Tag Archives: Neo-Darwinism

Do non-coding segments of the genome provide evidence for common ancestry?

From Evolution News.

Excerpt:

Darwin’s tree of life might be visible in DNA, if DNA didn’t conspire to scramble the signal.

Now that quite a few genomes have been published, a team from Australia and France went on a Darwin fishing trip in the gene pool. In the largest study of its kind to date, they examined microsatellite markers (tandem-repeated DNA motifs of 1-6 base pairs) that are widespread in eukaryotic genomes. If neo-Darwinism is correct, these non-coding stretches of DNA should reflect the tree of common ancestry by showing similar mutational patterns in related groups.

Well, they don’t. The paper by Meglecz, Neve, Biffin and Gardner in PLoS ONE is titled, “Breakdown of Phylogenetic Signal: A Survey of Microsatellite Densities in 454 Shotgun Sequences from 154 Non Model Eukaryote Species.” What went wrong?

As the title implies, the team checked 154 “non-model” species. Darwinian evolutionists tend to focus on the model species, like a particular roundworm, the fruit fly Drosophila melanogaster, and a species of watercress, because their genomes are complete and most researchers use them in experiments. Problem: they may or may not be representative:

Although information for model species is accumulating rapidly, it is insufficient due to a lack of species depth, thus intragroup variation is necessarily ignored. As such, apparent differences between groups may be overinflated and generalizations cannot be inferred until an analysis of the variation that exists within groupshas been conducted. In this study, we examined microsatellite coverage and motif patterns from 454 shotgun sequences of 154 Eukaryote species from eight distantly related phyla (Cnidaria, Arthropoda, Onychophora, Bryozoa, Mollusca, Echinodermata, Chordata and Streptophyta) to test if a consistent phylogenetic pattern emerges from the microsatellite composition of these species.

Sounds like a good test. After all, scientists shouldn’t generalize on overinflated signals, right? The team expected to find nicely behaved data interpolated between the model species. It wasn’t to be:

It is clear from our results that data from model species provide incomplete information regarding the existing microsatellite variability within the Eukaryotes. A very strong heterogeneity of microsatellite composition was found within most phyla, classes and even orders. Autocorrelation analyses indicated that while microsatellite contents of species within clades more recent than 200 Mya tend to be similar, the autocorrelation breaks down and becomes negative or non-significant with increasing divergence time. Therefore, the age of the taxon seems to be a primary factor in degrading the phylogenetic pattern present among related groups. The most recent classes or orders of Chordates still retain the pattern of their common ancestor. However, within older groups, such as classes of Arthropods, the phylogenetic pattern has been scrambled by the long independent evolution of the lineages.

There are two ways to interpret this anomaly. One is that microsatellites mutate too fast to maintain the phylogenetic signal. (This is known as a “post hoc rationalization.”)

The other is that Darwin was wrong. Data do not show a phylogenetic pattern; they show common design with some variation.

Read the rest here. I’m a skeptic on common ancestry, but not for religious reasons. I just don’t think that it’s compatible with the progress of science.

Melissa previews the new Illustra Media ID documentary

From Hard-Core Christianity.

Excerpt:

Last summer, I had the privilege of attending lectures by one of the scientists featured in the upcoming Illustra Media documentary, Metamorphosis. Dr. Paul Nelson explained the science behind this unique argument for intelligent design theory, and I’ve been waiting with bated breath for the film’s resease ever since!

The intelligent design argument presented by the film (which I understand isn’t discussed until the third part) is the enormous problem that insect metamorphosis poses for the theoretical neo-Darwinian descent pathways. In plain language, neo-Darwinism claims that random genetic mutations coupled with natural selection acting over greats spans of time are responsible for a caterpillar’s physical ability to transform into a butterfly. There’s an insurmountable obstacle for this alleged process, however.

When it enters the pupa phase, in which it forms a hard chrysalis around itself, the caterpillar’s body totally liquefies. Subsequently, an entirely new body plan is constructed from this chemical soup, and what emerges from the chrysalis is absolutely nothing like what went in. Now, according to neo-Darwinism, mutations that equip an organism for such a spectacular metamorphosis are cumulative. The mutations that dictate chrysalis formation would come first. Next would come mutations that cause body-liquefication. Next would come—uh-oh—do you see the problem here? If a caterpillar goes into a pupa stage without the necessary genetic information to build the new body structure and GET OUT OF the pupa stage (an “escape plan,” if you will), it would simply die inside the chrysalis, never to emerge. Thus, there is NO ADVANTAGE for natural selection to act upon, and the process of metamorphosis could never evolve. What would be needed here is for the caterpillar to acquire ALL the mutations necessary for the pupa phase and ALL the mutations necessary for the architecture of a survivable adult body plan AT THE SAME TIME. Based on what evolutionary biology teaches about how mutations accumulate, this simply isn’t going to happen. This is a case of all-or-nothing that argues strongly for intentional, intelligent design.

If you want to see the first three in the series, look here:

About Melissa:

Melissa is a graduate student at Biola University, studying for the Master of Arts in Science and Religion. She holds a Bachelor’s degree in biology and worked in biotechnology and pharmaceutical research for five years after obtaining her undergraduate degree. She has spent more than a decade studying the science and philosophy pertaining to the origins debate and is also currently working toward her certification in general Christian apologetics from Biola. She directs The Woodlands chapter of Reasonable Faith and welcomes opportunities to speak and teach on scientific apologetics.

She also is a homeschooling mom, which is the best kind of mom.

Assessing the evidence in favor of common ancestry

An article from Evolution News that takes a statement from an evolutionist who supports common descent, and then then refutes it point by point.

Here’s the case for common descent:

UCA is now supported by a wealth of evidence from many independent sources, including: (1) the agreement between phylogeny and biogeography; (2) the correspondence between phylogeny and the palaeontological record; (3) the existence of numerous predicted transitional fossils; (4) the hierarchical classification of morphological characteristics; (5) the marked similarities of biological structures with different functions (that is, homologies); and (6) the congruence of morphological and molecular phylogenies.

(Douglas L. Theobald, “A formal test of the theory of universal common ancestry,” Nature, Vol. 465:219-222 (May 13, 2010).)

And here’s a response to each of those points:

Before I read this post, I only knew about 3, 4, 5 and 6.

I thought that I would post this because I haven’t said much about common descent before. I’m against it.