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Author | Topic: An ID hypothesis: Front-loaded Evolution | |||||||||||||||||||||||||||||||||||||||||||||||
RAZD Member (Idle past 721 days) Posts: 20714 From: the other end of the sidewalk Joined: |
Hi Genomicus, and welcome to the fray.
I have abstained from participating thus far to see how things developed. At this point I have a simple question:
My question is -- how does this differ from the (deist) hypothesis that the universe is "front loaded" for life to develop on planets such as this, and evolve in the manner we have seen here, due to the "front loading" of all the mechanisms of physics, chemistry and biology to act in the way we have observed in this one instance? See Panspermic Pre-Biotic Molecules - Life's Building Blocks (Part I) for some additional information. quote: and Self-Replicating Molecules - Life's Building Blocks (Part II) for more information. quote: In other words, it appears that all this has occurred naturally, or it is all "front-loaded" to occur through the "front loaded" mechanisms involved. Note that this extends your hypothesis back further in time to the formation of pre-biotic molecules in space and methods\mechanisms to deliver them to the surface of planets, as well as broadening it to include the way that solar systems form and elements are created. Enjoy. by our ability to understand Rebel American Zen Deist ... to learn ... to think ... to live ... to laugh ... to share. • • • Join the effort to solve medical problems, AIDS/HIV, Cancer and more with Team EvC! (click) • • •
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RAZD Member (Idle past 721 days) Posts: 20714 From: the other end of the sidewalk Joined: |
Hi Genomics,
I think Percy (another deist btw) has the gist of it.
The FLU hypothesis simply posits that some intelligence seeded the universe with the subatomic forms that contained the necessary information to bias the formation of stars, planets, atoms, molecules in planned ways. I still see your concept as secondary to this process, like looking at the evolution of a toenail instead of the whole foot. When I look at what this means for the formation of life on earth, going to the toenail from the foot, if you will, I see front-loaded pre-biotic molecules distributed in space that carry the necessary chemical information to bias the development of life in planned ways. These are distributed throughout space in such a way that they will be readily delivered by front loaded mechanics (asteroids etc) to the surfaces of planets that are preloaded to support the formation of life, including earth. As far as evidence goes, we can look into deep space and see clouds of pre-biotic molecules, and we can find them in near earth orbits, but we don't see any good unequivocal evidence for space born cells, nor do we see any evidence for such cells in near earth orbits. See Panspermic Pre-Biotic Molecules - Life's Building Blocks (Part I) for more information in this regard: quote: Of course this means that earth and the life on earth are not special creations of some intelligent design but part of a larger process, and this does not bother me.
Well, that would be why deism is an honestly admitted faith\philosophy rather than an attempt at being a scientific hypothesis based on the faith\philosophy of a hypothetical interstellar vastly intelligent alien being acting like a god during the formation of life on earth. In my opinion ID would be in a much better intellectual position if it said:
Note that these hypothesis are not testable scientific hypothesis, but philosophical\theistic ones. One can assume that #1 and #2 are true for the sake of further argument, thus providing the basis for #3, but hypothesis #3 can only be considered testable if you can isolate natural means from non-natural means, ie - you need to show that x-y-z could not occur by natural means. Hence the attraction of Irreducible Complexity and it's off-spring.
By comparing them with other universes that have not been front loaded, the same way you would (ultimately) test for the existence of god/s. Admittedly that makes it difficult to test, and certainly not testable by current methodologies, and this is why it can only be considered an hypothesis at this point. Certainly one cannot claim that, just because x-y-z is predicted by the FLU hypothesis and we see x-y-z all around us, that this is evidence for the FLU - as opposed to a natural formation of the universe that just happens to have the physical etc characteristics so that x-y-z happens: one would need to be able to show that x-y-z cannot occur in a non-front loaded universe (NFLU) before one could make such a claim. Equally, however, one cannot claim that just because x-y-z occurs according to what are perceived as natural laws in a NFLU that this is evidence for the NFLU, yes?
So how do you test for it? Specifically how do you test that the occurrence of x-y-z in the early earth is necessarily due to front loading by an alien intelligence and not due to either natural NFLU processes or FLU processes?
Do you have evidence of x-y-z occurring that cannot be due to NFLU processes, and what is your filter\test to rule out NFLU processes? Enjoy. Edited by RAZD, : . by our ability to understand Rebel American Zen Deist ... to learn ... to think ... to live ... to laugh ... to share. • • • Join the effort to solve medical problems, AIDS/HIV, Cancer and more with Team EvC! (click) • • •
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RAZD Member (Idle past 721 days) Posts: 20714 From: the other end of the sidewalk Joined: |
Hi Genomics, thanks.
Fair enough. Admittedly I am interested in "the ultimate question of life, the universe, and oh, everything" to quote Douglas Adams, however I am also interested in explaining life on earth as part of that. Perhaps the difference is in focus angles (wide vs narrow).
While you assume it arose elsewhere and then was delivered here. We do know that at the early stages of earths formation there was no life that left any traces that we have found, and we do know that the oldest rocks known that could show fossil records of life do so - evidence for cyanobacteria - at some 3.5 billion years ago. A google search on cyanobacteria oldest life brings up a lot of hits: http://en.wikipedia.org/wiki/Evolutionary_history_of_life For example. What we don't know is how that life got there. Your delivery system requires a previously developed life\being while mine only requires observed systems for delivery of observed materials from space to the surface of a planet. With no evidence of your delivery system you must admit that this is an extremely weak link in your hypothesis: you have to assume that it existed.
You forget the age of these interstellar clouds - because of their distance from earth what we are seeing were there before the earth formed. Thus the absence of identifiable interstellar cells is problematic for a panspermia concept.
Now you are assuming that meteorites are your delivery system and that life arose on meteorites? Just saying.
So you would agree then that there is nothing special about life existing on earth?
While I am proposing that the initial pre-bionic molecules were made to act according to the designed laws of chemistry and evolution, to bias first the formation of life from the provided building blocks, and second what life evolved from the first cells. You say cells (origin unknown), while I say cells with some assembly required (together with instructions, assembly materials and some self-assembly systems).
And yet you are still only copying an existing system for making life. Building one that uses pre-biotic materials would confirm\validate my position that life was built from pre-biotic materials, would you not agree? Especially when you consider the work being done on self-assembly molecules and pre-cellular life systems. Being able to construct life from pre-biotic materials would be a prediction of FLU but not of FLE, yes? Does FLE predict that this will not be possible? It certainly seems to imply it to me, otherwise why is FLE necessary?
A scientific hypothesis, as opposed to a philosophical one, is based on objective evidence or objective observation (rather than on personal intuition: see Percy Message 210), AND it is testable. Objective evidence: pre-biotic molecules exist in space, both in distant interstellar clouds and on near earth asteroids, and they have been recovered from meteors impacting earth. Objective evidence: the earth formed 4.5 billion years ago, with lots of meteors impacting the surface in the early years, and life is known to exist 3.5 billion years ago, with no earlier record currently available for either life or precursors to life. Objective observation: the first life on earth occurred between 3.5 billion years ago and 4.5 billion years ago. Scientific hypothesis: life arose between 4.5 billion and 3.5 billion years ago from pre-biotic molecules via "natural (FLU or NFLU) laws" for chemistry and chemical evolutionary processes. Test: replicate how life could have formed to see if it can form as hypothesized. Faith: some unknown being made and delivered a designed front-loaded life system to earth. Test: believe it.
Curiously, I'm pointing out that your hypothesis is not testable - or at least you have not demonstrated how it could be properly tested.
There's also the joke about a flea and a fly in a flu were imprisoned, so what could they do; said the fly let us flee said the flee let us fly so the flew through a flaw in the flu.
But you have to admit that it is not a scientific hypothesis, but an assumption based on personal intuition\opinion\wish\hope, and that your FLE hypothesis is founded on that assumption. You might as well assume that god/s exist and that god-did-it to provide the first cellular life on earth, yes?
If the prediction is for something that could not occur under FLU or NFLU, then confirmation of a prediction would be evidence in favor of it. If the prediction is for something that cannot differentiate FLE from FLU or NFLU, then confirmation of a prediction just means that it is not falsified, while the validity of the hypothesis is not tested. You should also have a falsification test for something that could occur via FLU/NFLU natural laws but would not occur under FLE -- do you have such a test?
Methinketh there is a flaw in the FLE (or three) here ... First, what is your evidence for "deep homology" and how is this specifically predicted by FLE as opposed to being a post hoc ergo propter hoc observation? (ie -- if it is something known before your hypothesis was developed, then it would be, should be, relegated to the objective evidence used to form the hypothesis not to test it). You need to predict something unknown and then test for it. Second, how do you know that "deep homology" is not predicted by FLU or NFLU? (ie-- by "natural (FLU/NFLU) laws"). Just stating that it isn't does not meet scientific criteria. The process of Microevolution involves changes in the composition of hereditary traits, and changes to the frequency of their distributions within breeding populations from generation to generation, in response to ecological challenges and opportunities. The process of Divergent Speciation involves the division of a parent population into two or more reproductively isolated daughter populations, which then are free to (micro) evolve independently of each other. The Theory of Evolution (ToE), stated in simple terms, is that the process of Microevolution, and the process of Divergent Speciation, are sufficient to explain the diversity of life as we know it, from the fossil record, from the genetic record, from the historic record, and from everyday record of the life we observe in the world all around us. The ToE predicts that divergent speciation results in a pattern of nested hierarchies of descent from common ancestor breeding populations, of clades within clades, and this pattern necessarily results in "deep homologies" within the branches of each of the clades, and the deeper you go into the nested hierarchy ancestry the deeper you go into the "deep homologies" that are present. | Homologies shared by a, b, c, d,and e are "deep homologies" predicted by ToE. Thus the ToE predicts "deep homologies" necessarily develop from microevolution plus divergent speciation. The ToE also predicts that "deep homologies" shared by a and e but not by b will also not be shared by c and d. This pattern is not predicted by FLE, as I understand it, but is observed to occur. Can you explain this apparent omission? Third, the ToE also predicts derived traits, where a trait from an ancestral population is modified via microevolution into a variation that does not occur in the parent population. The ToE predicts that these derived traits will be homologous in descendant populations. Thus b will have derived traits that are not shared with a (or e) but which are shared with c and d AND that these derived traits have predecessors in a that have been modified in b, rather than appearing de novo. Does your FLE predict this? Then there is the issue of convergent evolution: why take two paths to reach a single front loaded result? Is this predicted?
Curiously, I've only been told this by people pushing their beliefs as an hypothesis, rather than people talking about scientific hypothesis and how they are properly tested. Amusingly, they also tried to use evidence used to develop an hypothesis as evidence that it was correct.
No, it is just evidence that the hypothesis is not invalidated, a seemingly minor but important distinction, and that it has not been tested to differentiate it from hypothesis B. Particularly if you have not show that it is not predicted by hypothesis B. Similarly if hypothesis A predicts x-y-q does NOT occur, and B does not predict the occurrence of x-y-q then the non-existence of x-y-q neither confirms nor invalidates hypothesis A or B.
No, it would just confirm that either hypothesis could be correct. You need a prediction that occurs by A and not by B or one that occurs by B and not by A in order to differentiate which hypothesis is a better explanation of the evidence. The purpose of an hypothesis (and a theory) is to explain the evidence, so as long as B explains the evidence it is a valid (not invalidate) theory. Consider where each hypothesis predicts something the other does not, but does not rule out. Both predictions come true: which one is better than the other in explaining the evidence?
In your opinion. Curiously, opinion has been shown to have little effect on reality. To be a proper test of an hypothesis you need to predict something that cannot occur by the other hypothesis or vice versa. If we assume A and derive B from A, and B predicts C occurs, then occurrence of C is evidence for B If we assume notA and derive D from notA, and D does not prevent C from occurring, then the occurrence of C is not evidence against D Does A or notA exist? If you cannot tell, then the occurrence of C is not evidence that B is any more likely to be true than not true. Enjoy. Edited by RAZD, : added derived traits by our ability to understand Rebel American Zen Deist ... to learn ... to think ... to live ... to laugh ... to share. • • • Join the effort to solve medical problems, AIDS/HIV, Cancer and more with Team EvC! (click) • • •
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RAZD Member (Idle past 721 days) Posts: 20714 From: the other end of the sidewalk Joined: |
Hi Genomicus, excuse the length - we may need to break this down into subtopics if this goes on growing.
Please note that I added a section on derived traits and a question about convergent evolution before I saw your reply:
The weak link is your completely unevidenced assumption of an intelligence and that the process is directed and designed to front-load the system, and in this your thesis is considerably different from "plain ole' panspermia" or FLU ... PLUS your FLE relies entirely on this being true: that is your extremely weak link.
Been there, hence my comment being what it was. quote: They are not positively identified as interstellar cells or the remains of them. The possibility of constructs like buckyballs were not known by Hoyle and Wickramasinghe when they published in the 70's: quote: And likely many other patterns are possible for forming hollow shells, with the ones observed being more stable. I would expect that a dodecahedron pattern would also be stable and larger geodesic shapes may also be possible. The graph used by Hoyle and Wickramasinghe
As NASA's recent evidence for buckyballs is the same kind of evidence as the 40+ year old evidence used by Hoyle and Wickramasinghe, and is much more discrete in analyzing the signal (two peaks instead of one), my money is on fullerenes rather than cells as the more accurate explanation. Furthermore, fullerenes are now known to clump together into larger particles: quote: Stacked like a crystalline structure using buckyballs as the matrix molecules ... could we see superbuckyballs made of buckyballs? In addition, there are other problems for them being dried shells of bacteria: they are not necessarily living organisms (or spores) nor do they necessarily have functional DNA inside - the pattern is for hollow shells, not living cells --- that has to be assumed for your thesis. Do a google on buckyball panspermia and see how many advocates are trying to cram panspermia inside the buckyballs.
Yes, it makes mine more complete and comprehensive, while yours still rests on certain incompletely defined assumptions being true without any objective evidence in this area.
Because (a) otherwise the FLE is unnecessary and (b) the inability to produce results would tend to invalidate the concept of abiogenesis by "natural (FLU/NFLU) laws" - leaving the field open for life being "salted" on earth.
But it makes assumptions about the origin of the cells and their delivery to the earth, assumptions that are just assumed to be true without testing or validation.
First, we may see evidence in life occurring today of "key eukaryotic proteins sharing deep homology with functional but unnecessary prokaryotic proteins." Seeing as all these forms are current living organisms they do not necessarily make any claim about early life. We also know that unicellular life is rife with horizontal transfer of material from one organism to another, even across the designations of the major domains of life (the cells don't care what they are). The laws of an FLU would allow this horizontal transfer, but it should be completely unnecessary and certainly is not predicted by an FLE that has a complete package in the initial life. quote: Curiously, I would expect that the FLE would predict a single unequivocal tree structure at the roots of life without Horizontal Gene Transfer (HGT), including genes for the production of proteins. Second, proteins are proteins, they don't depend on any specific branch of life to exist, they just need to be combined from amino acids in roughly the same order by any type of cell so we would expect (deep) homologies from shared ancestors along with some variation accumulated over time. If they serve little or no function in the fully developed cell at this stage in the game of existence (3.5 billion years after the first life) we can assume that some variation would occur, such that the proteins are not as homologous across domains as they are within domains. quote: Similar but different, just as should be expected. Note also that we have {p, b, a}, {p, b, nota}, {p, notb, a}, and {notp, b, a} homologies, which looks a lot more like horizontal transfer than front-loading to me.
Curiously, you appear to using evidence that is known prior to the hypothesis formation as a validation test, when this is properly included in your review of the current state of knowledge in forming an hypothesis in order to explain all the known objective empirical evidence. That is not a true prediction of the hypothesis, instead it is a demonstration of consilience between the known objective evidence and the hypothesis. A proper prediction is for something not already known, something new, and preferably something that cannot occur without the hypothesis or theory.
But there isn't -- see above. There is objective evidence that cilia exist. The proper approach is to take your example of your purported FLE instance (cilia exist), show that this could not occur in a NFLE world, and then form your your hypothesis test. Unfortunately, for you, you have done the opposite - shown how the NFLE would work.
Disagree all you want, but show me the evidence. You're going to have to provide me with more information than this hopefully from professional journals such as you have already used for this "discussion" you have asserted. I'm betting it is about details rather than yes or no.
Except that these are, as already noted, predicted by ToE and our current knowledge of early life and horizontal transfer among unicellular life. In no case have you provided evidence of something predicted that was not previously known. That is not a prediction, it is a claim of consilience between the known objective evidence and the hypothesis. Seeing as any new hypothesis must explain all current known existing evidence, demonstration of consilience with that evidence is not the result of prediction, rather this is a necessary part of the effort, the homework, that needs to go into the formation of a new hypothesis - checking to see that it is consilient with all known data. What you need to predict is something not already known, something new, and preferably something that cannot occur without FLE.
See above where I explain how "conventional theory" does in fact predict "deep homologies" ... (and derived traits in the added sections of the previous message noted above, along with the question of convergent evolution). Curiously, the ToE makes no prediction that preserved elements need to be functional or necessary, just that they not be deadly.
Again, see above where I explain why ToE does predict the patterns of deep homologies regardless of how specific they are. You have not shown a specific instance of any element that cannot occur by "conventional theory" and in fact have said so ("This is, in essence, the non-teleological hypothesis for the origin of the eukaryotic flagellum").
If you can then show me how. I'm open to evidence based logical argument.
Repeating your assertion does not make it any more valid. Using A you make a prediction that you have not made by B So which is more valid? The function of a hypothesis or a theory is to explain the evidence, it doesn't matter if the evidence is new or old, predicted or covered by the mechanics that went into the development of the hypothesis or theory. The function of a prediction test is to predict something not already known, something new, and preferably something that cannot occur without the hypothesis or theory.
Really? A "flagellum second" hypothesis would be a counter hypothesis (antithesis) to the "flagellum first" hypothesis and it would predict that TTSS would be more prevalent than the flagellum, which would be a proper falsification test for the "flagellum first" hypothesis. This test failed to falsify "flagellum first" -- it's simple cladistics: | This is why I talk about having a notA prediction to validate your hypothesis. Passing this test (and others as the testing progresses) makes the hypothesis stronger than not being tested. It doesn't make it true, as no amount of testing can accomplish that, and it doesn't make other hypothesis invalid unless they are mutually exclusive. What horizontal gene transfer would predict is that both the flagellum and TTSS could be transfered via HGT from bacteria that posses these trait to ones that don't. Natural selection says that these with the transfered gene would be preserved if they expressed the gene and it provided survival and reproductive benefit. This would predict that we would have some "flagellum first" and some "flagellum second" bacteria (and that this could muddy the evidence). It would also predict that all the species of bacteria where the gene originated would have the gene but not all species of bacteria that received the transfer would (however, those 'with' would likely be classified as a new species that would all have the gene). Thus these hypothesis are not incompatible or exclusive, and both hypothesis could be working at the same time. HGT is not invalidated here as the explanation (and it has been validated elsewhere as occurring), and it's prediction is not tested. The true answer probably lies with a combination of both hypothesis to explain all the evidence. This puts the "sister group" hypothesis in the same position as String Theory (really an hypothesis) compared to the "standard model" in physics, ... and your hypothesis. An hypothesis that is tested by passing invalidation tests is stronger than one that has not. This applies to "the standard model" the "flagellum first" hypothesis, common descent and the ToE, but it does not apply to String Theory, the "sister group" hypothesis, ... or your hypothesis. Your hypothesis is still not tested by a proper prediction. You can't predict something already known to exist, you can just show how the hypothesis explains it.
Curiously, that's not what I said. What I said was that
A falsification test for common ancestry is the genetic data: specifically there should be no ERV's of the same kind in the same locations in the genes. The genetic analysis not only shows these occurring, but occurring with "deep homologies" in a nested clade hierarchy pattern, just as predicted by the ToE. You don't have a proper invalidation test, and you don't have a prediction for something not already known, something new, and preferably something that cannot occur without the hypothesis or theory.
Except that (a) the "creationism model" pretends to do science after "special creation" rather than whole sale tweaking of every piece of evidence (a position they are forced into by the increasing evidence for ToE), (b) that the existence of NHP alone does not explain the existence of ERV sharing, and when the "goddunnit" card gets played every time the "creationism model" runs into problems, then it is constantly being revised to include more "goddunnit" and less natural processes validating the model. This means overall validation by objective evidence is shrinking rather than growing, and (c) invalidation of one hypothesis or theory does not make a single other hypothesis or theory more valid. Enjoy (1) - NHP as in Non-Human Primate? by our ability to understand Rebel American Zen Deist ... to learn ... to think ... to live ... to laugh ... to share. • • • Join the effort to solve medical problems, AIDS/HIV, Cancer and more with Team EvC! (click) • • •
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RAZD Member (Idle past 721 days) Posts: 20714 From: the other end of the sidewalk Joined: |
Hi Genomicus,
Always a possibility. Let me see if I can state it properly and you can correct me where I am wrong: premise 1: aliens of vast intelligence (or god/s) designed a cell Is that a fair assessment?
And yet your hypothesis is unable to remove a single premise above without falling to pieces. It does not matter whether these premises are stated or unstated, as each one is critical to the formation of the front-loading element in your hypothesis. Remove front-loading from your hypothesis and it reverts to pansperia as an explanation for first life, from which all life subsequently evolved by natural (FLU or NFLU) laws. You need all those premises included before you can get the cells to be front-loaded in your hypothesis. The premises aren't there to explain panspermia, OOL, or evolution, but to explain the front-loading of your hypothesis.
But how the front-loading originated is of critical importance to your FLE hypothesis. Let us posit that the appearance of front-loaded cell life was through the action of purely naturalistic (whether FLU or NFLU) laws, then evolution would be naturally' biased rather than design biased, yes? We can call this the NFLE hypothesis (antithesis). Thus to posit a design element, you need to posit a source for that design, and a method to realize the design and you need a means to test for it against the NFLE.
The question is how the front-loading originated. If we assume the NFLE hypothesis, then this would require life originating from some other source, one of which could be the construction of life from pre-biotic chemicals, and evidence of this being possible would be evidence for the NFLE rather than the FLE. I'm following your hypothesis to logical conclusions: if FLE is responsible for life on earth then no other mechanism for origins should exist.
The NFLE makes no prediction regarding the genome size or complexity of LUCA, it could be large or small. Confirmation that it is large and complex does not rule out NFLE, thus such a prediction does not differentiate FLE from NFLE. If if provides anything it provides for confirmation bias rather than open-minded skeptical validation. Furthermore, a smaller size and complexity of LUCA does not rule out the existence of "deep homologies" existing in the offspring of LUCA.
Whether evolution is via FLE or NFLE is not important to the FLU, and the special FL design of the FL cell is not necessary to the FLU. If you don't want to discuss FLU aspects, the we can concentrate on the differences between your FLE and a NFLE hypothesis, and how your testing proposes to differentiate one from the other. In NFLE we don't have a front-loaded cell, so evolution occurs purely by NFLE means and processes, including evolution as currently defined and used in science: (1) The process of Evolution involves the change in the frequency distribution and composition of hereditary traits within breeding populations from generation to generation, in response to ecological challenges and opportunities. This means that from generation to generation many traits are preserved within the populations (even if their frequency distribution changes), but that some may be altered and adapted. This means that there would be homologous traits preserved from generation to generation, and there would also be the appearance of derived traits (that can then become homologous in following generations). Thus the NFLE does not rule out deep homologies which you claim FLE predicts, and it also predicts deep derived traits that can then become deep homologies in later generations. As far as I can see your FLE does not predict deep derived traits nor do you have a test to separate original deep homologies from ones from deep derived traits and I also have to ask if deep derived traits are not counter to your front-loading hypothesis (as they should not be necessary if everything necessary was provided in the original front-loaded cells, yes?). Thus deep derived traits would seem to be a falsification test for FLE, yes? | Shared homologies in all populations (a thru m) would be deep homologies occurring via NFLE evolution. Shared homologies only in populations b thru f would also be deep homologies occurring via NFLE evolution from the deep derived traits in b that separate b from g, while shared homologies only in populations g thru m would also be deep homologies occurring via NFLE evolution from the deep derived traits in g that separate g from b. Curiously, it is just this pattern of deep deep homologies and deep derived traits that form the nested clade hierarchy pattern predicted by evolution in a NFLE world. For an FLE hypothesis I would expect to see homologies between b and g for unused copies of what otherwise appear to be deep derived traits, and logically this would also apply for all other appearances of derived traits in all later populations (ie no trait is ever derived, just expressed and used or not expressed and not used). This not only means a large and complex LUCA, as you state, but a large and complex descendant at every stage of evolution.
Likewise. I'm just trying to explore what differentiates your FLE from a NFLE, in order to better understand your hypothesis, the tests you have proposed, and what the evidence actually shows. Let me know where I've gone wrong eh? Enjoy Edited by RAZD, : ngls, subtitle Edited by RAZD, : clrty Edited by RAZD, : trying to remove curiously occurring extra spacing by our ability to understand Rebel American Zen Deist ... to learn ... to think ... to live ... to laugh ... to share. • • • Join the effort to solve medical problems, AIDS/HIV, Cancer and more with Team EvC! (click) • • •
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