really is not worth the time. If you guys want to make a joint response article that deals openly with all the points we made, feel free. I’m done spending time hashing it out here in this forum. I don’t see any further use.

All that means is that the genome is more interlinked and can’t be represented by a set of swtiches directly connected to red/green bulbs. But it can be represented by a set of switches connected to red/green bulbs where each bulb is controlled by a combination of switches. This in no way affects the reasoning the analogy is used to represent, so the point illustrated by the analogy remains valid.

As for your letters analogy, if the initial genome is HOUSEHOLD, then H->M giving MOUSEHOLD and D->E giving HOUSEHOLE would both be detrimental on their own, but having either one of them present makes the other beneficial since together they lead to the alternative adaptive peak MOUSEHOLE. Either mutation will change the ratio of possible detrimental vs beneficial mutations, contrary to the assumptions of GE.

(And comments about MOUSEHOLE being worse than HOUSEHOLD will be ignored due to being based on the assumption that initial genomes were perfect. MOUSEHOLE is just as valid a word as HOUSEHOLD).

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He’s doing no such thing. If anything, he’s seeing that genetic entropy contradicts astronomy and geology, comparing their respective evidential support, and noting (as we all are) that astronomy and geology are well -supported while genetic entropy is a hodge-podge of fallacies, unjustified assumptions, misunderstandings and falsehoods.

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It has certainly been worth my time.

What’s the point if those points have been thoroughly addressed here and not stood up to scrutiny.

I agree. There is no point in rehashing already debunked arguments.

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That completely ignores both reproduction and selection. If you’re going to model evolution as changes to a single organism it’s no wonder you reach faulty conclusions.

And that one is faulty. Programs such as Tierra show that you keep adding typoes to computer programs indefinitely without completely destroying it, and that you can get engineering by randomly throwing changes together.

Paging Edmund Blackadder…

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Speculation? You keep using that word. I do not think it means what you think it means.

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Pure assertion, and empirically demonstrably false. Organisms generally have demonstrably very real fitness-differences between them.

I’m sorry but you still can’t just declare things to be true by merely repeating the same assertion. And in any case we’re talking about fitness here. Some times reductions in function come with gains in fitness, or the other way around. Your simplistic analogies and metaphors simply won’t do.

This is why I want to talk about real biochemistry and molecular biology, and you totally neglect to actually speak about the examples I give, such as the activity of enzymes, or the relationship between metabolic gains and fitness.

When the enzyme encoded by a gene no longer accelerates a reaction, the locus really does just drift neutrally. Eventually mutations will produce a new function. Random DNA is usually only a few mutations away from gaining a promoter function, for example:

And expressed random DNA can frequently exhibit positive fitness effects:

Bzzzt, stop. You can’t begin the second sentence with “so”, because nothing you go on to state follows from the previous sentence. How complex an organism is in relation to a computer (by what measure, by the way?) is simply not relevant to the statement you make.

Disagree? Then where is your equation for change-tolerance where the measure of complexity is a factor?

No. This is biology, not cupper wires printed on glass fiber sheets, with little resistors, transistors, and capacitors soldered on to them.

In biology things are usually bendy, stretchy, and soluble in either water or fats, and they grow larger until they divide, or fuse and meld together. Individual cells and most tissues are soft, sludgy mixtures of oily and watery constituents that are mixed together, with many of them more or less freely floating around under diffusion. Contents will loosely associate, attach and transiently stick together, wiggle around under brownian motion, and even some times re-associate if separated, or regrow if damaged. Organisms are governed by the rules of water and oil chemistry and physics, and are more like soap bubbles than sheets of glass fiber.

In computers, nothing exhibits these properties. Stop obsessing about your computer metaphors and learn some real biology please.

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From Reddit, @PDPrice hails us:

Following our joint article (creation.com/genetic-entropy-defense), the forum chatter has of course continued. Stern Cardinale has posted a “response”, such as it is, in a couple places, and true to form it ignores basically everything that was said and continues to rehash the same arguments as before. As usual, the other antagonists can maintain an illusion of unity by saying as little as possible.

All this endless back-and-forth forum bickering has, I think, outlived its usefulness. I’ve literally been treading the same paths for years on this topic. I am glad we were able to catalogue the responses and tackle them directly.

My proposal for the antagonists is this: if you want to keep up the discussion about GE, don’t just keep sniping from the forums. Get together (like I, Carter and Sanford did) and write a joint response article. Don’t take cheap shots. Don’t bring in unrelated issues to try and “score points”. Just honestly deal with the arguments. Then publish your article online, not in a forum, but on a website. Make it official.

Then, if it is deserving of further comment, perhaps the useful debate can continue. But this endless pot-shot-taking from the forums is enough already. It’s not worth anybody’s time anymore.

https://www.reddit.com/r/Creation/comments/kea7ij/an_invitation_to_a_higher_discourse_on_genetic/

I linked to this thread, and pointed out:

The response was quite cogent, and I am puzzled you did not link to it.

u/PaulDouglasPrice A blog response is a good idea. I’ve also wanted this to be more orderly, and even suggested the same thing to you. Are you, Rob Carter, and John Sanford now ready for a phone call to discuss this? If not, why not?

I personally am not willing to respond much if there is going to be pot shots on our credentials and unwillingness to even take a phone call.

@dsterncardinale this is close to your area of expertise. If you would like to write a blog post / preprint summarizing the critiques of GE, we can (1) manage a peer review of it, (2) publish it on the blog, and (3) typeset it into a PDF and give it a DOI.

At this time, however, I am closing this thread.

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