I find it very revealing that the evolutionists here have been ducking and dodging simple questions, making excuses for being unable to provide a series of transitionals from 99.9% of the fossil record, obsessing on polyploids and guessing (wrong) about my motives for excluding them, and so on.
I had hoped to take this process step-by-step and get evolutionists to define the terms, chart what was reasonable and what wasn't, so that there would be no argument when we reached the conclusions that I had made up my own terms. But the evolutionists here are so terrified of saying anything that could be used as ammunition that they refuse to answer questions directly or deal with very simple issues and instead attempt to obscure the issues with meaningless terminology.
Unfortunately, my workload has just increased quite a bit so I can't play this game for a while. So here are some of the simple points I hoped to make:
Speciation: Evolutionists on this board repeatedly assert that speciation means reproductive isolation (the biological speciation concept) which is the first step toward macroevolution. Unfortunately for evolutionists, this cannot apply to (most) plants, because one of the mechanisms of change in plants is cross-breading, which produces polyploids with increased morphology due to the fact that these are natural hybrids. In these cases, you have what are already defined as TWO DIFFERENT SPECIES and they interbreed naturally, and create a THIRD new species. It violates the BSC definition during cross-breeding and again after the new species emerges, because it's entirely possible for the new species NOT to be reproductively isolated. Since this happens in 20-80% of all plants, this argues quite strongly that the whole concept of speciation is purely arbitrary, and can be redefined as needed to suit whatever argument for evolution you want to make. This is typical of evolutionist thinking - create definitions that support the theory and that way you can use them to declare the theory to be a fact.
Fossil record: I also wanted to exclude polyploids because they are clearly a different genetic mechanism of morphology than what one would have to assume is responsible for most evolution in just about anything but plants. (There are some polyploids in amphibians, etc., but these are rare.)
One would assume that just because plants are easily subject to cross-breeding doesn't mean they are immune to the other genetic mutations supposedly responsible for evolution in vertebrates. So if one wants to "test" the evolution of plants and invertebrates for the OTHER genetic mechanisms of adding information (morphology) in vertebrates (as in our reptile-to-mammal series), then one must exclude cross-breeding between different species as the most common means of creating new species and look at the remaining evidence to see if there is an equivalent reptile-to-mammal transition that occurred. If so, then one could confirm that this same mechanism (or some other non-polyploid mechanism) of mutation was occurring that could apply to vertebrates, plants and invertebrates.
Obviously, this didn't matter because nobody was able to come up with any meaningful series of transitions anyway.
But the bottom line is that IF the vertebrate series are dependable, and vertebrates make up 0.01% of the fossil record, then it should be EASY to find a better, more complete series with more fine-grained transitionals from the 99.9% of the record that includes invertebrates and plants. But the lack of evidence speaks for itself. Nobody was able to come up with such a series, and I doubt if anyone ever will.
THAT should tell you something right there. How can anyone believe in a theory that leave no evidence in 99.9% of the fossil record, but miraculously leaves evidence of transitions which we assume are true based on incomplete fossils (sometimes only one bone) gathered from scattered locations throughout the world (the creatures migrated from location to location as they evolved, I guess)? Because evolution didn't happen, but evolutionists will believe just about anything in order to salvage this crock.
Anyway, enjoy all your ad-hominem attacks, etc. I have other work to do.
I had hoped to take this process step-by-step and get evolutionists to define the terms, chart what was reasonable and what wasn't, so that there would be no argument when we reached the conclusions that I had made up my own terms. But the evolutionists here are so terrified of saying anything that could be used as ammunition that they refuse to answer questions directly or deal with very simple issues and instead attempt to obscure the issues with meaningless terminology.
Unfortunately, my workload has just increased quite a bit so I can't play this game for a while. So here are some of the simple points I hoped to make:
Speciation: Evolutionists on this board repeatedly assert that speciation means reproductive isolation (the biological speciation concept) which is the first step toward macroevolution. Unfortunately for evolutionists, this cannot apply to (most) plants, because one of the mechanisms of change in plants is cross-breading, which produces polyploids with increased morphology due to the fact that these are natural hybrids. In these cases, you have what are already defined as TWO DIFFERENT SPECIES and they interbreed naturally, and create a THIRD new species. It violates the BSC definition during cross-breeding and again after the new species emerges, because it's entirely possible for the new species NOT to be reproductively isolated. Since this happens in 20-80% of all plants, this argues quite strongly that the whole concept of speciation is purely arbitrary, and can be redefined as needed to suit whatever argument for evolution you want to make. This is typical of evolutionist thinking - create definitions that support the theory and that way you can use them to declare the theory to be a fact.
Fossil record: I also wanted to exclude polyploids because they are clearly a different genetic mechanism of morphology than what one would have to assume is responsible for most evolution in just about anything but plants. (There are some polyploids in amphibians, etc., but these are rare.)
One would assume that just because plants are easily subject to cross-breeding doesn't mean they are immune to the other genetic mutations supposedly responsible for evolution in vertebrates. So if one wants to "test" the evolution of plants and invertebrates for the OTHER genetic mechanisms of adding information (morphology) in vertebrates (as in our reptile-to-mammal series), then one must exclude cross-breeding between different species as the most common means of creating new species and look at the remaining evidence to see if there is an equivalent reptile-to-mammal transition that occurred. If so, then one could confirm that this same mechanism (or some other non-polyploid mechanism) of mutation was occurring that could apply to vertebrates, plants and invertebrates.
Obviously, this didn't matter because nobody was able to come up with any meaningful series of transitions anyway.
But the bottom line is that IF the vertebrate series are dependable, and vertebrates make up 0.01% of the fossil record, then it should be EASY to find a better, more complete series with more fine-grained transitionals from the 99.9% of the record that includes invertebrates and plants. But the lack of evidence speaks for itself. Nobody was able to come up with such a series, and I doubt if anyone ever will.
THAT should tell you something right there. How can anyone believe in a theory that leave no evidence in 99.9% of the fossil record, but miraculously leaves evidence of transitions which we assume are true based on incomplete fossils (sometimes only one bone) gathered from scattered locations throughout the world (the creatures migrated from location to location as they evolved, I guess)? Because evolution didn't happen, but evolutionists will believe just about anything in order to salvage this crock.
Anyway, enjoy all your ad-hominem attacks, etc. I have other work to do.