A question for TEs

pshun2404

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All biological systems demonstrate plan and purpose, both in their being and in how they function. A plan is typically a list of processes foreseen or built in that if followed, using timing and resources, intends to achieve some objective. It can also be a predetermined strategy or any set of intended actions through which one achieves their goal. Purpose is an objective toward which one strives (in form or function), or for which something is devised or exists. A planned purpose precludes intent. Inanimate matter has no inherent ability to intend or plan such purpose. Do you agree that "Inanimate matter has no inherent ability to intend or plan such purpose?"

Thanks

Paul
 

Papias

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All biological systems demonstrate plan and purpose, both in their being and in how they function. A plan is typically a list of processes foreseen or built in that if followed, using timing and resources, intends to achieve some objective. ....

Thanks

Paul



Wrong from the get go. The various structures of all biological systems are easy to arrive at by mutation and natural selection.

That's very good news for us Christians, because time and again we see really stupid designs in the animal world.

To say that God directly micromanaged every detail all would mean that God would have to be pretty bad.

One example is poor giraffe’s neck – it has only 7 vertebrae, just like it’s horselike anscestors, so it can’t easily bend it’s neck to drink. Stupid design - not to mention running a nerve 15 feet longer than a direct route would require. Our eyes are put together upside down, which gives us a blind spot. An engineer would be fired for designing an eye like that. The panda’s thumb is rigged from a deformed wrist bone – and so it can’t even bend. The Dodo had useless, shriveled wings – why “design” entire wings that serve no purpose and don’t even work? Whales grow teeth in the womb, only to reabsorb them before birth – why? It’s because they evolved from land animals with teeth, but now it’s just a stupid waste to make the teeth.

That brings up a good way to find these examples - look first at creatures that evovled in one environment, but then moved to another, like whales, sea turtles, ostriches, penguins, etc. Who but an idiot or a sadist would make sea turtles and whales have to breathe....... air?!?!?! Or lay their eggs on land?


There are hundreds of examples like this, many in the human body. For God to purposefully design this, he would have to be incompetent or cruel.

Of all the kinds of life on earth, most of them are parasites. Ouch. If you were a good god, would you design most kinds of life to be parasites?


Why design cruel things, like the wasp that paralyzes the spider, and then lays eggs on it so the larvae slowly eat the spider alive? Can you imagine what it would be like to be slowly eaten alive by worms inside your own body?

Speaking of the human body, some of the best examples come from that - and not just diseases or malfunctions. For instance, look at the idiotic design of the eye, with the nerves coming off the retina into the eye, then needing to punch a hole to get back out again! An engineer would be fired for being so incompetent a designer. Or the birth canal - why not route it out the belly, like a natural C-section? simple. Or the stupid plumbing of the prostate gland - causing urination problems? Just plumb it around the gland instead of through it. Duh. But no, we are left with these incompetent designs and others, like the throat prone to choke, the backwards freshwater kidneys (see http://www.talkorigins.org/origins/postmonth/may05.html), "wisdom" teeth that no longer fit our evolved, shorter jaw, and so many more.


It still amazes me that the people who blame God for all of this incompetent, infernal, or incomplete design (http://www.geocities.com/lclane2/id2.html) are those who claim to worship this God. Creationism leads to a direct indictment of God, something that Jesus himself warns us Christians to avoid.

In Christ-

Papias
 
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-57

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Wrong from the get go. The various structures of all biological systems are easy to arrive at by mutation and natural selection.

Arrive at this by mutation and natural selection.

motorprotein.jpg
 
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-57

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Arrive at it by intelligent design.


Processes such as described below show that on a subcellular level evolution won't work and ID is required.


Cells carefully monitor the amount of misfolded proteins. An accumulation of misfolded proteins in the cytosol triggers a heat-shock response, which stimulates the transcription of genes encoding cytosolic chaperones that help to refold the proteins.


You break one portion of this pathway and the correction fails.


For those of you familiar with the following game..the concept can be easily understood.



To build a molecular motor or molecular machinery you need information for building the protein parts out of which the machines and motors are made. To do this, sequencing and folding the smaller parts of amino acids is required to occur in just the right precise way to create these 3D complex structures. The folding instructions come from information coded in the DNA…..How did a process of undirected random chance produce such a complicated code? How did the DNA code gain the ability to correct a misfolded protein?


Once everything is folded and assembled correctly...the machine must now carry out its function. The motor linked to above needs to travel across a microtubular in order to reach its destination and deliver the "package".


An animation of the process can be seen here.


A single breakdown in the chemical process that anchors then propels the organell along the tubular...will cause it to stop dead in its tracks. The process has to be complete and fully functional as the exaptation of incipient stages will not allow for the transportation process to function.


The tubular must also be told where to construct itself. A signaling process of complex metabolic-pathways could not have "evolved" through a process of random chance...triggering one function to trigger another, through a chain of sequences..to tell the tubular ...how, where and when to construct then deconstruct itself.


This is just the beginning. Irreducible complexity on the sub-cellular level shows evolutionism to be impossible.


PSA 139:14 I praise you because I am fearfully and wonderfully made; your works are wonderful, I know that full well.


ROM 1:20 For since the creation of the world God's invisible qualities--his eternal power and divine nature--have been clearly seen, being understood from what has been made, so that men are
 
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Papias

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This is just the beginning. Irreducible complexity on the sub-cellular level shows evolutionism to be impossible.

A IC is a concept that was first recognized by scientists, and seen to be evidence in favor of evolution. It was called "interlocking complexity" then, and it's evidence in favor of evolution because evolution can easily craft IC things by first building up a complex system, then removing parts that are no longer needed. This is why Behe himself admitted that IC isn't evidence against evolution.

B Even if IC systems weren't evidence in favor of evolution, and even if we didn't know how they evolved, they still wouldn't be evidence that evolution didn't happen - they would only be evidence of our ignorance. That's why every IC anti-evolution argument boils down to "Because I am ignorant of biology, I want you to reject evolution." It's the classic argument from ignorance fallacy.

C

To build a molecular motor or molecular machinery you need information for building the protein parts out of which the machines and motors are made.

False - in many of the IC examples, we know quite well how they could have evolved, step by step, with some later steps including the removal of parts to make it IC. Here's how your molecular motor evolved:




D

Also - You didn't respond to all the examples I gave earlier of the many stupid designs in nature. To say that God micromanaged these designs is to say that God is stupid. Let's not do that, OK?

In Christ-

Papias
 
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-57

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A IC is a concept that was first recognized by scientists, and seen to be evidence in favor of evolution. It was called "interlocking complexity" then, and it's evidence in favor of evolution because evolution can easily craft IC things by first building up a complex system, then removing parts that are no longer needed. This is why Behe himself admitted that IC isn't evidence against evolution.

B Even if IC systems weren't evidence in favor of evolution, and even if we didn't know how they evolved, they still wouldn't be evidence that evolution didn't happen - they would only be evidence of our ignorance. That's why every IC anti-evolution argument boils down to "Because I am ignorant of biology, I want you to reject evolution." It's the classic argument from ignorance fallacy.

C



False - in many of the IC examples, we know quite well how they could have evolved, step by step, with some later steps including the removal of parts to make it IC. Here's how your molecular motor evolved:




D

Also - You didn't respond to all the examples I gave earlier of the many stupid designs in nature. To say that God micromanaged these designs is to say that God is stupid. Let's not do that, OK?

In Christ-

Papias

Papias, nice try...but you're wrong.
Anyone can say..if we add this, then this, then this...and finally we have cemplexity is presenting nothing more than a comic book version.
Your problem is in the precise folding and positioning of the proteins used to make the organelle. All throgh a process that requires random chance mutations. Just to make the protien you need amino acids to chain together. Those amino acids have to chain together and make a protein...which need to work in conjunction with each other to construct an organelle. Often organelle are used to make other organelle. How does your process involving random chance mutations account for that? The proteins are made up of molecules. The molecules are made up of atoms. It's all coded for in the DNA.
Now, if you want to go down this route claiming a mutation happening by chance in DNA has the ability to control the atoms..to make molecules...that group together to make amino acids..that string together to make proteins...that join together with other proteins to make organelle ...that work in conjunction with each other following yet another DNA code to make other organelle....have at it. Evolutionism clearly fails.
 
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Papias

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Papias, ...

Whoa, I see you ignored nearly all of my post.

You ignored these points. So do you agree?

A. That IC is evidence in favor of evolution, not against it. This was established nearly 100 years ago, long before Behe was out of diapers.

B. That your argument of "I don't understand how it evolved, so it must have been poofed into existence." is simply an argument from ignorance, and hence fallacious.

D. Even if designed, the examples given previously show that many of the designs are really stupid. That's not something that we, as Christians, want to blame God for.

The only one you responded to was C - about the feature itself. You wrote:


Anyone can say..if we add this, then this, then this...and finally we have cemplexity is presenting nothing more than a comic book version.

But someone didn't "just say it". It's based on evidence by actual experts, such as Dr. Matzke. It's presented in a bunch of peer reviewed papers by people who not only understand this stuff well, but have spent their whole lives understanding it. That's why your comment above is like a 5 year old telling an experienced neurosurgeon that brain surgery is impossible because the gears are too hard. Not that it matters, but even Behe, who first came up with the idea that the bacterial flagellum is some kind of problem for evolution, now admits that it can easily evolve.


Your problem is in the precise folding and positioning of the proteins used to make the organelle. All throgh a process that requires random chance mutations. Just to make the protien you need amino acids to chain together. Those amino acids have to chain together and make a protein...which need to work in conjunction with each other to construct an organelle. Often organelle are used to make other organelle. How does your process involving random chance mutations account for that? The proteins are made up of molecules. The molecules are made up of atoms. It's all coded for in the DNA.

No, that's not my problem. That's basic, well understood biochemistry. To understand it, you could take a class at any local community college. Here's one - is it near you?

http://www.austincc.edu/support-and...-students/career-services/majors/biochemistry

Or you could take an online course.


Now, if you want to go down this route claiming a mutation happening by chance in DNA has the ability to control the atoms..

This sounds again like you don't understand basic biochemistry, or even now DNA works. It's lucky for you, and for most of us, that we don't have to know how our DNA is working every moment of every day for it to do so, or we'd all collapse into a pile of molecular fragments.

In Christ-

Papias
 
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-57

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Whoa, I see you ignored nearly all of my post.

You ignored these points. So do you agree?

A. That IC is evidence in favor of evolution, not against it. This was established nearly 100 years ago, long before Behe was out of diapers.

B. That your argument of "I don't understand how it evolved, so it must have been poofed into existence." is simply an argument from ignorance, and hence fallacious.

D. Even if designed, the examples given previously show that many of the designs are really stupid. That's not something that we, as Christians, want to blame God for.

The only one you responded to was C - about the feature itself. You wrote:




But someone didn't "just say it". It's based on evidence by actual experts, such as Dr. Matzke. It's presented in a bunch of peer reviewed papers by people who not only understand this stuff well, but have spent their whole lives understanding it. That's why your comment above is like a 5 year old telling an experienced neurosurgeon that brain surgery is impossible because the gears are too hard. Not that it matters, but even Behe, who first came up with the idea that the bacterial flagellum is some kind of problem for evolution, now admits that it can easily evolve.




No, that's not my problem. That's basic, well understood biochemistry. To understand it, you could take a class at any local community college. Here's one - is it near you?

http://www.austincc.edu/support-and...-students/career-services/majors/biochemistry

Or you could take an online course.




This sounds again like you don't understand basic biochemistry, or even now DNA works. It's lucky for you, and for most of us, that we don't have to know how our DNA is working every moment of every day for it to do so, or we'd all collapse into a pile of molecular fragments.

In Christ-

Papias
I think you need to learn how to present your case. So far I presented how complicated the celluar level is...and you blew it off with a link.
You post said I don't know how DNA works...that was your claim...and all you have is a link?
Explain to me....in your own words...seeing as if you have some sort of knowledge of how DNA works, show me how a motor protein could have evolved through a process that contains random mutations where only a small fraction of a percent would be considered as beneficial.
So far all you have given me is an argument based upon faith. Faith in what you have been forced fed in school about "evolutionism" is actually correct.

If I presented you with a 5-10 min long video showing how certain orgenelle are made...would you watch it, or would I be wasting my time?
 
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Papias

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-57, it seems you didn't read nor respond to the points presented. Here there are again for your convenience.



Whoa, I see you ignored nearly all of my post.

You ignored these points. So do you agree?

A. That IC is evidence in favor of evolution, not against it. This was established nearly 100 years ago, long before Behe was out of diapers.

B. That your argument of "I don't understand how it evolved, so it must have been poofed into existence." is simply an argument from ignorance, and hence fallacious.

D. Even if designed, the examples given previously show that many of the designs are really stupid. That's not something that we, as Christians, want to blame God for.

The only one you responded to was C - about the feature itself.

........

You wrote:


I think you need to learn how to present your case.

I did. I showed that your whole argument was not only factually incorrect, but also based on the fallacy of the argument from incredulity. That means that you have no case.


So far I presented how complicated the celluar level is...and you blew it off with a link.

No, only presented those facts from the experts in case you actually wanted to understand. I had already pointed out that your argument was invalid because it was fallacious. There was no blowing of any reasonable argument.



Explain to me....in your own words...seeing as if you have some sort of knowledge of how DNA works, show me how a motor protein could have evolved through a process that contains random mutations where only a small fraction of a percent would be considered as beneficial.

It's clear from your posts that you don't have a clue how actual evolution based on mutation and natural selection works (not to mention basic grammar and spelling), and thus won't be able to understand biochemical evolution until you first understand some of the basics of evolution itself. Of the many obvious falsehoods you've posted, your statement above shows that you don't understand the basic idea of natural selection, which shows that the greater frequency of harmful mutations is irrelevant. So I'll start there. Here is a basic description of why a greater number of harmful mutations than beneficial mutations still allows evolution to work well.

Take a population of, say, 100,000 (which is really quite small, the population of deer just in Michigan is over 2,000,000 - 20 times as much). So the mutations will usually be on separate individuals, not on the same individual. Thus, the mutations will or will not be transmitted to the next generation according to the common sense observation of whether they help or hurt.


So let's try an example:


So, out of that population of 100,000 there will be around 20 to 80,000 births in one breeding season, depending on the species. (actually, it's much higher in many species that have litters of more than 2 babies). Of those 50,000 say there are 5000 harmful mutations and 50 beneficial mutations (that's 100 to 1 harmful to beneficial). So those 5,000 fail to reproduce (they're hampered by harmful mutations), the population isn't affected (only 10,000 of the babies will reproduce anyway, most just lose the competition even being unmutated), and most importantly, of course those 50 beneficial mutants are more likely to reproduce, so say that 40 of them do so, giving just 3X babies, or 120.

**
Now, next generation. Remember that you had 40 with good mutations. You get another batch of 50,000 babies, and we'll assume the same mutation rates. So that gives:

5,000 new harmful mutations.
50 new beneficial mutations
120 offspring from the previous generation's good mutations
0 offspring from the previous generation's harmful mutations

So, just like before, let's look at the competition phase next.
Those with harmful mutations fail to reproduce (they're hampered by harmful mutations), the population isn't affected (only 10,000 of all babies will reproduce anyway), and most importantly, of course those 170 beneficial mutants (120 + 50 new ones) are more likely to reproduce, so say that 150 of them do so, giving 450 babies (again, only 3X, a conservative number since it's much higher in many species).

**
Now, next generation. Remember that you had 450 with good mutations. You get another batch of 50,000 babies, and we'll assume the same mutation rates. So that gives:

5,000 new harmful mutations.
50 new beneficial mutations
450 offspring from the previous generation's good mutations
0 offspring from the previous generation's harmful mutations

So, just like before, let's look at the competition phase next.
Those with harmful mutations fail to reproduce (they're hampered by harmful mutations), the population isn't affected (only 10,000 of all babies will reproduce anyway), and most importantly, of course those 500 beneficial mutants are more likely to reproduce, so say that 400 of them do so, giving 1,200 babies (again, only 3X, a conservative number since it's much higher in many species).

**
Now, next generation. Remember that you had 1,200 with good mutations. You get another batch of 50,000 babies, and we'll assume the same mutation rates. So that gives:

5,000 new harmful mutations.
50 new beneficial mutations
1200 offspring from the previous generation's good mutations
0 offspring from the previous generation's harmful mutations

So, just like before, let's look at the competition phase next.
Those with harmful mutations fail to reproduce. Those 1,250 beneficial mutants are more likely to reproduce, so say that 1000 of them do so, giving 3,000 babies.

**
Now, next generation. Remember that you had 3,000 with good mutations. You get another batch of 50,000 babies. So that gives:

5,000 new harmful mutations.
50 new beneficial mutations
3,000 offspring from the previous generation's good mutations
0 offspring from the previous generation's harmful mutations

So, just like before, let's look at the competition phase next.
Those with harmful mutations fail to reproduce. Those 3,050 beneficial mutants are more likely to reproduce, so say that 2,700 of them do so, giving 8,000 babies.

**
Now, next generation. Remember that you had 8,000 with good mutations. You get another batch of 50,000 babies, and we'll assume the same mutation rates. So that gives:

5,000 new harmful mutations.
50 new beneficial mutations
8,000 offspring from the previous generation's good mutations
0 offspring from the previous generation's harmful mutations

So, just like before, let's look at the competition phase next.
Those with harmful mutations fail to reproduce. Those 8,050 beneficial mutants are more likely to reproduce, so say that 7,000 of them do so, giving 21,000 babies.

**
Now, next generation. Remember that you had 21,000 with good mutations. You get another batch of 50,000 babies, and we'll assume the same mutation rates. So that gives:

5,000 new harmful mutations.
50 new beneficial mutations
21,000 offspring from the previous generation's good mutations
0 offspring from the previous generation's harmful mutations

So, just like before, let's look at the competition phase next.
Those with harmful mutations fail to reproduce. Those 21,050 beneficial mutants are more likely to reproduce, so say that only 18,000 of them do so, giving 54,000 babies.

Hold on though. Our land can only support 50,000 babies per generation, so we only get 50,000 of those.

But look at what has happened! Even though there were always 100 harmful mutations to only 1 good mutation, what one would naively think is an overwhelmingly bad rate, yet at the end of the day we have seen that the good mutations have now spread to every single member of the population, and the harmful mutations are gone!

You can run this again and again with different ratios of good to bad mutations, different mutation rates, and so on. I've changed all those numbers, and you know what? Biologist have too, both by looking at different actual animal populations, and by computer simulations. Both the real world and the simulations show that same things. Those are:

1. The higher the overall mutation rate, the faster the good mutations add up.
2. The faster the reproduction, the faster the good mutations add up.
3. The rate of harmful mutations has no effect. 3 to 1 bad to good, or 20 to 1, or 50 to 1, or 100 to 1 or whatever, has no effect because the harmful mutations are removed by selection anyway. Try it for yourself and see.
4. The larger the total number of good mutations, the faster they spread though the population, but this is less important than conclusion #2.

Does that all help? Looking at it in detail shows that it's all common sense, nothing that's hard to understand.

If I presented you with a 5-10 min long video showing how certain orgenelle are made...would you watch it, or would I be wasting my time?

Being that you won't take 5-10 minutes to watch a video showing what really happens according to those who actually understand it, who have spent literally dozens of thousands of hours in this research, I guess I can't be surprised that you don't know the basics of biology. The description above is at least a start. And I'm still waiting on responses for points A-D.
In Christ-

Papias
 
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-57

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-57, it seems you didn't read nor respond to the points presented. Here there are again for your convenience.





You wrote:




I did. I showed that your whole argument was not only factually incorrect, but also based on the fallacy of the argument from incredulity. That means that you have no case.




No, only presented those facts from the experts in case you actually wanted to understand. I had already pointed out that your argument was invalid because it was fallacious. There was no blowing of any reasonable argument.





It's clear from your posts that you don't have a clue how actual evolution based on mutation and natural selection works (not to mention basic grammar and spelling), and thus won't be able to understand biochemical evolution until you first understand some of the basics of evolution itself. Of the many obvious falsehoods you've posted, your statement above shows that you don't understand the basic idea of natural selection, which shows that the greater frequency of harmful mutations is irrelevant. So I'll start there. Here is a basic description of why a greater number of harmful mutations than beneficial mutations still allows evolution to work well.

Take a population of, say, 100,000 (which is really quite small, the population of deer just in Michigan is over 2,000,000 - 20 times as much). So the mutations will usually be on separate individuals, not on the same individual. Thus, the mutations will or will not be transmitted to the next generation according to the common sense observation of whether they help or hurt.


So let's try an example:


So, out of that population of 100,000 there will be around 20 to 80,000 births in one breeding season, depending on the species. (actually, it's much higher in many species that have litters of more than 2 babies). Of those 50,000 say there are 5000 harmful mutations and 50 beneficial mutations (that's 100 to 1 harmful to beneficial). So those 5,000 fail to reproduce (they're hampered by harmful mutations), the population isn't affected (only 10,000 of the babies will reproduce anyway, most just lose the competition even being unmutated), and most importantly, of course those 50 beneficial mutants are more likely to reproduce, so say that 40 of them do so, giving just 3X babies, or 120.

**
Now, next generation. Remember that you had 40 with good mutations. You get another batch of 50,000 babies, and we'll assume the same mutation rates. So that gives:

5,000 new harmful mutations.
50 new beneficial mutations
120 offspring from the previous generation's good mutations
0 offspring from the previous generation's harmful mutations

So, just like before, let's look at the competition phase next.
Those with harmful mutations fail to reproduce (they're hampered by harmful mutations), the population isn't affected (only 10,000 of all babies will reproduce anyway), and most importantly, of course those 170 beneficial mutants (120 + 50 new ones) are more likely to reproduce, so say that 150 of them do so, giving 450 babies (again, only 3X, a conservative number since it's much higher in many species).

**
Now, next generation. Remember that you had 450 with good mutations. You get another batch of 50,000 babies, and we'll assume the same mutation rates. So that gives:

5,000 new harmful mutations.
50 new beneficial mutations
450 offspring from the previous generation's good mutations
0 offspring from the previous generation's harmful mutations

So, just like before, let's look at the competition phase next.
Those with harmful mutations fail to reproduce (they're hampered by harmful mutations), the population isn't affected (only 10,000 of all babies will reproduce anyway), and most importantly, of course those 500 beneficial mutants are more likely to reproduce, so say that 400 of them do so, giving 1,200 babies (again, only 3X, a conservative number since it's much higher in many species).

**
Now, next generation. Remember that you had 1,200 with good mutations. You get another batch of 50,000 babies, and we'll assume the same mutation rates. So that gives:

5,000 new harmful mutations.
50 new beneficial mutations
1200 offspring from the previous generation's good mutations
0 offspring from the previous generation's harmful mutations

So, just like before, let's look at the competition phase next.
Those with harmful mutations fail to reproduce. Those 1,250 beneficial mutants are more likely to reproduce, so say that 1000 of them do so, giving 3,000 babies.

**
Now, next generation. Remember that you had 3,000 with good mutations. You get another batch of 50,000 babies. So that gives:

5,000 new harmful mutations.
50 new beneficial mutations
3,000 offspring from the previous generation's good mutations
0 offspring from the previous generation's harmful mutations

So, just like before, let's look at the competition phase next.
Those with harmful mutations fail to reproduce. Those 3,050 beneficial mutants are more likely to reproduce, so say that 2,700 of them do so, giving 8,000 babies.

**
Now, next generation. Remember that you had 8,000 with good mutations. You get another batch of 50,000 babies, and we'll assume the same mutation rates. So that gives:

5,000 new harmful mutations.
50 new beneficial mutations
8,000 offspring from the previous generation's good mutations
0 offspring from the previous generation's harmful mutations

So, just like before, let's look at the competition phase next.
Those with harmful mutations fail to reproduce. Those 8,050 beneficial mutants are more likely to reproduce, so say that 7,000 of them do so, giving 21,000 babies.

**
Now, next generation. Remember that you had 21,000 with good mutations. You get another batch of 50,000 babies, and we'll assume the same mutation rates. So that gives:

5,000 new harmful mutations.
50 new beneficial mutations
21,000 offspring from the previous generation's good mutations
0 offspring from the previous generation's harmful mutations

So, just like before, let's look at the competition phase next.
Those with harmful mutations fail to reproduce. Those 21,050 beneficial mutants are more likely to reproduce, so say that only 18,000 of them do so, giving 54,000 babies.

Hold on though. Our land can only support 50,000 babies per generation, so we only get 50,000 of those.

But look at what has happened! Even though there were always 100 harmful mutations to only 1 good mutation, what one would naively think is an overwhelmingly bad rate, yet at the end of the day we have seen that the good mutations have now spread to every single member of the population, and the harmful mutations are gone!

You can run this again and again with different ratios of good to bad mutations, different mutation rates, and so on. I've changed all those numbers, and you know what? Biologist have too, both by looking at different actual animal populations, and by computer simulations. Both the real world and the simulations show that same things. Those are:

1. The higher the overall mutation rate, the faster the good mutations add up.
2. The faster the reproduction, the faster the good mutations add up.
3. The rate of harmful mutations has no effect. 3 to 1 bad to good, or 20 to 1, or 50 to 1, or 100 to 1 or whatever, has no effect because the harmful mutations are removed by selection anyway. Try it for yourself and see.
4. The larger the total number of good mutations, the faster they spread though the population, but this is less important than conclusion #2.

Does that all help? Looking at it in detail shows that it's all common sense, nothing that's hard to understand.



Being that you won't take 5-10 minutes to watch a video showing what really happens according to those who actually understand it, who have spent literally dozens of thousands of hours in this research, I guess I can't be surprised that you don't know the basics of biology. The description above is at least a start. And I'm still waiting on responses for points A-D.
In Christ-

Papias

Papias, there's a line in the Meatloaf song Paradise by the Dashboard light which says....STOP RIGHT THERE!!!...

In your post you said..."Of those 50,000 say there are 5000 harmful mutations and 50 beneficial mutations"

Did you make those numbers up or can you back them up with scientific data?
I think you made them up...which invalidates your entire post. When you have real numbers, please try again.
 
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-57

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-57, it seems you didn't read nor respond to the points presented. Here there are again for your convenience.
Papias,
Disregarding your numbers you assume the beneficial mutations will occur in a fashion that will enhance the fitness of the species. What you fail to realize is that in order for beneficial mutations to accumulate ove the generations and evolve a new body organ, appendage, trait etc. is where the mutation must occur in the DNA.

In the so-called evolution of a walking land animal into a dolphin the mutations must occur in the portion of the DNA that codes for the gene that will produce the unique features of a modern dolphin. For example a mutation to the flipper producing genes will not effect the changes required to produce the features of the blowhole.

The human has about 2.5 billion base pairs. I don't know how many base pairs a proto-dolphin would have but I know it would be like a human quite large. It's so large that if each base pair was a mile wide they would stretch from Earth to Pluto. (at its closest)

For a species to evolve or build upon a particular trait a so-called beneficial mutation must occur in just the right place at just the right time so it can enhance a so-called beneficial mutation that happened in a previous generation. The odds of a so-called beneficial mutation via a process that contains random chance is extremely low. In my opinion very close to zero.

I know of no one who believes in evolutionism that would suggest it would take one or two mutations to move the nostril to the top of the head and form a blowhole. Nor do I know of any evolutionist that would suggest it took several mutations to create the mechanism in the blowhole system that produces the clicking sound that the dolphin uses for echo-location.

In order for a trait to enhance or be created so-called beneficial mutations must occur over and over again, many, many times to realize the complexity of the dolphins echo-location system. You have not demonstrated this is possible.

To complicate things even more for the person that believes in descent with modification many of the systems must "evolve" in harmony with each other. With the dolphin the forehead must take on the shape of an accustic lens which acts in conjunction with an oily melon....as well as the clicks derived by the blowhole system. You have not described how a process containing so few so-called beneficial mutations through a process containing random chance has the ability to overcome the problems presented above....and we still haven't addressed the receiving capabilities of the dolphins echo-location system.

All you and other evolutionist have done is claim so-called beneficial mutations occur, survive and produced the many varieties of species we see today with all of their distinct variation, complex, sophisticated systems and traits.

You closed with this question...."Does that all help? Looking at it in detail shows that it's all common sense, nothing that's hard to understand."
My answer is no. Common sense doesn't suggest how you must overcome the problems I presented above. You have not presented the common sense that shown how the T.O.E can produce and add to a trait. All you have done is thrown made up numbers at me and then suggest they can produce the modern dolphin and all the differences between them and a walking land animal.
 
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Papias

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First and foremost, -57, it looks like we've got some Gish Gallop going on here. Please start responding to the many topics you've brought and then abandoned, or it will be pointless to address the new topics.

Specifically,

Whoa, I see you ignored nearly all of my post.

You ignored these points. So do you agree?

A. That IC is evidence in favor of evolution, not against it. This was established nearly 100 years ago, long before Behe was out of diapers.

B. That your argument of "I don't understand how it evolved, so it must have been poofed into existence." is simply an argument from ignorance, and hence fallacious.

D. Even if designed, the examples given previously show that many of the designs are really stupid. That's not something that we, as Christians, want to blame God for.

The only one you responded to was C - about the feature itself. You wrote:​


Papias, there's a line in the Meatloaf song Paradise by the Dashboard light which says....STOP RIGHT THERE!!!...

In your post you said..."Of those 50,000 say there are 5000 harmful mutations and 50 beneficial mutations"

Did you make those numbers up or can you back them up with scientific data?
I think you made them up...which invalidates your entire post. When you have real numbers, please try again.

As I said, it's a basic description so you can understand natural selection. Since you are apparently unclear on what a basic description is, I'll let you know. A basic description is a simplified way of explaining a concept, that generally is constructed to explain the concept, being consistent with real data. If you want real examples of natural selection being demonstrated, there are tons of those too - a good place to start would be the Grant's work with Finches, for instance. I can provide links if you are unable to find their work, which is easily available.


Papias,
Disregarding your numbers you assume the beneficial mutations will occur in a fashion that will enhance the fitness of the species. ....

The human has about 2.5 billion base pairs. ......
For a species to evolve or build upon a particular trait a so-called beneficial mutation must occur in just the right place at just the right time so it can enhance a so-called beneficial mutation that happened in a previous generation. The odds of a so-called beneficial mutation via a process that contains random chance is extremely low. In my opinion very close to zero.

I know of no one who believes in evolutionism that would suggest it would take one or two mutations to move the nostril to the top of the head and form a blowhole. Nor do I know of any evolutionist that would suggest it took several mutations to create the mechanism in the blowhole system that produces the clicking sound that the dolphin uses for echo-location.
....

Wow, there are so many complete falsehoods and misunderstandings in there for me to know where to start. Plus, as per the Gish Gallop, you still haven't finished with any of the other topics being ignored, and have now brought up dolphins. They are a great example, and could be a good discussion, but how about we finish the several topics already started, first?

In Christ-

Papias
 
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-57

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First and foremost, -57, it looks like we've got some Gish Gallop going on here. Please start responding to the many topics you've brought and then abandoned, or it will be pointless to address the new topics.

Specifically,

Whoa, I see you ignored nearly all of my post.

You ignored these points. So do you agree?

A. That IC is evidence in favor of evolution, not against it. This was established nearly 100 years ago, long before Behe was out of diapers.

B. That your argument of "I don't understand how it evolved, so it must have been poofed into existence." is simply an argument from ignorance, and hence fallacious.

D. Even if designed, the examples given previously show that many of the designs are really stupid. That's not something that we, as Christians, want to blame God for.

The only one you responded to was C - about the feature itself. You wrote:​




As I said, it's a basic description so you can understand natural selection. Since you are apparently unclear on what a basic description is, I'll let you know. A basic description is a simplified way of explaining a concept, that generally is constructed to explain the concept, being consistent with real data. If you want real examples of natural selection being demonstrated, there are tons of those too - a good place to start would be the Grant's work with Finches, for instance. I can provide links if you are unable to find their work, which is easily available.




Wow, there are so many complete falsehoods and misunderstandings in there for me to know where to start. Plus, as per the Gish Gallop, you still haven't finished with any of the other topics being ignored, and have now brought up dolphins. They are a great example, and could be a good discussion, but how about we finish the several topics already started, first?

In Christ-

Papias
I've read your post and noticed one thing....you said a lot of nothing.
NEXT
 
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