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Author Topic:   What is the mechanism that prevents microevolution to become macroevolution?
Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 139 of 301 (346431)
09-04-2006 12:14 PM
Reply to: Message 137 by Quetzal
09-04-2006 9:40 AM


Re: On predictions and tests.
If now you are changing the subject to decrease in genome size, how easy would it be to identify the death of a gene?
I'm not the one making the claim. Ask MJ - it's his assertion. You tell me...
Actually, I doubt he made the assertion that every speciation involves the loss of a gene or genes, which was your claim in your Message 108. Kindly reference this.
Edited by Faith, : No reason given.
Edited by Faith, : No reason given.

This message is a reply to:
 Message 137 by Quetzal, posted 09-04-2006 9:40 AM Quetzal has replied

Replies to this message:
 Message 141 by Quetzal, posted 09-04-2006 1:09 PM Faith has replied

Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 142 of 301 (346461)
09-04-2006 2:29 PM
Reply to: Message 136 by Quetzal
09-04-2006 9:11 AM


Why is showing divergence of relevance to our discussion?
Because they are discussing divergeance in genotype. We're not talking here about phenotypical differences - they're using 16s and mtDNA sequence differences between the populations to show that genetically these populations are diverging. Some of them, indeed, as in the second article I linked to, are very different from each other. Not just 'cause one population has different stripe patterns, or whatever.
The divergence of genotypes is the same as the divergence of phenotypes as far as what I'm saying goes. I expect both to diverge. I expect speciation or incipient speciation to be occurring in the two subspecies at the far ends of the territory. I've been saying this in the last few pages. I have been arguing that this divergence of phenotypes AND genotypes is the result of the differing frequencies of alleles between the two populations, and most likely the loss of some alleles as well in one or both populations which is what "reduced genetic diversity" means.
In other words, divergence of both phenotype and genotype is no refutation of anything I've said but a confirmation of it. And since this appears to be the whole supposed refutation offered by that article, it fails; in fact it confirms my view and not yours.
Why is showing greater genetic divergence across greater distance of relevance to our discussion?
Well, for one thing, the greater the geographic distance between the populations, the less gene flow there is - which calls into question your contention that the differences seen are due only to recombination or some kind of skewed frequency distribution.
This does NOT refute what I'm saying, but the opposite, it confirms it, as I've already said. I have repeatedly said that I EXPECT greater divergence with greater distance, and that gene flow would INTERFERE with speciation --- the reduction or absence of gene flow ENHANCES the speciation processes. It appears that you haven't even made the slightest effort to follow the argument. You are describing this article as proving exactly what I've been saying, yet you are claiming it refutes me.
I suppose it is that you have such a totally evolution-focused bias that you can't hear this thing I'm saying no matter how many times I say it.
In addition, the most distant populations (from each other) contain novel alleles not found in the populations closer to each other, which leads to the question: "Where did these sequences come from?".
There is no reason whatever to assume that these alleles are novel in the sense of brand new. My argument has been from the beginning that when you have a strong shift in allelic frequencies, which in ring species is very likely to include the loss of some alleles, you get VERY new allelic combinations, new genotypes, new phenotypes. The novel alleles are not novel in the sense of brand new to the species, they were simply suppressed or latent or of very low frequency in the original combined population, and may very well now be completely absent except in the population where they are noted -- why? Because they were low frequency to begin with. Merely sampling a few individuals would likely miss their existence too if they continue to exist in low frequency.
PLEASE point to where you or this abstract have shown how genetic diversity is increased.
How about the very first line of the abstract?:
quote:
The analysis of interactions between lineages at varying levels of genetic divergence can provide insights into the process of speciation through the accumulation of incompatible mutations.
So what you mean by "increased genetic diversity" is merely mutations.
But absolutely nothing in anything you have said about what the article is about demonstrates that mutations have any part whatever in any of it.
The mere fact of divergence or incipient speciation, and the presence of some supposedly novel alleles, seems to be enough to prove in your mind that mutation must have a part, but this is merely assumed. Nothing has been said to demonstrate that this is the case.
What is actually described of the circumstances fit MY scenario -- the divergence of phenotypes and genotypes, the lack of gene flow, the appearance of previously suppressed alleles, all that proves what I have been saying from the beginning. It is all thoroughly explained by allelic shuffling and reduction of genetic diversity (loss of alleles).
Mutation has no necessary role in any of this, and there is not one iota of evidence that it actually does in this case, in anything you've said or the article has said.
It seems to be the case that mutation is merely assumed to have a role because you aren't grasping the fact that it is not necessary, that when there is reduced gene flow and clear divergence between the populations, or incipient speciation, changed allele frequencies including previously suppressed alleles now being expressed, and lost alleles (or loss of genetic diversity), explain it perfectly.
Since you aren't grasping that, or refuse to believe it, being evolution-focused, you stick mutation in there to explain it. But you must SHOW that mutation has contributed to this at all instead of assuming it. You haven't done this, nor has the article. The fact is mutation isn't involved, you and the article are simply projecting it into the scene by assumption.
AND...
quote:
We compared the genetic structure across two transects (southern and northern Calaveras Co.), one of which was resampled over 20 years, and examined diagnostic molecular markers (eight allozyme loci and mitochondrial DNA) and a diagnostic quantitative trait (color pattern).
All of which is apparently focused on proving that divergence and even incipient speciation has occurred, which is far from disputed by me.
The full article goes on to discuss - in some detail - the reasoning behind this. Since the full article isn't on-line (unless you have a subscription), you can see a similar set of research in the PNAS article I provided (which is available free). I can also provide other, similar, references if it makes you feel any better. The point is molecular/genetic level studies of diverging populations (incipient speciation) show genotype differences that simply cannot be accounted for by changes in frequency distribution of pre-existing alleles. These are not hypothetical examples, but examinations of real-world populations.
But none of what you've said actually demonstrates that the genotype differences can't be accounted for as I've claimed, you have merely asserted it. All completely hollow claims. The entire scenario is easily explained by allelic shuffling. I can't even understand why you doubt this. There is nothing in the scenario itself to suggest it can't occur as I've described.
You, and the article, are simply *asserting* that alleles are novel without proving they are novel (just because they didn't turn up in a sampling of the population left behind?), and merely *asserting* that mutation is bringing about the genotypic diversity instead of proving it, and so on. Again, you seem to think that the mere facts of divergence and reduced gene flow are evidence enough, although they are evidence for what I'm saying instead.
AGAIN, despite your offering of evidence, there is no ACTUAL evidence for your position in any of this, because everything you have actually provided supports MY position instead.
The mere existence of one identifiable mutation would not prove that increased genetic diversity caused the divergence, and nothing you have said shows that reduced genetic diversity which produces new phenotypes is not the explanation.
You stated things along these lines several times, so I'll ask you again: how does "reduced genetic diversity" create "new phenotypes"? This contention is so completely counterintuitive that I'm half convinced I'm missing something in what you're trying to say.
Thank you for asking, I appreciate it very much, and you ARE missing what I'm trying to say despite my many repetitions of it.
So let me try it again to say it clearly, God willing:
What I'm claiming is that a reduction in genetic diversity (loss of alleles) is the OVERALL trend over time in all the processes that lead to speciation. These are the same processes that bring about change in allele frequencies, only from time to time the change is a reflection of alleles having been lost altogether. This is clearly the case in bottleneck which is why the cheetah keeps coming up -- a dramatic unusual extreme case of speciation that involves great loss of genetic diversity that I bring up to illustrate the principle. I also bring up domestic breeding of animals such as dogs, because it is also demonstrable there that a loss of alleles brings about a new breed, and that no amount of inbreeding of that type would turn up a whole raft of alleles that other dog breeds possess. The absence of these alleles is part of the definition of the breed, a part of the process of developing a new phenotype, genotype, organismal type etc.
Many events that bring about a new phenotype are merely the shuffling of alleles rather than outright loss of diversity through loss of alleles, but the ONLY cases where an increase in numbers of kinds of alleles occurs is hybridization. Gene drift may increase the frequency of some and reduce the frequency of others, but an actual increase in alleles only happens with hybridization or the recombination of previously isolated populations. Since hybidization is the ONLY situation in which an increase in genetic diversity occurs, and you think an increase is necessary to speciation, then hybridization should be where you would look for evolution to occur. But it isn't where you look. You look where there is no increase or even a decrease, but without recognizing this decrease as intrinsice to the processes of speciation.
In none of these processes except hybridization does the production of a new phenotype involve an increase in genetic diversity (increase in kinds of alleles). Population splits either do not reduce genetic diversity, simply changing frequencies, or they DO reduce genetic diversity through loss of alleles, which must happen quite frequently when populations split off in a series of splits as in the example of ring species, so that the farthest apart populations would have alleles that the other doesn't have at all or has at very low frequencies.
The point is that since increase in diversity is of absolutely no use in speciation (unless you want to count hybridization as THE track to evolution), but decrease allows formerly suppressed alleles to produce new phenotypes, the overall trend of speciation processes is reduction of genetic diversity.
These are all the normal processes that bring about speciation. Nothing new is needed. There are plenty of alleles for all kinds of variations of most species. But out at the extremes of speciation there will be fewer alleles per locus, and this also no doubt accounts for the inability to interbreed with other populations of the same species.
Again these are the NORMAL proceses of speciation.
Now you want to introduce mutation into a process that doesn't need it for starters. You think genetic diversity must increase for speciation to occur, the opposite is counterintuitive as you say. I suppose it is. You have to get rid of alleles for others to form new phenotypes, that's all. Otherwise a population will stay pretty much the same or slowly change through gene drift as frequencies change due to internal influences. Change in phenotype/genotype requires a new allelic collection that reduces or gets rid of the old in order to allow the expression of something new and different.
ENTER MUTATION. But where does it enter into this scenario? It appears that evolution merely assumes it, because it assumes that all alleles were once brought about by mutation. It is not needed for speciation. Certainly it occurs, perhaps now and then it is selected, I wouldn't deny that, I just haven't seen that it actually contributes anything necessary or important to speciation, which follows from allelic shuffling quite well.
I hope that's clear for the umpteenth time.
The abstract is too technical for me to read.
So, actually reading the research is probably out of the question?
I'd have to look up a dozen words, have to study to understand their whole context of usage in science, so yes, it is probably out of the question.
But you won't take my word for what the articles say when I try and use simpler terms to explain it? That being the case, I ask you again "Where do we go from here?"
I did take your word for it. I took what you said about it completely straight, and I answered, more than once by now, that it is not proving what you think it proves.

This message is a reply to:
 Message 136 by Quetzal, posted 09-04-2006 9:11 AM Quetzal has not replied

Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 143 of 301 (346462)
09-04-2006 2:30 PM
Reply to: Message 141 by Quetzal
09-04-2006 1:09 PM


Re: On predictions and tests.
I'm not accusing you of making stuff up, merely misreading.
In Message 34 he is talking about a loss of alleles of ten genes, not a loss of genes:
MJF writes:
Let's suppose we have a species that possesses 30,000 genes. Two populations form from this species that become geographically isolated. Originally, there's a lot of genetic redundancy (or overlap). So let's suppose that of the original 30,000 genes, all the alleles are present for 29,990 genes. But for a small number of genes (10 in this case) there is geographic isolation, no overlap between populations. This occurs purely by chance, remember. So, is there a reduction of genetic diversity? Not really, the sum population still possesses the full diversity of alleles among its 30,000 genes. However there has been a reduction of genetic diversity as seen in each population.
I'm a bit unclear about what he is saying about what is isolated from what, but it's not at all unclear that he's not talking about a loss of ten genes but a loss of alleles for those ten genes.
Edited by Faith, : No reason given.
Edited by Faith, : No reason given.

This message is a reply to:
 Message 141 by Quetzal, posted 09-04-2006 1:09 PM Quetzal has not replied

Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 145 of 301 (346554)
09-04-2006 9:02 PM
Reply to: Message 88 by RAZD
09-01-2006 9:30 PM


Re: are bottlenecks tied to speciation?
What I'm saying is that a bottleneck is simply an extreme version of a number of the selecting and population-splitting processes that cause new traits to appear in the phenotype
The question is whether it must always result in this. I don't think so.
Considering how many alleles must be no longer available, forcing the few that got bottlenecked to define the new organism / phenotype /genotype, I hardly see how it could avoid bringing about new traits.
Speciation may cause a bottleneck, if it is of the founding population variety and the population is small.
Well, I suppose it's possible that the bottleneck simply might select out the very alleles that are already most expressed in the population and there would be little phenotypic change. I can't think of another way this might happen.
It may make no selection of alleles at all. Think of a population of 10,000 individuals and 1 in 10 survive a random catastrophe by luck not genetics\selection -- they just happened to be in the right place.
I used "selection" in the informal sense of "random selection" -- I guess that can be confusing. I didn't mean anything like the alleles were chosen, only that they did just *happen* to get bottlenecked. But there certainly is a different collection of alleles from the original population since many must have had to be left behind.
The distribution of alleles in both populations is the same, both in kinds of alleles involved and in their relative number -- say a bell curve distribution -- so that the shape of the distribution is the same, just the total population is reduced. The result is the same degree of diversity (the same bell curve) just fewer individuals.
The species will still have the same distribution of alleles.
Well, but the whole point of the bottleneck (and founder effect) example is that it is not at all likely that you would get anything like the same distribution as was in the original population, because the new population is so much smaller. Two alleles per gene might be the total available in such a case, whereas there might have been even a dozen or more for the same genes in the original population. So unless the original population was already very allele-poor you are not going to get anything like the same diversity, you are going to get something dramatically different from the original after a few generations of inbreeding in the new population with the very few allelic possibilities.
Yes, drift is the situation of no population split which we've been acknowledging may change the phenotype without reduction in diversity. It's the natural playing out of changing allelic frequencies in the population that brings this about in this case.
Speciation without bottleneck, bottleneck without speciation, therefore not necessarily related. It's like a grid:
----------------------------------
| no-speciation | speciation |
| bottleneck | bottleneck |
----------------------------------
| no-speciation | speciation |
| no-bottleneck | no-bottleneck |
----------------------------------
Any population can fall into any one of those four quadrants at different times.
There are other factors involve that make a strict relationship problematical, imh(ysa)o.
Well, I'm trying to avoid being all that strict, I'm trying to argue a TREND here, a trend TOWARD speciation that involves overall reduction of genetic diversity, normally over many generations, not a clearcut formula for instant speciation. The usefulness of the bottleneck and founder effect examples is that they cut to the chase -- they are examples of a drastic reduction in genetic diversity while at the same time they should be expected to demonstrate the formation of a new phenotype or even speciation as a result of this reduction.
Only mutation. Nothing else.
No, mutation has no bearing on whether population fall into one quadrant or another -- there are other factors that affect which quadrant they are in that can override any relation between speciation and bottlenecks. The only way that a strict relationship could exist is if two corners of the grid could not be populated with different species at different times.
I don't know why you are focused on a "strict relationship" since I've been trying to say that this is trend, not a strict anything. Overall you get a reduction in genetic diversity along with the development of new phenotypes. But there are situations where such a reduction doesn't happen of course, such as gene drift within a population or a population split in which both are quite numerous, or any form of selection that simply reduces the frequency of alleles in a population without eliminating them. To get the genetic reduction I'm talking about alleles are totally eliminated, they no longer figure in genotypes for their traits so new traits from other alleles take their place and gradually shape the new phenotype.
Again, the bottleneck simply demonstrates this process of reduction of alleles at an extreme. Most situations simply shuffle alleles rather than eliminating them altogether.
But in neither case is there an increase in alleles. All these processes that lead toward speciation either shuffle or reduce alleles. The only situation in which there is an increase in alleles is hybridization but this does not introduce anything new, it simply recombines formerly separated alleles.
My remark about mutation was that mutation is absolutely the only thing that could possibly ADD alleles. All the processes of speciation otherwise over time involve reduction of alleles.
But there is definitely a loss of diversity IN the subpopulations and this is what we are talking about. If they can't interbreed then they can't recombine their alleles so the diversity they share between them is meaningless.
It does NOT reduce the diversity in the total population of life on the planet, and it allows the now separated populations to expand their population diversity with subsequent mutation, thus ending up with more diversity than the total population of life on the planet started with: that is the issue.
I haven't claimed that genetic diversity is reduced for anything but the population being discussed, in which it brings about new phenotypes and even speciation.
The idea that mutation now takes over and produces new alleles is pure fantasy, an assumption dropped into the story without any warrant whatever. For starters, mutation is not needed for speciation, since the shuffling of preexisting alleles alone can bring it about, most especially the expression of formerly suppressed alleles when others are lost to the population -- this is all it takes to form new species or variations out of the existing collection of allelic possibilities. Mutation is absolutely NOT needed. Again, while mutations do occur, and are occasionally selected, it has not been shown that they contribute anything beyond negligible (or destructive) to the formation of new species.
{EDIT: EXCEPT OF COURSE IN BACTERIA. And here's an answer to that one, Crash, if you're paying attention. You are dealing with ONE cell there. You get a mutation that allows that cell to survive a threat and multiply. But multicelled creatures do not get mutations in all their reproductive cells all that predictably, do they? They don't get mutations at anything like a rate that would contribute useful traits, and as you have said many times MOST of such mutations are either supposedly useless or a bad thing.}
So there does seem to be this idea that speciation CAUSES bottlenecks.
That is the other problem with the supposed relationship - in some cases {A} can happen before {B} and in some cases {B} can happen before {A}. That makes it hard to show that {A} causes {B} eh?
Sorry I am not following you. Bottlenecks MAY cause a new species, but I don't see how species cause bottlenecks, they may simply exemplify them.
some speciations cause bottlenecks in daughter populations
some speciations don't cause bottlenecks in daughter populations
some bottlenecks cause speciation
some bottlenecks don't cause speciation
Conclusion: bottlenecks and speciation are not necessarily related events.
Um, I hope the above has clarified what I was saying since none of this represents it.
{Edit: First, I haven't said that bottlenecks are CAUSED BY speciation at all, this is your own thing completely. And second, I'm sure bottlenecks don't always cause speciation, but it would be very unusual if they didn't bring about new phenotypes in the new population with its drastically reduced genetic diversity (numbers of alleles available per gene.)
Edited by Faith, : No reason given.
Edited by Faith, : No reason given.
Edited by Faith, : No reason given.
Edited by Faith, : No reason given.

This message is a reply to:
 Message 88 by RAZD, posted 09-01-2006 9:30 PM RAZD has replied

Replies to this message:
 Message 254 by RAZD, posted 09-09-2006 8:37 PM Faith has replied

Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 146 of 301 (346571)
09-04-2006 11:37 PM
Reply to: Message 6 by Archer Opteryx
08-26-2006 11:54 AM


Re: what is the mechanism inhibiting change?
Rereading this thread, realized I could answer some contentions a little more clearly perhaps:
Research has proven genetic changes due to mutation. Research has proven that some genetic mutations enable an organism's survival in its environment. Research has shown that subsequent generations exhibit further genetic changes. There is no reason to doubt that changes accrue over time.
Creationists deny that small genetic changes can accrue over time.
This is false. We are constantly affirming that genetic changes accumulate, creating new varieties or breeds as a regular thing, even to the point of speciation. What we deny is that this goes beyond the Kind and that it involves mutations. All it takes is the playing out of the given complement of allelic possibilities, as I spend this entire thread, and a few other threads, explaining.
Creationists are obligated to show what would prevent this, if they wish their ideas to be treated seriously as science.
We have no interest in demonstrating that small genetic changes don't accrue over time; we affirm that they do. We merely deny that they accrue beyond the Kind, and in this thread I'm arguing where the barrier to further evolution / divergence /variation /speciation beyond the Kind is to be found.
Edited by Faith, : No reason given.

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 Message 6 by Archer Opteryx, posted 08-26-2006 11:54 AM Archer Opteryx has not replied

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 147 of 301 (346586)
09-05-2006 1:41 AM
Reply to: Message 136 by Quetzal
09-04-2006 9:11 AM


Endangered species = reduced alleles
It isn't hard to find discussions of these common phenomena in relation to conservation programs with endangered species, that is, the reduction in genetic diversity through population isolation. What they usually leave out of the discussion is that these processes are related to speciation, certainly at least the development of new genotypes and phenotypes, or divergence of populations phenotypically one from another, which is a step on the way to speciation.
As the article you linked is concerned to prove, the geographically isolated populations of Ensatina can probably be termed incipient species or possibly even species due to their lack of contact with one another or lack of gene flow between them. This means that each is inbreeding with its own different frequencies of alleles and possibly even an absence of some that the other population retains. This gets called incipient speciation in that article. Perhaps Ensatina is not yet on the verge of extinction, but a few more splits off the existing populations, leaving more alleles behind, and it could very well go in that direction.
Anyway, what I've been talking about all along is this common pattern which leads to the endangerment of species (in the very process of differentiating them). Here's one discussion of this pattern.
Page not found – Essig Museum of Entomology
Population Genetics and Endangered Species
In applying the principles of population genetics to the field of endangered species conservation, biologists are interested primarily in genetic variation, in particular its distribution and maintenance. In general genetic diversity is considered to be a good thing, and the more the better. In terms of population structure, multiple large populations of a species which are in some way in contact with each other provide a good situation for maintaining variation.However, in the case of endangered species, we are generally faced with the opposite situation: a small number of populations which are isolated from one another, each containing a small number of individuals.
...Connectedness is generally measured by examining the frequencies of different alleles, or forms of a specific gene, at several different genes. If the frequencies differ significantly between two areas, it is likely that there is some restriction in gene flow between them.
Which is what the article about Ensatina identifies.
If it appears that there is no difference in frequencies from one area to another, it may be supposed that there is some genetic connection preventing differentiation (other interpretations are, of course, possible). The interpretation of genetic connectedness is difficult as its significance is situation dependent. Strong interpopulational connectedness (presumably through frequent migration) will be good for promoting the maintenance of overall genetic diversity; rare alleles are less likely to disappear in a larger population.
Isolation, which leads to formation of new phenotypes or incipient speciation, not mentioned here but think about it, is BAD for genetic diversity which bodes ill for the prospects of the species in a fallen world.
And if mutation were anywhere near the power claimed for it, so many species would not be on the verge of extinction as a result of becoming isolated and changing in the ways that may be called incipient speciation or outright speciation.
Edited by Faith, : No reason given.
Edited by Faith, : No reason given.
Edited by Faith, : No reason given.

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 148 of 301 (346590)
09-05-2006 2:11 AM
Reply to: Message 147 by Faith
09-05-2006 1:41 AM


Re: Endangered species = reduced alleles
Here's the problem I'm talking about in the context of domestic breeding. From the very first sentence it ought to be clear that the very processes of developing a new breed or species lead to reduction in genetic diversity. Speciation=reduction in genetic diversity. BUT this is bad for the species' survival prospects so they are trying to encourage breeders to avoid this usual speciation process:
Too many breeders follow the "breeding for extinction" paradigm. Start with too few founders, close the registry to new imports, inbreed and breed your preeminent males as many times as possible. It is a guaranteed recipe for degrading the gene pool. Breeders will visit the Diversity web site, read some of the information, and come away still believing that what I propose will lead to deterioration of their line, often insisting that the best and most successful breeders don't breed this way. They don't see the relevance of the strategies for saving endangered species or populations, and maintain that the factors taken into consideration for the Mexican or Ethiopian wolf don't apply to Canis familiaris.
http://www.lhasa-apso.org/health/wolves.htm
It's rather odd that this common fact that reduced genetic diversity is associated with the development of new species is not easily recognized among evolutionists. They put all their hopes on this phantasm called mutation, yet have never shown that mutation occurs in any degree or quality that could overcome the effects of the inevitable downside of speciation -- the trend to extinction. Mutation occurs, it sometimes gets selected, and all their focus goes there.
Meanwhile, species speciate further and further and get closer and closer to extinction, and conservationists have to deal with the nitty gritty reality that speciation is NOT a healthy development. The implication from this fact that there's no way that evolution could ever be built on such a reality seems never to enter any evolutionist's mind. They just claim that it's all saved by .... The Mighty Mutation, this fantasy that can't be demonstrated to do anything like what is claimed for it.
Meanwhile, again, conservationists are working to UNDO the effects of speciation, because, well, it just plain doesn't go in the direction of evolution, it goes in the direction of extinction. Imagine that.
Because loss of genetic diversity in endangered species is often associated with inbreeding and a reduction in reproductive fitness (Reed and Frankham 2001), efforts to increase the genetic diversity of the endangered Korean goral should be considered as a high priority for conservation of this species.
Cross-Species Amplification of Bovidae Microsatellites and Low Diversity of the Endangered Korean Goral | Journal of Heredity | Oxford Academic
The fact is that all living things were given a genetic package back at the Creation and it has simply been playing out ever since, losing much of its contents over the centuries and millennia, but still capable of a lot of variation. Only now more and more species are getting out to the speciation limits of their Kind where extinction threatens.
Edited by Faith, : No reason given.

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 Message 147 by Faith, posted 09-05-2006 1:41 AM Faith has not replied

Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 151 of 301 (346606)
09-05-2006 4:40 AM
Reply to: Message 149 by PaulK
09-05-2006 2:28 AM


Re: Endangered species = reduced alleles
I don't see how this is supposed to help your argument in any of the points under dispute. The fact that the bottleneck in itself has not instantly converted the isolated populations into new species in itself for instance suggests that there is something more to speciation than a bottleneck.
My argument is that reduction in genetic diversity is the inevitable inexorable trend of all natural processes towards speciation, and all species undergo these processes. It's a trend, not an "instant conver[sion]" to new species. I don't think a bottleneck always leads to speciation, but it may in fact, meaning it may lead to a new phenotype / genotype that can no longer interbreed with others of its kind -- if any near relations are even still around. I think that nowadays it is most likely to lead to this condition, however, because of the overall depletion of genetic diversity across pretty much all species. That's a guess, but as a principle, no, speciation isn't a necessary result of a bottleneck, merely likely. Bottleneck is merely a way to illustrate the situation of severe genetic reduction caused by population reduction. The kind of domestic breeding programs that simply aim to get the best of a type without regard to its survival prospects bring about the same condition, the kind that a quote I gave above called "breeding to exinction." What is breeding but a step on the way to speciation if not speciation itself? You select, you change genetic frequencies and if you get down to a few founders you certainly remove lots of alleles / genetic diversity from your new breed. That's how you GET the new breed.
(As should be obvious - if there were no new alleles every individual in the "new" species would have been possible in the original species)
Yes, they are possible in the original species, but the traits of some alleles are not expressed much or at all, and could be said to be "latent," either because they occur in very low frequency or are recessive or affected by other genetic conditions I wouldn't know a lot about. These are the ones that breeders breed FOR after all, the unusual trait, the low frequency trait. These are the ones that pop up and surprise by their seeming newness in a drastically reduced new population that happened to contain them. All this newness does not require anything really new, at all, just the coming to expression of formerly suppressed or latent traits, because of the removal or reduction of competition from other alleles that formerly dominated in the original population.
And if mutation were anywhere near the power claimed for it, so many species would not be on the verge of extinction as a result of becoming isolated and changing in the ways that may be called incipient speciation or outright speciation.
But this is BEYOND the power attributed to mutation. Mutation is not credited with the power to automatically rescue populations from the immediate consequences of a depleted gene-pool. It takes time (the cheetahs are still recovering, slowly, for instance).
The simple fact is that neither extinction nor salvation through mutation are inevitable in such a situation. Small isolated populations just have a harder time surviving.
The point is just that it is very hard to get across this fact of inexorable genetic depletion through the normal processes of variation and speciation, because mutation keeps being assumed to take up the slack of this depletion. In fact it simply doesn't. Evolutionists automatically think in the direction of mutation as the driving force of evolution, by its supposedly increasing genetic diversity, producing new alleles and new traits to be selected, and it is very hard to get the focus off mutation and onto the fact that all the OTHER processes that affect genetic diversity are working to decrease genetic diversity. Mutation has to be able to occur at a prodigious rate with prodigiously useful effects to overcome this inexorable reduction, if the ToE could possibly be true, and so far what has been demonstrated of mutation just doesn't meet the challenge.

This message is a reply to:
 Message 149 by PaulK, posted 09-05-2006 2:28 AM PaulK has replied

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 Message 153 by PaulK, posted 09-05-2006 6:08 AM Faith has replied

Faith 
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Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 154 of 301 (346612)
09-05-2006 6:42 AM
Reply to: Message 152 by Wounded King
09-05-2006 5:42 AM


Re: what is the mechanism inhibiting change?
This is false. We are constantly affirming that genetic changes accumulate, creating new varieties or breeds as a regular thing, even to the point of speciation. What we deny is that this goes beyond the Kind and that it involves mutations.
This makes no sense. You must have a completely novel definition of 'genetic change' if it is somehow dissociated from mutation.
Well, I was using the term Archer Opteryx used, and took it in a rather generic sense as he seemed to be using it, speaking simply of observable changes accruing over time, which is certainly not disputed by creationists. You seem to want to insist that the term must imply mutation, and I suppose it probably does for evolutionists, but simply descriptively there is no reason why it should. I guess I could drop the "genetic" if that helps, and simply say that we do not deny all the observed changes that evolutionists say accumulate in species, we simply explain them differently. But these changes occur both in the phenotype and the genotype and involve alleles shuffling -- and I guess I'm back at "genetic changes." Don't really see how to give up the term even if evolutionists mean something different by it than I do.
The sort of changes in allelic frequency you have been discussing are not genetic changes as that term is understood scientifically, they are changes in a populations genetics which is quite different.
Again, I have no other word for it in order to answer what was clearly meant by Archer O, since clearly he meant that we deny the accumulation of new traits toward speciation, and the fact is that we do not deny that.
So if you think that all of the variation we see below the level of 'kind' is due to the reduction of allelic variation which was already present in the breeding pairs which got of the Ark then you clearly are denying the existence of small genetic changes.
Well, as long as you insist that "genetic changes" = "mutation" then of course I am denying them. But those genetic changes as a matter of observed fact I do not deny, merely the explanation for them.
All it takes is the playing out of the given complement of allelic possibilities, as I spend this entire thread, and a few other threads, explaining.
But there is considerably less evidence for the sort of superallelic variation you posit, than there is evidence for the ability of genetic mutation to create variation.
There is nothing "super" about it. It's all normal well-known shuffling of alleles you can find described in any basic genetics course or certainly on domestic breeding sites. Surely there is a ton of evidence that the alternating of different alleles for a gene produces variation. Perhaps it is so ubiquitous and taken for granted it is simply hard to recognize. Mutations create variation but at nowhere near the rate of allelic substitutions and most of it is useless to the organism.
All you are explaining is an ad hoc fantasy without a shred of evidence to support it. Why assume a vast amount of completely undemonstrable lost genetic information over a clearly demonstrable facility for genetic material and its machineries of reproduction to produce genetic variation.
"Undemonstrable lost genetic information?" What's undemonstrable about the effect of changing alleles? If you have a dozen alleles in a population for a particular gene, you get very different traits from each. If 6 of those alleles are left behind in a population split you'll have 6 in each new population that will come to characterize each population as they spread and sort through it over time, and both populations will eventually look appreciably different from each other and from the original population that had 12 alleles -- certainly a step toward speciation or divergence between the two. Genetic effect of the most common gardenvariety kind. No role here for mutation.
The sort of alleles we see in populations are completely consistent with the sort of genetic mutations we see regularly ocurring, where does the need to posit some other origin for these alleles come from other than from a religious pre-conviction, what evidence suggests we should adopt your hypothesis?
Well, an allele looks like an allele I guess, and if mutations make alleles then why would they look different? I'm not selling a religious belief, I'm arguing evidence. I would say that the evidence I've given on this thread ought to make you realize that speciation does not require mutation, even if it occasionally makes a small contribution to it, and that nothing more than that has yet been evidenced. All the changes are all quite easily explained by the most ordinary common normal genetic operations. This does lead to suppositions about a beginning point in the past, but stick to the evidence itself. You don't have to follow me there. The evidence will lead you there.

This message is a reply to:
 Message 152 by Wounded King, posted 09-05-2006 5:42 AM Wounded King has replied

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 Message 155 by RickJB, posted 09-05-2006 6:48 AM Faith has replied
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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 159 of 301 (346622)
09-05-2006 8:33 AM
Reply to: Message 155 by RickJB
09-05-2006 6:48 AM


Oh but the argument is FINE. Open your eyes
Chutzpah I've got, in a way, but it's simply based on seeing how what I'm arguing is true, even if I get some of it cockeyed here and there. I'm not particularly clever, I'm arguing a pretty straightforward point, but I do pray a lot to be able to understand it and convey it. However, what I've given IS evidence. All you have to do is follow the reasoning. It's all there.
Edited by Faith, : No reason given.
Edited by Faith, : No reason given.

This message is a reply to:
 Message 155 by RickJB, posted 09-05-2006 6:48 AM RickJB has replied

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Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 166 of 301 (346797)
09-05-2006 6:41 PM
Reply to: Message 162 by EZscience
09-05-2006 12:22 PM


Re: mutation pressure
I had not heard the term used to imply asymmetry in forward/backward mutation rates. I was objecting to its use by Faith in the context of some sort of driving force in speciation.
I've never once used the term "mutation pressure." I have no idea what it means.
The only way I've used "driving force" I got off a definition of mutation at Wikipedia: mutation as the driving force of evolution.
{Edit: OK I see where you recognized your error, that you should have imputed it to Philip instead of me}
Edited by Faith, : No reason given.
Edited by Faith, : No reason given.

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 Message 162 by EZscience, posted 09-05-2006 12:22 PM EZscience has not replied

Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 167 of 301 (346808)
09-05-2006 7:15 PM
Reply to: Message 165 by crashfrog
09-05-2006 4:52 PM


No, it's not just a matter of subtracting phenotypes
The cheetah is a NEW phenotype
I don't see how it is, or at least, I don't see how it's a "new phenotype" that arose through a reduction in allelic diversity.
The "cheetah body plan", or the traits that we recognize as the definitive morphological character of cheetahs, didn't arise because of the bottleneck event; they were already there in the population. The pre-bottlenect population of ur-cheetahs would have included individuals that looked like modern cheetahs, and individuals that looked differently.
Not necessarily at all. The particular alleles for the traits that characterize the cheetah were there in the population, but the particular combination of them that is the cheetah may not have been, and in fact probably wasn't, it took the bottleneck to isolate them and combine them.
All the alleles for the Great Dane or the poodle or the spaniel were already there in the dog population hundreds or thousands of years ago, but there is every reason to believe that neither a Great Dane nor a poodle nor a spaniel ever existed until recently. All the alleles for all the modern breeds were there even if the dogs all looked like wolves or mutts.
The bottleneck didn't give rise to anything new, it simply removed other phenotypes, so that the current cheetah "specification" was the only one left.
No, it removed alleles, and left those that put together the cheetah.
How is that a new phenotype? That's simply the loss of the old ones - a loss of phenotypic diversity, which is exactly what I've been telling you is the consequence of a loss of allelic diversity.
Well, others here seem to be disagreeing with you more than I am even. They tell me that I can't even talk on the level of the phenotype at all, that all the processes I'm talking about are about the genotype -- or something like that; I guess I'll eventually get around to those posts. I think that's wrong since the genotype codes for the phenotype and it's the phenotype we have in mind when we talk about evolution.
But in any case I disagree with your picture as I just explained. The cheetah phenotype did not exist until the bottleneck. It came about as the result of the alleles for it being isolated and recombined by inbreeding in the new population.
The phenotype is now completely defined for those particular traits by those single alleles. It is a NEW phenotype compared to the population it was bottlenecked from
No, it's not, because it was in the old population, too.
Not so, only the alleles for it were, and they were most likely mixed up among all the other alleles, and could only make the cheetah when they were isolated out. They could have been selected, for the special adaptive abilities of the fast cheetah for instance, but in this case they were bottlenecked. It's POSSIBLE that the cheetah in basic form did exist and the bottleneck merely streamlined it, but that's not necessarily the case, and the virture of the example of the bottleneck for my purposes is as a demonstration that dramatically new phenotypes can be put together by drastically reduced genetic diversity.
Let's say that we have a population of tall people and short people, and that that's determined, as it is in pea plants, by a single gene that is dominant for tall.
Now, imagine that aliens come down from space and because they hate tall people, they vaporize everybody who is tall. That leaves only the people who lack any tall alleles, who only possess the short allele. That's a loss of diversity, a loss of an allele (the tall one.)
Yes, if you focus on only one allele you can say the phenotype was already there, although it's even possible then that a recessive just never got expressed at all, or at least very very rarely in the population and it took a bottleneck for it to get expressed -- that would mean that the bottleneck just happened to isolate a pretty rare combination though, but it could happen. In any case, it's the combination of all the alleles of all the genes that make up the cheetah that wasn't there. Or probably wasn't.
So, all humans are now a lot shorter. But how is that "new"? All those short people where there in the old population, before the alien bottleneck. So there's no "new" phenotypes - only a loss of old ones. A loss of physical diversity that stemmed from something that reduced genetic diversity.
Well but even in that case you can talk of having an entirely new population even if the phenotype for that population did occur occasionally in the old. But again, it's a more complicated combination of many traits and their alleles that happens in reality, such that the new phenotype really has never been seen before.
{Edit: Not that it stops looking like its predecessors in any case, but that it is a new version of them, of course. All the new species that arise still have most things in common with all the others of their Kind. Whether this comes about as I am describing or by totally novel mutations, nothing newer than a variation on the theme happens phenotypically}
No, it's not. I've already referred to the direct experimental evidence that this is not the case. Alleles increase in diversity over time; that's the trend.
I don't know where you think you've proved this. The occasional mutation certainly wouldn't prove it.
Specific events might remove alleles, selection might do that (although for statistical reasons it's actually fairly hard to completely select out an allele, especially if it's recessive. The fewer number of individuals that possess an allele, the harder it is to select against.)
Yes.
But the overarching trend is always one of allelic increase, not decrease. That's been consistently borne out in observation and experiment, and mutations are known - known, Faith! Known like we know lightning is made of electricity! - to be the cause.
But Crash, you've said this many times and have NOT shown it to be the case in anything but the onecelled bacteria, and I'm not even certain in what sense the allele that pops up there is really "new." In multicelled creatures and sexually reproducing creatures, however, you are *assuming* that mutation brought about all the genetic material, but you haven't shown anything like that, not even the beginning of it.
and new phenotypes are certainly produced by this loss
If what you're saying is that they're "new" not because they're actually something different than has come before, but merely "new" because now they represent a greater fraction of individuals, that's pretty dumb.
I'm not. See above. Consider dog breeding.
Edited by Faith, : changed select to isolate
Edited by Faith, : No reason given.

This message is a reply to:
 Message 165 by crashfrog, posted 09-05-2006 4:52 PM crashfrog has replied

Replies to this message:
 Message 169 by crashfrog, posted 09-05-2006 8:04 PM Faith has not replied

Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 176 of 301 (347010)
09-06-2006 3:34 PM
Reply to: Message 175 by crashfrog
09-06-2006 2:42 PM


Re: Mutation Fallacies in Macro-ToE
You say "genetic adaptation" like it's a different thing than a mutation. What is the adaptive mechanism operating on genetics if it isn't selection operating on random mutations?
Here's my answer. It's selection operating on the pre-existing alleles in a population. "Selection" in the broad sense. It can mean natural selection, or sexual selection, or the random selection processes of geographic isolation, migration etc etc etc. But it all operates on pre-existing genetic potentials, that is, the variety of alleles available.

This message is a reply to:
 Message 175 by crashfrog, posted 09-06-2006 2:42 PM crashfrog has replied

Replies to this message:
 Message 178 by crashfrog, posted 09-06-2006 3:50 PM Faith has replied
 Message 181 by RickJB, posted 09-06-2006 4:07 PM Faith has replied

Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 177 of 301 (347013)
09-06-2006 3:44 PM
Reply to: Message 172 by crashfrog
09-06-2006 1:15 PM


Re: From alpha centari?
No, maybe it was already in the gene pool but unexpressed.
What kept it from being expressed? What turned it on only in this one Italian village?
It was probably not very numerous in the population at large, and to be expressed probably had to get paired up with another of the same, a low probability occurrence. Other people could be carriers of it without expressing it, if this is how it operates.
If we sequence the gene and find no evidence of it in anybody else - random members of other populations - is that sufficient to conclude that this is recent, rather than an ancient, mutation?
No. It could be an allele that used to be very numerous but has been destroyed by deleterious mutations {Edit: or by one of those "neutral" mutations that "don't do anything" because their effect isn't detectable unless you know what the allele that got destroyed was supposed to do}. So this allele in its original form only survives in small numbers here and there. A random sample could all too easily fail to pick it up.
Maybe it was expressed but not noticed. (It wasn't until the last decade or less).
Why wouldn't we notice it if it were in other populations besides the one in Italy?
What's to notice? Are you checking everybody's DNA? Some people live longer than others. Are you checking the DNA of all of those? You can't even identify them UNTIL they've lived longer. Maybe they live longer because they have this allele but there could be other factors. How are you going to identify who has this allele if it's rare?
Edited by Faith, : No reason given.
Edited by Faith, : No reason given.

This message is a reply to:
 Message 172 by crashfrog, posted 09-06-2006 1:15 PM crashfrog has replied

Replies to this message:
 Message 180 by crashfrog, posted 09-06-2006 4:07 PM Faith has not replied

Faith 
Suspended Member (Idle past 1474 days)
Posts: 35298
From: Nevada, USA
Joined: 10-06-2001


Message 179 of 301 (347017)
09-06-2006 3:55 PM
Reply to: Message 178 by crashfrog
09-06-2006 3:50 PM


Re: Mutation Fallacies in Macro-ToE
How does that apply to this case? The trait is dominant. You can't hide a dominant trait, you can only lack it by being homozygous recessive.
If an individual has a trait that is dominant, but neither of the parents have the trait, then either the gene came about through mutation or the parents aren't who you think they are.
Do you have a link to a discussion of these factors in this case?
Edited by Faith, : No reason given.

This message is a reply to:
 Message 178 by crashfrog, posted 09-06-2006 3:50 PM crashfrog has not replied

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