How does the data from the Cambrian Explosion argue for/against the evolutionary model(s)?
What is special about the Cambrian explosion is the relatively short time in which life seems to have evolved. The question for evolutionists is, how did such a wide range of life evolve in so short a period of time?
The earliest morphological evidence for life is 3.5 billion years old, fossils of stromatolites (colonies of cyanobacteria) and single, undifferentiated cells, or Prokaryotes. For 1.6 billion years these simple cells were the only kind of living organism, until the arrival of Eukaryotes, or single cells with differentiated nuclei and cell organelles. Although representing a large leap in complexity, the Eukaryotes were still only single cells or cell aggregates. It was another 1.4 billion years before complex, multicellular life made an appearance in the form of the Ediacaran faunas (see fossils), followed by all the variety of the true Cambrian animals about 550 million years ago.
Therefore 80% of the history of life on Earth is exclusively single or undifferentiated multi-cellular. 3 billion years went by before complex multicellular life appeared, but when it did it only took between 5 and 10 million years for all the basic body plans of the organisms we see around us today to be established. This is why the origin of multicellular life, in particular the metazoans or large animals with complex body plans, is termed the Cambrian explosion.
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The Cambrian explosion
Though dates vary, the Cambrian layer roughly started 550 MYA and lasted roughly 50 million years. Within the Cambrian period is the Cambrian explosion that is estimated to have lasted between 5 and 17 million years. In this time, most all the modern phyla are found in the Cambrian. The estimates of the number of phyla vary, but generally is around 50.
The Cambrian Explosion is the radiation of animal phyla that started about 570 million years ago, which is 30 million years after the beginning of the Cambrian geologic period, and lasted between 5 and 17 million years through much of the early Cambrian.
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Wikipedia
The Cambrian is a geologic period that began around 542 million years ago and ended about 490 million years ago. The Cambrian Period is the earliest period in whose rocks are found numerous large, distinctly-fossilizable multicellular organisms more complex than sponges or medusoids. During this time, roughly fifty separate major groups of organisms or "phyla" (including almost all the basic body plans of modern animals) emerged suddenly, in most cases without evident precursors. This radiation of animal phyla is referred to as the Cambrian Explosion
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Free Dictionary
50 is the number of phyla found in the Cambrian layer, but only 38 exist currently. So, there was actually
more phyla in the past than now. This poses a serious anomaly for proponents of common descent. Common descent should predict that more phyla would evolve over time, not an immediate explosion of phyla and a decrease over time.
A simple way of putting it is that currently we have about 38 phyla of different groups of animals, but the total number of phyla discovered during that period of time (including those in China, Canada, and elsewhere) adds up to over 50 phyla. That means [there are] more phyla in the very, very beginning, where we found the first fossils [of animal life], than exist now.
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Explosion of Life
Probably the only peer-reviewed article challenging evolutionary theories in regards to the evidence of the Cambrian explosion was just published this year by SC Meyer -
The origin of biological information and the higher taxonomic categories Proceedings of the Biological Society of Washington, 117[2]:213-239, August 4, 2004.
It makes for interesting reading and has (predictably) caused quite a
reaction among evolutionary proponents.
SC Meyer wrote:
The "Cambrian explosion" refers to the geologically sudden appearance of many new animal body plans about 530 million years ago. At this time, at least nineteen, and perhaps as many as thirty-five phyla of forty total (Meyer et al. 2003), made their first appearance on earth within a narrow five- to ten-million-year window of geologic time. Many new subphyla, between 32 and 48 of 56 total (Meyer et al. 2003), and classes of animals also arose at this time with representatives of these new higher taxa manifesting significant morphological innovations. The Cambrian explosion thus marked a major episode of morphogenesis in which many new and disparate organismal forms arose in a geologically brief period of time.
He argues that it is highly improbable for random mutations alone to account for the development of complex life forms in the period of the Cambrian explosion. Life would have had to have evolved in many different ways, including protein evolution, cell evolution, and body plan evolution.
Regarding protein evolution, the chance of just a 150 residue protein producing a functional protein by mere chance is 1 in 10E77.
Thus, the probability of finding a functional protein among the possible amino acid sequences corresponding to a 150-residue protein is similarly 1 in 10E77.
Given these odds, just for a 150 residue protein to have evolved in less than 50 million years is highly improbable. Of course, life contains proteins much more complicated than this, so the odds increases even more to explain what we see in the Cambrian explosion.
Some can argue that random mutations will have mostly neutral effects and the functional mutations will gradually increase over time. However, mutagenesis experiments show that there is more functional loss over time than functional gain.
Thus, Axe's results imply that, in all probability, random searches for novel proteins (through sequence space) will result in functional loss long before any novel functional protein will emerge.
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.
For a new cell to arise, new combinations of proteins must arise simultaneously from either existing proteins or new proteins. This further decreases the statistical probability of the origin of new cells.
Thus random variations must, again, do the work of information generation--and now not simply for one protein, but for many proteins arising at nearly the same time. Yet the odds of this occurring by chance alone are, of course, far smaller than the odds of the chance origin of a single gene or protein--so small in fact as to render the chance origin of the genetic information necessary to build a new cell type (a necessary but not sufficient condition of building a new body plan) problematic given even the most optimistic estimates for the duration of the Cambrian explosion.
So, he states that the Cambrian explosion does not give evolution enough time to produce all the life that is found in the Cambrian layer.
The sensitivity of proteins to functional loss, the need for long proteins to build new cell types and animals, the need for whole new systems of proteins to service new cell types, the probable brevity of the Cambrian explosion relative to mutation rates--all suggest the immense improbability (and implausibility) of any scenario for the origination of Cambrian genetic information that relies upon random variation alone unassisted by natural selection.
He also brings up that genetic mutation is not sufficient for morphological changes.
Significant morphological change in organisms requires attention to timing. Mutations in genes that are expressed late in the development of an organism will not affect the body plan. Mutations expressed early in development, however, could conceivably produce significant morphological change (Arthur 1997:21). Thus, events expressed early in the development of organisms have the only realistic chance of producing large-scale macroevolutionary change (Thomson 1992). As John and Miklos (1988:309) explain, macroevolutionary change requires alterations in the very early stages of ontogenesis.
Yet recent studies in developmental biology make clear that mutations expressed early in development typically have deleterious effects (Arthur 1997:21). For example, when early-acting body plan molecules, or morphogens such as bicoid (which helps to set up the anterior-posterior head-to-tail axis in Drosophila), are perturbed, development shuts down (Nusslein-Volhard & Wieschaus 1980, Lawrence & Struhl 1996, Muller & Newman 2003).
This problem has led to what McDonald (1983) has called "a great Darwinian paradox" (p. 93). McDonald notes that genes that are observed to vary within natural populations do not lead to major adaptive changes, while genes that could cause major changes--the very stuff of macroevolution--apparently do not vary. In other words, mutations of the kind that macroevolution doesn't need (namely, viable genetic mutations in DNA expressed late in development) do occur, but those that it does need (namely, beneficial body plan mutations expressed early in development) apparently don't occur.6 According to Darwin (1859:108) natural selection cannot act until favorable variations arise in a population. Yet there is no evidence from developmental genetics that the kind of variations required by neo-Darwinism--namely, favorable body plan mutations--ever occur.
Developmental biology has raised another formidable problem for the mutation/selection mechanism. Embryological evidence has long shown that DNA does not wholly determine morphological form (Goodwin 1985, Nijhout 1990, Sapp 1987, Muller & Newman 2003), suggesting that mutations in DNA alone cannot account for the morphological changes required to build a new body plan.
These considerations pose another challenge to the sufficiency of the neo-Darwinian mechanism. Neo-Darwinism seeks to explain the origin of new information, form, and structure as a result of selection acting on randomly arising variation at a very low level within the biological hierarchy, namely, within the genetic text. Yet major morphological innovations depend on a specificity of arrangement at a much higher level of the organizational hierarchy, a level that DNA alone does not determine. Yet if DNA is not wholly responsible for body plan morphogenesis, then DNA sequences can mutate indefinitely, without regard to realistic probabilistic limits, and still not produce a new body plan. Thus, the mechanism of natural selection acting on random mutations in DNA cannot in principle generate novel body plans, including those that first arose in the Cambrian explosion.