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Prominent NAS member trashes neo-Darwinism

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Natural selection …is not the fundamental cause of evolution.

Masatoshi Nei

Science continues to destroy Darwinism. A prominent member of the National Academy of Sciences, Masatoshi Nei, trashed neo-Darwinism in the recent peer-reviewed article: The new mutation theory of phenotypic evolution.

Haldane’s dilemma showed mathematically that natural selection could not be the major driving force of evolution. Haldane’s dilemma lead in part to the non-Darwinian theory of molecular evolution known as the “neutral theory of molecular evolution”. Neutral theory asserted natural selection was not the principal driving force of molecular evolution. However, when molecular neutral theory was presented to the world in the 1960’s, it was politically incorrect to assert the obvious consequence of the neutral theory of molecular evolution, namely: morphology, physiology, and practically anything else made of molecules would NOT be principally shaped by natural selection either.

In What are the speed limits of naturalistic evolution?, I pointed out:

And if Haldane’s dilemma were not enough of a blow to Darwinian evolution, in the 1960’s several population geneticists like Motoo Kimura demonstrated mathematically that the overwhelming majority of molecular evolution was non-Darwinian and invisible to natural selection. Lest he be found guilty for blasphemy, Kimura made an obligatory salute to Darwin by saying his non-Darwinian neutral theory “does not deny the role of natural selection in determining the course of adaptive evolution”. That’s right, according to Kimura, adaptive evolution is visible to natural selection while simultaneously molecular evolution is invisible to natural selection. Is such a position logical? No. Is it politically and intellectually expedient? Absolutely!

But now 4 decades later, the inevitable consequence of Haldane’s dilemma and Kimura’s neutral theory may be ending the uneasy truce between neo-Darwinists and neutralists.

Nei writes:

For the last six decades, the dominant theory of evolution has been neo-Darwinism, which was developed by the three founders of theoretical population genetics, Fisher (1), Wright (2), and Haldane (3), and was later supported by various evolutionists (4). Neo-Darwinism asserts that natural selection is the driving force of evolution,
….
In the last four decades, the study of molecular evolution has shown that a majority of amino acid substitutions in proteins are neutral or nearly neutral

However, most evolutionists still believe in neo-Darwinism with respect to phenotypic evolution and are not interested in neutral evolution (19,22).

Mayr (23) stated that neutral mutations apparently occur at the molecular level, but because they do not affect phenotypic characters, they are of little interest to evolutionists.
….

By contrast, Nei (17, 24, 25) argued that because phenotypic characters are ultimately controlled by DNA sequences, both molecular and phenotypic evolution must occur in similar [non Darwinian] ways. He also suggested that a considerable portion of morphological evolution is caused by neutral or nearly neutral mutations, and the driving force of evolution is mutation at both molecular and phenotypic levels.
….
As mentioned in the introduction, a majority of current evolutionists believe in neo-Darwinism. In one of the most popular textbooks on evolution, Futuyma (ref. 20, p. 10) states that evolutionary change is a population process in which one genotype replaces other ones, and for this process to occur, mutation is quite ineffective because of its low rate of occurrence, whereas even the slightest intensity of natural selection can bring about substantial change in a realistic amount of time. He also states “Natural selection can account for both slight and great differences among species, and adaptations are traits that have been shaped by natural selection.” Although this type of statement is quite common in the evolutionary literature, it is obvious that any advantageous genotype is produced by mutation including all kinds of genetic changes. Natural selection occurs as a consequence of mutational production of different genotypes, and therefore it is not the fundamental cause of evolution.

Historically, the word mutationism was used to refer to William Bateson’s saltationism or similar ideas, in which natural selection plays little role. Later Morgan (109) presented a more reasonable form of mutationism taking into account the role of natural selection. His view was abstract and based on a few lines of speculative arguments. However, recent molecular studies of phenotypic evolution support the basic ideas of his view and have extended it to a more comprehensive view presented in this article. If the new form of mutation theory described here is right, even in its crudest form, more emphasis should be given on the roles of mutation in the study of evolution.

Notes:

1. ID sympathizer Dr. John Davison, who has spent much of his recent life promoting the works of William Bateson, should be much encouraged with these developments. It was through Davison I learned of Bateson’s wonderful ideas.

2. Richard Dawkins wrote of Kimura in Blindwatchmaker. Dawkins argued Kimura’s ideas wouldn’t overturn Darwinism since Darwinism operated at the higher level of adaptation whereas Kimura’s non-Darwinian theory operated at the lower level of molecules. But the reductionists are now getting taste of their own medicine. If the Darwinism doesn’t operate at the molecular level, then why should we expect it to operate at much higher levels like morphology and physiology either?

3. Lewontin gives a powerful example of neutral evolution at the morphological level. Rhinos have either 1 horn or 2 horns. Did natural selection cause the evolution of one horn in one case, and 2 horns in another? Unlikely.

4. Salthe pointed out a fundamental contradiction in Fisher’s fundamental theorem of natural selection. Selection is the enemy of diversity. Salthe realized the obvious problem of trying to account for the abundance of diversity through a mechanism which reduces diversity.

5. At least 3 signatories of the Discovery Institute’s Dissent from Darwin list anticipated these recent developments. Davison, Salthe, and Ho. Ho managed to present echoes of these ideas 30 years ago in a peer-reviewed journal. See: An eloquent but bogus non-review by Dawkins.

a relative lack of natural selection may be the prerequisite for major evolutionary advance

Mae Wan Ho

Comments
ARN points out this by Dawkins:
The crucial passage in The Edge of Evolution is this: "By far the most critical aspect of Darwin's multifaceted theory is the role of random mutation. Almost all of what is novel and important in Darwinian thought is concentrated in this third concept." What a bizarre thing to say! Leave aside the history: unacquainted with genetics, Darwin set no store by randomness. New variants might arise at random, or they might be acquired characteristics induced by food, for all Darwin knew. Far more important for Darwin was the nonrandom process whereby some survived but others perished. Natural selection is arguably the most momentous idea ever to occur to a human mind, because it - alone as far as we know - explains the elegant illusion of design that pervades the living kingdoms and explains, in passing, us. Whatever else it is, natural selection is not a "modest" idea, nor is descent with modification.
Unfortunately for Dawkins, someone more knowledgeable says otherwise:
Natural selection …is not the fundamental cause of evolution. Masatoshi Nei
scordova
July 20, 2007
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Joseph: 500/3=166.67 amino acids. Don't want the anti-ID lurkers to think we have a problem doing division, do we? I apologize. You are obviously right. I was writing in a hurry, and from (misled) memory. The number 500 is in reality the number of bits, not of nucleotides. Dembski's UPB is 1 to 10^150, and corresponds roughly to 500 bits of information, which is the same as about 115 aminoacids (20^115), that would be, as you correctly remarked, 345 coding nucleotides (indeed, 4^345 is more than 10^200, but that's because of the redundancy of the genetic code). Anyway, 115 aminoacids are really a very small quantity of biological information if their possible random computation would exhaust all the resources of the whole universe! Again, I apologize. And, please keep it secret and just don't tell darwinists, but sometimes I do have problems doing division...gpuccio
July 20, 2007
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Jerry: For once it would be refreshing for them to admit that they don't have anything but just beleive it will be forthcoming. And what, exactly, is your problem with "science via promissory notes"? :)Joseph
July 20, 2007
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gpuccio: But the problem is, “any” neutral mutation is free to accumulate, or alternatively be lost. Even the most beneficial mutation has the chance of being lost. NS acts each and every day on each and every organism. Those which aren't lost are then free to accumulate. (I am just giving you their version, not that I believe it) At risk of being repetitive, Dembski's UPB is of “only” 500 nucleotides, or roughly 100 aminoacids. 500/3=166.67 amino acids. Don't want the anti-ID lurkers to think we have a problem doing division, do we? Behe's arguments, which deal with true mutations in real life, show that even a coordinated mutation of a few aminoacids is beyond any reasonable chance, if there is no step by step selection. There isn't any coordination. Just a bunch of lucky mistakes that happen to make something of themselves. And that is why the premise is unscientific. And now neutralist are claiming that the whole genome, or most of it, derives from the accumulation of neutral mutations, totally random, without practically any relevant selection… I must miss something in their reasoning. Magical mystery mutations. Magical because they do things that have never been directly observed. And mystery because they still elude us. When I first started studying electricity and electronics back in the early 70s we used to call it "friggin' magic". That term can now be aplied to the theory of evolution.Joseph
July 20, 2007
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gpuccio, You said "and now neutralist are claiming that the whole genome, or most of it, derives from the accumulation of neutral mutations, totally random, without practically any relevant selection… I must miss something in their reasoning." They never have any reasoning only conjecture and "just so stories". Evolutionary biology is the only science without empirical backing. Whenever you ask for reasoning you get speculation. Whenever you ask for evidence you get silence or in its place rhetoric or sophistry or irrelevant answers. It is always fun to watch them ignore, evade or distract. That is all they can do other than their ad hominem comments. The real interesting question is what psychological make up leads to such an approach. For once it would be refreshing for them to admit that they don't have anything but just beleive it will be forthcoming. My guess is to admit the obvious is like surrendering to an enemy.jerry
July 20, 2007
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Bob, You said to my comment "All novelty must come from some mechanism as yet undetermined" "Mutation." Any examples? Behe just shot down mutations; they do nothing but trivial stuff. Whay can you offer other than faith and a few simple examples?jerry
July 20, 2007
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joseph: "Neutral mutations- those which do not convey an advantage or disadvantage- are then free to accumulate." I understand that's the general idea. But the problem is, "any" neutral mutation is free to accumulate, or alternatively be lost. So, we are left with the whole configuration space, with the total of possibilities. At risk of being repetitive, Dembski's UPB is of "only" 500 nucleotides, or roughly 100 aminoacids. And believe me, Dembski's UPB is really, really a generous limit. Behe's arguments, which deal with true mutations in real life, show that even a coordinated mutation of a few aminoacids is beyond any reasonable chance, if there is no step by step selection. And now neutralist are claiming that the whole genome, or most of it, derives from the accumulation of neutral mutations, totally random, without practically any relevant selection... I must miss something in their reasoning. Acquiesce: I agree with what you say. I have suggested myself, in a previous post somewhere in UD, that really evolution seems to implement more the need to "express" higher functions than the need for survival. There is no doubt that increasing complexity is, everywhere, a cause of incresing weakness. That is particularly true of information and of software. The more the complexity, the more the problems, errors, bugs, etc. But, indeed, complexity can perform "new" functions. That's its real value. On the same line, it seems that evolution is constantly trying to express higher complexity, and an astonishing level of diversification, creativity and beauty, "in spite" of the inherent challenges to survival and fitness. While I remain convinced that the highest fitness belongs to stones, there is no doubt that bacteria are more fit than any other living being. And just try to compare mosquitos and rats with chimps and human beings... The whole idea that biological complexity arises from the need for survival is totally wrong. Biological complexity is an astonishing, utterly unlikely design through which some intelligent and artistic force is trying to express something new, some new interesting quality or function, some further creative adventure. Regarding NS, it is obvious that it can act only to select a new relevant function after it has appeared. That's why its role is so limited, because complex functions are not deconstructable in step by step subfunctions. In other words, practically any significant new function, new protein, new network, is in essence IC. But there is more. Even if NS has a role, it cannot really be "heuristic" in any way. NS is, by definition, blind. That's why it is, in reality, practically random. All the examples made by darwinists (see Methinks it's a weasel and similar) are examples of intelligent selection, where a very definite knowledge of the aim to be obtained is already present in the "selector". That's why they can work. A very good example of "intelligent" selection is the mechanism by which antibody affinity is increased after an immune response. That's an almost perfect model of how an intelligent mechanism can determine evolution through random mutation. A random mutation process (an intense and intentional random mutation process) is aimed at a target which is already near to the desired result in the configuration space (the low affinity antibody of the primary immune response, which is selected from a natural repertoire through its affinity with the antigen). The variations in affinity are then accurately tested against the available information (the antigen itself), and only the clones with higher affinity are selected, while the others are inhibited. That's really intelligent selection. Even if the organism does not know which DNA/aminoacids sequence is the best to react with the antigen, it can use a random search and carefully select the results aaccording to a specific complementary information (the antigen). The procedure is higly purposeful, and it can succeed only because it has already most of the necessary information (the antigen itself). If the organism did not know the antigen, or if it had to test the efficacy of all the new anibodies "in the wild", that is by darwinian mechanisms, waiting to see if any new variant of the antibody gives some survival advantage, no higher antibody spcificity could be found in million of years. Instead, the organism checks each result with a known target, by an informational algorithm performed by specific cells (probably the antigen presenting cells in network with other T cells, of the helper and suppressor kind), and useful results are reached in a short time, exactly like in the "methinks it's a weasel" example. Intelligent selection can perform miracles: it only has to know in advance what it has to find.gpuccio
July 20, 2007
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Atom [33] It is easier to get the protein in many small steps, if each step is indeed selectable, than getting it all at once.
Well that's highly debateable after all we know proteins have an invariant core, rubisco (a protein used in photosynthesis) comprises 476 aminos, 105 of these are totally invariant. In edition 110 other animos can only be substituted by one alternative, and nearly 189 others by one of three alternatives. So for NS to produce this protein it must have a substantial amount of the sequence correct, which means it cannot proceed in ‘many small steps'. But the point I was making was merely an attack on NS. NS doesn't make the arrival of a new trait any more likely, all it does is potentially fixate it into the population.Acquiesce
July 20, 2007
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Bob [42] Acquiesce - you're evidently not aware of the idea of a trade-off. Just to give one example, a reduction in the number of offspring can lead to a higher fitness if the offspring are more likely to survive.
Actually, I'm fully aware of it, that's why I specifically made the point that not only are bacteria the fittest organisms on our planet, but are the fittest organisms in whatever environment they live in. So your point that a reduction in the number of offspring can lead to higher fitness seems strange. Maybe you name me an organism, other than bacteria, which are fitter than bacteria in any particular environment? In other words, what offspring are more likely to survive than those of bacteria? This is precisely the point I'm making.
Bob [42] Incidentally, point 6 is silly: it's not the same bacteria that live everywhere. You don't find viable populations of E. coli on the skin of humans, for example.
That's why I just said bacteria. Whats the point your making here? Bears are quite diverse, the polar, the grizzely, the panda – they're not the same bear. But they're still a bear, and you wouldn't find them living near sea vents with temperatures around 600F.
Bob [42] specialisation (e.g. on one food source) can be advantageous if it means you can exploit it better, and that you don't loose out too much in trying to eat everything.
Now, I didn't say it wasn't advantageous. I said that increasing specialzation, such as predominance to a certain food source, in the case of the panda, shows how NS takes generalizations, produces specializations. which lead ultimately to extinction through lack of generalization. I think that's common sense.Acquiesce
July 20, 2007
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Acquiesce - you're evidently not aware of the idea of a trade-off. Just to give one example, a reduction in the number of offspring can lead to a higher fitness if the offspring are more likely to survive. Another example: specialisation (e.g. on one food source) can be advantageous if it means you can exploit it better, and that you don't loose out too much in trying to eat everything. Incidentally, point 6 is silly: it's not the same bacteria that live everywhere. You don't find viable populations of E. coli on the skin of humans, for example. BobBob O'H
July 20, 2007
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All novelty must come from some mechanism as yet undetermined...
Mutation.Bob O'H
July 19, 2007
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What are you missing? Magical mystery mutations! But anyway: From the “Contemporary Discourse in the Field Of Biology” series I am reading Biological Evolution: An Anthology of Current Thought, edited by Katy Human (perhaps related to Mike Gene ;) ).
The old, discredited equation of evolution with progress has been largely superseded by the almost whimsical notion that evolution requires mistakes to bring about specieswide adaptation. Natural selection requires variation, and variation requires mutations- those accidental deletions or additions of material deep within the DNA of our cells. In an increasingly slick, fast-paced, automated, impersonal world, one in which we are constantly being reminded of the narrow margin for error, it is refreshing to be reminded that mistakes are a powerful and necessary creative force. A few important but subtle “mistakes,” in evolutionary terms, may save the human race. -page 10 ending the intro
Can evolution make things less complicated?:
Instead, the data suggest that eukaryote cells with all their bells and whistles are probably as ancient as bacteria and archaea, and may have even appeared first, with bacteria and archaea appearing later as stripped-down versions of eukaryotes, according to David Penny, a molecular biologist at Massey University in New Zealand. Penny, who worked on the research with Chuck Kurland of Sweden's Lund University and Massey University's L.J. Collins, acknowledged that the results might come as a surprise. “We do think there is a tendency to look at evolution as progressive,” he said. “We prefer to think of evolution as backwards, sideways, and occasionally forward.”
Joseph
July 19, 2007
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There isn't any direction. Right. And there isn't any heuristic that would seem to bias evolution toward a baboon instead of toward bacteria. So, how is NS useful in the process again? And yet Dawkins' Mount Improbable seemed to assume that evolution would climb toward the peak. Still, with no direction and no heuristic, that seems to leave us with a comprehensive search of the problem space, in which case, man is just an incredibly lucky guess. What am I missing?Phinehas
July 19, 2007
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An arm must be a bad arm first before becoming a good wing. NS does not have the foresight to overcome such problems. Sal, Sal, Sal. A bad arm riding the NS wave of good legs, good sight and good everything else, will survive because the deficiancy it raises is outweighed by the over-performance of other innovations. ;) To Acquiesce: Please read Wobbling Stability To Phinehas: There isn't any direction.
Natural selection is the simple result of variation, differential reproduction, and heredity—it is mindless and mechanistic. It has no goals; it's not striving to produce “progress” or a balanced ecosystem.
http://evolution.berkeley.edu/evosite/evo101/IIIE6Nonrandom.shtmlJoseph
July 19, 2007
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An arm must be a bad arm first before becoming a good wing. NS does not have the foresight to overcome such problems. Indeed. And it doesn't seem to me that appealing to flying squirrels is much help in this regard, since at some point on the continuum between arm and wing, it seems likely that you will have something that doesn't function very well as either. And the something would be selected against by NS. So, it seems to me that there are two sides to the NS problem for Darwinists. (1) NS as a heuristic cannot seem to account for how a baboon is more fit than bacteria, and (2) NS would likely cull the vast majority of those changes that might have proved helpful in moving toward a novel function, but not yet providing it.Phinehas
July 19, 2007
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The problem is Blindwathcmaker heuristics lead down the wrong path. An arm must be a bad arm first before becoming a good wing. NS does not have the foresight to overcome such problems.scordova
July 19, 2007
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Acquiesce, I've been pondering the same issue, only from a different perspective. As a video game designer, I am familiar with various path-finding algorithms. Some algorithms, such as Dijkstra's, do a comprehensive search of the space in order to discover the shortest path from one spot to another. An algorithm like A* differs from Dijkstra's in that it has a heuristic that helps direct the search. For instance, a simple heuristic will give preference to nodes that are closer to the goal point (as the crow flies, so to speak, even though there could be intervening barriers). So, I've tended the think of NS as a kind of heuristic, helping narrow the search space, or helping direct the search toward a specific direction. But then I stumble on the realization that the NS heuristic only moves toward life. If we take a look at Dawkins' Mount Improbable, we see an analogy that purports to show how gradualism solves the problems that Darwinian evolution faces in taking life from bacteria to man. Setting aside CSI for the moment, I'm not sure I really see how gradualism is such a great solution. I keep wondering why Dawkins assumes life will climb Mount Improbable in the first place, as opposed to rolling down the gradual slope. Surely the Darwinist would say that it is NS that propels life up Mount Improbable. But isn't the mountain one of complexity? I can see how NS can function as a heuristic guiding toward life, but how does it function as a heuristic guiding toward complexity? It seems to me that at any point up on that gradual slope of Mount Improbable, you have life to the left, to the right, and down the slope behind you. So why must NS lead straight ahead, up the slope? What heuristic is it that pushes toward the complex life that is man vs. toward the simple life that is bacteria? And if you don't have NS as a heuristic guiding toward complex man, aren't you left with a comprehensive search of the problem space? I would really like to understand the Darwinists perspective on this. Anyone?Phinehas
July 19, 2007
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Finally, someone has accused me of misrepresentation! I point to a good critique (though I disagree) by Dr. N. Wells, a geologist/paleontologist at ARN here. He argues neutral theory can be absorbed into Neo Darwin synthesis. I took some pains to point out there is a quantitative estimate which proceeds from one of the founders of neo-Darwin synthesis (Haldane) which puts a limit on how much an organism is shaped by natural selection. I pointed out about 700 of the 4 Billion base pairs might be subject to selection at any time for creatures like humans, and this is being generous. Natural selection explains only about 700/4 billion of what makes us human... With those figures it's like trying to say a piece of canvas car cover can cover a Corvette (or Lamborghini), therefore isn't the canvas wonderful, and the canvas can explain the entire Corvette. This is what is done when arguments are made that Neo Darwin synthesis can accommodate any possible stream of new and inconvenient facts -- just argue Natural Selection influences all of biolgical reality, therefore one gives the impression it therefore explains biological reality. Gravity influences all of biological reality, it certainly doesn't explain it. In fact, a canvas is too generous. Saran wrap is a better metaphor.scordova
July 19, 2007
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Acquiesce, You raise valid points concerning Darwinism. I have wondered myself, for example, how anything other than bacteria (super-replicators) can be expected from RM/NS, since going from uni-cellularity to multi-cellularity results in a fitness hit, as does moving to sexual reproduction (even when factoring in possible benefits from recombination...the short-term 50% hit is way too high to overcome with a subtle, long-term benefit). On a side-note, your last comment makes reference to a specific protein (1 in 10^130 chance) and NS. The reason NS is brought in is because if any sub-set of that protein has function/selection value, it will spread and allow cumulative selection to help get the final product. It is easier to get the protein in many small steps, if each step is indeed selectable, than getting it all at once. PS Has anyone read Jon Saboe's The Days of Peleg advertised on the side-bar? I'm reading it right now and it is a verrrry good, fun read. I had the opportunity to build with Jon as well, a very nice guy.Atom
July 19, 2007
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On a side point, NS, let's remember, can only select a trait once it adds some selective value, which means functionality. So if it's one chance in 10^130 to get a specific protein molecule by RM, it will still be one chance in 10^130 even when NS is factored in. All NS can do is potentially fixate the trait into the population once it has arisen, and even that's not a given.Acquiesce
July 19, 2007
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So basically what I'm saying is that even if we grant Darwinists NS and RM the likelihood is that NS would only direct RM in producing traits which further increase fitness. So its doubtful NS would ever go beyond simple, fast reproducing organisms such as bacteria. Of course the Darwinists would contend that this argument is flawed because, you guessed it – higher organisms with reduced fitness do exist. Spot the circular nature of that response, which I've had many times.Acquiesce
July 19, 2007
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I genuinely would love to know how NS can direct the evolution of higher organisms, all of which process a reduced level of fitness – compared to their first primitive ancestor. For example, at some point NS must select these traits: 1. Reduced reproductive fecundity (i.e. reduced numbers of offspring) 2. Reduced population size (from tillions to, for example, pandas) 3. Reduced resistance to poisons, temperature and environmental changes/conditions 4. Increased generation times (bacteria can reproduce every 20 minutes) 5. Increased gestation times (i.e. elephants 22 months) 6. A reduction in livable environments (bacteria live virtually everywhere) 7. Sexual reproduction (a 50% hit in fitness alone) If NS really did direct the process of evolution then it must, at some point, have selected traits which lead to one or more of these effects. How therefore does NS select in the direction of higher complexity, when it appears that higher complexity necessitates a reduction in fitness? In regards to NS without constructive mutations, then clearly all it can do is take generalizations and produce specializations, which eventually go extinct though lack of, you guessed it – generalization. The panda is a fine example. Becoming more specialized for its peculiar lifestyle it has totally lost generalization – if the bamboo (which consists of well over 90% of its diet) goes extinct, it goes extinct.Acquiesce
July 19, 2007
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"Budda-bing, budda-boom" is technical evolutionary jargon... :)Joseph
July 19, 2007
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I'll probly mess this up but here goes: gpuccio asks: Can anyone explain to me how evolution based on neutral mutations and/or genetic drift is supposed to work? Neutral mutations- those which do not convey an advantage or disadvantage- are then free to accumulate. This accumulation will then lead to DNA sequences that will then do something good or bad for the organism. That is when NS takes over. The good is kept and the bad dies with its owner. Budda-bing, budda-boom, a novel function is created.Joseph
July 19, 2007
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Bob, As you say NS can never create novelty. The process only selects, not creates. All novelty must come from some mechanism as yet undetermined and NS just chooses from what is presented and then eventually eliminates possibilities. So why should anyone really study NS for anything other than the obvious or the trivial? It is only a study of what is potentially in a genome. Sort of like intellectual dog breeding.jerry
July 19, 2007
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On Nei, he's just adding to the debate over the relative strengths of different evolutionary forces. It's actually a debate that my PhD supervisor was involved in (in a different context) about 15 years ago. Nei wants to argue that mutation is important, and we should pay more attention to it. I'm not convinced by his arguments, partly because I don't think he makes a strong case: there's too much arm-waving, but also because it's not clear what exactly he thinks we should be looking for. At one level, he's right that mutation is important: novelty has to arise through mutation. Hence, a lineage may become dominant simply because the key novelty arose by mutation in that lineage, and not another one (I think this is the message of his discussion about humans and chimps). But one could argue from the same data that selection is important, because that is what will fix most mutations that have a phenotypic effect. So, it's more a problem of which perspective you want to take. And a lot of that will depend on the sorts of problems you are looking at, and aspects such as the time scales you are looking over: he criticises Fisher, Wright and Haldane, but they were mainly thinking over shorter timescales, and not so much about the long-term evolution of novelty. I think we've moved on a lot since then, and the sorts of problems Nei raises are being studied much more now, and we're getting quite a good understanding of the processes. So, the bottom line: this is nothing to get excited about, unless you're interested in the details of the subject: it's part of the process of assimilating the new empirical process. BobBob O'H
July 19, 2007
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gpuccio, Just a comment. Natural Selection is over hyped as a force in evolution. All it can do is select among already existing alleles. It cannot create any new information, only select amongst the information structure already present. And over time actually decrease information by eliminating alleles. So in no case can NS, by definition, ever increase information. This is basic NDE 101. Increasing information can only come from the origin of new alleles through some mechanism. So the real Achilles heel of gradualism is the origin of new alleles. Mutations are the gradualist's only hope and as Behe just showed, this is a forlorn hope. Where are they to go. Hype a meaningless process such as NS or pray for more meaningful mutations. The answer is "prayer."jerry
July 19, 2007
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OK, Sal. Now I see where you're coming from. A couple of comments: 1. (this is trivial) Usually the selection coefficient is calculated relative to the least fit allele. Hence my confusion. 2. Is there any evidence that there are 700 genes where there is an allele reducing viability like this? It sounds high to me, although that is just my intuition - I don't have any evidence. OK, I'd better get back to Nei before this thread is totally derailed. BobBob O'H
July 19, 2007
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10:04 AM
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Natural selection …is not the fundamental cause of evolution. Masatoshi Nei
I've surveyed the Darwinist blogsphere. They haven't done their usual and accuse me of quote mining yet. They're becoming slackers. What's taking them so long. By now I would have expected to hear venom and vitriol spewing forth. Man, I'm dissappointed with their non reaction. :-)scordova
July 19, 2007
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gpuccio asked: How are they supposed to explain CSI? How are they supposed to explain any complex function? Are the proponents of this kind of “evolution” completely unaware of the mathematical impossibilities of obtaining CSI by purely random methods? Have they never read any serious ID source? Or are they simply not interested in the question?
Though it's rather hard to glean it in the somewhat rambling paper by Nei, the explanation for CSI or the appearance of progress is that it is an artifact of our post-dictive projections, much like us projecting and seeing human faces in the sky. To some like Nei, asking why certain clouds evolved to look like human faces is like asking why neutral mutations evolved to look like functional machines.
The teleological view of evolution has been out of fashion for more than a century. Yet, human minds appear to be susceptible to this view consciously or unconsciously. In the evolutionary literature, it is not uncommon to see such phrases as ‘‘making of Homo sapiens'' M. Nei
The Universal Probability Bound (UPB) suggested by Dembski actually refutes much of the post-diction arguments, but how UPB does this when combined with a 500-bit specification is a bit subtle and probably beyond the scope of this thread. But briefly, there are only so many 500-bit (or more than 500-bit) specifications humanity can conceive of because of memory storage issues. These specifications are patterns. If the patterns can be demonstrated to be independent and not post-dictive and are 500 or more bits, then Nei's arguments are refuted. One way to demonstrate a pattern is not post-dicitve is to see how these patterns emerged independently in the engineering discipline or even every day life. The lock/key or login/password metaphor is an independently given pattern. Why do we see these patterns in biology. We call such things protein-protein binding sites, but this analogy would not be possible if biology were a product of neutral evolution. This of course is a very difficult and subtle math argument, but I believe ultimately correct. The neutralists (even though wrong) are much less wrong than the Darwinists. It takes a more subtle argument to refute the tenets of neutralism. Heck, most people don't even know there exists neutralism, much less an argument to refute it.scordova
July 19, 2007
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