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Author Topic:   The Origin of Novelty
mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


Message 644 of 871 (692641)
03-06-2013 6:42 AM
Reply to: Message 638 by Tempe 12ft Chicken
03-05-2013 11:47 AM


Re: Evidence again
Do you still need more information on the Pocket mice and the fact that they definitely show a new feature arriving via mutation (actually through different mutations that both resulted in dark fur and the ability to produce melanin)?
Thanks for posting the links. I still haven't read the early part of the thread, kept too busy by everyone since my first post here.
I readily admit mutations can cause improved fitness and novel functions. These are REDUCED complexity mutations, ie disabled regions. The insertion mutation of these mice caused the promotor to disable. A similar example is the duffy gene, where disabling mutations can increase fitness in humans exposed to malaria. Thus organisms can gain a net fitness and new function, even while losing some functionality and losing some complexity (they lose activity in a gene that in more normal circumstances would have some benefit). This loss of complexity over time, although one of the processes of evolution, cannot explain the appearance of modern life-forms.
Edited by mindspawn, : No reason given.

This message is a reply to:
 Message 638 by Tempe 12ft Chicken, posted 03-05-2013 11:47 AM Tempe 12ft Chicken has not replied

Replies to this message:
 Message 648 by Taq, posted 03-06-2013 9:22 AM mindspawn has replied

  
mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


Message 646 of 871 (692646)
03-06-2013 8:27 AM
Reply to: Message 623 by bluegenes
03-02-2013 5:28 AM


Re: Novel protein coding gene in an Antarctic fish
I'm not sure if you've quite understood the paper, but that last sentence of yours is correct. It produces them randomly all the time.
It's producing useful duplications that we were discussing
Rather than me not understanding the paper, it seems you did not quite understand my comments. If in a laboratory they choose a particular organism that is lacking amplification, when the normal state of the species is known to be amplified, then they are pre-empting expected results by artificially creating amplification where nature already has it. They are just copying nature. Just the fact that they chose the place in the genome that is already known to have duplicates as their position to produce artificial duplicates, makes their conclusions about the value of coding duplicates doubtful.
You're welcome, and you're getting there! I don't know what you mean by "rare". Duplication + neofunctionalization wouldn't have to be an every day, every year, or every generation happening in order to account for the increase in number of protein coding genes in a population group from 1,000 to 20,000 (the scenario you were discussing in your debate with RAZD). The completion of such an event in one individual organism in the group every 10,000 years on average would get you there in 200 million years, and things have been evolving for far longer than that.
By rare, I mean in dispute, never convincingly observed. The e.coli example of novel genetic function is close, involves the promoter and not the gene, and mimics a close relative , the staphylococcus. Is it a new function? Or did the mutation re-activate a silent aerobic promoter that always existed in the active state of that gene in the staphyylococcus?
Shall we look for relatives to test the hypothesis that genes, like organisms, come in families with nested heirarchies?
Please! I'm happy with any proof or even schoolbook illustration of long-term nested hierarchies, I believe in short term hierarchies but everyone just seems to make sweeping statements in overconfident fashion on this site. I prefer a more scientific approach with examples of actual long-term nested hierarchies, instead of unproven philosophy.
Or do you mean high copy numbers in a created population 6,500 years ago? I'd expect there to be considerable variation 6,500 years ago in an evolutionary scenario, and before. 300 generations is not a long time to create much variation. A clue to another of the problems for your model is in the word "copy". In that paper about adaption to heat that you enjoyed, there were duplication events in 3 of the cultures that all included the same key genes. But the duplications were all different. When genes are duplicated, it's in this messy kind of way. If the AMY1 duplications look as though they are on messy randomly inserted stretches of DNA, wouldn't it be reasonable for you to ask yourself if your creator wasn't trying to make things look as though they were products of mutation? You won't find lots of neat little AMYs sitting in a row, looking pretty.
Nevertheless, if its nature copying itself badly, or nature losing genes, neither process involves new coding genes.
Let me explain it this way, not to argue from evidence, but for you to understand my view on the matter. The biblical view is a move from an exclusive vegetarian pre-flood diet (includes starch) to a protein filled diet. Thus to start off the post-flood world with many individuals with high copy numbers , and then de-selection of those with high copy numbers makes perfect sense for a vegetarian population that subsequently becomes a hunter gatherer population in certain communities. If these hunter gatherer populations undergo urbanization in modern society, and a return to a less protein filled diet (expensive meat, no hunting) those rare individuals who have retained high copy numbers will become selected into greater proportions of the population. Thus we have a change in copy numbers merely through sexual variation, and not through mutational duplication.
IF some individuals undergo a duplication mutation in the same region, this would be duplicating what nature has already produced, high copy numbers in that area. This would explain the "messy" arrangements, but this is re-establishing sequences already there, the over-producing of proteins has never been observed to add to fitness.
Deletions and duplications don't look the same. And there are far too many human CNVs to have occurred in the last 300 generations of evolution. I think you need all the deletions and duplications that you can get! You also need a very high mitochondrial DNA mutation rate for a 6,500 year old Eve. Which brings me on to the next subject.
This is what I like, to get to actual numbers. You are stating a fact here "And there are far too many human CNVs to have occurred in the last 300 generations of evolution". Could you kindly back this up with exact figures please, or alternatively refrain from making sweeping statements.
'You also need a very high mitochondrial DNA mutation rate for a 6,500 year old Eve" - this statement also needs actual figures to back it up.
If you look at the true haplogroups, rather than just at those used to illustrate population spread outside Africa, you can see that the true ones are an indicator of diversity, although they can be misleading. As the paper you linked to mentioned, older haplogroups can have arrived in an area relatively recently.
So, once again, which area of the world has the greatest diversity?
I'm happy with the information I have presented. I feel that the fact that most haplogroup maps show that the greatest diversity is in the Middle East, is satisfactorily convincing. The only evidence I have seen against this is that the DNA from Africa shows more mutations, and is therefore older. This logic is incomplete because it is a well known fact that mutation rates are higher during prolonged sun exposure, and so the higher mutations in African DNA does not necessarily reflect the older population. Without evidence presented from you, the argument favors the Middle East, although some would generalize the origin of humans from South-Western Asia.

This message is a reply to:
 Message 623 by bluegenes, posted 03-02-2013 5:28 AM bluegenes has replied

Replies to this message:
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 Message 702 by bluegenes, posted 03-13-2013 2:24 AM mindspawn has replied

  
mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


Message 666 of 871 (692687)
03-06-2013 2:17 PM
Reply to: Message 640 by Blue Jay
03-05-2013 3:07 PM


You started out arguing that birds and bats were functionally distinct, designed to fill specific, different niches. But, now, you're arguing that they are functionally redundant, as a failsafe plan..
Exactly! Does anything in your evolutionist deductive reasoning require mutual exclusivity of the two concepts? But not just a failsafe plan, creativity and variety and beauty are also goals in their own right. Not everything has a practical purpose, some things in nature are beautiful, some are amazing in their sheer uniqueness.
These explanations make opposite predictions. Yet, you have said that both would be evidence of extreme cleverness on the part of the Designer. You've constructed your theory such that it cannot be falsified, even if it's actually wrong.
Not actually, I'm constructing nothing, I'm merely expressing the obvious regarding the nature of the Creator. It would be natural that our Creator creates in logical patterns, and yet also produces amazing exceptions to standardized patterns. If creationism cannot be contradicted by reality, it is a strength, not a weakness of the theory.
You may not believe it, but I actually am fully willing to accept Intelligent Design. I'm under significant pressure from my family to do so, and it would make my life a hell of a lot easier if I could just give in and accept it.
But, I can't accept an idea that's based entirely around an unfalsifiable framework of ad hoc rationalizations; so, I need to see that Intelligent Design is actually capable of making successful predictions, and I need to see evidence that its proponents are willing to reject it when its predictions are unsuccessful
The evolution/creation debate is more likely to be solved by mathematicians. Genome sequences have to be compared to current observed rates of mutations to see which position is more mathematically tenable. Certainly each view has the potential to be falsifiable, but proven mutations, and proven mutation rates have to be defined. Under evolutionary assumptions, most genomes are accumulated mutations, under creationism they are created with few mutations. Comparisons can be made, mutations are being more clearly defined. I believe that the evidence will increasingly point to creationist time frames, let's see what the future holds.

This message is a reply to:
 Message 640 by Blue Jay, posted 03-05-2013 3:07 PM Blue Jay has replied

Replies to this message:
 Message 675 by Taq, posted 03-06-2013 4:49 PM mindspawn has replied
 Message 683 by Blue Jay, posted 03-06-2013 5:48 PM mindspawn has replied

  
mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


Message 667 of 871 (692688)
03-06-2013 2:56 PM
Reply to: Message 655 by Admin
03-06-2013 11:00 AM


Re: Moderator Suggestion
If the things wrong are not described then it isn't possible to become aware of them.
Maybe you should say the same to Bluegenes regarding his so-called superior view on human diversity which he seems reluctant to describe.

This message is a reply to:
 Message 655 by Admin, posted 03-06-2013 11:00 AM Admin has replied

Replies to this message:
 Message 670 by Admin, posted 03-06-2013 3:56 PM mindspawn has replied

  
mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


Message 668 of 871 (692689)
03-06-2013 3:09 PM
Reply to: Message 658 by Taq
03-06-2013 11:18 AM


If you want to work ahead you can do a comparison of the human and chimp genomes. The differences between those genomes contain the beneficial mutations that were responsible for the novel functions found in humans and chimps.
Humans and chimps evolved, therefore their differences are evolved, therefore their differences are proof that novel functions evolve?? What an interesting circular argument!!!
Someone please help this guy with deductive reasoning......
(ps moderators, I'm not being personal here, I am merely pointing out his complete failure to reason his point to any degree that makes any sense. Maybe a little moderator public guidance will help him, it seems to be freely given here to Bolder-dash)
Edited by mindspawn, : No reason given.

This message is a reply to:
 Message 658 by Taq, posted 03-06-2013 11:18 AM Taq has replied

Replies to this message:
 Message 674 by Taq, posted 03-06-2013 4:45 PM mindspawn has replied

  
mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


Message 669 of 871 (692690)
03-06-2013 3:27 PM
Reply to: Message 647 by Taq
03-06-2013 9:20 AM


Re: Evidence again
Complete and utter speculation that just doesn't add up. Color vision is a result of having multiple types of photoreceptors that react to a narrow spectrum of light. Humans have three such receptors for blue, green, and red. There is absolutely no reason why a forward facing retina could not support color vision, or be able to support adequate perfusion of blood
HAHA even I said I was speculating, so your comment that I'm speculating is perfectly true and already admitted by me, so you are a little late in pointing it out. You seem to be have been distracted from my real point.
This is what I said, my point stands:
I'm just guessing here, my point is I do not know enough about biology and for you to say your designs would be better than my Intelligent Designer when most biologists know how little we know about biology seems a little overconfident.
If you feel you can confidently mix and match parts of the human eye with parts of the octopus eye, and guarantee an improvement, I would see you as overconfident when we do not yet know all the facts about biology.
Edited by mindspawn, : No reason given.

This message is a reply to:
 Message 647 by Taq, posted 03-06-2013 9:20 AM Taq has not replied

  
mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


(1)
Message 671 of 871 (692695)
03-06-2013 4:04 PM
Reply to: Message 648 by Taq
03-06-2013 9:22 AM


Re: Evidence again
Taq, what makes you sure that there is a mutation, rather than merely changed alllele frequencies? If differing alleles already exist in the mouse population, some for light color, some for dark color, don't you think its only natural via adaptation through variation and selection that the new allele frequencies of both light and dark populations would reflect the best allele combinations for that region respectively?
The best way to detect mutations is to isolate a population and then check for absence of mutations in the original population. When this isolated population then shows genetic changes, this is proof of mutation. No such study was done with the mice, the results of the study could merely be a reflection of changed allele frequencies and nothing more. The dark alleles are dominant with the dark mice, the light alleles dominant with the light mice. Simple as that. Evolutionists over estimate the predominance of mutations due to their assumption that most of the genome is there from mutations.

This message is a reply to:
 Message 648 by Taq, posted 03-06-2013 9:22 AM Taq has replied

Replies to this message:
 Message 673 by Taq, posted 03-06-2013 4:42 PM mindspawn has replied

  
mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


Message 672 of 871 (692699)
03-06-2013 4:36 PM
Reply to: Message 670 by Admin
03-06-2013 3:56 PM


Re: Moderator Suggestion
Please don't follow Bolder-dash's example. He is extremely reluctant to follow moderation.
I just like fairness to both sides. Not following anyone's example.
Looking at Bluegene's last post (Message 623), it seems very detailed and nothing at all like Bolder-dash's (paraphrasing), "There are at least 3 or 4 reasons you are wrong, all too boring to go into here...". I see no similarity at all.
the wording is different, the point he was scolded for is the same:
If the things wrong are not described then it isn't possible to become aware of them
I wish Bluegenes just stated which region he thinks has more human diversity and why, instead of indicating I am wrong and yet being mysterious about his correct answer. I've nothing against his silence on the matter, if he doesn't wish to defend his view that's fine by me, what I don't like is that a creationist is advised against holding back his views, yet the evolutionist is not advised against holding back his evidence.
The impression you give is that you are intervening in the debate on behalf of evolutionists because you think it will be in their favor if Bolder-Dash gives detail. This is the impression I have of you.
Moderation here is not biased
An honest truth is that the least biased among us realize its impossible for the human mind not to have bias. Once you realize this, you are more able to eliminate your most biased reactions, knowing that a lifetime of trying will never eliminate bias. Maybe this advice will help you in future dealings with creationists.
Edited by mindspawn, : No reason given.

This message is a reply to:
 Message 670 by Admin, posted 03-06-2013 3:56 PM Admin has replied

Replies to this message:
 Message 682 by Admin, posted 03-06-2013 5:29 PM mindspawn has not replied

  
mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


Message 676 of 871 (692704)
03-06-2013 4:52 PM
Reply to: Message 673 by Taq
03-06-2013 4:42 PM


Re: Evidence again
If you don't mind, I will copy and paste my reply to Faith who asked the very same question:
+++++++++++++++++++
1. Selection pressure. They surveyed many regions across the desert spanning Arizona and New Mexico. This survey included two black lava fields (one in Arizona and one in New Mexico) separated by 750 km, the areas immediatly around each lava field, and the desert between the two lava fields. What they found is that in between the lava fields there were no black mice. Even more, there were no alleles associated with dark fur even though light fur is the recessive allele (it only takes one dark allele to have dark fur). On the lava fields, the vast majority of mice had dark fur, and the dark allele was very, very common. In the areas directly around the dark lava fields there was a mixture of the two phenotypes. Right away, one thing is very appararent. There is extremely strong negative selection against the dark allele in the light colored desert that separates the two lava fields. If the dark allele had emerged in the light colored desert it would have disappeared in just a few generations. The only way that the allele could survive is if the mice carrying the mutation moved into the black lava fields.
2. Variation of the alleles. From the paper, "Finally, the pattern of nucleotide variation observed among Mc1r alleles from the Pinacate site suggests the recent action of positive selection. Thirteen polymorphic sites are variable among the light haplotypes, whereas only one site is variable among the dark haplotypes (Table 1). " This means that the dark allele had gone through a much more recent selection event than the light allele. Therefore, the dark allele emerged after the light allele.
3. Age of the lava fields. As was demonstrated above, you need black lava fields in order to have the dark allele. So how old are the lava fields? Very recent, geologically speaking. They are around 1 million years old, much younger than the desert landscape that the ancestral populations adapted to. As shown by both the nucleotide variation and selection pressures, the recent appearance of the lava fields is just one more piece of evidence showing that the dark allele arose through recent mutations in a population that did not have dark fur.
++++++++++++++++++++
You evolutionists sometimes think that just by REPLYING you have made some sense, your answer did not deal with the question at all. It points to selection pressure on favorable alleles, which is actually MY point.
But just as a general question, what is it about the differences in the dark allele that make it impossible to produce through random mutations?
Good point, if you could convince me that these types of substitutions do occur naturally you would have an argument that beneficial mice mutation can be observed, even if not in the mice study presented. How exactly does the substitution occur in nature?

This message is a reply to:
 Message 673 by Taq, posted 03-06-2013 4:42 PM Taq has replied

Replies to this message:
 Message 677 by Taq, posted 03-06-2013 4:56 PM mindspawn has replied

  
mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


Message 678 of 871 (692707)
03-06-2013 4:56 PM
Reply to: Message 675 by Taq
03-06-2013 4:49 PM


None of which explains why life falls into a nested hierarchy. Paintings and sculptures are beautiful, but they do not fall into a nested hierarchy. Hand tools are useful, but they do not fall into a nested hierarchy.
What nested hierarchies? You fail to show me any. (or are you referring to the mole/reptile?)

This message is a reply to:
 Message 675 by Taq, posted 03-06-2013 4:49 PM Taq has replied

Replies to this message:
 Message 679 by Taq, posted 03-06-2013 4:58 PM mindspawn has replied

  
mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


Message 680 of 871 (692709)
03-06-2013 5:03 PM
Reply to: Message 677 by Taq
03-06-2013 4:56 PM


Re: Evidence again
Did you read the reply?
Right away, one thing is very appararent. There is extremely strong negative selection against the dark allele in the light colored desert that separates the two lava fields. If the dark allele had emerged in the light colored desert it would have disappeared in just a few generations. The only way that the allele could survive is if the mice carrying the mutation moved into the black lava fields.
So how old are the lava fields? Very recent, geologically speaking. They are around 1 million years old, much younger than the desert landscape that the ancestral populations adapted to.
And that is just one of the points illustrating that the allele came about through mutation in an ancestral population that did not have that allele.
Aaaah , so your whole theory is based on your ASSUMPTION that the original population did not travel far even over a million years. You are assuming the entire planet had a light landscape and so only light alleles existed. Mice can travel far in a thousand years, let alone a million years, logically all the alleles were not confined to that region. Your conclusions are a Huge assumption, and not a logical one either.

This message is a reply to:
 Message 677 by Taq, posted 03-06-2013 4:56 PM Taq has replied

Replies to this message:
 Message 681 by Taq, posted 03-06-2013 5:09 PM mindspawn has replied

  
mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


Message 685 of 871 (693213)
03-12-2013 3:56 PM
Reply to: Message 679 by Taq
03-06-2013 4:58 PM


Start here:
Animals
Is that all? I fail to see anything there that would favor long term hierarchies over design "groupings". But I keep saying this, and you keep claiming this great "nested hierarchy" argument without any backing. Why don't you show a tree of apes becoming humans and chimpanzees and orangutans? That would be more convincing.
Edited by mindspawn, : No reason given.
Edited by Admin, : Fix quote.

This message is a reply to:
 Message 679 by Taq, posted 03-06-2013 4:58 PM Taq has replied

Replies to this message:
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mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


Message 687 of 871 (693215)
03-12-2013 4:05 PM
Reply to: Message 674 by Taq
03-06-2013 4:45 PM


But perhaps you can actually answer my question. Which of the differences between the human and chimp genomes could not be produced by the observed mechanism of mutation?
The "observed mechanism of mutation" generally causes observed damage to organisms. Mutations are favorable only when genes are damaged, or when in laboratory conditions they mimic areas of the genome that are widely known to have multiple copies. Thus there is NO OBSERVED mechanism that could produce the differences observed between the chimp and human.

This message is a reply to:
 Message 674 by Taq, posted 03-06-2013 4:45 PM Taq has replied

Replies to this message:
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 Message 700 by NoNukes, posted 03-13-2013 12:07 AM mindspawn has replied

  
mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


Message 689 of 871 (693220)
03-12-2013 4:35 PM
Reply to: Message 681 by Taq
03-06-2013 5:09 PM


Re: Evidence again
This is also backed up by the lack of sequence variation within the dark allele compared to the light allele.
The lack of sequence variation could also be an indicator of a recent common ancestor for most of the dark mice (an allele that was introduced into the population) and all the dark mice in that area are descended from this outsider.
If what you claim is true then we should see the same mutations in both populations, but we don't.
You evolutionists seem to have a fixation with mutations. I guess you have to because you believe 95 percent of genomes are there through mutations so any flimsy argument is good enough for you. Its possible that brand new combinations of alleles are being created through variation via sexual reproduction, and any new favorable combination can be bred into a population. Thus what you see as definitely two mutations I see as two new allele combinations or new introductions from outside populations. You have not yet convinced me that these regions were always dry, isolated and always devoid of darkness (ash falls across the desert ) over your entire period. There is always a chance that during wetter or "darker soil" periods of history a darker breed of mice bred into the local population. These interbreeding moments between isolated populations of a species are commonly observed compared the rarity of favorable mutations. To assume a rare mutation rather than a common interbreeding moment reveals bias based on the evolutionary assumption that beneficial mutations were common.
Edited by mindspawn, : No reason given.
Edited by mindspawn, : No reason given.

This message is a reply to:
 Message 681 by Taq, posted 03-06-2013 5:09 PM Taq has replied

Replies to this message:
 Message 691 by Taq, posted 03-12-2013 4:49 PM mindspawn has replied
 Message 703 by NoNukes, posted 03-13-2013 3:21 AM mindspawn has replied

  
mindspawn
Member (Idle past 2689 days)
Posts: 1015
Joined: 10-22-2012


Message 692 of 871 (693225)
03-12-2013 5:44 PM
Reply to: Message 683 by Blue Jay
03-06-2013 5:48 PM


For evolution, the coin actually has heads and tails. In the bats and birds example, the hypothesis based on evolution is that birds and bats evolved flight independently. This hypothesis predicts that bats' flight apparatus is derived from mammalian features, and that birds' flight apparatus is derived from avian/dinosaurian features. If some bats had flow-through lungs or feathers, or some birds had wing membranes or a diaphragm (i.e., if the coin landed on tails), I would be forced to reject my evolution hypothesis
Now would you REALLY reject your evolution hypothesis if some organisms were found to have features of unknown origin? You would not, you would retain faith in your beliefs and hope that some transitionary fossils would back up evolution one day.
I love bats, they are truly unique, and have no known common ancestor with any other mammal. Where is the wing transition in the fossil record of mammals?The unique shoulder blade common ancestor? Why do mega-bats neural pathways resemble primates but microbats neural pathways do not? Does this mean the mega-bat has a common ancestor with a primate, yet the micro-bat does not? If they both evolved separately, where are their transitional fossils. The fossil evidence points towards a fully intact bat with no transitional forms. Evolution makes up fictional half-bats with no evidence for such a creature.
Evolution is fiction based on a well written book by Darwin , who observed layers of proliferation (different taxonomic classes dominating different eras) and observed microevolution, and unfortunately related the two observations in a well written very logical manner. Just because his logical book became popular and is taught as fact does not make the theory of evolution empirically superior.
Your idea, on the other hand, is not falsifiable. So, you're effectively flipping a double-headed coin, and patting yourself on the back when you make it land on heads. This is a wonderful construct for protecting your cherished beliefs from criticism, but surely you can see that it's an inappropriate and dishonest way to determine whether an idea is accurate.
You seem to have ignored my point that the debate will be solved by actual observations of true mutation rates, and comparing actual mutations with the two theories. ie with enough neutral studies one of the theories can become falsifiable. In the meantime us creationists have to endure evolutionary imagination when it comes to mythical transitional forms, making your theory temporarily unfalsifable. Its easy to make up a new tree every time genome sequencing proves an old tree false, and its pretty amusing to us creationists to see the evolutionist scramble to be the first to reclassify a n organism when genome sequencing shows the old tree to be false. Amusing, but sad for science.

This message is a reply to:
 Message 683 by Blue Jay, posted 03-06-2013 5:48 PM Blue Jay has replied

Replies to this message:
 Message 693 by Taq, posted 03-12-2013 5:55 PM mindspawn has replied
 Message 698 by Blue Jay, posted 03-12-2013 11:16 PM mindspawn has replied

  
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