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Why do I have a sudden urge to go read up on Thalidomide?
..Once you have changes that will produce a new species, there is nothing to stop multiple speciations spread thru time producing humans from "another form of life"...
Wah, woah, what? You seem to show you understand the theory, but then come out with this strange non sequitur. The principle doesn't become invalid just because there's no evidence for it. And besides, there is evidence for it. Do you deny that there are such things as mutations?Most of evolution theory can be rechecked and tested for viability. The parts that can't are those that take more multiple human generations to produce substantial change from random or directed random mutations. Suffice to say that if mutations were good, then species exposed to larger amounts of radiation would be better adapted than those shielded from mutation causing radiation. Since we have no evidence for that, then the whole "random mutations as a source of new life forms" is invalid.
New chromosomes do indeed get added by mutation, and we've seen it happen. Ever heard of Down's syndrome? While it's obviously a detriment, it's nonetheless proof that a mutation that increases the number of chromosomes isn't necessarily fatal. Chromosome replication that is either beneficial or neutral would exist in subsequent generations, and mutations on this 'bonus' chromosome would eventually lead to it being unique and distinct among the genome: instead of being a redundant clone, it now holds vital genetic information.Natural selection and forced selection of varieties of species can produce changes in populations. Dogs have been bred with certain characteristics for certain desired uses. While a DNA has been selected from the variations, no new DNA has been added. Evolution theory covers how changes occur to DNA but does not cover how DNA was formed or how new chromosomes get added to create different forms of life.
Well, we've seen it happen. It follows directly from theoretical analysis of genetic flow in population dynamics, and we've seen it happen naturally in the wild, accidentally in human habitat, and artificially in the lab.Evolutionists are at their boldest (and stretching) when stating that one species can evolve into another.
No, we don't, because we know that it isn't meant to. That's like saying germ theory doesn't explain how atoms behave; well, yea, of course it doesn't, but it's not meant to. Atomic behaviour is dealt with by other theories. Likewise, the origin of life and DNA is dealt with by abiogenesis, a distinction Creationists can't seem to get their heads around.That's not saying much. And it certainly doesn't explain the origins of DNA, why DNA works so hard to correct errors, the adding of chromosomes, or the creation of new forms of life. But they have faith that it does.
DNA has self-repair mechanisms that repair most all changes.
There certainly are DNA repair enzymes, for instance for repair of thymine dimers induced on sun exposure. People with defective DNA repair enzymes have a condition known a Xeroderma pigmentosum and must carefully avoid even the slightest sun exposure or they develop multiple basal cell and squamous cell carcinomas. However, these enzymes are not 100% efficient or no one would get sun induced skin cancer. But these mutations are not passed on in any case. It is obvious that many mutations in the germ line are passed on or there would not be be huge number of single nucleotide and other polymorphisms in the human genome.DNA has self-repair mechanisms that repair most all changes.
There certainly are DNA repair enzymes, for instance for repair of thymine dimers induced on sun exposure. People with defective DNA repair enzymes have a condition known a Xeroderma pigmentosum and must carefully avoid even the slightest sun exposure or they develop multiple basal cell and squamous cell carcinomas. However, these enzymes are not 100% efficient or no one would get sun induced skin cancer. But these mutations are not passed on in any case. It is obvious that many mutations in the germ line are passed on or there would not be be huge number of single nucleotide and other polymorphisms in the human genome.
There certainly are DNA repair enzymes, for instance for repair of thymine dimers induced on sun exposure. People with defective DNA repair enzymes have a condition known a Xeroderma pigmentosum and must carefully avoid even the slightest sun exposure or they develop multiple basal cell and squamous cell carcinomas. However, these enzymes are not 100% efficient or no one would get sun induced skin cancer. But these mutations are not passed on in any case. It is obvious that many mutations in the germ line are passed on or there would not be be huge number of single nucleotide and other polymorphisms in the human genome.
There certainly are DNA repair enzymes, for instance for repair of thymine dimers induced on sun exposure. People with defective DNA repair enzymes have a condition known a Xeroderma pigmentosum and must carefully avoid even the slightest sun exposure or they develop multiple basal cell and squamous cell carcinomas. However, these enzymes are not 100% efficient or no one would get sun induced skin cancer. But these mutations are not passed on in any case. It is obvious that many mutations in the germ line are passed on or there would not be be huge number of single nucleotide and other polymorphisms in the human genome.
Any beneficial mutations you can point to that show promise of improving the organism that failed to destroy the mutant DNA first?
I've read this 3 times now and it still doesn't make any sense.
SW, how much do you know about DNA and genetics?
Sickle-cell anaemia. A mutation that helps fight malaria. It is more likely to occur in those of sub-Saharan descent (i.e., places where malaria is strong).I agree. I can't figure out the beneficial mutations claim either.
Go figure.
"I can now assure you that the ability to comprehend descent with modification, natural selection, speciation, and other related concepts can be easily taught to kindergartners and first-graders. "
I suggest making the clearest case at a 10th grade level.
Do you know why your doctor tells you to finish your antibiotic even though you think you may be over your disease?I agree. I can't figure out the beneficial mutations claim either.
Go figure.
Maybe this is your problem"I can now assure you that the ability to comprehend descent with modification, natural selection, speciation, and other related concepts can be easily taught to kindergartners and first-graders. "
I suggest making the clearest case at a 10th grade level
Because of adaptation?Do you know why your doctor tells you to finish your antibiotic even though you think you may be over your disease?
Most of evolution theory can be rechecked and tested for viability. The parts that can't are those that take more multiple human generations to produce substantial change from random or directed random mutations.
Suffice to say that if mutations were good, then species exposed to larger amounts of radiation would be better adapted than those shielded from mutation causing radiation.
Since we have no evidence for that, then the whole "random mutations as a source of new life forms" is invalid.
Natural selection and forced selection of varieties of species can produce changes in populations. Dogs have been bred with certain characteristics for certain desired uses. While a DNA has been selected from the variations, no new DNA has been added.
Evolution theory covers how changes occur to DNA but does not cover how DNA was formed
or how new chromosomes get added to create different forms of life.
Evolutionists are at their boldest (and stretching) when stating that one species can evolve into another. That's not saying much.
And it certainly doesn't explain the origins of DNA, why DNA works so hard to correct errors
the adding of chromosomes, or the creation of new forms of life.
But they have faith that it does.
Which can occur through either horizontal gene transfer from other bacteria but also occurs because of mutations that produce antibotic resistance in the orginal bacteria. If you don't treat long enough you can leave a small pool of organisms that have some resistance to the antibiotic and they can give you an infection that will require a different antibiotic. You can also get some surprises. After taking a fairly long course of oral erythromycin for an infection, which was cured, We were able to culture a significant population of erythomycin resistant bacteria from swabs of the skin on my face. This probably came from the drug since I don't normally use antibacterial soaps or lotions on my face.Because of adaptation?
And so the point is what? that man came before whales, contrary to what the Bible says?Which can occur through either horizontal gene transfer from other bacteria but also occurs because of mutations that produce antibotic resistance in the orginal bacteria. If you don't treat long enough you can leave a small pool of organisms that have some resistance to the antibiotic and they can give you an infection that will require a different antibiotic. You can also get some surprises. After taking a fairly long course of oral erythromycin for an infection, which was cured, We were able to culture a significant population of erythomycin resistant bacteria from swabs of the skin on my face. This probably came from the drug since I don't normally use antibacterial soaps or lotions on my face.
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