Evolution: the Facts.

I can understand perfectly well why biologists would have made those claims. I just don't agree that showing that sections of an organism's DNA previously thought to be "junk DNA" is actually functional does anything to dismantle this line of argument. If we find genuine "junk DNA" tomorrow, evolutionary theory predicts that this will show the same pattern as functional DNA, i.e., that taxa closely related in the true tree will be more likely to have sequences more similar to each other than would taxa that are more distantly related on the true tree.

The argument that "junk DNA", if found, will show this property is still, theoretically, a very strong argument in favour of evolution, as we would expect "junk DNA" to behave the same way as functional DNA, albeit perhaps at a different speed. The fact that what was previously thought to be "junk DNA" turned out to be functional mean precisely one thing: that the specific examples given of "junk DNA" conforming to the theory of evolution are not examples of "junk DNA" doing so. They do remain examples of functional DNA showing the exact same thing. The strength of the evidence does not lie in the label we attach to the data, but to the actual data. Arguing otherwise betrays only your intimate lack of knowledge of the field.

Your point would have some merit if you could show that the very same people who argued that "junk DNA" is strong evidence in favour of evolution also argued that all other forms of DNA, whether structural, coding or whatever, are not strong evidence in favour of evolution, and that this is actually the case. This is the only case in which your argument has merit, as this is the only case in which data would be moved from the "evidence basket" to the "not evidence basket". As long as the very same data shows the same pattern regardless of what we call the data, it remains as strong a piece of evidence for or against evolutionary theory as it was before. If, as I have seen you write elsewhere, you truly want to look at the data and see what the data tells you, then you should agree that the labeling of the data is irrelevant to what the data actually says.



Can you show that creationists and other non-biologists argued that similarity in a given alignment of supposed "junk DNA" sequences from different species did not indicate common descent, and that when this piece of supposed "junk DNA" was shown to be functional, it turned out that the data actually didn't indicate common descent in the group? In other words, can you show for instance a phylogeny which was based on supposed "junk DNA" sequences which, when discovering that the specific sequences used were not in fact "junk DNA", altered so that no common descent was indicated?



So this will be challenge number two, then: show me a list of these predictions ID has made with regards to a single group of animals which have been shown to be correct, and I will endeavour to do the same using scientific scenarios, and we will see which is most numerous. Pick whichever group of organisms you want, list the predictions ID has made regarding the relationships and whatever else you want for this group (as well as the basis for this prediction), show the methods used to test these predictions, and what the results are (i.e. to what extent their predictions have been supported by the data and their analyses of the data), and, after you have told me what group you will be looking at, I will do the same using evolutionary predictions and evolutionary data.

This is, of course, in addition to the first challenge, which was that if I randomly select a sample of phylogenies, you will be able to to show that it contains groupings of species that would not be predicted by the theory of evolution? I have developed a quick method for removing most of the bias with regards to what phylogenies will be selected, and could proceed with this whenever you give the signal. The proposed method of phylogeny selection:

1. Load random pages on Wikipedia.

2. Every time a page is on an animal taxon (1), I will go to Google Scholar and make a search for "[taxon name] + phylogeny".

3. Using a ten-sided die (possibly an electronic one) I will select which phylogeny is to be studied. If the die shows a four, and article number four is not available to me, I will take the next one, and continue going down the page until I reach a paper I have access to.

4. To remove some bias, I will not select the following taxa, as I am more intimately familiar with those due to my own research: Phthirapteran lice, Clitellate worms, and Charadriiform shorebirds. If requested, I will also remove the following taxa that I have not worked with, but with which I am nonetheless quite familiar: Passeriform birds, Anuran amphibians, Vespid wasps, Psocopterans, and all polychaetes. If any such taxon is generated in the Wikipedia search, I will just discard this result and do a new one.

5. I also propose to remove all studies which are on a below-species level, as these, typically being concerned with shorter time periods and smaller geographical areas, would tend to bias the study in my favour. If the die suggests a paper of this nature, I will proceed as under point 3 above.

6. I will write down all search results in Wikipedia, including all discarded searches, as well as all initial and modified search results in Google Scholar. If necessary, I will provide you (and anyone else who wants them) with all the selected phylogenies (in case you don't have access to them yourself).

7. I will then give you as much time as you require to read through the papers and detail in which of them groupings of species occur that would not be predicted by the theory of evolution. After you have presented your case, I will look through it and get back to you as soon as possible.

Please comment on this method, as I may have overlooked flaws that would bias the process in my favour. I will start this test as soon as you give the signal (although I will be away during most of the weekend, and will not therefore not have time until Monday).



You will need to detail this picture more comprehensively, as I can see no such picture forming when I look at the data. Assuming I am the one with bias, I would ask you for more detail, and also to clarify what your claim actually is. As "phylum" is a label given to groups of animals which have a very long common history, and have been separated from all other groups of animals for a long time, this by necessity means that this label will be given only to groups of animals that formed a long time ago. More recent groups have other labels attached to them.

This does in no way imply that "phylum", "family" or any other taxonomic label is anything that exists in nature; these are all within-science terms used for communication, and has no external existence. However, certainly there are groupings referred to as, e.g., families that are more recent than other groupings having the same rank label. As taxon labels are only terminology, they are not comparable between higher taxa. A bird family is not necessarily as inclusive or as old as a wasp family, as the very term is just a label we use for a certain grouping we feel is significantly closely related to warrant it. How inclusive a taxon in differs widely between higher taxa, mainly because it is comparatively rare for people to work on multiple taxa, and because different taxa offer different levels of resolution, and have different number of differently skilled people working on them.



We will (and have) certainly found groups of organisms which have evolved more recently than the "Cambrian explosion". Whether you call these "phyla" or "classes" or even "orders" is just a matter of taste, as the recent restructuring of the Platyhelminths and several other large groups should show adequately.

However, I will concede that it is unlikely that a group that diverged from a known phylum within the last 10 million years or so would be referred to as a phylum. This, however, is just because of the way taxonomy and systematics works, and has no bearing on the theory of evolution.



If they show evolution in action, they are certainly good examples of it, and should be used as such. However, it is imperative to understand the limits of using such examples.

Again, evolution does not necessitate change measurable to humans over any given period of time. It also does not oblige any given taxon to evolve into something else (2), and certainly not if the niche a given organisms occupies at a given point in time is more or less stable for extended periods of time, and the organism is already highly adapted to that niche.




This is not true. One instance of early speciation followed by a long period to time during which both sister taxa survive and evolve is sufficient for the development of differences significant enough for us to place the two sister taxa in different higher taxa, without the need for any speciation past the initial event. Granted, a widely distributed pair of sister taxa in a natural environment is likely to yield speciation within their respective lineages, but nothing in the development of higher taxa presupposed or requires speciation past the initial event. There are several phyla which contain only a handful of known species.



Of course there is a reason for that. There are, in fact, plenty, the most obvious one being that different groups of organisms reproduce in different ways, and therefore cannot be expected to divisible into smaller units in the same fashion. The animal kingdom alone exhibits more variations of reproduction than most people can comprehend. However, de Queiroz and some others are very close to establishing a combined species concept which may work on any given higher taxon, so this may not be so much of a problem in the future.



How fitting, then, that you are the first person to mention this fact. This is nothing that has ever been argued by a biologist in possession of a basic evolutionary knowledge.

However, evolutionary theory does contain a continuum, but it is temporal rather than spatial. We predict that a given extant individual of a given species would theoretically be able to breed with its direct antecedents. These, in turn, would be able to breed with theirs, that is, the first species grandparents. Let this continue backwards in time, and you will find a temporal continuum. However, evolutionary theory predicts that we will eventually reach a point at which the extant individual could no longer breed successfully with an ancestor of a given generation, provided they were given the opportunity. This ancestor could then be given the status of a different taxon, and could be the starting point of a new continuum going either backwards to the next point in time where interbreeding between taxon 2 and its direct (but not immediate) ancestor is at least theoretically impossible, or forward where another of taxon 2's descendant lines are followed.



This is a simplification, as mere chance can also be the basis of speciation, as is the case in sympatric speciation. I don't see how this is in any way a critique of evolutionary theory, however, as this is something that is well known.



No, you have not. What you have said is:



This was followed by what I refer to above as the "first challenge", which you sidestepped because you feel a greater urge to appear clever than to actually appear intellectually honest. I refer to this post:



At no point have you actually suggested a phylogeny we could inspect together. Above, you will see that I am inviting you to do so more formally. If you truly believe what you are arguing, I see no reason for you not to accept the test I outline above (or any variation you believe is more fair).



I do not see these attempts as a problem, as evolutionary theory is robust enough to handle cases where the biological species concept can be said to work (or approximated to work). As long as we know the mode of reproduction of a given taxa randman may chose to discuss, who cares if we are discussing it on "his terms"? Example taxa where the BSC is valid (or approximately valid) can be discussed on these terms, and taxa where it is not valid are simply not eligible for discussion under the assumption that the BSC is valid.



This would entail having to assume that lack of known fossil subtaxa within a given higher taxon is evidence of actual lack of these taxa. I am not prepared to make this assumption, but if you want to make a case for this, I would be willing to discuss it.



I find it amusing that you can argue this, and still argue that there is a huge qualitative difference between calling a certain section of DNA "junk DNA" or functional DNA, not to mention your parade of ignorance when it comes to taxonomy.



However, past the initial split of an ancestral taxon into two, no further speciation is actually required by the theory of evolution for it to hold true. It is certainly a very likely consequence, and we would certainly predict that it would happen in most natural populations, but it is not at all a requirement.



One is what biologists call themselves, the other is what non-biologists call biologists. I take "evo" to be short hand for "evolutionist", which is a synonym for "biologist".

---
(1) This is for practical purposes. I am more familiar with what journals on animal taxa my university has access to, and it will therefore be easier to obtain these phylogenies. If you object to this, I can easily include non-animal taxa as well.

(2) Which, in any case, is a taxonomic impossibility.

Vry nice!
 
We will (and have) certainly found groups of organisms which have evolved more recently than the "Cambrian explosion".
Perhaps. There are two things at work here: First, "higher taxa" are really just older clades. The further back in time you go, the more decendants each population has. Second, there's speculation that there was something different at work in the past--less restrictions on bauplans, for example, or changes in ocean chemsitry--which allowed for more varieties of bauplans (the reason I keep using that word si that in Linnaean classification phyla ARE bauplans). So what is considered in Linnaean taxonomy to be a class or order may one day be considered a phyla, but we're not sure.
 

Certainly we have. The taxon "Aves", for instance, did not exist during the Cambrian explosion, even if its ancestors did.

There are two things at work here: First, "higher taxa" are really just older clades. The further back in time you go, the more decendants each population has. [...] So what is considered in Linnaean taxonomy to be a class or order may one day be considered a phyla, but we're not sure.

Which is more or less the same as the sentence that followed the one you quoted:

Whether you call these "phyla" or "classes" or even "orders" is just a matter of taste

Though I would say that there is nothing to "be sure" about, as it is all just labeling, and there is no single correct answer for where you draw the line between, e.g., phylum and class, as this is just an arbitrary distinction with no foundation in the natural world.

(Also, that essay you wrote in the other thread was great! Thank you!)
 
Kotatsu said:
Certainly we have. The taxon "Aves", for instance, did not exist during the Cambrian explosion, even if its ancestors did.
I wasn't saying that no new taxa have arisen--I want to say that bryozoans arose after the C. Explosion, though I'm not 100% sure that's the right phylum; at any rate, one new one did arise. And, you know, the whole amphibian/reptile/mammal/bird clade. I was more thinking out loud about a few papers I've read concerning channelizaiton in bodyplans, and the reasons for the observed channelization. There's a bit of a debate in paleontology as to whether or not new bodyplans can arise anymore--there really hasn't been a major revision since the CE (let's face it, all vertebrates are basically the same), though personally I suspect that this has more to do with biases and lack of material than actual evolutionary history. But to be fair, I often overestimate the amount of data lost to paleontology (I'd rather be proven wrong by someone showing that we do in fact have the data than be proven wrong because my conclusions overstep what my data can support).

(Also, that essay you wrote in the other thread was great! Thank you!)
As was your post. :)
 
Vry nice!

Now who's got what in the draw for how randman is going to avoid answering the questions/challenges put to him? I think I'm going to go for answering one small part of the post with an irrelevancy and pretending that that's an answer to the rest of it. Who's got "doesn't post in the thread again" and "leaves the message board all together"?
 
So we have a continuum in many ways other than sickle cell anemia, but in this case we can have breeding populations that vary on amounts of members that have the following three states:
1. No sickle cell anemia
2. Half a trait of sickle cell anemia
3. Full trait of sickle cell anemia

Now before I proceed to discuss how a continuum proceeds to divergent populations that can no longer breed,

Note the bolded part. You admit such a thing as divergent populations exist.

I rest my case.
 
So I will try to spiel it out for you but I will try to go at a pace that maybe will stop your rhetorical posturing and hand waving behavior.

I was trying to establish a simple principle:
-accumulation of traits within divergent lines in a breeding population.

So in this example I was talking about sickle cell anemia and how you can have the expression of the trait in this case as
-no trait
-half trait
-full trait

Do you agree that this is possible in this discussion of this trait of sickle cell anemia?
Yes or no, If no please state your reasons.

Now some traits are going to be more complex so say we have a trait that is manifested in a two gene sites as two alleles, so we would have 1,1/1,2/2,1/2,2 so in this simple example we have four possible states for the expression of our model trait.

Do you agree that this is possible in this model trait?
Yes or no, If no please state your reasons.



Now for the next step we look at eight possible traits, but for the sake of the model we will give them just an on/off designation, rather than a more realistic model.

So we have eight traits that are either present or not so there are 28 possible configurations of the ten traits or 256 the set being
00000000, 10000000, 01000000, 11000000... 01111111, 11111111.
So in this model the possible number of states in the ten traits is 256.

So do you agree that this is possible in as there being 256 potential configurations of these ten traits?
Yes or no, If no please state your reasons.


So sticking with this last model of ten traits that have a binary expression it is easy to see how we can look at these ten traits as being a sequence that has 256 configurations going from no expression of these ten traits to expression of all ten traits.

Now can we arrange these 256 possible configurations as gradations between two members of our model breeding population?

The math one would be to just sort the 256 states 1-256 with 00000000=0, 10000000=1, 01000000=2, 11000000=3...01111111=255 and 11111111=256.

So in this case we can just assign a set order to the possible expression of the ten traits, and if we have any two members of our model breeding population we can just grade them through where they fall in this ordered set.

Do you agree that is a possible way to order the possible combination and grade the differences between two members of our model breeding population?
Yes or no, If no please state your reasons.


Now that is a very arbitrary and mathematical way to sort between two members our model breeding population, the way that humans more usually sort things would be to just take the ten traits and compare them so you would usually sort them as being similar or dis-similar.

So if the share no traits their similarity is 0, if they share all traits then the score of similarity would be ten.

So if we compare two members of our model breeding population we can give them a similarity score based upon ten traits as a range from 1-10.

Do you agree that we can compare and grade the traits between two members of our model breeding population in this fashion?
Yes or no, If no please state your reasons.


So again I am setting this up to be a discussion of divergence in breeding sets within a breeding population.

Please answer, then I can hopefully engage in a discussion with your of the next part, how do you get from the continuum of traits to two sets within the breeding pool that can no longer breed with each other.
Waste of time because absolutely nothing you posted is relevant to the discussion. Maybe this will help?

Regardless of any of those questions, NeoDarwinism posits sequential speciation as the process of evolving all species and all biota.

Do you admit that or not? Do you see why discussing changes within a breeding population that does not evolve into a new species is of little value to assessing whether new species did or did not emerge?

It's a simple question.
 
Now who's got what in the draw for how randman is going to avoid answering the questions/challenges put to him? I think I'm going to go for answering one small part of the post with an irrelevancy and pretending that that's an answer to the rest of it. Who's got "doesn't post in the thread again" and "leaves the message board all together"?
Avoid answering challenges? Kind of like a 1st grader challenging you to eat more ice cream than them, or who can fart louder?

You guys have not even grasped the most basic aspects of evolutionary theory. You even deny your own theory which you are largely ignorant of posits sequential speciation is how all biota evolved.
 
I think this is wrong and will explain why. Though the paper does emphasize the loss of genes in the lineages leading to flies and worms, they still also mention one reason for their surprise based on the relative simplicity of the organization of the cellular structure of the coral. Since they would be aware that evolution can happen via loss of genes, the findings would not be that surprising. One reason I included the quote from the author is to help illustrate that acknowledgement of the "intrinsic" beliefs of evolutionists thinking greater genetic complexity emerges with greater morphological complexity.

The findings were surprising because two model animals of separate lineages both lost this set of genes, while a third, vertebrates, did not. I cannot comment of the quote because you have failed to provide the source for it, in context. Greater morphological complexity does require greater genetic complexity, nothing has changed about that.

A review of the history of evolutionary thought might be helpful. One reason Darwin's idea caught on is it appealed to prevailing beliefs of the day such as progress, racism and a desire for a simple mechanical explanation of things. The idea of progressive evolution "upward" was long a staple but in more recent years, that has been deemphasized to say evolution does not have a direction per se.

It also explained a lot of observations about life. Regardless, this is irrelevant because scientific models change over time. Darwin did not know about DNA, but he did predict variation and heritability.

Nevertheless, the general patten of increasing complexity remains. Evolution does not predict a human being, for example, at the root of the phylogenetic tree, but a very simple organism. Why is that? Because life is thought to have begun with something simple and evolved into greater complexity through evolution splitting off new species and so forth. The mechanism for this is that genetic changes would be selected for and so genetic complexity (origin of new genes for greater function) would emerge with greater morphological complexity. That's really the prediction of the mechanism and at the heart of Darwinism, that we see simpler organisms at the beginning of life, and they adapted via mutation, etc,...being selected for through natural selection acing on a population.

Things start out simple and then may increase in complexity. They may also decrease in complexity or they may remain at the same complexity. The important concept is that complexity is built up over time. At the emergence of animals life had already had almost 3 billion years of evolution to build up the complexity of LCA.

In fact, evos back in the 90s used to explicitly say NeoDarwinism predicted simpler organisms would have simpler genomes and actually went on quite a bit on sites such as Infidels about that.

What does simple mean? In general, less complex organisms have much smaller genomes than more complex organisms.

So whereas NeoDarwinism makes room for evolution via loss of genes, it would be surprising to see it occur from the LCA through a "massive loss" of genes because the LCA was thought to be not that genetically complex. It's important to realize that the concept of genetic complexity emerging through morphological complexity predates any of the molecular studies and genome mapping, but is an idea going back to the very beginning. It had been modified some but is actually being turned over completely now.

Wrong. You are missing the point that I made earlier. The predictions for the genes of LCA were based off the available sequences of model organisms, not some core concept of evolutionary theory in isolation. Nothing is being turned over at all. It's the same theory with an additional data point added. The new data point changes a few things, but that isn't a big deal. There were so few data points to start that it is expected that things will change.

Keep in mind there other studies not just this one paper. So if the LCA is now thought to be incredibly complex genetically,

It's not. You are using weasel words. It is now thought to contain some genes that were previously thought to be vertebrate specific. That does not in any way translate to "incredibly genetically complex."

that begs the question of how much of a driver environmental pressures are to the origin of novel genes and to evolution itself. Maybe Pierre Grasse and others were right to deride NeoDarwinism so much and insist evolution was internally driven. The picture emerging is very different than what the NeoDarwinian narrative suggested it should be.

No, it's not. You fail to understand what the previous predictions were based on and to understand the new data in it's appropriate context.



Maybe so. I am not sure that's necessarily proven but I think your point here is that since these genes have function there, they must have evolved through NeoDarwinian means. One problem is we don't know how the first genes got there in the first place. I am sure in the future evos will argue that between the original common ancestor and LCA, that all this genetic evolution took place producing a very genetically complex LCA, and then we see where it ran backwards so to speak (I use that term just in reference to the old concept of increasing complexity). In other words, a massive build-up of types of genes following a decrease in available types of genes. Already, some researchers are saying the precursors to plants and animals had available to them more types of genes than are available to plants and animals today.

The problem of the first genes goes all the way back to the origin of life, not the origin of animals. We know how new genes arise once life has started.

LCA is not predicted to be "very genetically complex" and it is not predicted to be more complex than the fly or even worm. The loss of a subset of genes, does not in anyway imply a loss of complexity over the time scales we are talking about. There is no implication of running backwards from LCA to worms or flies. There are known instances of 'running backwards' in other model systems, however, and it's not a big deal.

But this is still a big departure from what evos envisioned, and we have no evidence of how the first genome came about. Who is to say it came about through neodarwinism? If the further back our studies will allow an estimation, we see greater complexity genetically, why do we assume even further back there is somewhere at some time genetic simplicity?

Maybe you are confused. We are talking about the origin of animals, not the origin of life, do not conflate the two issues. Again, we do not see greater complexity the further we look back. You are reading to much into this study without understanding what it actually means.
 
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Greater morphological complexity does require greater genetic complexity, nothing has changed about that.

Thank you for responding. This is an interesting comment which I think the data says is not true, but even more interesting is why this should be true.

Why do you think this is the case?
 
We know how new genes arise once life has started.

LCA is not predicted to be "very genetically complex" and it is not predicted to be more complex than the fly or even worm. The loss of a subset of genes, does not in anyway imply a loss of complexity over the time scales we are talking about.

2 questions related to those above before going further.

1. Do we know how new genes arise? If so, how? Can this be tested as a general pattern?

2. The LCA is not predicted to be genetically complex? I agree. What does that mean if it is?
 
Avoid answering challenges? Kind of like a 1st grader challenging you to eat more ice cream than them, or who can fart louder?

No, like someone who is claiming to want honest scientific debate being asked to demonstrate his assertions are true. You've been given an easy and fair protocol with which to do so, and have been given license to modify this protocol or design one of your own if you consider the one put forth to be unfair or biased in any way. If you're confident that your assertions are true, why would you not want to demonstrate this fact?

You guys have not even grasped the most basic aspects of evolutionary theory. You even deny your own theory which you are largely ignorant of posits sequential speciation is how all biota evolved.

Did I have "post an irrelevancy and pretend it's an answer"? I think I did. I win! Go me!
 
Avoid answering challenges? Kind of like a 1st grader challenging you to eat more ice cream than them, or who can fart louder?

You guys have not even grasped the most basic aspects of evolutionary theory. You even deny your own theory which you are largely ignorant of posits sequential speciation is how all biota evolved.

You misinterpret what is going on. Neither of the two challenges in any way relies on my understanding or lack of understanding of evolutionary theory. Let me make it clearer to you.

The first challenge is for you to show that some phylogenetic trees, either chosen randomly or chosen by you, contain groupings which would not be predicted by evolutionary theory. I have proposed what I perceive to be a more unbiased way to chose these trees, but if you have some candidates with which you are familiar, you are free to suggest them. While I will concede that as a second step in this challenge, I (or someone else) will attempt to interpret these trees from an evolutionary perspective, the first step of this challenge is actually entirely independent on our (that is, everyone but you) understanding of evolutionary theory, phylogenetics, evolutionary history, biology, or any other aspect. It depends entirely on your understanding of these matters. If, as you claim, you can find these groupings not predicted by evolutionary theory in most phylogenetic trees, you should be able to do so regardless of if you are discussing them with experts of novices. Our skills and knowledge does not come into this challenge until at a later stage, where you have already presented the evidence for your claim.

For the second challenge, you are required to show a list of predictions ID and related fields have made in natural history for a group of animals of your choice, list the basis for these predictions, and show the data and analyses performed to test these predictions, and show the results of these tests. Your claim is that ID and related fields have "often been more predictive of results than Darwinism", which is what I challenge you to provide data for. This challenge is also independent of my or anyone else's knowledge of evolutionary theory, speciation, and biology in the initial stage, and relies instead entirely on your intimacy with the predictions of ID and related fields, your familiarity with the scientific literature, and your knowledge of evolutionary theory.

To fail to accept, or even discuss, these challenges based on asserted -- but not demonstrated -- shortcomings in my understanding of evolutionary theory is dishonest at best, and most likely cowardly. Neither of them relies on my understanding of evolutionary theory, but relies heavily on your understanding of it. If, as you claim, we have misunderstood the theory and the data, this would be a great opportunity to show this conclusively. Otherwise, no more likely explanation readily suggests itself than that you are a coward, a braggart, a mental troglodyte, and a liar.
 
The first challenge is for you to show that some phylogenetic trees, either chosen randomly or chosen by you, contain groupings which would not be predicted by evolutionary theory.

None of them do.
 
None of them do.

As in, "none of the trees contain groupings that would not be predicted by evolutionary theory"? If so, what did you mean when you wrote:

Even looking at phylogeny, the pattern of how species seem to be grouped together, it's not what "evolution" in the sense of Darwinism would predict, but you have to take the time to look at the patterns and consider the arguments closely.
 
Note the bolded part. You admit such a thing as divergent populations exist.

I rest my case.

That is strange, I never said they did not, I wonder what my posts are pointing to? The acumulation of traits, then we can talk about the split of populations into divergent lines, and then how populations that come from similar backgrounds are likely to develop similar traits even after seperation.

The point is divergent traits within a breeding population at this time.

However considering you have made your point clear, it seems strange you would claim to have a case.
 
Waste of time because absolutely nothing you posted is relevant to the discussion. Maybe this will help?

Regardless of any of those questions, NeoDarwinism posits sequential speciation as the process of evolving all species and all biota.
And considering that you have yet to show a source for this claim, and we can discuss that source and claim separately, this is very strange of you.

I am discussing the continuum that can exist for a range of traits.

Which you made some silly statement about.
Do you admit that or not? Do you see why discussing changes within a breeding population that does not evolve into a new species is of little value to assessing whether new species did or did not emerge?
It has everything to do with evolution and speciation. Which is the point, there multiple consequences of the theory of evolution through the natural selection of traits by reproductive success.

You seem to be monomaniacal. first we were talking about front loading and I am still addressing that point, then you made some statement that a continuum of traits was not possible, so I am addressing that.

Your monomania seems to shift focus.

So do you agree the evolution or naturals election through reproductive success, can lead to divergent traits, even without speciation?
It's a simple question.

It may be a simple question but the answer is not simple.

Um, I am continuing to discuss what we discussed back in the beginning of the thread.

So I go back to one of my original points, does evolution include the development of populations that have divergent traits but are still the members of same species?
 
Avoid answering challenges? Kind of like a 1st grader challenging you to eat more ice cream than them, or who can fart louder?

You guys have not even grasped the most basic aspects of evolutionary theory. You even deny your own theory which you are largely ignorant of posits sequential speciation is how all biota evolved.

Considering that it can be shown that you seem to make false claims about evolutionary theory that you can't substantiate or source, I would recommend that you stay away from claims about what evolutionary theory is. Otherwise I can keep asking you to show where in evolutionary theory it is stated that a continuum on a range traits doesn't exist.

Of course the solution is for you to admit that perhaps you don't really understand what other people are discussing and just assert that you do.

There is no continuum under Darwinism. There is separation and reproductive isolation of populations. If you have been taught otherwise and actually believe there is a continuum, that's kind of sad really. Everyone knows, say, a cat cannot mate with a dog. Even a child knows that. There is no continuum as if all living, sexually reproducing creatures can still mate with one another. That's absolute lunacy.

No the possibilities are rather limited here randman:

1. You misunderstood that I was talking about a continuum of traits within a breeding population.
2. You started arguing about a point that I was making and so did still not understand what I was talking about.
3. You just respond to words that you see in posts without reading for context.
4. You lack the ability or desire to try to understand what other posters are trying to discuss.
5. You are just here to make a monologue without actual discussion.
6. You seem to make lots of assertions about what evolutionary theory is but never back them up.

So I was talking about a continuum of traits that can exist within a breeding population.

So explain what happened please?

1. Did you misunderstand?
2. Did you try to make some rhetorical point because I used the word continuum?
3. Do you misunderstand that evolutionary theory has a possibility for a continuum of traits within a breeding population?
4. That you changed the topic I was addressing to make some other point?
5. Insert your explanation.

Well randman which is it?
 

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