Evolution use the fossil record and DNA sequencing as proof of morphological changes. This is good science because it shows it happened somehow. However, IMO evolutionist have not explained the cause of this morphological change. They have theories and hypothesis but no proof. For example, small incremental steps are not a viable mechanism for large morphological changes. Evolutionist have new theories that explain how large changes can happen all at once. For example,1. Mutation of a switch: The switch mutation affects the way whole groups of genes are affected by one mutation. (Evo-devo)We could get into it on your Jonathan Wells tract, but what would be the point? The general scientific point - that small changes occur in populations due to selective pressure - isn't even at issue for the most devout creationist.
Though maybe you could follow this up and accuse Miller and Urey of fraud.
2. That there is part of our DNA that we thought wasn’t used. Rather, some believe it is used and is like an empty hard drive. It builds up information until it becomes useful.
3. Gene or DNA duplication: This is similar, because this duplicated DNA can build up useful mutations and has some starting point. This has been discussed some above.
4. Early mutations. A mutation early in an embryo’s development process has a better chance of causing morphological changes rather than mutations latter in the embryonic process.
According to scenarios 2-3, non-coding sections of the genome, or duplicated sections of coding regions, can experience a protracted period of “neutral evolution” during which alterations in nucleotide sequences have no discernible effect on the function of the organism. Eventually, however, a new gene sequence will arise that can code for a novel protein. At that point, natural selection can favor the new gene and its functional protein product, thus securing the preservation and heritability of both.
Stephen Myer quote from this article link
One problem with the isolated DNA strands, items 2 and 3, it that it relies on random mutation alone. There is no survival of the fittest mechanism. We have to wait until the whole process is finished by completely random events. In this way, the process resembles abiogenesis rather than a typical evolutionary process. They do the mathematics which shows absurd improbabilities. Dawkins has noted that scientific theories can rely on only so much “luck” before they cease to be credible.Stephen Myer quote from this articleThis scenario has the advantage of allowing the genome to vary through many generations, as mutations “search” the space of possible base sequences. The scenario has an overriding problem, however: the size of the combinatorial space (i.e., the number of possible amino acid sequences) and the extreme rarity and isolation of the functional sequences within that space of possibilities. Since natural selection can do nothing to help generate new functional sequences, but rather can only preserve such sequences once they have arisen, chance alone--random variation--must do the work of information generation--that is, of finding the exceedingly rare functional sequences within the set of combinatorial possibilities. Yet the probability of randomly assembling (or “finding,” in the previous sense) a functional sequence is extremely small.
In my own words, negative mutations add up and are cumulative in any isolated stand of DNA. The mutations end up destroying the genes functionality and its specific folding that made it functional. Also, the new protein has to fit into a new system or creating a new system by pure random events. Again, we do not have a survival of the fittest mechanism in isolated DNA. This adds a significant hurtle to the isolated DNA scenarios.Thus, although this second neo-Darwinian scenario has the advantage of starting with functional genes and proteins, it also has a lethal disadvantage: any process of random mutation or rearrangement in the genome would in all probability generate nonfunctional intermediate sequences before fundamentally new functional genes or proteins would arise. Clearly, nonfunctional intermediate sequences confer no survival advantage on their host organisms. Natural selection favors only functional advantage. It cannot select or favor nucleotide sequences or polypeptide chains that do not yet perform biological functions, and still less will it favor sequences that efface or destroy preexisting function.
Evolving genes and proteins will range through a series of nonfunctional intermediate sequences that natural selection will not favor or preserve but will, in all probability, eliminate (Blanco et al. 1999, Axe 2000). When this happens, selection-driven evolution will cease. At this point, neutral evolution of the genome (unhinged from selective pressure) may ensue, but, as we have seen, such a process must overcome immense probabilistic hurdles, even granting cosmic time.
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