In the link below are the abstracts with links to the papers presented at the International Conference on Creationism 2018 in Pittsburgh, PA July 29-August 1, 2018. Those presenting are professors at Christian colleges, professors already expelled from secular colleges, or professors at secular colleges who (by God’s grace) can’t be expelled. 🙂
http://www.creationicc.org/icc18_abstracts.php
A topic I will raise among the population geneticists there (John C. Sanford, Rob Carter, Nathaniel Jeanson, and others) is the issue of heteroplasmy in mtDNA as they are presenting on these topics.
Mature human cells have 100,000 to 600,000 mitochondrion. So how can a cell be mostly homoplasmic yet have mtDNA mutations that are reflected in lineages whereby an individual has a mostly homoplasmic mtDNA that enable us to identify the 7 daughters of Eve (to quote Oxford Geneticist Bryan Sykes).
I would think we would have not-so-discrete-one-or-the other situation but substantially more degrees of heteroplasmy given there are 100,000-600,000 mitochondrion in a cell.
One possible solution that was unwittingly suggested by an NIH grant is that some gametes have only 1-3 mitochonrion by extreme accident, hence we can have an mtDNA change in an lineage.
These issues must be considered when trying to calibrate mtDNA clocks by direct sampling of grandparents and grand children. Also, what is the effect of somatic mutations in the calibration of the clock since we usually sample somatic cells to calibrate the speed of germline mutations of mtDNA. I do not have answers to these questions, so this thread is a place marker for discussion for what I hope to glean at ICC 2018 regarding mtDNA.
Speaking of the Seven Eves:
Welcome back Sal!
I hope you are well…
Have you expanded your knowledge of QM? 😉
Thanks J-mac. Nice to see you again.
I actually need to re-learn QM before even expanding knowledge on that front. I’ve been having to focus, in connection with Dr. Sanford’s work, on other things in the meantime.
My posts here at TSZ might now become insufferably boring because of the technical nature of some of the topics I bring up. I bring them up because they are of interest to the 3 people I named in the OP and maybe I could actually get an expert commentary on the issue I raised.
So, apologies in advance for my new boring persona at TSZ.
sal:
Not true at all.
Want to try another number? (hint: you are about 2 orders of magnitude off)
PeterP,
Thank you for your response. I’ve seen numbers for gametes around 100, but for somatic cells 100,000-600,000.
Did I mis-interpret this. Thanks in advance:
https://www.researchgate.net/publication/16900133_Mitochondrial_DNA_copy_number_in_bovine_oocytes_and_somatic_cells_1
Yes.
Why the switch from your claim of mature human cells to bovine oocytes?
No worries Sal…It’s good to have you back… I mean it 😉 While we disagree on some issues, I really would like to attend the conference and meet you in person (provided you don’t post my picture here. It would ruin all the fun… 😉
We have more than boring OPs here including some of mine but I found that the simpler the subject is presented (if possible) the more likely it is to be popular…
Just look at the “Why does the soul need the brain? OP… it has almost become as popular as Daytona 500 also called Gruppcio 500 by Joe Felsaintstain…
J-Mac, to Sal:
For once, I actually feel a little sorry for Sal.
Do you really feel that anyone here cares what you have to say? We all know you can’t “feel’ anything…Why would we care? Don’t you get it?
Your god evolution made you what it should have made you: crap
But, logically, given that’s not at all what you think happened you should in fact be questioning your foundation for saying the world that your presumed deity/Intelligent Designer made contains a crap thing.
Keiths is exactly as your guiding intelligent wanted him to be. Agree or disagree?
Cows are mammals, that was the one reference where I saw the large number. I thought I saw numbers for human oocytes 100,000-600,000 somewhere, but I don’t remember the reference.
Anyway, this is not me promoting an idea, I’m soliciting information. So thanks for pointing out errors on my part.
https://embryo.asu.edu/pages/mitochondrial-dna-mtdna
So what does that figure mean? That’s obviously the same one I used in the OP. I’m not an embryologist or developmental biologist.
Oocyte is not a somatic cell right, so somatic cells lose mitochondrion numbers???
Sal,
I suggest a disguise so that J-Mac won’t recognize you at the conference.
You mean like my casino pimp outfit? 🙂
I thought more on the problem that inspired me to post. The problem is estimating mutation rates in the germ line in a way that we factor out the effect of somatic cell mutations since, as far as I know we test somatic cells like say between mother and daughter, not the actual germ line cells. So the germline might have gone 1 generation, but the somatic cells???? maybe 60-120 based on the Haflick limit? Is that right? Does that make sense?
Sal,
Your reasoning and reading comprehension skills are pitiful.
Sal:
PeterP:
Sal:
PeterP:
Sal:
So your reasoning is “cows are mammals, therefore bovine oocytes are human somatic cells”? You make the baby Jesus cry when you reason like that, Sal.
Then Sal finds a quote that applies to humans:
So your reasoning is “human oocytes contain 100,000 to 600,000 mitochondria; therefore human somatic cells contain 100,000 to 600,000 mitochondria”?
Again, you’re making the baby Jesus cry.
That may be true, and that’s why I came here for brilliant guys like you to set me straight.
That’s what I thought, but so a variety of somatic cells are generated with on the order of 100 less mitochondrion than oocytes???
Unlike you I’m willing to re-orient my understanding and say I’m wrong, but it would be nice if a biologist chimed in offered some references. I mean that’s an enormous variation.
Here is the mechanistic issue. As I read it, at some stage maybe as little as 1-3 mitochondria exist in a reproductive cell, though typically it’s 100, then when it becomes an oocyte it goes to 600,000 and then a somatic cell it goes to 4000????? Is that right. If no more than “I tell you different” would be helpful.
From an NIH grant:
https://grants.nih.gov/grants/guide/pa-files/PA-16-087.html
Ok so, thanks to Keiths I see where I’ve confused my terms. Unlike Keiths, however I will say I was confused, I mis-interpreted, I was wrong. In contrast Keiths will go for thousands of posts defending his mistake. He’s so much fun to debate because he must save face at all costs and try to give the appearance he’s infallible.
A professor evolutionary biology over a Reddit disputed the meaning of this:
Mitochodria without mtDNA??????
Sal,
Assuming you meant to say “100 times fewer mitochondria than oocytes”, then yes. Why do you find that so astonishing?
Sal,
You acknowledged a mistake. That’s good. Why spoil it by immediately following it with a lie?
Sal,
No, all mitochondria have mtDNA. I think the author meant to write this:
Sal,
Presumably those that were expelled were also expelled because that’s what your god wanted to happen? So on the one hand you praise god for stopping their expulsions but on the other hand you seem to have forgotten to blame it for the explosions that did happen.
I guess it’s a bit like those people who praise de lard for saving them for a tornado, but never seem to question why de lard sent it in the first place.
Ok, let me state some my errors so far in this discussion and thus set a good example to Keiths how to behave rather than constantly try to save face:
Error 1:
The proper term is Ooocyte, it probably would not be considered a representative cell. According to wiki, the number is 4,000 for other cells, but to my credit, from a university website:
PeterP said I misinterpreted. Ok, so I misinterpreted. I was wrong wrong wrong.
There, see Keiths, it’s not so hard to say, “I’m wrong.” or “I mis-interpreted.” or “I was uninformed” or “I made a terrible mistake.” or “I certainly need to learn more.”
Hopefully in the process of me highlighting my errors you learned something from my shining example of humility. 🙂
So what’s the ulterior motive behind this seemingly innocuous discussion. Well it relates to this dispute posted by a professor of evolutionary biology:
stcordova,
There is always hope and I remain optimistic 🙂
Good to see you post here Sal. Have you read Ewert’s paper?
colewd,
I’ve read parts of it, I actually have a more far reaching hypothesis which extends Ewert’s ideas. I sketched it out in the link below. I call it the “Hackability Hypothesis.”
Nice to see you too! Nice to be back. I hope you are well.
Sal,
I know. I’ve been trying to get you to follow my lead for years.
I’m happy to see you doing so, and at the same time disappointed (but not at all surprised) that you immediately resort to lying in order to make the bitter pill of correction easier to swallow.
It’s a typically Cordova-ish move. Such behavior is among the many reasons you are so widely disrespected.
Start with this:
Birky C.W., Jr. Evolution and population genetics of organelle genes: Mechanisms and models. In: Selander R.K., Clark A.G., Whittam T.S. editors. Evolution at the Molecular Level. Sunderland, MA, Sinauer Assoc., 1991. p. 112-134.
Thanks John, much appreciated.
What are you talking about. You don’t admit when you are wrong or when you’ve misinterpreted something.
ETA:
Ah. I get it now.
Mung,
Sure I do. What is it with doofuses like you and Sal? Do you think you can alter the past simply by wishing for it to change?
I’m more interested in how you will act in the future. Whether you will ever admit your mistakes and learn from them. Your track record in that regard leaves something to be desired. The idea that someone can learn from you how to admit mistakes is hilarious.
Mung:
keiths:
Mung:
keiths:
For sure someone can mimic your words about how you admit your mistakes. I’m talking about actions. Where you actually do admit to making a mistake.
Christ, Mung. It happened just a few minutes ago:
Predicted Mung response, as indicated above:
LoL. You made a typing mistake. So you can admit when you make a typing mistake.
My bad.
Not just typos, of course.
But you’ve got to admit that it’s funny. You make a claim, not realizing that there’s a counterexample from just a few minutes earlier. Typical Mung fail.
I had a conversation with Nathaniel Jeanson over mtDNA.
First, there is a developmental bottlneck where cells have only 9 mitochondrion. It was one of the papers cited in Jeanson’s work. I don’t have it handy. THAT’S one piece of the puzzle I was trying to solve!!!! Whoohoo!
This is good news. We need more reasons to believe in a young earth.