Tag Archives: Common Ancestry

News

How biological convergence falsifies Darwinian evolution

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Cornelius Hunter, a software engineer / biologist with a Ph.D in bioinformatics from UIUC explains the latest discovery of biological convergence on his blog. (H/T Tweet from J. Warner Wallace)

Excerpt:

The theory of evolution states that the species arose spontaneously, one from another via a pattern of common descent. This means the species should form an evolutionary tree, where species that share a recent common ancestor, such as two frog species, are highly similar, and species that share a distant common ancestor, such as humans and squids, are very different. But the species do not form such an evolutionary tree pattern. In fact this expectation has been violated so many times it is difficult to keep track. These violations are not rare or occasional anomalies, they are the rule. Entire volumes have been written on them. Many examples are the repeated designs found in what, according to evolution, must be very distant species. Such evolutionary convergence is biology’s version of lightning striking twice. To explain this evolutionists must say that random mutations just happened to hit upon the same detailed, intricate design at different times, in different parts of the world, in different ecological niches, and so forth. The idea that the most complex designs we know of would spontaneously arise by themselves is, itself, not scientifically motivated and a real stretch of the imagination. But for the same intricate designs to arise independently by chance is even more of a stretch. That is why evolutionist’s claim this week that they have found evidence for convergent evolution was so intriguing.

[…]Though evolutionists sometimes deny biological convergence, it is a scientific fact. And a paper from this week added yet another example:

In mammals, hearing is dependent on three canonical processing stages: (i) an eardrum collecting sound, (ii) a middle ear impedance converter, and (iii) a cochlear frequency analyzer. Here, we show that some insects, such as rainforest katydids, possess equivalent biophysical mechanisms for auditory processing. Although katydid ears are among the smallest in all organisms, these ears perform the crucial stage of air-to-liquid impedance conversion and signal amplification, with the use of a distinct tympanal lever system. Further along the chain of hearing, spectral sound analysis is achieved through dispersive wave propagation across a fluid substrate, as in the mammalian cochlea. Thus, two phylogenetically remote organisms, katydids and mammals, have evolved a series of convergent solutions to common biophysical problems, despite their reliance on very different morphological substrates.

It is another curious example of biological convergence, so rather than attempt to deny the undeniable, evolutionists now claim it as another confirmation of evolution.

I’m a software engineer, and we re-use components all the time for different programs that have no “common ancestor”. E.g. – I can develop my String function library and use it in my web application and my Eclipse IDE plug-in, and those two Java programs have no common ancestry, but they do have a common designer. So you find the same bits in two different programs because I am the developer of both programs.

Previously, I blogged about another example of convergence reported by Science Daily. One of the predictions of intelligent design theory is that examples of convergence, which is really just re-use of common code by the designer, will be everywhere in nature. And that predictions just keeps getting confirmed as science marches forward, and the primitive religion of naturalism retreats.

News

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

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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.

Commentary

Is common descent supported by evidence from biogeography?

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Just FYI, I am delaying my mean anti-feminist post until 6 PM at least to check it over.

Mysterious Jonathan writing at Uncommon Descent.

Here’s his thesis:

Recently on this blog, I have been exploring and examining some of the genomic arguments for common descent. As I have been documenting in recent weeks, while the case for common ancestry — on the face of it — looks mightily strong, closer inspection reveals that the arguments don’t, in fact, stand up under more rigorous scrutiny. In the vast majority of instances, the corroborative data is very carefully cherry picked from the pertinent data set, and the non-congruent evidence is discarded or ignored.

And here’s a snippet:

One popular argument for common descent is the case from the discipline of biogeography — that is, the study of the geographical and historical distribution of species in relation to one another. The argument is based largely around the observation that species are related in accordance with their geographical proximity with respect to one another.

And here is the problem – this is dynamite:

So, when the biogeographical data does not accord with the predictions and expectations made by common descent, one always has ‘oceanic dispersal’ as an ad hoc fudge factor — including the rather remarkable claim that Monkeys made it across the Atlantic from Africa to South America! As Casey Luskin notes here, molecular studies claim that the South American monkeys diverged from the African monkeys around 35 million years ago. But Africa became an isolated island continent around 80 million years ago!

Apparently, monkeys rode on the back of the Flying Spaghetti Monster from Africa to South America.

I actually thought that the evidence for common descent was fairly good, because Behe accepts it and he is not a Darwinist. I didn’t like it, but facts are facts. But I’m glad that Jonathan is shedding some light on this issue. I would like to be able to argue against it, if the evidence is there.