Why do so many christian deny evolution?
There are observed instances of speciation within drosophila - nonetheless, you still end up with two populations of fruitfly (which can't interbreed) and I can see an objection there along the lines of not being sufficiently distinct, I just don't know how it would be worded (other than in a "I'll know it when I see it" kind of way).
I mean we've seen the evolution of species that can no longer interbreed, we've seen how different dogs can look, we've seen bacteria create novel proteins -- it doesn't take much imagination to see where this all leads. And then when you look underground and find exactly what you were imagining, you'd almost have to be crazy to continue to deny evolution. (Not that I'm saying you deny evolution, but I think that understanding Concerto's objection as quoted doesn't encompass the full picture.)
I mean we've seen the evolution of species that can no longer interbreed, we've seen how different dogs can look, we've seen bacteria create novel proteins --
it doesn't take much imagination to see where this all leads.
more like, it doesnt take much imagination to come up with a decent hypothesis that is yet to be proven wrong.
wow i really feel bad for concerto after reading these last 2 pages.
wow i really feel bad for concerto after reading these last 2 pages.
Concerto,
You can honestly tell me that you would be saying the same exact stuff itt if the bible mentioned something that was clearly what we know as ToE? (when i say clearly let's imagine over 90% of all Christian sects believe it's true)
You can honestly tell me that you would be saying the same exact stuff itt if the bible mentioned something that was clearly what we know as ToE? (when i say clearly let's imagine over 90% of all Christian sects believe it's true)
Enough for our purposes. Essentially, it means reproductively incompatible. Though one has to exclude the sort of reproductive incompatibility that results from processes that can only continue for a few generations, like chromosome doubling. This is fair because the terminating nature of such processes does not allow them to extend to the sort of diversity evolutionists are attempting to account for anyway.
In other words, there are two sorts of reproductive incompatibility: 1) the sort associated with "sufficient distinction" of overall morphology and 2) the sort only a few steps removed from the parent population. In practice, there is enough of a gap between the two classifications to justify the difference.
In the second paragraph, what makes you think 1) and 2) are necessarily distinct? I think this is the heart of my question - drosophila have been observed to split into two mutually distinct species in the sense that the two populations can no longer interbreed, yet are viable going forward. I can accept they're not "distinct enough" - but what's the criteria for determining that?
It still depends on your definition of 'species' and 'new'. I can't proceed without a fixed definition of both.
I introduced increasing infertility as an example of the vast set of potential obstacles to the indefinite accumulation of mutations which handwavy "evolutionist" magicians have left unaccounted for.
In that case, you pick two species A and B, where A evolved to B, that you consider taxonomically distinct enough to be an instance of whatever process you claim can produced the observed biological diversity.
Say what now?
thats right, hes started creating his own biological concepts
ToE provides mechanisms for how speciation occurs. Concerto's objection seems to be ‘prove to me that these mechanisms will never ever stop!’ (1). He’s incapable of ever accepting evolutionary evidence because his requirements for evidence are to show that 2 species ‘sufficiently different’ had a common ancestor(2).
He claims ‘sufficiently different’ means reproductively incompatible (3). Then when hes shown that the species are reproductively incompatible he’s basically said ‘well, I don’t consider them distinct organisms’(4). He’s using definitions of species not used in biology (5) and hes making up biological concepts (6).
Concerto, you are a lunatic.
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He claims ‘sufficiently different’ means reproductively incompatible (3). Then when hes shown that the species are reproductively incompatible he’s basically said ‘well, I don’t consider them distinct organisms’(4). He’s using definitions of species not used in biology (5) and hes making up biological concepts (6).
Concerto, you are a lunatic.
1.
Originally Posted by Concerto
Okay then. Show there is no natural mechanism to stop the accumulation of effects of the actually observed mechanisms of diversity occurring.
Originally Posted by Concerto
One of my views is that no two sufficiently distinct populations (roughly: different species) have an ancestor in common.
Originally Posted by Bunny
Is sufficiently distinct well defined
Originally Posted by Concerto
Enough for our purposes. Essentially, it means reproductively incompatible.
Originally Posted by Concerto
It's not a matter of number of generations. It's about distinct organisms being produced.
Originally Posted by Concerto
reproductive incompatiblity is only a necessary condition....[I require] A demonstration of the sustainability of a candidate mechanism of speciation to the extent of producing something like the observed diversity of life.
Originally Posted by Concerto
...there are two sorts of reproductive incompatibility: 1) the sort associated with "sufficient distinction" of overall morphology and 2) the sort only a few steps removed from the parent population.
and I don't see the justification for this.
In the second paragraph, what makes you think 1) and 2) are necessarily distinct? I think this is the heart of my question - drosophila have been observed to split into two mutually distinct species in the sense that the two populations can no longer interbreed, yet are viable going forward. I can accept they're not "distinct enough" - but what's the criteria for determining that?
Exhaustive? No, not given time constraints. For our purposes here, macro-evolution has occurred if both 1) the descendent population is reproductively incompatible with an ancestor population and 2) the mechanism of that reproductive incompatibility can be repeated within the descendent population to produce another descendent population that is reproductively incompatible with the first descendent population, etc indefinitely.
That's what we see: two types of reproductive incompatibility.
To start with, a simple quantification of the differences. The two underlying categories of reproductive incompatibility correspond to vastly different orders of magnitude of genetic separation between parent and descendant. More importantly, a causal continuity between the types in which one leads to the other by reiteration of the first has not been demonstrated.
I think this is the heart of my question - drosophila have been observed to split into two mutually distinct species in the sense that the two populations can no longer interbreed, yet are viable going forward. I can accept they're not "distinct enough" - but what's the criteria for determining that?
For our purposes here, macro-evolution has occurred if both 1) the descendent population is reproductively incompatible with an ancestor population and 2) the mechanism of that reproductive incompatibility can be repeated within the descendent population to produce another descendent population that is reproductively incompatible with the first descendent population, etc indefinitely.
The determination of reproductive incompatibility type is made by asking, "Could the operation that produced this reproductively incompatible population be repeated on it to produce from it a subsequent reproductively incompatible population, an arbitrary number of times on successive populations?" The answer must be yes for a candidate mechanism of macro-evolution to be viable, but such has not been demonstrated.
That is not how the determination of type is made. The "distinct enough" property is a justification of the categorization by showing it fits into a broader biological scheme.
The determination of reproductive incompatibility type is made by asking, "Could the operation that produced this reproductively incompatible population be repeated on it to produce from it a subsequent reproductively incompatible population, an arbitrary number of times?" The answer must be yes for a candidate mechanism of macro-evolution to be viable, but this has not been demonstrated.
The determination of reproductive incompatibility type is made by asking, "Could the operation that produced this reproductively incompatible population be repeated on it to produce from it a subsequent reproductively incompatible population, an arbitrary number of times?" The answer must be yes for a candidate mechanism of macro-evolution to be viable, but this has not been demonstrated.
Drosophila has been observed to evolve into two distinct, viable species. You and I agree that this in itself is not enough to demonstrate humans came from sludge. What would be enough? If one of the new drosophila had an extra couple of legs? Could distinguish color? Breathed water?
If your category of "distinct enough" is to mean anything I think these kinds of questions need to be answerable. (Is this tied up with the meaning of type I asked about above?)
The two types of reproductive incompatibility I am referring to here are macro-evolution versus whatever meets only the first criterion.
Drosophila has been observed to evolve into two distinct, viable species. You and I agree that this in itself is not enough to demonstrate humans came from sludge. What would be enough? If one of the new drosophila had an extra couple of legs? Could distinguish color? Breathed water?
If your category of "distinct enough" is to mean anything I think these kinds of questions need to be answerable. (Is this tied up with the meaning of type I asked about above?)
If your category of "distinct enough" is to mean anything I think these kinds of questions need to be answerable. (Is this tied up with the meaning of type I asked about above?)
Oh, so you're going with that and ignoring the other part where I mention the fossil evidence? Well done, continue to mischaracterize my quotes in order to make your argument.
ToE provides mechanisms for how speciation occurs. Concerto's objection seems to be ‘prove to me that these mechanisms will never ever stop!’ (1). He’s incapable of ever accepting evolutionary evidence because his requirements for evidence are to show that 2 species ‘sufficiently different’ had a common ancestor(2).
He claims ‘sufficiently different’ means reproductively incompatible (3). Then when hes shown that the species are reproductively incompatible he’s basically said ‘well, I don’t consider them distinct organisms’(4). He’s using definitions of species not used in biology (5) and hes making up biological concepts (6).
Concerto, you are a lunatic.
He claims ‘sufficiently different’ means reproductively incompatible (3). Then when hes shown that the species are reproductively incompatible he’s basically said ‘well, I don’t consider them distinct organisms’(4). He’s using definitions of species not used in biology (5) and hes making up biological concepts (6).
Concerto, you are a lunatic.
In other words, there are two sorts of reproductive incompatibility: 1) the sort associated with "sufficient distinction" of overall morphology and 2) the sort only a few steps removed from the parent population. In practice, there is enough of a gap between the two classifications to justify the difference.
Exhaustive? No, not given time constraints.
And then we have an absolute doozy like this:
What would be enough is a function of the extrapolatability of the operation (or set of operations) that produced the observed "speciation" such that the operation could be repeatedly applied to the extent of giving rise to something like the current biodiversity. That is what has to be demonstrated, not a minimum difference of morphology necessarily.
...yeah. I think I'm done here, pending an update from Professor Concerto.
All reproductive incompatibility has been "real" in this discussion.
A basis for categorizing a given reproductive incompatibility is the operation (mechanism, combination of mechanisms, etc) that caused it.
Just like there are felt-tip markers that are black verses those that are not, and times of day when the sun is up verses those when it is not, there are, I suggest, reproductive incompatibilities caused by operations that can be continually applied to produce successive populations where each is reproductively incompatible with its predecessor, and those that cannot.
So far, the former type of reproductive incompatibility inducing operation, which is essential to the evolution hypothesis, has not been shown to exist.
All of which has what, exactly, to do with speciation 'associated with "sufficient distinction" of overall morphology'?
The explanation in my previous post replaces "sufficient distinction" since that approach did not seem to get the meaning across.
Whatever. Have a good one.
What would be enough is a function of the extrapolatability of the operation (or set of operations) that produced the observed "speciation" such that the operation could be repeatedly applied to the extent of giving rise to something like the current biodiversity. That is what has to be demonstrated, not a minimum difference of morphology necessarily.
Fruit flies have been shown to evolve into species which are not able to interbreed with sibling populations*. One reason this may be said to be 'not reproducible to the extent of giving rise to something like the current biodiversity' is due to the morphological similarity between the two resultant, viable populations. How else are you saying that those incremental changes are not sufficient to 'give rise to the current biodiversity'?
*You havent also directly addressed this - but requiring that it be demonstrated with parent populations is an unnecessarily strict prescription. If a parent population can be shown to have resulted in humans and possums it is enough to show those two can't interbreed, it's not necessary to identify a parent population and demonstrate neither sibling can interbreed with that.
In fact, on the talkorigins page which was linked to refute my use of the quote, it is said:
Patterson goes on to acknowledge that there are gaps in the fossil record, but points out that this is possibly due to the limitations of what fossils can tell us. He finishes the paragraph with:
". . .Fossils may tell us many things, but one thing they can never disclose is whether they were ancestors of anything else."
It is actually this statement which is the key to interpreting the Sunderland quote correctly; it is not possible to say for certain whether a fossil is in the direct ancestral line of a species group.
". . .Fossils may tell us many things, but one thing they can never disclose is whether they were ancestors of anything else."
It is actually this statement which is the key to interpreting the Sunderland quote correctly; it is not possible to say for certain whether a fossil is in the direct ancestral line of a species group.
It seems talkorigins concedes my use of the quote. For a person to make up stories about what the fossils mean is like making up stories about Santa--how do you put that to the test? The question should rather be how to prove positively the claim, yet in many circles the unproven stories are accepted and it's assumed the fossils do more than they can. Above, both talkorigins and Patterson make salient points which if applied to evolutionary theory consistently would go a long way towards demonstrating its insufficiency.
The only difference between micro and macro evolution is the level at which the changes are ‘noticed’. The underlying mechanism of both are the same. Microevolution encapsulates changes below the species level. Macroevolution encapsulates changes above the species level.
Different species are defined as such if they’re unable to produce fertile offspring when they interbreed. Are you suggesting that if we take 2 monkeys of the same species, regardless of the number of mutations one of them experiences, they will always be able to interbreed together to produce fertile offspring? I hope not, since it is factually incorrect.
Why must microevolution stop before it begins to have an affect above the species level? You’re incorrectly assuming micro and macro evolution are totally separate things driven by totally different mechanisms. They’re not.
Different species are defined as such if they’re unable to produce fertile offspring when they interbreed. Are you suggesting that if we take 2 monkeys of the same species, regardless of the number of mutations one of them experiences, they will always be able to interbreed together to produce fertile offspring? I hope not, since it is factually incorrect.
Why must microevolution stop before it begins to have an affect above the species level? You’re incorrectly assuming micro and macro evolution are totally separate things driven by totally different mechanisms. They’re not.
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