The coelacanth genome has been sequenced, which is good news all around…except that I found a few of the comments in the article announcing it disconcerting. They keep calling it a "living fossil" — and you know what I think of that term — and they keep referring to it as evolving slowly
The slowly evolving coelacanth
The morphological resemblance of the modern coelacanth to its fossil ancestors has resulted in it being nicknamed 'the living fossil'. This invites the question of whether the genome of the coelacanth is as slowly evolving as its outward appearance suggests. Earlier work showed that a few gene families, such as Hox and protocadherins, have comparatively slower protein-coding evolution in coelacanth than in other vertebrate lineages.
Honestly, that's just weird. How can you say its outward appearance suggests it is slowly evolving? The two modern species are remnants of a diverse group — it looks different than forms found in the fossil record.
And then for a real WTF? moment, there's this from Nature's News section.
It is impossible to say for sure, but the slow rate of coelacanth evolution could be due to a lack of natural-selection pressure, Lindblad-Toh says. Modern coelacanths, like their ancestors, "live far down in the ocean, where life is pretty stable", she says. "We can hypothesize that there has been very little reason to change." And it is possible that the slow genetic change explains why the fish show such a striking resemblance to their fossilized ancestors.
Snorble-garble-ptang-ptang-CLUNK. Reset. Does not compute. Must recalibrate brain.
None of that makes sense. The modern fish do not show a "striking resemblance" to their fossilize ancestors — they retain skeletal elements that link them to a clade thought to be extinct. This assumption that Actinistian infraclass has been unchanging undermines their conclusions — the modern species are different enough that they've been placed in a unique genus not shared with any fossil form.
Then the argument that they must live in a stable environment with a lack of natural-selection pressure is absurd. Selection is generally a conservative process: removing selection pressures from a population should lead to an increase in the accumulation of variability. Do they mean there has been increased selection in a very narrowly delimited but stable environment?
But even that makes no sense. We should still be seeing the accumulation of neutral alleles. Increased selection is only going to remove variability in functional elements, and most of the genome isn't. I suppose one alternative to explain slow molecular evolution would be extremely high fidelity replication, but even that would require specific selection constraints to evolve.
This article broke my poor brain. I couldn't see how any of this could work — it ignored the fossil evidence and also seemed to be in defiance of evolutionary theory. It left me so confused.
Fortunately, though, the journal BioEssays came to my rescue with an excellent review of this and past efforts to shoehorn coelacanths into the "living fossil" fantasy, and that also explained the molecular data. And it does it plainly and clearly! It's titled, "Why coelacanths are not 'living fossils'", and you can't get much plainer and clearer than that.
First, let's dismiss that myth of the unchanging Actinistian. Here's a phylogeny of the coelacanth-like fossils and their one surviving species.

Comparison of extant and selected extinct actinistians, commonly known as coelacanths. A phylogeny of Actinistia; schematic sketches of body outlines and approximate body length (given in metre) illustrate the morphological diversity of extinct coelacanths: some had a short, round body (Hadronector), some had a long, slender body (Rebellatrix), some were eel-like (Holopterygius) whereas others resembled trout (Rhabdoderma), or even piranha (Allenypterus). Note that the body shape of Latimeria chalumnae differs significantly from that of its closest relative, Macropoma lewesiensis.
Love it. I've been looking for a diagram like this for a long time; creationists often trot out this claim that coelacanths haven't changed in hundreds of millions of years, and there you can see — divergence and variation and evolution, for hundreds of millions of years.
In addition, we can look in more detail at the skull and limbs of these animals. This drawing is comparing modern Latimeria with its closest fossil relative, and even here there are dramatic differences in structure.
Comparison of the skeleton of extant and selected extinct coelacanths. A-D: Latimeria and its sister group Macropoma show numerous skeletal differences. A, B: Overall view of the skeletal organisation of the extant coelacanth and of its closest relative. A: Latimeria chalumnae. B: Macropoma lewesiensis. Relative to the body length, in L. chalumnae the vertebrae are smaller, the truncal region of the vertebral column is longer and the post anal region is shorter than in M. lewesiensis. In the latter region, the hemal arches (ventral spines) extend more ventrally in M. lewesiensis than in L. chalumnae. In addition, the swim bladder is ossified in Macropoma but not in Latimeria, and the basal bone of the first dorsal fin is characteristic of each genus. C, D: Comparison of the skulls of L. chalumnae and M. lewesiensis. C: In L. chalumnae, the mouth opens upward, the articular bone (yellow) is long and narrow, the parietonasal shield (red) is short, the premaxillary bone (orange) is devoid of denticle ornamentation, the dorsal part of the cleithum (light brown) is spiny, and the scapulocoracoid (green) is located on the ventral side. D: In contrast, in M. Lewesiensis, the mouth opens forward, the angular bone (yellow) is triangular, the parieto-nasal shield (red) is long, the premaxillary (orange) protrudes and forms a hemispherical snout which is ornamented with prominent denticles, the dorsal part of the cleithrum (light brown) is thick, and the scapulocoracoid, (green) is located more medially. Modified from [3]. E: Pectoral fin skeleton of L. chalumnae (above) and Shoshonia arctopteryx (below). The three first preaxial radials are numbered from proximal to distal. In L. chalumnae the fin appears nearly symmetrical because radial bones (orange) are arranged nearly symmetrically about the fin axis. The proximal preaxial radials 1-2 are extremely short and bear no fin ray, and the preaxial radial 3 is short and fractionated. In contrast, in S. arctopteryx the fin is strongly asymmetrical chiefly because proximal preaxial radials are long and all bear fin rays.
The authors make it clear that this idea of morphological conservation of the Actinistians is simply bogus.
In addition, an examination of the skeleton of the fossil genus Macropoma (approximately 70 Ma), the sister group of Latimeria and the only known fossil actinistian record from the Cretaceous to the present, shows some interesting differences. Not only are the extant coelacanths three times larger than their closest extinct relatives (about one and a half metres vs. half a metre), but there are also numerous structural differences. The swim bladder is ossified in Macropoma but filled with oil in Latimeria, indicating they were probably found in different types of environments. There are also noticeable differences in the vertebral column (the post anal region is shorter and ventral spines extend less ventrally in M. Lewesiensis compared with L. chalumnae), and in the attachment bones of the fins. In addition, Macropoma and Latimeria have distinctly dissimilar skull anatomies, resulting in noticeable differences in head morphology.
Finally, it should not be forgotten that external morphological resemblances can be based on a very different internal anatomical organisation. The most often emphasised resemblance between coelacanths is that they all have four fleshy-lobed-fins. Until recently, the anatomy of the lobed fins of coelacanths was only known in Latimeria, in which the pectoral fin endoskeleton is short and symmetrical. In 2007, Friedman et al. described the endoskeleton of the pectoral fin of Shoshonia arctopteryx, a coelacanth species from the mid Devonian, and therefore contemporary with Miguashaia. They showed that this earliest known coelacanth fin endoskeleton is highly asymmetrical, a characteristic that is probably ancestral since it resembles the condition found in early sarcopterygians such as Eusthenopteron, Rhizodopsis or Gogonasus. This result is additional support, if needed, that extant coelacanths have not remained morphologically static since the Devonian.
Well, so, you may be wondering, what about the molecular/genomic data? Doesn't that clearly show that they've had a reduced substitution rate? No, it turns out that that isn't the case. Some genes seem to be more conserved, but others show an expected amount of variation.
However, a closer look at the data challenges this interpretation [of slow evolution]: depending on the analysed sequence, the coelacanth branch is not systematically shorter than the branches leading to other species. In addition, most phylogenetic analyses - including analysis of Hox sequences - do not support the hypothesis that the Latimeria genome is slow evolving, i.e. they do not place coelacanth sequences on short branches nor do they detect low substitution rates. The clearest example, which involves the largest number of genes, is a phylogeny based study of forty-four nuclear genes that does not show a dramatic decrease, if any, in the rate of molecular evolution in the coelacanth lineage. What we know about the biology of coelacanths does not suggest any obvious reason why the coelacanth genome should be evolving particularly slowly.
So why is this claim persisting in the literature? The authors of the BioEssays article made an interesting, and troubling analysis: it depends on the authors' theoretical priors. They examined 12 relevant papers on coelacanth genes published since 2010, and discovered a correlation: if the paper uncritically assumed the "living fossil" hypothesis (which I've told you is bunk), the results in 4 out of 5 cases concluded that the genome was "slowly evolving"; in 7 out of 7 cases in which the work was critical of the "living fossil" hypothesis or did not even acknowledge it, they found that coelacanth genes were evolving at a perfectly ordinary rate.
Research does not occur in a theoretical vacuum. Still, it's disturbing that somehow authors with an ill-formed hypothetical framework were able to do their research without noting data that contradicted their ideas.
Maybe a start to correcting this particular instance of a problem is to throw out the bad ideas that are leading people astray. The authors strongly urge us to purge this garbage from our thinking.
Latimeria was first labelled as a 'living fossil' because the fossil genera were known before the extant species was discovered, and erroneous biological interpretations have grown and reports still show little morphological and molecular evolution. A closer look at the available molecular and morphological data has allowed us to show that most of the available studies do not show low substitution rates in the Latimeria genome, and furthermore, as pointed out by Forey [3] long before us, the supposed morphological stability of coelacanths from the Devonian until the present is not based on real data. As a consequence, the idea that the coelacanth is a biological 'living fossil' is a long held but false belief which should not bias the interpretation of molecular data in extant Latimeria populations. The same reasoning could be generalised to other extant species (such as hagfish, lamprey, shark, lungfish and tatuara, to cite few examples of vertebrates) that for various reasons are often presented as 'ancient', 'primitive', or 'ancestral' even if a lot of recent data has shown that they have many derived traits [58-64]. We hope that this review will contribute to dispelling the myth of the coelacanth as a 'living fossil' and help biologists keep in mind that actual fossils are dead.
But of course we also shouldn't let that color our data. If analyses showed a significantly reduced substitution rate in the evolution of a species, it ought to get published. If nothing else, it would be an interesting problem for evolutionary theory. Coelacanths, though, don't represent that problem.
Amemiya CT, Alföldi J, Lee AP, Fan S, Philippe H, Maccallum I, Braasch I, Manousaki T, Schneider I, Rohner N, Organ C, Chalopin D, Smith JJ, Robinson M, Dorrington RA, Gerdol M, Aken B, Biscotti MA, Barucca M, Baurain D, Berlin AM, Blatch GL, Buonocore F, Burmester T, Campbell MS, Canapa A, Cannon JP, Christoffels A, De Moro G, Edkins AL, Fan L, Fausto AM, Feiner N, Forconi M, Gamieldien J, Gnerre S, Gnirke A, Goldstone JV, Haerty W, Hahn ME, Hesse U, Hoffmann S, Johnson J, Karchner SI, Kuraku S, Lara M, Levin JZ, Litman GW, Mauceli E, Miyake T, Mueller MG, Nelson DR, Nitsche A, Olmo E, Ota T, Pallavicini A, Panji S, Picone B, Ponting CP, Prohaska SJ, Przybylski D, Saha NR, Ravi V, Ribeiro FJ, Sauka-Spengler T, Scapigliati G, Searle SM, Sharpe T, Simakov O, Stadler PF, Stegeman JJ, Sumiyama K, Tabbaa D, Tafer H, Turner-Maier J, van Heusden P, White S, Williams L, Yandell M, Brinkmann H, Volff JN, Tabin CJ, Shubin N, Schartl M, Jaffe DB, Postlethwait JH, Venkatesh B, Di Palma F, Lander ES, Meyer A, Lindblad-Toh K. (2013) The African coelacanth genome provides insights into tetrapod evolution. Nature 496(7445):311-316.
Casane D, Laurenti P (2013) Why coelacanths are not 'living fossils': A review of molecular and morphological data. Bioessays 35: 332-338.
103 Comments
DS · 20 April 2013
Thanks PZ.
It is always important to remember that morphological and molecular evolution may be coupled or uncoupled. This is undoubtedly due to the complex relationship between genetics and morphology, given the complexity of developmental pathways.
Does anyone know if the complete genome sequence sheds any more light on the phylogenetic relationships between coelacanths, lungfish and tetrapods? Was this covered in the article? For many years the question proved hard to address. I had the impression that the consensus was that coelacanths are less closely related to tetrapods than lungfish. Does this relationship hold up given the new sequence data?
https://me.yahoo.com/a/JxVN0eQFqtmgoY7wC1cZM44ET_iAanxHQmLgYgX_Zhn8#57cad · 20 April 2013
Well why are there still fossils, if coelecanths evolved from fossilized ancestral forms (or anyway, from relatives of those)?
See, there are always questions for evilutionists.
Glen Davidson
Eric Finn · 20 April 2013
Posts like this one are the reason I keep on lurking at Pandas Thumb.
The issue discussed in this opening post has bothered me. It is indeed true that sometimes (or often) it has been indicated in public that a body shape that remains almost the same indicates either lack of evolution or slow evolution also at genetic level.
On the other hand, I do not remember anyone drawing a conclusion that the genetic makeup of ichthyosaur, dolphin and tuna fish should be highly similar.
According to the answer given here, there is no reason to assume that.
Moreover, even the body shape is not quite as stable as sometimes indicated, at least not in the case of coelacanths.
Just wanted to tell that a layman might possibly have understood something about what you said.
Mike Elzinga · 20 April 2013
I have not been able to find an answer to a question that I have been curious about for quite a few years now.
Have there ever been studies done on the rates of genetic change in creatures that have lived for thousands of years at low temperatures?
The reason I ask this is that there are some fundamental physic/chemistry notions behind the probabilities of mutations. The probability of a “jump” to another state is proportional to exp(-φ/kT), where φ is the height of a potential barrier between different configurations or states of a molecule.
If the general rule for rates of molecular evolution in living organisms is that they are pretty much “temperature independent,” then that would suggest that those barriers are large relative to kT. For example, room temperature kT is on the order of 1/40 of an electron volt.
I would expect that the barriers to molecular changes involved in genetic evolution would be at least 10 to 100 times larger; thus I would not expect any measurable differences in rates of molecular evolution given that the temperatures for life here on earth lie primarily within the range of liquid water.
Down at those geothermal vents, kT is greater because water is superheated under pressure; but one can also imagine that molecular configurations for extremophiles could be “more robust” – i.e., have slightly higher φ’s – also. They also live at considerably higher pressures.
I’m guessing that it is not likely that there will be measurable differences in molecular evolution rates across the entire spectrum of life. There is not much room for φ and T to vary without destroying the organism.
apokryltaros · 20 April 2013
EvoDevo · 20 April 2013
EvoDevo · 20 April 2013
robert van bakel · 20 April 2013
Are there examples of living animals (birds,insects,sharks etc) that DO resemble their respective fossil ancestors extremely closely? So closely in fact that selection seems to have been made redundant by the stability of the environment.
Really, just asking!
Robert Byers · 20 April 2013
Wait a minute. Lets think about this.
If My Myers is saying past and present, very present, scholarship on these things is so poor then creationists are right to lack and teach lack of confidence in anything from evolutionary biology.
Its not just this fish!
If its a Coel and has relatives in fossils said to be so long ago then the differences are so small to in effect say its unchanged.
They even invoked here about size. What does that matter? Irrelevant.
Mr Myers is stressing small differences to press the point this fish type has been evolving with the best of them.
Its very little different from what i read here.
There is indeed no living fossils because this presumes the fossils indicates ancient ages.
Its just a more common type that survived from a greater diversity living a few thousand years ago as the great flood took place.
there are many types of creatures unchanged from fiossil relatives in strata below the k-pg line.
My Myers is right however about modern literature in science fails to do a good job in origin issues.
We know that fossil is still unmorphed.
Scott F · 20 April 2013
Scott F · 20 April 2013
harold · 21 April 2013
DS · 21 April 2013
apokryltaros · 21 April 2013
Mark Sturtevant · 21 April 2013
I have been following the recent spate of postings about the Coelacanth genome. This is the most useful one of 'em all. So I am ready to expunge the idea of 'living fossil' for the coelacanth in my mind. What about horseshoe crabs? Any thoughts?
Dave Luckett · 21 April 2013
There is also the idea that some mutations are caused by radiation - nuclear and ultraviolet. Coelacanths live in deep water, below 100 meters, down to at least 500. There must be less EMR down there to cause mutations.
Or is this pure nonsense?
Marilyn · 21 April 2013
EvoDevo · 21 April 2013
Mark Sturtevant · 21 April 2013
harold · 21 April 2013
Ray Martinez · 21 April 2013
phhht · 21 April 2013
DS · 21 April 2013
stevaroni · 21 April 2013
harold · 21 April 2013
Ray Martinez · 21 April 2013
phhht · 21 April 2013
Ray Martinez · 21 April 2013
DS · 21 April 2013
DS · 21 April 2013
If Ray wants to discuss science he can get to it. IF not he can piss off. No one is interested in his religious delusions.
So mister immutabalist, how do you explain the numerous skeletal differences observed between the fossil and modern coelacanths. Sure don't look immutable to me.
DS · 21 April 2013
Mike Elzinga · 21 April 2013
apokryltaros · 21 April 2013
KlausH · 21 April 2013
John Harshman · 21 April 2013
Steve P. · 21 April 2013
apokryltaros · 21 April 2013
DS · 21 April 2013
apokryltaros · 21 April 2013
apokryltaros · 21 April 2013
stevaroni · 21 April 2013
Just Bob · 21 April 2013
So Steve, that island where you live and work: was it pretty much the same 200 years ago? Same population, same urbanization, same agriculture, same degree of forestation, same type of pressure on the fisheries?
How about 1,000 years ago? 5,000?
Do you seriously think the SAME environmental niches are available today as then? Don't you think that if you looked, you could see new niches open or old ones close; or available niches EVOLVE in their ability to provide resources and protection ...within a very few years or even months in a modern, industrialized, technologically advanced region like Taiwan?
And as niches evolve, guess what their inhabitants have to do.
https://me.yahoo.com/a/JxVN0eQFqtmgoY7wC1cZM44ET_iAanxHQmLgYgX_Zhn8#57cad · 21 April 2013
stevaroni · 21 April 2013
Joe Felsenstein · 21 April 2013
Rolf · 22 April 2013
Bhakti Niskama Shanta · 22 April 2013
Does Current Biology have the Misfortune of Owning an Unreliable Clock?: http://scienceandscientist.org/Darwin/2013/04/20/does-current-biology-have-the-misfortune-of-owning-an-unreliable-clock
TomS · 22 April 2013
DS · 22 April 2013
John Harshman · 22 April 2013
ogremk5 · 22 April 2013
John Harshman · 22 April 2013
Henry J · 22 April 2013
Does this mean that their DNA copying mechanism is slightly more accurate than the average for other species? Or do they just reproduce less often than a lot of other species?
Omar · 22 April 2013
Evolution is false because it does not match the fossil record. The fossil record shows species appearing suddenly, it does not show small and minor changes. An example of this is the Cambrian Explosion, which was the fast appearance of most major animal phyla. This was 542 million years ago. Pro evolutionists claim that evolution requires diversity whereas this could not happen with small isolated populations. That's why the morphological resemblance of the modern coelacanth to its fossil ancestors that has resulted in it being nicknamed 'the living fossil' cannot be true.
matthew.s.ackerman · 22 April 2013
Mike Elzinga · 22 April 2013
DS · 22 April 2013
Ray Martinez · 22 April 2013
phhht · 22 April 2013
TomS · 22 April 2013
DS · 22 April 2013
Ray Martinez · 22 April 2013
phhht · 22 April 2013
Ray Martinez · 22 April 2013
phhht · 22 April 2013
PA Poland · 22 April 2013
DS · 22 April 2013
Steve P. · 22 April 2013
Steve P. · 22 April 2013
Dave Luckett · 22 April 2013
Only that's totally wrong, Steve. It's just non-fact that you're making up and writing down, because you'd like to believe it. But it's simply not true. Environments change, and populations of living things evolve to fit them. Yes, some of that change is cyclic - oscillating, as you put it. But some of it is continuous change in one direction over very long periods of time.
Mountain ranges rise and erode over tens of millions of years. That means, and it must mean, that the climates around them change. Old niches close, new niches open. Organisms migrate, form new populations, and these change the environments and the biosphere in the colonised region, permanently. Continental drift opens new oceans, separating new continents, or closes them, joining lands. What were shallow seas become ocean depths, or low-lying shores. Species adapt by evolutionary change, and that adaptation itself changes the environment, permanently.
Large-scale, long-term change is not an assumption or a conjecture. It is demonstrated fact, and you are simply wrong.
phhht · 22 April 2013
Rolf · 23 April 2013
apokryltaros · 23 April 2013
magically poofIntelligently Design the lizards to magically transform into scaly goats with the ability to magically make their own cellulase without the aid of cellulase-digesting symbiotes?apokryltaros · 23 April 2013
DS · 23 April 2013
DS · 23 April 2013
DS · 23 April 2013
Stevie is once again trying to disrupt a thread with his incessant, mindless babbling. Time for another dump to the bathroom wall.
DS · 23 April 2013
If anyone is interested in lizard cecal valve evolution here is a summary:
http://www.sciencedaily.com/releases/2008/04/080417112433.htm
So large changes were directly observed in natural populations in a short period of time. Stevie concludes that this disproves evolution! What a moron.
DS · 23 April 2013
Here is a scientific reference, complete with phylogenetic analysis:
http://www.ncbi.nlm.nih.gov/pmc/articles/pmc2290806/
DS · 23 April 2013
PZ discusses the topic here:
http://scienceblogs.com/pharyngula/2008/04/23/still-just-a-lizard/
Steve P. · 23 April 2013
Steve P. · 23 April 2013
PA Poland · 23 April 2013
apokryltaros · 23 April 2013
apokryltaros · 23 April 2013
Steve P. · 23 April 2013
apokryltaros · 23 April 2013
Evolution is actually measured in increments of generations, Steve P.
That, and if the lizards' cecal valves magically disprove Darwin's "slow evolution" (sic), then why don't the papers about the lizards mention disproving it?
DS · 23 April 2013
DS · 23 April 2013
DS · 23 April 2013
And yet that's exactly what we have in the case of whale evolution, and tetrapod evolution and human evolution and bird evolution and many other lineages as well. You ignorance is evidence of nothing but your ignorance. Deal with it already.
Rolf · 23 April 2013
Jon · 24 April 2013
Wrote this article on ceolocanths and lungfish yesterday:
http://www.policymic.com/articles/37403/this-new-genome-shows-how-all-land-vertebrates-evolved-including-ourselves
DS · 24 April 2013
DS · 24 April 2013
The original article includes a phylogenetic analysis for 251 genes demonstrating the slow rate of molecular evolution in coelacanths relative to lungfish. It also includes a detailed analysis of hox gene evolution, complete with an analysis of cis regulatory regions and transgenic experiments. Perhaps PZ could start another thread concentrating on these issues.
apokryltaros · 24 April 2013
DS · 24 April 2013
Hey Steve, how about this, why don't you look up "punctuated equilibrium" and see what you find? If after that you still think that the fact that evolution can occur slowly or quickly is a problem you can explain why. If after that you still think that this somehow disproves Darwin you can explain why. If you then think that Gould should be venerated as a saint instead of Darwin you can explain why. Until you educate yourself, your ignorant opinions are worthless, as usual.
The last straw has slipped through your fingers and your you are grasping at air.
TomS · 24 April 2013
Wikipedia has an article which discusses this: Italian wall lizard.
scienceavenger · 24 April 2013
SteveP's comments re fast or slow evolution reminds me of AGW deniers who represent the scientific case as "wanting it both ways", thus "warming proves AGW and cooling proves AGW". It's as if there is something inherent in the science-denying mind that demands reality be simple and conducive to one-sentence rules.
Henry J · 24 April 2013
Or like they don't know what "average" means?
apokryltaros · 24 April 2013
Karen S. · 28 April 2013
Just noticed today at the American Museum of Natural History that the coelacanth is referred to as a living fossil. They also say that it has changed little. Old habits die hard!
Ray Martinez · 29 April 2013
PA Poland · 29 April 2013