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The Cambrian "Explosion"


Abstract

This page describes the metazoan (animal) evolutionary phenomenon popularly known as the "Cambrian explosion." The apparent discrepancy between divergence ages implied by genetic calibration techniques and a literal interpretation of the fossil record is discussed.

Keywords: Cambrian, Cambrian biota, Cambrian explosion, Cambrian radiation, fossil record, evolution, Metazoan radiation

Introduction

The base of the Cambrian System and Period is defined at a certain locality in Newfoundland, at a horizon where a particular trace fossil, known as Trichophycus (formerly Phycodes) pedum, makes its first appearance. This horizon has been reliably dated as 543 ± ?? million years (Ma) old. There are very few fossil animals of this age, here or anywhere else in the world. The earlier, widespread Ediacaran assemblage has all but disappeared, leaving only a few, general tiny, shelly organisms, collectively known as the small shelly fauna, on stage for the next ~13 Ma: the strangely quiescent Nemakit-Daldynian Age. Then, apparently very suddenly, starting at the beginning of the Tommotian Age (~530 Ma), almost all of the animal phyla known today appear in the fossil reocrd in rapid succession.

This abrupt appearance of a diverse and highly derived fauna in the brief Tommotian and Atdabanian Ages of the Early Cambrian is widely known as the 'Cambrian Explosion.' Although that particular phrase only came into common usage in the early to mid 1970s, the event itself has long been recognised as a phenomenon demanding some accommodation from evolutionary theory. As early as 1859, Charles Darwin drew attention to the matter in Origin of Species, and it is probable he had considered the matter for many years prior to that.

However, despite the rapid proliferation of evolutionary novelties which undoubtedly occurred at this time, at least some of the phenomenon is attributable to the acquisition of preservational characteristics - 'hard parts' - and multiple lines of evidence reveal that life was already highly diversified prior to the Tommotian.

The fossil record is continually yielding more and better evidence of pre-Tommotian life, from the earliest biochemicals extracted from ~3,800 Ma cratonic rocks of southwest Greenland, through the perplexing grotesquery of the Ediacarans. Yet despite these finds, paleontological evidence does not generally corroborate molecular clock studies which almost invariably indicate animal origins lying very deep within the Proterozoic  (contrary to the almost bizarre view expressed in Ayala et al. 1998). Bruce Runnegar (1982, p. 397) notes: "Few of the known late Precambrian animals have been closely related to Cambrian organisms, and none of the associated or coeval trace fossils has been thought to have been produced by the animals observed more directly. … What the trace fossil record does tell us, is that there were few large, mobile, bottom-dwelling animals before the end of the [Vendian]."

[Also see Xiao & Knoll 2000, top of p. 785a.]

 
 

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The Tommotian and Atdabanian Ages (530 to 519 Ma)

The oldest known shelly fossils, simple tubes of the family Cloudinidae, first appear very near the end of the Proterozoic. Shelly fossils become more common and more diverse in the basal Cambrian – comprising the so-called ‘small shelly fauna’ – but this radiation is modest compared to the explosive diversification of the late Early Cambrian, a phenomenon which has come to be known as the Cambrian Explosion.

"This explosion is perhaps the most striking single event documented by the fossil record. In the strict sense, the explosion refers to a geologically abrupt appearance of fossils representing all except two of the living [animal] phyla that had durable (easily fossilizable) skeletons. One of those two phyla is the Porifera (sponges), which was present in the fossil record at an earlier time. The other is the Bryozoa, a phylum that contains some soft-bodied groups and may well have been present but not yet skeletonized. A number of enigmatic organisms of obscure relationships also appear during the explosion, enriching the early Cambrian fauna. Precision dating indicates that the explosion began at 530 Ma (million years ago) and ended before 520 Ma" (Bowring et al. 1993 ???).
For a very long time, non-shelly fossils were unknown or poorly understood, the metazoan status of the Ediacarans was famously a matter of debate, and other lines of evidence had yet to be discovered. Thus, as far as anybody could be sure, the shelly fossil record was a literal record of metazoan evolution, and it seemed to be telling us that in the late Early Cambrian animals diversified explosively from almost nothing to approximately the full range of basic archetypes known today, in as little as 10 million years.
However, "[t]he presence of true, though soft-bodied, triploblasts is now documented by worm burrows, by radular markings and body impressions of early mollusks, and by phosphatised embryos, of Vendian age" (Seilacher et al. 1998, p. 80). Some, such as Kimberella and Parvancorina, can even be tentatively assigned to extant phyla. Nevertheless, although recent discoveries have greatly extended the record of sponges and bilateral animals, the earliest unequivocal paleontological evidence of metazoan life is no more than 600 Ma (Bromham et al. 1998, p. 12386).
Whereas a literal interpretation of the Cambrian fossil record requires the near-simultaneous, ‘late arrival’ of nearly all metazoan phyla, recent genetic evidence reveals a different pattern, sometimes known as the ‘slow burn’ or ‘early arrival’ hypothesis. Age estimates derived from calibrated gene divergence studies tend to vary considerably today – the science is new – but a consistent pattern emerges, nevertheless. These studies all conclude that the major animal groups became separated from one another hundreds of millions of years before the Cambrian. Some studies (e.g. the classic Wray et al. 1996) place the age of the primary division of animals into protostomes and deuterostomes at around 1,200 Ma – much more than twice the age of the Cambrian Explosion.
The Cambrian Explosion documents a real and dramatic radiation of skeletal morphologies, which might represent the parallel uptake of skeletonisation by numerous pre-existing, soft-bodied lineages or, alternatively, a rapid diversification within a relatively few already-skeletonised lineages. The resulting morphological disparity – as measured by the number of major animal types – was at least as great as the present. "Analysis of animal skeletons in relation to the multivariate, theoretical ‘Skeleton Space’ has shown that a large proportion of these options are used in each phylum. [The] structural elements deployed in the skeletons of Burgess Shale animals (Middle Cambrian) incorporate 146 of 182 character pairs defined in this morphospace. Within 15 million years of the appearance of crown groups of phyla with substantial hard parts, at least 80 percent of skeletal design elements recognised among living and extinct marine metazoans were exploited" (Thomas et al. 2000, p. 1239). However, the species diversity produced by the Cambrian radiation, judged at the familial and generic levels, was much below that of succeeding periods (there are more than four times as many marine families today).
"The Early Cambrian metazoan radiation was accompanied by a marked diversification of organic-walled microorganisms. Early Cambrian protists include prasinophyte and dasyclad green algae, benthic foraminifers, and a diversity of acritarchs. Prokaryotes are represented by the carbonaceous and calcified remains of cyanobacteria, as well as by biogeochemical signatures, both isotopic and molecular" (Knoll 1996, p. 51).

Duration

"A span of 40 million years embraces the appearance of the first small, simple shells that may have been secreted by metazoans and the subsequent exuberant diversity of Chengjiang and the Burgess Shale. This is not so short a time for an evolutionary ‘explosion.’ However, the proliferation of animals with well-differentiated hard parts characteristic of specific metazoan phyla was largely restricted to the last 15 million years of this interval" (Thomas et al. 2000, p. 1239).

The application of absolute dates "to the boundaries of the Stages of the Lower Cambrian remains a difficult stratigraphic problem, but it is likely that the most critical Stages, the Tommotian and Atdabanian, are probably only 8-10 [million years] in duration; over 50 metazoan orders first appear in the [fossil] record during that interval (Valentine et al. 1991)" (Valentine 1995, p. 89). As noted above, precision dating has now constrained the major Cambrian radiation to the interval 530 to 520 Ma (Bowring & Erwin 1998).

Genes or Skeletons?

Charles Darwin (1859, p. 308) recognised that the sudden appearance of a diverse and highly derived fossil fauna in the Cambrian posed a problem for his theory of natural selection, "and may be truly urged as a valid argument against the views here entertained." Two obvious possibilities are that animal life did, indeed, evolve very abruptly about that time, or, alternatively, had existed long before, but that, for whatever reason, we have failed to find fossil evidence: the "late-" and "early-arrival" models, respectively.

The two patterns – Cambrian Explosion versus a very long (though obscure) metazoan history – are not necessarily incompatible, because they are based upon different criteria. The genetic evidence documents lines of descent and inheritance, irrespective of morphology, whereas the fossil record documents only the external expression of the genes.

Late-Arrival Models

The ‘late arrival’ model embodies a literal interpretation of the fossil record: that the evolution of the main animal groups took place both late in Earth’s history, and as we now know, extremely rapidly.

What kind of mechanisms could have prompted such an accelerated pace of evolution? Various proposals have been advanced over the years, including:
  • A response to the evolution of Hox genes (Erwin et al. 1997).
  • A rise in macroscopic predation perhaps leading to an ‘arms-race’ style of evolution (Conway Morris 2000). Note, however, that the specific suggestion by Parker (2003) that such an arms race could have been fuelled by the acquisition of high-resolution vision in one or more groups, seems highly implausible (see the review by Conway Morris for a detailed critique).
  • Finally, perhaps we can look to the lifting of some external constraint such as insufficient atmospheric oxygen (Runnegar 1982; Brasier 1998, p. 548; Adouette et al. 2000, p. 4455).
Nowhere is the late-arrival model more eloquently discussed than in Stephen Gould’s Wonderful Life (Gould 1989), though nearly everyone would now agree that, in this book, Gould overstated his case by some orders of magnitude.

(Read more.)

Early-Arrival Models

Darwin himself preferred the early-arrival explanation, noting that "before the lowest Silurian [the Cambrian system had not yet been recognised] stratum was deposited, long periods elapsed, as long as, or probably far longer than, the whole interval from the Silurian age to the present day; and that during these vast, yet quite unknown, periods of time, the world swarmed with living creatures" (Darwin 1859, p. 307).

Today we might regard Darwin’s views as wonderfully prescient, for numerous Precambrian fossils have now indeed been collected, and modern techniques – impossible in Darwin’s day – such as ‘molecular clock’ studies, strongly indicate metazoan evolutionary events having occurred deep within the Precambrian.
There can be little doubt, on the basis of trace evidence alone, that bilaterian metazoans existed in the Vendian, and possibly early in the Vendian. Although some traces are simple, rather featureless, winding trails, "others display transverse rugae and contain pellets that can be interpreted as of fecal origin. The bilaterian nature of these traces is not in dispute. Furthermore, such traces must have been made by worms, some of which had lengths measured in centimetres, with through guts, which were capable of displacing sediment during some form of peristaltic locomotion, implying a system of body wall muscles antagonized by a hydrostatic skeleton. Such worms are more complex than flatworms, which cannot create such trails and do not leave fecal strings" (Valentine 1995, p. 90).
"The lack of any evidence of horizontal burrowing in rocks older than about 575 Mya and of vertical burrowing in rocks older than 543 Mya is a strong argument that there existed no animals about 1 cm or longer that were capable of disturbing sedimentary layers before this time. When they do appear, these bilaterian traces indicate the presence of animals that had AP [anterior-posterior] differentiation, but there is no evidence of limbs" (Erwin & Davidson 2002, p. 3023, but note these authors were apparently unaware of Arenicolites).
Sets of paired hypichnial ridges strongly hint at an arthropod s.l. presence. [Where and when? Reference?]

An entirely independent line of study is reported in Lieberman 2003. Here, the results of a phylogenetic biogeographic analysis of Early Cambrian olenellid trilobites are calibrated by a tectonic event, the breakup of Pannotia at 600 to 550 Ma, providing evidence that "trilobites likely had evolved and begun to diversify minimally by between 550 to 600 Ma" (Lieberman 2003, p. 231).

In preserving evidence of bilaterians, the Vendian record provides constraints on the protostome-deuterostome (P-D) divergence. If Kimberella is indeed a mollusc, as suggested by Fedonkin & Waggoner 1997, or certain trace fossils recorded from the Ediacara Hills and Zimnie Gory are correctly interpreted as radula scratches, we have evidence for derived protostomes at 555 Ma. Similarly, if Arkarua adami (from the Pound Subgroup, South Australia; Gehling 1987) is correctly interpreted as an echinoderm, we have evidence for a derived deuterostome of similar age. In either case, it follows that the protostome-deuterostome split must have occurred well before 555 Ma, which is consistent with most ‘molecular clock’ studies.
The latter, however, mostly favour a P-D split far deeper in the Precambrian: some as early as 1,200 Ma (table 1). If correct, then the Cambrian explosion is clearly an artefact.
Authority

Eukayote Divergence

Fungi/Plant+Animal

P-D Divergence

Wray et al. 1996

 

 

1,200 Ma

Doolittle et al. 1996

~2,000 Ma

965 Ma

670 Ma

Feng et al. 1997

2,188 Ma

1,272 Ma

850 Ma

Ayala et al. 1998

 

 

670 Ma

Bromham et al. 1998

 

 

>680 Ma

Wang et al. 1999

 

1,576 Ma

 

Heckman et al. 2001

 

~1,600 Ma

1,000 Ma

Table 1: Divergence dates offered by various authorities.
The nature of the last common P-D ancestor (PDA) is explored in Erwin & Davidson 2002 which concludes that the last PDA must have been an extremely simple organism because there is no fossil trace evidence of complex bilaterians prior to 555 Ma, yet the mollusc interpretation of Kimberella requires the PDA to be older than this (though see de Robertis & Sasai 1996 and Holland 2002 for other perspectives).
The usual counter-argument, for a complex PDA, is met with the observation that "[a]lthough the heads, hearts, eyes, etc., of insects, vertebrates and other creatures carry out analogous functions, neither their developmental morphogenesis, nor their functional anatomies are actually very similar if considered in any detail. … [Whereas t]he regulatory processes that underlie development of specialized differentiated cells are indeed very old, conserved, plesiomorphic features. In contrast, the morphogenetic pattern formation programs by which the body parts develop their form are clade-specific within phyla or classes" (Erwin & Davidson 2002, p. 3025)
Not only is a very simple PDA consistent with the increasingly dependable and well-resolved fossil record, taking a developmentally explicit view of evolution, it seems inconceivable that a complex organism could survive the mutation which reversed the polarity of the blastopore. The characters involved in an ontogenetically early development like this, subsequently become so ‘developmentally networked’ (Arthur 1997, p. 47, or ‘generatively entrenched’ in the nomenclature of Wimsatt 1986) that the requirement for internal coadaptation ‘freezes’ them in, preventing any viable change. This view is consistent with Nielsen’s observation (2001, p. 85) that the mouth openings of the … Protostomia and Deuterostomia, cannot a priori be regarded as homologous."
Nielsen considers that a through-gut was "probably ancestral" (Nielsen 2001, p. 83). Erwin & Davidson 2002 also favour a PDA with a through-gut (p. 3029); I, however, do not.

Causal Explanations

Regardless of when the principal metazoan (and other) lineages diverged, early or late, a major radiation certainly did occur in the Cambrian. What drove it?

  • Runnegar’s paper on oxygen
  • Normal ‘rebound’ after an extinction event (Kerr 2002)

(Also see Valentine’s 1995 paper.)

Why No New Baupläne After the Cambrian?

Knoll (2003) favours an ecological explanation: "as the world filled ecologically, evolutionary opportunities for further new body plans dwindled" (p. 223).

I don’t find this explanation totally satisfying. Rather, I think it is only a partial explanation, adequate to account for the failure of new multicellular organisms to arise de novo from unicellular ancestors. But I believe it is internal coadaptation – Arthur’s ‘developmental networking’ – which prevents complex existing phyla from diverging any further. The necessary early-stage mutations are simply lethal.

Conclusion

The abrupt entry of a diverse and highly derived fauna into the fossil record, during the brief Tommotian and Atdabanian ages of the Early Cambrian, has long been recognised and is now widely known to paleontologists and laymen alike, as the ‘Cambrian Explosion.’ However, despite the rapid proliferation of evolutionary novelties which undoubtedly occurred at this time, at least some of the phenomenon is attributable to the acquisition of preservational characteristics – ‘hard parts’ – and multiple lines of evidence reveal that life was already highly diversified prior to the Tommotian.

It is to be expected that morphologically diversity should lag behind genetic diversity. This is especially true of organisms which are morphologically simple to begin with. Bacteria and Archaea look very much alike and, prior to genetic sequencing, they were classified together even though their genes now tell us they are as different as elephants and pond scum – maybe more so.
This expectation is borne out by the generally much greater ages attributed to the divergences of all megascopic lineages by molecular clock methods than is revealed by the fossil record.
Representatives of different high level taxa diverge from one another very early in ontogeny. It is at least intuitively reasonable that the ancestral organisms which experienced the ‘homologous’ phylogenetic divergences, were very simple. For example, the last common protostome-deuterostome ancestor is unlikely to have been a morphologically complex animal. Moreover, once one of these ‘early’ mutations has occurred, it is soon ‘frozen’ in by subsequent internal coadaptation.
These realisations permit us to reconcile diverse observations, such as:
  • The very early evolution of life generally (> 3,500 Ma), and eukaryote life in particular (> 1,200 Ma);
  • Molecular and microfossil evidence for an ancient (~ 1,000 Ma) diversification of eukaryotes;
  • Our failure to find convincing fossil evidence of advanced, megascopic eukaryotes, especially animals, until after ~600 Ma;
  • The apparently rapid origin of very many crown group metazoans in the ~35 million year interval from ~565 Ma to ~530 Ma (the misnamed Cambrian Explosion);
  • The observation that few fundamentally new metazoan body plans (some would say none) have arisen since.

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