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I saw an article on George W. Bush the other day, and it showed pictures of him as a baby, at age 6, at age 9, at age 18, at age 25, and at his present age. Did he grow up in a continuum, or did he abruptly go from being a baby to age 6?
You know, people say that Star Wars was shot using real actors, but if you look at the actual reels of film, you just see a series of discrete photos, each slightly different from the next. Does that mean that the whole film was actually animated?
Have you ever seen all the transitional forms from Eohippus to Equus, laid out in a row?
Let me put it this way: do you believe in paternity tests? Do you believe that use of DNA fingerprinting can establish whether people are related? Because very sophisticated forms of DNA fingerprinting have not only reconstructed the family tree of living things, but that tree agrees with the one constructed from the fossil evidence.
Let’s also suppose you compare the DNA from humans and, say, chimps. The number of silent mutations will be greater than the number of mutations which actually have an effect.
There are also things called pseudogenes, which are genes that got eroded away by mutations because there was no selectional pressure to keep them. For example, the common ancestor of primates ate a lot of fruit, and didn’t need the gene to synthesise vitamin C, so that gene got switched off by deleterious mutations. If you look at pseudogenes across species, you see that the pseudogenes are precisely where you would expect them to be if they were being inherited as new species arose from pre-existing species. Moreover, the portions of the pseudogene which used to be coding regions have accumulated a number of mutations intermediate between what you see for normal coding regions and for silent mutations.
There are also processed pseudogenes. When a gene is activated, a copy of it is made from RNA and it undergoes a number of different kinds of processing. Sometimes it accidentally gets spliced back into DNA as a pseudogene. If you look at the DNA of different species, you see, once again, that these pseudogenes are inherited by new species just as children inherit their parents’ genes.
As for segregational load:
remember Mendelian genetics, where species could have a dominant allele “A” and/or a recessive allele “a” at a particular genetic locus? Let’s suppose (to take a real-life example) that there is a species of butterfly which can have a gene “A” for red forewings or a gene “B” for blue hindwings at a particular locus. The butterflies can then be homozygous, and be “AA” (and have red forewings) or “BB” (and have blue hindwings.) They can also be heterozygous, and be “AB” (and have red forewings and blue hindwings.) “AB” butterflies look like a different species of poisonous butterfly, so birds don’t eat them. The problem is that if two AB butterflies mate, some of their offspring will be AB, but some will also be AA and BB. AA and BB butterfiles get eaten, because they don’t have the full camouflage. The birds don’t mistake them for poisonous butterflies, so the extra coloration just makes them stand out. This is called “segregational load”; heterozygotes have a big advantage, but since some of their offspring will always be homozygous, a lot of their offspring end up getting killed.
If a chromosomal rearrangement duplicates the genetic locus, then that produces a big evolutionary advantage for the butterfly, because its offspring can be AA at one copy of the locus and BB at the other copy of the locus. Eventually all the butterflies will have the duplicate locus, because all of their offspring will be able to have both the A gene for red forewings and the B gene for blue hindwings.
So the question is, if creationism is true, why did God create organisms which have segregational load?
-Ben