Showing posts with label Ring Species. Show all posts
Showing posts with label Ring Species. Show all posts

Saturday, March 10, 2012

Loss of Genetic Diversity same as Loss of Information: Both prevent macroevolution. Evolution Defeats Evolution

[NoNukes says]: A creationist might state that nature cannot create the "information" required to produce novel features and "macroevolution" . Dog breeding includes human intervention which can be viewed as being similar to an ID agent stepping in to add information allowing new features like wiener-dog legs.

I don't really grasp the context of the issue of "novel" characteristics so I'm not sure how to address that, but I can respond to the idea of "information" at least.

Apparently this is easily misunderstood, and I have to agree that the very term "information" is vague or even cryptic in a way. The idea is really pretty simple though, from a creationist point of view anyway. You have a given built-in genetic recipe from the Creation for each species, so the possibility of that species evolving into another would require the addition of whatever is lacking in the first that the second needs. That's the "information" that would have to be added to the genome for it to macroevolve. Perhaps I don't even need to invoke the original Created species for this to make sense. It should be apparent to all that each species does have its own genome, many of which are in the process of being sequenced, and they are being sequenced AS being specific to the particular species they belong to. The DNA for each species has its own characteristics peculiar to that species, genes that aren't found in some other species but only this one, a certain number of chromosomes particular to the species and so on and so forth, with of course occasional exceptions. The genes pertain to the particular trait, perhaps eye color, the alleles define the different qualities of that trait, in this case the color. Wherever there are many alleles for a trait you can get a great variety from the genome as given for that species, you don't need to add alleles. Macroevolution requires getting from these recognizable species to something completely outside the particular genetic recipe, whether you think of them as having evolved to their present identity or been created independently at the Creation. You still have to posit the addition of NEW information that is not already present in the current genome.

New genes at least. New alleles isn't enough. New alleles for extant genes could only give variation to the trait the gene instructs for.

So has anybody ever shown the formation of a new gene? Is there even a theory about how that might come about?

In any case, the whole idea of the need for more information really starts as an observation that the processes of evolution ELIMINATE INFORMATION rather than adding it, and that fact means that evolution is moving in a direction that makes evolution less rather than more possible.

But I think it's clearer to say that evolution reduces genetic diversity. It's really the same observation. Evolution eliminates alleles at the very least and at some extremes may eliminate ALL alleles for a given gene which effectively kills the gene and most probably makes it a corpse in the genetic graveyard known as Junk DNA.

This IS the natural direction of all evolutionary processes. In order to get a new phenotype, especially one that sticks and becomes characteristic of a new population or variation or breed, other alleles for the same traits that give a different character MUST GO. That's LOSS OF INFORMATION, or REDUCED GENETIC DIVERSITY.

THIS LOSS IS THE VERY MACHINE OF EVOLUTION ITSELF.

Now here comes RAZD answering NoNukes:

Curiously, the mutations that cause short legs are fairly common in many species, including humans - it's called Dwarfism.
So is RAZD saying these mutations are NEW information?

I must ask, how does he know these are mutations? He gives no evidence, he merely CALLS the allele that bring about this trait mutations. Evidence please. I'm willing to consider this a mutation myself just because dwarfism must be thought of as a disease process, which I KNOW mutations produce. But are all shorter legs caused by dwarfism or is it simply possible to get a combination of naturally occurring (built-in) genes/alleles that naturally produce shorter legs? Evidence please.
The difference is between a random mutation occurring and it being spread into the breeding population is selection.
Pure theory, which is all evolution ever has to offer. Is he talking about useful / beneficial mutations, and if so nobody has ever shown that they even occur except in very rare and problematic instances, they are merely ASSUMED to be the source of all change in the genome. But if we are talking about nondeleterious variations the most likely scenario is that a rare normal allele simply comes to expression, and then yes, it will spread in the population if it is selected in the reproductive lottery. If not, it won't. But to call it a mutation is simply to beg the usual questions.
Within the ecological challenges and opportunities imposed by artificial selection, there is a survival and reproductive benefit to having short legs for the dogs being bred that have them, and not having them would be detrimental. This is a rather demanding ecology to survive in, yes?
Could be, depends I suppose. But we still don't know if this is a mutation or simply a normal-occurring healthy allele.
Now the problem with the creationist\IDologist claim about information is that they don't define what the concept means
Well, it's difficult, but I believe I may have succeeded in defining it above. And I vote for substituting the concept of reduction or loss of genetic diversity as being easier to grasp.
or even more importantly, how it can be measured.
As I've proposed, do a DNA sampling of the first and last populations in a ring species, one you find in nature or one you create in the lab. You should find obvious reduced genetic diversity in the last population and probably a progression of reduction in intermediate populations as well. Lots of homozygosity in the last population, a lot more heterozygosity in the first. Go gather a bunch of salamanders from the California ring species, label them and sample their DNA especially the genes for the patterns on their skin.

He goes on to give an irrelevant self-fulfilling chart he claims falsifies the claim about loss of information. He's probably misreading a built-in allelic possibility as new information but it's all just an exercise in proving what he wants to prove.

No, do what I suggest above, see that there really is loss of genetic diversity (same as loss of information) when species evolve. That kills MACROevolution right there.

Evidence for Reduced Genetic Diversity as Necessary Component of Evolution

You want some evidence for the claim that evolutionary processes always involve the reduction of genetic diversity? It's pretty simple, OUGHT to be obvious, and it's all about the reduction of heterozygosity to homozygosity or even less: This is from Wikipedia on Zygosity:
A cell is said to be homozygous for a particular gene when identical alleles of the gene are present on both homologous chromosomes.[2] The cell or organism in question is called a homozygote. True breeding organisms are always homozygous for the traits that are to be held constant.
In nature the same thing applies. Once you get a new variety, a subpopulation that is reproductively isolated from its parent population or other populations of the same species, even the result of a "speciation" event, and especially after it has inbred over some generations, its traits are going to be or become fixed. For a new trait to stick, or continue to characterize the new population, competing alleles for that trait must have been eliminated from that gene pool. THIS IS THE NECESSARY REDUCTION IN GENETIC DIVERSITY THAT ALLOWS A NEW TRAIT TO COME TO CHARACTERIZE A NEW BREED OR POPULATION IN THE WILD, THIS MUST OCCUR FOR A NEW TRAIT TO DEVELOP AND STICK IN A NEW POPULATION.

If they are "true breeding", they will be homozygous for their characteristic traits. This HAS to be true whether the population is the result of natural processes such as natural selection or genetic drift, migration and so on, or domestic breeding decisions.

HOMOZYGOSITY MEANS ONLY ONE ALLELE FOR THE GENE, ALL THE OTHER ALLELES HAVING BEEN ELIMINATED FROM THAT PARTICULAR GENE POOL. THAT'S THE SEVEREST CASE OF DECREASED GENETIC DIVERSITY (except for hemizygosity and nullizygosity, mentioned in the article below) AND IT'S NECESSARY TO GETTING A "TRUE BREED." AND WHAT IS A TRUE BREED BUT A NEW PHENOTYPE OR "SPECIES," A SPECIATION EVENT IN ITSELF, THE SUPPOSED STEP ON THE WAY TO OPEN-ENDED EVOLUTION FROM ONE SPECIES TO ANOTHER ACCORDING TO EVOLUTIONISTS.

Take dogs. If you want a Dachshund you have to eliminate all the alleles that specifically produce Great Danes or Golden Retrievers or Chihuahuas etc. If any of those alleles show up in the Dachshund breeding program you'll get a less perfect Dachshund. They make the breed less than what it is supposed to be.

It works the same way in nature, maybe through Natural Selection but probably more often through random events that simply happen to separate a population into two or more subpopulations. A particularly marked salamander emerges because the other markings are genetically decreased by comparison to those for the new marking. The markings of the last species to develop in a ring species of such salamanders should be genetically homozygous. Same with the genetics underlying the last species in the ring of green warblers and so on. You should find decreased genetic variability and probably a lot of homozygosity, just because this is what evolution DOES.

It's NECESSARY to evolution, and if evolutionists weren't always imagining nonexistent mutations into the mix it ought to be obvious even to THEM. The only mutations that are involved are those that contribute diseases to the mix and interfere with the health of the most genetically reduced populations, even to extinction in some cases.

In nature the introduction of disease elements may simply eliminate a new variety, Natural Selection in operation at its most severe, but if the new variety finds a niche it can adapt to it will survive just as a good domestic breed will.

The new variety necessarily comes through a reduction in genetic diversity. That's how evolution WORKS, really, though such an obvious necessity, that must lead to LESS ability to evolve, is simply ignored by believers in evolution who go on spinning evolution out of imaginary mutations.

To repeat the point: If circumstances are such that the populations remain reproductively separate, meaning without gene flow or the sharing of alleles between them, each will develop its own particular characteristics, and as long as there remains no gene flow or reproductive contact between the populations those characteristics will remain. For them to remain means that the alleles for different characteristics have been eliminated. That's what decreased genetic diversity MEANS. This may amount to actual speciation, but at least certainly at the extremes you do get speciation, where the new characteristics are preserved because there is a complete lack of interbreeding with former populations.

Evolutionists regard bottlenecks as events that interfere with the processes of evolution, but they shouldn't. The elephant seal and the cheetah which were produced by severe bottlenecks -- reduction of their former populations to just a few individuals -- that severely reduced their genetic diversity -- really ought to be considered to be examples of speciation, nature doing what domestic breeders do. Bottlenecks are really just one way new varieties or breeds are brought about in nature or in domestic breeding. ALL the processes of evolution tend in the same direction, genetic drift, migration, natural selection, just not as rapidly. Domestic breeding in the past could be described as the artificial creation of genetic bottlenecks for the purpose of developing desired traits for new breeds. You select the desired character and take pains to breed only with others that possess that character. Since a rigid adherence to this formula also usually brings disease problems into the breed, breeders today take care to avoid the most severe bottleneck methods with the most severely decreased genetic variability by mixing with more vigorous but less desirable animals as far as the target trait is concerned, but if it weren't for the threat of disease, these severe methods would be considered the most reliable way of producing the best breeds. SPECIATION.

Yet here we have RAZD at EvC carrying on as if the evolution processes just go on and on producing new phenotypes or varieties or breeds, even past speciation which he treats as the end point of microevolution and beginning of macroevolution, but afterward the same changes continue without a hitch in his scenario.
What separates (micro) evolution from the macro view of evolution (macroevolution) is the process of speciation, as evolution occurs within the breeding population, and nested hierarchies are formed by speciation events, and macroevolution is just a macro view of what occurs over several generations via evolution and speciation.

If we look at the continued effects of evolution over many generations, the accumulation of changes from generation to generation may become sufficient for individuals to develop traits that are observably different from the ancestral parent population. This lineal change within species is sometimes called phyletic change in species. This is also sometimes called arbitrary speciation in that the place to draw the line between linearly evolved geneological populations is subjective and because the definition of species in general is tentative and sometimes arbitrary.
See, he's simply ASSUMING the open-endedness of evolution, the phenotypic changes just go on and on, a neverending ACCUMULATION of changes. He has no evidence for this, though he has charts that give it an aura of authority that are simply meaningless reflections of his false belief. Actually, they are ILLUSTRATIONS of what he believes, they provide nothing in the way of evidence for any of it. And everything he says is also all assumption without evidence. Dawkins does the same thing with his ridiculous computer models of how evolution works, simply programming in his own bias, his assumption of open-ended changes. Sometimes you'll see an evolutionist acknowledging that reduced genetic diversity can sometimes be a problem but they keep that information off in a separate mental compartment, it's something that occurs only with bottlenecks, in extreme scenarios that interfere with evolution, not with evolutionary processes themselves.

Just for the record, here is the most pertinent part of the Wikipedia article on Zygosity:
Types
The words homozygous, heterozygous, and hemizygous are used to describe the genotype of a diploid organism at a single locus on the DNA. Homozygous describes a genotype consisting of two identical alleles at a given locus, heterozygous describes a genotype consisting of two different alleles at a locus, hemizygous describes a genotype consisting of only a single copy of a particular gene in an otherwise diploid organism, and nullizygous refers to an otherwise-diploid organism in which both copies of the gene are missing.

Homozygous
A cell is said to be homozygous for a particular gene when identical alleles of the gene are present on both homologous chromosomes.[2] The cell or organism in question is called a homozygote. True breeding organisms are always homozygous for the traits that are to be held constant.

An individual that is homozygous-dominant for a particular trait carries two copies of the allele that codes for the dominant trait. This allele, often called the "dominant allele", is normally represented by a capital letter (such as "P" for the dominant allele producing purple flowers in pea plants). When an organism is homozygous-dominant for a particular trait, the genotype is represented by a doubling of the symbol for that trait, such as "PP".

An individual that is homozygous-recessive for a particular trait carries two copies of the allele that codes for the recessive trait. This allele, often called the "recessive allele", is usually represented by the lowercase form of the letter used for the corresponding dominant trait (such as, with reference to the example above, "p" for the recessive allele producing white flowers in pea plants). The genotype of an organism that is homozygous-recessive for a particular trait is represented by a doubling of the appropriate letter, such as "pp".

Sunday, November 7, 2010

The ToE has been Falsified many times over but residents of Wonderland need not notice; and a note about forensics

I keep thinking I'm going to run out of interest in the evolution debate again soon or just run out of topics to keep me going, but EvC is a goldmine of such topics at the moment. Somehow I'd overlooked this thread inviting Potential Falsifications of the Theory of Evolution .

As I've been saying so frequently lately, all Evolution has is Hypotheses, it has no other credentials from the Scientific Method, it's nothing but a subjectively elaborated mental exercise in the end. THEREFORE it cannot be falsified. But by asking for falsification they give the illusion that it is science and that it's those who can't come up with an ironclad falsification who are at fault, not the theory.

Again, this is a competition of hypotheses, it's a matter of judgment calls not science, not any of the methods of science. Creationists have the better hypotheses and the better judgment calls but since it's all a matter of who believes which system this can forever go unnoticed. It's all a matter of who has the power and Old Earth and Evolution have the power.

The geologic timetable is laughable and without it the foundations of evolutionary theory are destroyed but they don't need to notice because there is no way to scientifically prove or disprove any of this. The Flood beautifully and elegantly accounts for all the phenomena that are so awkwardly and ridiculously interpreted by evolutionists as time periods, the disparate layers undisturbed until all were in place, for instance, but this need not be noticed because there is no way to scientifically prove or disprove it one way or the other, It remains observation and hypothesis. It SHOULD falsify evolution just because it's a better explanation, the observation is rational as evolution's is not, and the hypothesis makes sense while evolution's is a weird concoction, but since they are deluded that any of this has anything to do with the Scientific Method they've protected themselves from ever having to recognize it.

The fossil record is beautifully explained by the worldwide Flood, as there is no other way so many living things could have been buried so as to meet the conditions for fossilization, and the immense variety of fossilized life forms, many of which no longer exist, is completely in keeping with the Biblical record of the Flood, but again, since there is no way to scientifically prove this no matter how much more reasonable an explanation it is than the geo timetable /evolution explanation, they can go on blindly in their delusion. Again, this SHOULD falsify evolution just because it's a better explanation, but since they require creationists to meet impossible criteria that they themselves can't even meet, though they think they do, alas, they can sustain their fantasy by aggressive ridicule and flat-out assertion forever.

And then there is the genetic delusion as well, that mutations just keep on a-building the genetic code although the evidence in hand is clearly against this assumption -- and it is, as usual, nothing BUT an assumption, again at best a hypothesis, upheld by belief in it, not evidence. The evidence shows that in small populations genetic deterioration is the norm, but they still believe that in bigger populations mutation saves the day although there is NO evidence for this and simply studying the DNA in ring species would show their assumption to be wrong.

All these things falsify the Theory of Evolution but since the Theory of Evolution is constructed out of pure fantasy like the Emperor's New Clothes, they simply can't see the falsification because their fantasy is so beautiful and so real -- really, so NECESSARY -- to them.

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Interesting, a contributor to that same thread, named Michael McBride, has said pretty much what I've said above but unfortunately instead of keeping to the particulars of evolution he went way back to the origin of the universe to make his point. It's the same point, which is that the past is not subject to the Scientific Method, so that all evolution can be is a theory / hypothesis (so is Creationism but it's the better hypothesis and we have a written document on our side too). Alas, the poor lock-step pedantic evolutionists aren't going to give him the slightest benefit of the doubt. I suppose, to be fair, that they can't, simply because they ARE locked into their assumptions and their false belief that SCIENCE has anything to do with any of this.

Sorry, Michael McBride. Good try. Start a blog. It's wonderful for exploring the truths that the world rejects.

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Oh but then a bunch of them jumped on him with all their smug pedantic irrelevant pronouncements about how it's not just that the ToE can't be proven, it's that science itself can't be proven, falsely implying that the ToE is science. Some science IS proven, if not to the unrealizable perfection these pedants keep insisting on, at least proven in a way the ToE can never be proven, because real science is subject to the Scientific Method while the ToE is not, and Newton's law IS an example of real science. The ToE simply IS NOT SCIENCE and IS "just a theory" in a sense Newton's Law is not, but they'll NEVER EVER stop to see how that is true, they'll just go on with their prissy definitional / credal chants on the word "theory" and miss the whole reality.

Anyway, here's another bit of Evo pedantry, or sophistry, that needs to be taken down, by subbie in Post #71:
There is no way to Observe the origin of the universe
There is nothing preventing us from observing the evidence left behind from the origin of the universe and develop scientific theories based on those observations. In the exact same way, there's nothing preventing us from observing the evidence left behind from the history of life on this planet and develop scientific theories based on that evidence.
Right, you can make those observations and you can develop theories / hypotheses about them, both about the origin of the universe and about the history of life on this planet, AND THAT IS THE END OF WHAT YOU CAN DO SCIENTIFICALLY.

You CANNOT TEST THEM because you cannot REPLICATE them, you cannot do EXPERIMENTS to prove or disprove them. The only conclusions and consensus you can achieve are purely a matter of subjective persuasion, politics, NOT SCIENCE. You cannot, in a word, subject them fully to the Scientific Method. You are left ONLY with your theories in the end, and with theory in a sense that Newton's Laws were not, or that Einstein's were not, or any of the rest of the "hard" sciences whose propositions are testable and replicable, because they CAN apply the Scientific Method in full and others can replicate their work.

It's irrelevant that new data might eventually change the scientific picture in those cases, because what is in hand CAN BE SUBJECTED TO THE SCIENTIFIC METHOD and valid conclusions can be drawn to the extent of current knowledge; but THAT CANNOT BE DONE WITH THE PAST, whether with the history of life on the planet or with the origin of the universe and it is sheer delusion that the scientific method applies here as applies to the laws of physics. If you apply what you know about the present to the past you are making an unwarranted leap of pure blind assumption because you have no way of knowing how different the past might have been.

If you'd just PAY ATTENTION to what Creationists have been TRYING to say forever, and really THINK about it instead of just rattling off your nitpicking objections and your canned creeds, you might NOTICE that we are saying something you need to hear.

But I won't hold my breath.

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And on a similar point, let's see if we can put to rest another bit of sophistry that keeps coming up in this regard, the idea that criminal forensics is the right scientific model:
Why can't the origin of the Universe be observed?
time travel hasn't been invented yet
Police solve crimes that have no eyewitnesses all the time. Things that have actually happened leave evidence behind.
First it needs to be pointed out when you resort to forensics for your model that you are abandoning classic Scientific Method -- you know, the observation-hypothesis-conclusion-testability-replicability-falsifiability-consensus model. I probably got some of that out of order but you get the idea. Forensics is a COMPLETELY DIFFERENT investigative model. So which is it, Scientific Method or Forensics?

Well, the Scientific Method cannot be applied to questions about the UNWITNESSED past.

So let's see if the Forensics method can be.

You say the crime leaves evidence behind. And so do events in the very distant unwitnessed past. So far so similar. Maybe we're on the way to abandoning the Scientific Method conceit if nothing else.

However, there are huge clues available to criminal forensics that are not available to the study of the distant past because the crime occurred in a present in which other crimes are known. The investigator can't perform tests to be replicated, but he can count on other cases he's studied for clues, hundreds of them. He can remember and usually go back and read about all those in which similar patterns are discernible. There is no such thing for the distant past, there are no anchor points, you are in completely unknown territory.

The criminal investigator can make reasonable guesses amounting to assumptions about the habits and motivations of people who live in his own time and place. This isn't the case for the investigator of the distant past. Even the historically known past can't be approached without a lot of study of history, and then your own experience often has to be set aside in order to understand situations that are radically unfamiliar in your own contexts. Then when you are studying a past that has not been recorded in history at all (except of course in the Bible which you all discount), the origin of species for instance, you have nothing to go on. Nothing. As far as observation is concerned, Natural Selection takes you no further than microevolution, known for millennia, you have only unverifiable/unfalsifiable assumption that makes the leap to macroevolution.

The criminal investigator is most likely familiar with any objects that happen to occur in connection with the crime and if he's not he has sources of information he can go to for help. Even human artifacts from the distant historical past may take lifetimes of study to comprehend and there is no guarantee that they will ever be understood. But even the creatures found in the fossil record are different from what we are familiar with today and we have NO examples of fossilization on such a scale, or sedimentary layering on such a scale, and no matter how much we know about DNA in the present, all extrapolations to the past are pure guesswork since we don't know how different DNA may be now from what it was thousands of years ago. YOu think you have an objective measure in various atomic dating methods but how can you when you can't know anything about how THEY behave in the past either? EVERYTHING you assume about the past is ONLY an assumption and not subject to the methods of science so not falsifiable, and forensics methods can't offer any more reliable information either.

I'm sure I can come up with more differences that make the forensics model just as useless to justifying evolution as the scientific method but I'm getting tired and this should go a long way to making the point as is.

However, I do think creationists do better forensic reasoning about the distant past than evolutionists do. More later.

Tuesday, November 17, 2009

No, those aren't Transitionals.

(Not yet getting to the topic of the ape and human genomes. I'll get there eventually. Meanwhile:)

On that video that was the topic of the previous post, Kenneth Miller is discussing how they have all kinds of transitional species so the constant complaint that they don't is ridiculous. But they don't have transitionals. What they have is complete creatures, not transitionals or intermediates in the sense the theory needs in order to validate it.

They have something they claim is a whale with feet for instance, Ambulocetus Natans. (However, there's an article at Talk Origins that denies that it's a whale at all, says it's rather some sort of land animal.)

But the question about transitionals is really a question about transitional FEATURES, not whole animals, however nicely they may seem to fit between other types of animals, but features that were passed on (according to the theory) because they conferred some advantage even in their undeveloped condition, and then developed further as they continued to be passed on.

I think always of antlers. Doesn't evolution imply that they would have started as hardly recognizable small bumps on the head, which for some reason were passed on and which then grew over time into some of the very impressive kinds we see on some deer, moose, elk etc.? The problem is that there's no reason to think anything in such vague beginning stages would confer an advantage so there's no reason to think it would be passed on and develop into the full-grown result we see today.

But of course if the idea of incremental acquisition by natural selection IS the theory, then MANY features of all creatures SHOULD be found in various stages of vague underdevelopment by the bazillions, shouldn't they? Some of no value -- or harmful effect either -- to be eventually discarded, some to be passed on and developed further? In fact ALL creatures should ALL be "transitional," and all appear "unfinished" in some sense or other, shouldn't they? Should there ever BE a clearcut Species at all? Each stage is supposed to be functional, however, MUST be functional if it's to be passed on or selected, isn't that the rule? In reality how is that going to happen?

I think this idea of incremental stages to completed function describes the missing transitionals creationists are always referring to, a fact that keeps getting lost as evolutionists respond with a completely different idea of what a transitional is that confuses things.

That is, there shouldn't be a whale and a whale with feet, there should be thousands of whale-type skeletons with all sorts of half-developed appendages, perhaps some tending to adaptations for land, some for water, but some utterly unrelated to either -- this last category is necessary if we are really to take seriously the idea that evolution is blind and goal-less and that mutations come up with experiments that natural selection may potentiate or completely ignore as it were. There should be things perhaps that look like antennae in the bud, or antlers even -- on a whale? why not if evolution is blind? -- or budding wings or whatnot, it seems to me, in keeping with the expectations that evolution theory raises as it is often stated.

ALL creatures should be found in similar stages of experimentation, with many features in various stages of change all at once.

Actually, isn't the unlikelihood of there being such transitional features -- not to mention the observed nonexistence of them -- the reason some have postulated great leaps in evolution -- "punctuated equilibrium" -- as opposed to incremental development? But that defies explanation on any known rule of genetic transmission, besides which, why should neat adaptations suddenly appear by great leaps either, if evolution is blind?

In spite of themselves, evolutionists DO think teleologically about how evolution works, that is, they assume change is all tending toward a particular goal that they have in mind even if they aren't aware of it. Then they'll rear up when you point this out and inform you that no, it doesn't have any goals at all and deny their own tendency to think as if it does.

Go back and look at the ring species example. There you have a series of subspecies that are completely whole and functioning creatures in themselves -- there's nothing transitional about any of the designs, no features that suggest something in the process of development. They form a series so that each type may be intermediate between those before and after in appearance but not intermediate in the sense of there being anything unfinished about any of them. In fact they aren't even necessarily intermediate in appearance, they are independent designs unto themselves.

Clearly all variations are already present, are BUILT INTO the genome from the beginning, they do NOT appear by experimentation or mutation. The rules of genetics allow for wonderful variations, they do not allow for transitionals, AND, of course, I repeat for the hundred-umpteenth time, selection processes ALWAYS reduce genetic diversity even as they produce new subspecies, and that means the very processes evolution supposedly depends on lead to a dead end for evolution.

Evolution defeats evolution.

Saturday, November 14, 2009

What exactly is proved by Ring Species? A CREATIONIST'S PROPOSITION FOR A SCIENTIFIC TEST

[Source of diagram=PBS Evolution Library]
Thoughts about ring species. I've argued many times that this phenomenon demonstrates the inexorable reduction in genetic diversity with each "speciation event" or formation of a new variety of a Kind (new phenotype). It's a great example because many stages of variation (or change or evolution or speciation) are present, from a population that is probably fairly similar to the original to a population at the end of the ring that demonstrates the most changes from the original and may even be incapable of interbreeding with the original or others toward the beginning of the ring. Since reproductive isolation from the earlier populations is one of the definitions of evolution according to the theory, this is called Speciation in the strict sense and considered strong evidence that this is genuine macroevolution.

"Ring species" is the term for a series of more or less isolated populations of somewhat different versions of the same creature, chipmunks and salamanders being examples I've seen discussed, that are distributed all around a geographic barrier such as a mountain or mountain range or a body of water (the illustration shows salamanders found around the Joaquin Valley in California), each population descended from the previous in the ring. Such series demonstrate some of the principles of evolution (or speciation or variation) and are often taken as evidence for evolution.

It is apparently possible to identify the progression from one population to another, which follows a sequential path around the ring (or sometimes separately on each side of the barrier), as well as point to visible features that distinguish the populations from one another. There may or may not be complete reproductive isolation, meaning no interbreeding between the separate populations, and some interaction (or gene flow) may be retained in some cases, but for purposes of understanding the principles involved it's fair to describe each separate population as an isolated species or subspecies unto itself.

[The illustration to the right shows different variations of seagulls distributed around the northern Atlantic and Arctic oceans, and the picture below shows members of two different populations or subspecies at the opposite extremes of the ring]













So there's the concept. I hope it's clear.

Now. I've been arguing that whenever a new population or "species" or variation is formed, whether by natural selection or accidental selection by unpredictable events (bottleneck, founder effect) or by the migration of a part of one population to a new territory, where the new population becomes isolated and inbred among its own members, you get a new type of the creature, a variation, AND you always get it along with the loss of some genetic possibilities, specifically some that defined the previous population that are now changed in the new population and soon set it apart visibly from the previous.

So, if the former population had gray wings (or brown skin in the case of salamanders) you may now have a population with white wings (or striping in the case of salamanders) and changes in other traits as well. Genetically speaking what has happened is that alleles for the old coloring are now suppressed or even eliminated altogether in the new population while formerly unexpressed alleles are now being expressed in the new phenotype. The alleles that form the new traits may or may not be "mutations" but useful mutations are very rare and mutations are not needed for speciation in any case -- AND the same fate would meet the mutation as meets any other allele anyway, whether it is expressed in the new population or left behind in the old, the overall effect is still always reduction in genetic diversity in the new population as a whole.

The changes from the old to the new population demonstrate the famous definition of evolution as "a change in the frequency of alleles." But what is usually not taken into account in this definition is the fact that this change in frequency necessarily reflects a reduction in SOME of the alleles, at the extremes a complete elimination of them, and the only increase is merely a matter of the difference in proportions present in the different populations, the coming to expression of formerly suppressed alleles that were already present in the old population. That is, there is no actual increase in the alleles available, there are simply more of a kind, PROPORTIONALLY, of which there used to be proportionally fewer in the former population, but there is always a decrease in some alleles that defined the original population and in some cases a complete elimination of those formerly expressed alleles and this means an overall loss in genetic diversity.

As this process is repeated around the ring, perhaps over long periods of time though no more than enough years to establish a large and phenotypically homogeneous population, one established population becoming the basis for the migration of a few of its members to a new territory to form a new population, these few members as a group necessarily possess an even more limited complement of alleles from the former population, and the new frequency of alleles becomes the basis for a new phenotype that eventually emerges from the inbreeding of all the members. This is due to the isolation and inbreeding among members of the new population, again forming an identifiable new "species" or subspecies. And this "speciation" event is of course again accompanied by the expected REDUCTION in genetic possibilities, because the change in gene frequency that occurs with the founding of each new population REQUIRES that some of the alleles that characterized the phenotype of the former population are LOST to the new population, at least suppressed.

By the time many such migrations have occurred and there are many populations forming a ring, many alleles from the original population that started the ring are likely to be lost altogether in the more recently formed populations and certainly in the very last in the ring.

YOU DO NOT GET SPECIATION WITHOUT REDUCTION-TO-COMPLETE LOSS OF GENETIC VARIABILITY.

EVOLUTION DEFEATS EVOLUTION is my slogan. This expresses the observation that the very processes that form new phenotypes through change in gene frequency, are ALWAYS accompanied by a corresponding reduction in genetic diversity that ultimately reaches a point after many population splits beyond which no further variation/evolution/speciation is possible at all. If complete reproductive isolation occurs at this point then further evolution is completely impossible, though it may often still be possible for reproduction to be resumed with members of some former populations, but overall the tendency is always out to less variability and never to more and this contradicts all the expectations for the theory of evolution. The genetic situation ought to reflect this and ought to be measurable.

This is my claim.

NOW. Although I believe this is pretty close to a fact that ought merely to be recognized by anyone who will think it through, a fact I believe is supported by many observations made by conservationists at least, and very much the same genetic situation that domestic breeders face every time they try to isolate a highly specialized new breed, it ought to be possible to test this claim I've been making, only I don't have any way to do it myself.

It seems to me that ring species ought to be a very accessible proving ground for this claim. The claim predicts that whatever remains of the original population in a ring should have more genetic diversity among its members than the last in the ring, and there should be correspondingly less and less genetic diversity in each new population that is formed sequentially around the ring.

This ought to be testable. Proposed Method: All you need to do is analyze the genomes of whatever number of members of each of the populations in the ring will show what's needed to prove this one way or the other.

Prediction: The newest population should show quite a lot less genetic diversity than the oldest or first population, possibly even homozygosity at some gene loci, or radical total inability to vary in some characteristics beyond that point.

Intermediate populations should show incremental reduction of genetic diversity from the original to the newest population.

Conservationists know about the loss of diversity from migration and even natural selection and anything that isolates a small portion of a population from the greater population. They deal with practical consequences of this all the time. They don't want a few salmon, for instance, to break off from the main river population and head up a small tributary to breed because that will change the character of the fish in ways they don't want to happen by accident, and because this is a bottleneck situation that usually so drastically reduces the genetic variability of the new population that forms that it is vulnerable to environmental threats in a way the more diverse larger population is not.

This ought to be testable. I would really like to see it tested. Who do I talk to?

Perhaps the necessary observations of the genomes of the different populations in ring species have already been made in the service of some other scientific investigation and can just be brought out and looked at specifically for this purpose. That would be nice and easy.

I've dreamed up laboratory tests but they appear to be way too cumbersome. You start with a cage of mice (or whatever creature would work best for this purpose), let them breed among themselves for enough generations to establish a definitive phenotype for the population (which will unfortunately probably number in the thousands by that time, at least hundreds), then you send a few of them to another cage to inbreed among themselves until again a recognizably new homogeneous population is formed with a recognizably different appearance from the former population, and then you send a few from that new population to a new cage and so on until you have a dozen or more well-established new populations of mice that should show some pretty clear differences in characteristics from one another (by this time the mice will have taken over the laboratory), and then you take a look at their genomes. As I say for the above version of the experiment in the field, the newest population should show quite a lot less genetic diversity than the oldest or first population, possibly even homozygosity at some gene loci, or radical total inability to vary in some characteristics beyond that point; and there should be a graded series of reductions in genetic diversity from the original to the end population.

I really think this is obvious and shouldn't really need special testing but since it's doubted whenever I argue it in evolutionist venues it ought to be tested and it is obviously testable.

I would really like to see it tested. Any rich creationists out there who would like to fund this project?

(Yes, of course the evolutionists are going to rush in and assure us all that GIVEN ENOUGH TIME, like bazillions of years, mutation will overcome this effect anyway. It's a big fat delusion but we'll deal with that when we get there (though I've already answered the charge somewhere above). Meanwhile at least the claim that the phenomenon of Ring Species demonstrates macroevolution, and all similar and related arguments, should be dead and buried by this test.)

---CJA

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P.S. I think some of my terminology and description are probably not precisely accurate but I also think anyone who knows about the phenomena I'm trying to describe should understand what I'm getting at and perhaps be able to put it in more precise language. And it doesn't affect the mechanics of the test I'm proposing anyway.