Starting today August 7th, 2024, in order to post in the Married Couples, Courting Couples, or Singles forums, you will not be allowed to post if you have your Marital status designated as private. Announcements will be made in the respective forums as well but please note that if yours is currently listed as Private, you will need to submit a ticket in the Support Area to have yours changed.
MewtwoX said:No, we haven't learned that Gradualism is "dead" (or at least, the version of "gradualism" you appear to be referring to), but rather that Punctuated Equillibria plays as an additional "mechanism" in Evolutionary Development.
Again wrong, as this process has been shown time and again to lead to the development on beneficial mutations. Your previous attempts at disproof were shown false.
Does "transduction by retrovirus" mean anything to you?
The ToE does not go out of its way to specify all mutations that occur will be pure and perfect randomness; this is you trying to make a strawman. There's more to mutation than just copying errors, however the bulk of mutations are copying errors.
Your use of the term "gradualism" at the end of this point suggests that you don't have a firm understanding of what "gradualism" means.
Completely ridiculous.
Of COURSE.... no Evolutionary Biologist spends time discussing the nature of mutations in Evolution and its mechanics...
*cough*
http://www.talkorigins.org/faqs/mutations.html
http://www.talkorigins.org/faqs/information/infotheory.html
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=16908036&query_hl=1&itool=pubmed_docsum
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=16913914&query_hl=1&itool=pubmed_docsum
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=16893475&query_hl=1&itool=pubmed_docsum
*cough*
As for beneficial mutations...
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=16903693&query_hl=3&itool=pubmed_docsum
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=16882283&query_hl=3&itool=pubmed_docsum
Just two things to think about, in addition to the usual examples for beneficial mutations, mmkay?
It has been shown to you... time and again.
Very poor understanding of genetics. Single nucleotides can have larger affects, depending on what they change, whether they are alterations, indel or perhaps even whether they are naturally caused (tautomers) or not.
Think about this: A change in one amino acid of the Haemoglobin product leads to the development of Sickle Cell anemia.
one amino acid.
Also, think about this:
http://www.talkorigins.org/indexcc/CB/CB100.html
Its a short summary, but it introduces one idea you haven't talked about yet: the affects of Sexual reproduction on mutation rates.
Actually, I believe he is incorrect. There are mutations that lead to double stranded separation.
Translocations of entire chromosomes have occured and on a much lower scale, some indel mutations function by nucleotides being broken off by radiation.
http://en.wikipedia.org/wiki/Chromosomal_translocation
http://en.wikipedia.org/wiki/Transposable_element
Even by a logical deduction, if one mucleotide is changed, leading to a different amino acid, which has a chain reaction of effects (IE. the Sickle Cell Anemia example I showed you before) then a "single nucleotide" can be selected for.
O RLY?
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&dopt=AbstractPlus&list_uids=16893475&query_hl=3&itool=pubmed_docsum
It is known that phenotypes can change for non genetic reasons. It is also known that there are variations in phenotype for reasons outside of genetic and environmental reasons. We attribute these differences to developmental noise.
(An example: http://www.medscape.com/medline/abstract/12782415 )
No, the connection between the change and the genetic difference is established in experiments. In papers that do not account for this possibility, the only possible outcome is a shredding by the Peer Review committee.
Naked Assertion.
Fallacy of Composition.
Obviously hasn't been paying much attention to the scientific papers. Odd for a Geneticist, aint it?
Worth considering, for the number of claims that no "beneficial information" was made:
http://www.talkorigins.org/indexcc/CB/CB101_2.html
As for the nylon bug... its pretty much set that the mutation was neomorphic. The only ones who dispute this are the usual brand of Creationists, who are dismanted in the following articles quite nicely:
http://www.nmsr.org/nylon.htm
Since the rest is essentially the same things dealt with above, I'll ignore it... except for this:
There's only so many times one can say this before it reflects badly on the individual.
Supersport, your arguments are starting to appear to be more vengeful then academic... Isn't this unsettling to you?
supersport said:I have no idea.
supersport said:all those links to nonsense sites...all those hand-waving refutes -- the fact is, you have no answer for common sense and truth.
supersport said:I don't know about your first example...but just from your descriptions I can tell your bottom two examples of mutations adding information are not random. Random would mean RANDOM -- not as a result of an enviornmental change.
supersport said:all those links to nonsense sites...all those hand-waving refutes -- the fact is, you have no answer for common sense and truth.
JohnR7 said:The genetic information was there all along, but they try to use their magic to demonstrate that it just showed up out of nowhere.
supersport, you obviously don't have the slightest idea about the things you post -or should I better say cut and paste -on a daily basis, and yet you act like the sole authority on the subject.supersport said:all those links to nonsense sites...all those hand-waving refutes -- the fact is, you have no answer for common sense and truth.
I thank you for bringing up the sickle cell thing though...that's one I forgot to mention that's always brought up when evolutionists start talking about mutations. What this has to do with cumulative selection of beneficial random mutations I have no idea.
There is no mutiple lines of evidence that the things they call mutations are mutations at all. They have not shown or demonstrated that a mutation has taken place and they admit that they can not tell the difference between a mutated gene and a gene that has never "mutated".c'mon sense said:multiple lines of evidence that we have.
They have observed mutations. But they have not been observed in all the various places they claim they are happening.Chalnoth said:Mutation's not a theory. It's an observational fact.
Ever heard of a thing called sickle cell anemia?JohnR7 said:There is no mutiple lines of evidence that the things they call mutations are mutations at all. They have not shown or demonstrated that a mutation has taken place and they admit that they can not tell the difference between a mutated gene and a gene that has never "mutated".
Perhaps it could be that science has made some progress since 1866.Far to often instead of using Mendels genetics to explain something they try to use Darwin's theory with no evidence at all to back up what they are claiming.
Yes, and Thomas Edison didn't use a microwave, so those can't possibly be working either.You never once heard mendal say that the gene must have become mutated so that the pea came out wrinkled. Yet that is the nonsense you hear today.
If it is a observed fact in the hampsters then show me your observations. Line up the 50 year old DNA and show me where the DNA has mutated in order for all the vast array of different fur colors to be able to manifest themselves. They have a perfect control group to demonstrate their theory.Chalnoth said:Mutation's not a theory. It's an observational fact.
Ever hear of a syrian hampster?MrGoodBytes said:Ever heard of a thing called sickle cell anemia?
I am wondering, why do you think that this was caused by a mutation? Because it can be "good" & "bad" or because you do not find it in everyone.MewtwoX said:This example also serves to illustrate the ambiguity in defining certain mutations as "good" or "bad". Good in one place can be bad in another...
JohnR7 said:I am wondering, why do you think that this was caused by a mutation? Because it can be "good" & "bad" or because you do not find it in everyone.
Or do you call it a mutation because you have a control group and you can demonstrate where a copy error first took place and the sickle cell first appeared?
Or do you just assume a mutation created the gene?
JohnR7 said:There is no mutiple lines of evidence that the things they call mutations are mutations at all. They have not shown or demonstrated that a mutation has taken place and they admit that they can not tell the difference between a mutated gene and a gene that has never "mutated".
Sexual recombination is not enough to explain genetic diversity. However, in the process of crossing-over, strange things can happen to chromosomes and genes thereon.JohnR7 said:Far to often instead of using Mendels genetics to explain something they try to use Darwin's theory with no evidence at all to back up what they are claiming.
You never once heard mendal say that the gene must have become mutated so that the pea came out wrinkled. Yet that is the nonsense you hear today.