Monday 24 September 2012

Plesiosuchus vs. Dakosaurus... Fight!


Last Tuesday (18.09.12) a paper was published in PLOS ONE on the metriorhynchid crocodile Dakosaurus, resurrecting the name Plesiosuchus manselii for a large specimen that had been synonymised with Dakosaurus maximus in the late 19th Century (Lydekker 1888). There is not necessarily any reason that this name change would be picked up by popular science, but there are a number of implications made by the authors (Young et al. 2012 a) which made it incredibly interesting. So much so that when given the opportunity to blog on the same subject matter after Lorna Steel's (Young et al. 2012 b) talk at SVPCA Oxford I decided to hold back until the paper came out...

Metriorhynchid crocodiles were a group of thalattosuchian crocodylomorphs with a temporal range (time span) from the Middle Jurassic to the Lower Cretaceous. The group was made up of fully marine crocodiles which were highly specialized for their marine environment. Fossil evidence shows that much like other secondarily marine tetrapods (four legged land animals) [i.e. ichthyosaurs, whales and dolphins] metriorhynchids had tale flukes, like those of sharks. In addition to this clear specialization, the metriorhynchids had hydrofoil-like forelimbs, large salt-glands and lost their armoured plates. These animals filled several niches in the marine environment, they developed numerous cranial and dental morphologies and varied in size greatly. Within the Metriorhynchidae two major radiations are persistently recovered by cladistic analyses; the Metriorhynchinae and the Geosaurinae. The members of the Geosaurinae are usually interpreted as being super-predators and among them, Dakosaurus is interpreted by Young et al. (2012 a) to be macrophagous: "an animal that could feed upon prey items of similar body size" (Young et al. 2012 a). Plesiosuchus is also interpreted to be a macrophagous predator, but differences in anatomy and dental morphology led the authors to suggest a different niche for this creature and to reject Lydekker's (1888) assertions that Plesiosuchus was synonymous with Dakosaurus. This renewed view of diversity is supported by a cladistic analysis (fig. 26 Young et al. 2012 a) [Fig. 1].
Fig. 1 (fig. 26 of Young et al. 2012) cladistic analysis of crocodylomorphs, showing Plesiosuchus (bold) separate from Dakosaurus (bold). Used with the permission of authors.

By comparing Dakosaurus and Plesiosuchus with modern killer whales and false killer whales, the research team have suggested that the smaller Dakosaurus is a possible suction feeder, or predated upon abrasive prey such as sharks, whereas Plesiosuchus predated upon other large marine reptiles. This interpretation is supported by evidence of the animals relative size, their tooth wear and the maximum gape of their jaws. It seems that the smaller Dakosaurus (~4.5 m) could tear up its prey and was not limited on the size of the prey that it could capture and consume. Distinctive wear patterns on the mesial and distal carinae (front and back cutting edges) of the teeth show that the teeth were shearing, capable of ripping chunks of flesh off their prey. Whereas Plesiosuchus (~6.8 m) was rather more limited by the size of its head, making it more specialized, but nonetheless a large predator sharing affinities with killer whales, which eat other marine mammals. Either way, both would have been fearsome predators of the Late Jurassic seas. However, despite Dakosaurus' incredibly efficient bite, it seems that it may have fallen victim to the larger, veracious Plesiosuchus.

Art work by Dmitry Bogdanov (fig. 30 of Young et al. 2012)


 See also:
The original paper
The NHM article



Lydekker, R. 1888. Catalogue of the Fossil Reptilia and Amphibia in the British Museum (Natural History), Cromwell Road, S.W., Part 1. Containing the Orders Ornithosauria, Crocodilia, Dinosauria, Squamata, Rhynchocephalia, and Proterosauria. London: British Museum of Natural History. 309 p.

Young, M.T. Brusatte, S.L. de Andrade, M.B. Desojo, J.B. Beatty, B.L. Steel, L. Fernández, M.S. Sakamoto, M. Ruiz-Omeñaca, J.I. Schoch, R.R. 2012 a. The Cranial Osteology and Feeding Ecology of the Metriorhynchid Crocodylomorph Genera Dakosaurus and Plesiosuchus from the Late Jurassic of Europe. PLoS ONE 7(9): e44985. doi:10.1371/journal.pone.0044985 

Young, M. Brusatte, S. de Andrade, M. Desojo, J. Beatty, B. Steel, L. Fernández, M. Sakamoto, M. Ruiz-Omeñaca, J. & Schoch, R. 2012 b. Comparative cranial osteology and feeding mechanics of two Late Jurassic macrophagous metriorhynchids from Europe. Programme and Abstracts, SVPCA, 60th Annual Symposium on Vertebrate Palaeontology and Comparative Anatomy. p.22

Thursday 20 September 2012

SVPCA Oxford- A review of some amazing palaeontology


It’s nearly been a week since the end of SVPCA Oxford. High time I made good with my promises and wrote the blog post. There was an unbelievable range of talks this year, working through them hierarchically, from jawless lower vertebrates (not Mesozoic) up to mammals, with the archosaur lineage stuffed in the middle. Not only was a large chunk of Vertebrata covered, but it was covered in a huge range of topics; phylogeny, function, morphology, functional morphology, trace-fossils and much more.
Perhaps one of the most pertinent papers for this blog was presented by Paul Barrett and co-authors (Barrett et al. 2012). The title was ‘The earliest known dinosaur?’ a bit of a punch line spoiler, but none the less an informative and entertaining talk ensued. To give a brief summary: the material, from the Triassic of Tanzania has been sat in drawers for years, but a renewed understanding of what it is that makes a dinosaur a dinosaur and a dinosauromorph a dinosauromorph allowed the research team to say that the specimen is definitely one or maybe the other. All joking aside, the specimen is fragmentary, comprising of a partial humerus and some hip and back vertebrae (sacral and dorsal), with some other referred material (originally assigned to separate genera and species) and from this the team established that this animal is either the earliest known dinosaur, or the closest known dinosauromorph to the Dinosauria. They also demonstrated that the bone growth of these specimens was rapid, much like that of dinosaurs, leaving me inclined to consider the material a dinosaur for now. This is great, because now we not only know what the earliest dinosaurs look like, but we can be fairly confident of where they come from and it closes up the ghost lineage on the cladogram. Even with a pinch of salt it certainly says a lot for the robustness of the current archosaur phylogenies, which are being corroborated by new fossil data.
Another impressive piece of work was by Falkingham and Gatesy (2012). The duo modelled track ways to establish the locomotion of small theropod dinosaurs. It sounds like a simple task that won’t return much information right? Well it’s not. They realised that the various morphologies of track ways available in the collections housed at the Beneski museum represented similar animals at different stages of penetration into a substrate. They found a stack which represented the same foot moving all the way through the substrate and tracked landmarks using a computer simulation. Lowe and behold a model of a foot emerged from this process. Not only did they have a foot that looked just like a small theropod’s, but they also had its range of motion, confirming that a small theropod dinosaur does indeed move like a modern bird/avian dinosaur.
In the world of pterosaur research, Dave Unwin presented a piece of research on the ontogenetic (growth) series of Darwinopterus (Unwin et al. 2012). Darwinopterus is a transitional pterosaur, between the derived pterodactyloids and basal forms. When originally described in 2010 (Lü et al. 2010) Darwinopterus was reported as being an example of modular evolution. Now, with the ontogenetic series studied by Unwin and company they have revealed one of the potential mechanisms by which the animals evolved. The suggested mechanism is heterochrony: the process of changing the developmental patterns of an animal, or removing them altogether. In Darwinopterus juveniles it was found that less caudal vertebrae were ossified and that they were shorter than in adults, therefore the short tails of early pterodactyloids such as Pterodactylus are interpreted as neotenous (retaining juvenile characters).
Frankly, there was too much great research to post on in one go, so I’ll briefly report on one more presentation and call it a day. Lorna Steel a curator at the NHM UK presented on behalf of Young and their co-authors (Young et al. 2012) on the metriorhynchid crocodiles Dakosaurus and Plesiosuchus. Metriorhynchids are fully marine crocodiles with tail flukes... pretty cool. Long story short they were huge and Plesiosuchus appears to have been a marine reptile predator, much like modern killer whales. I’m being supremely brief on this one, since it deserves its own post.
Also there is another crocodile paper to be reported on, but this will be reserved for when it is published.
So, all in all it was a great conference and we all have to be appreciative of what the organizers have done for us. They have kept a 60 year tradition going, allowing researchers to present cutting edge science on the clade Vertebrata.

Don't forget to follow me on Twitter.


Barrett, P. Nesbitt, S. Werning, S. Sidor, C. & Charig, A. 2012. The earliest known dinosaur? Programme and Abstracts, SVPCA, 60th Annual Symposium on Vertebrate Palaeontology and Comparative Anatomy. 6-7.
Falkingham, P. & Gatesy, S. 2012. Using penetrative tracks to reconstruct limb kinematics of bipedal dinosaurs traversing semi-fluid substrates. Programme and Abstracts, SVPCA, 60th Annual Symposium on Vertebrate Palaeontology and Comparative Anatomy. 11-12.
Lü, J. Unwin, D.M. Jin, X. Liu, Y. & Ji, Q. 2009. Evidence for modular evolution in a long-tailed pterosaur with a pterodactyloid skull. Proceedings of the Royal Society, Biological Sciences, 277: 383-389.
Unwin, DM. Lü, J. Pu, C. Wu, Y. 2012. A short tale: Darwinopterus, ontogeny and pterosaur evolution. Programme and Abstracts, SVPCA, 60th Annual Symposium on Vertebrate Palaeontology and Comparative Anatomy. 24.
Young, M. Brusatte, S. de Andrade, M. Desojo, J. Beatty, B. Steel, L. Fernández, M. Sakamoto, M. Ruiz-Omeñaca, J. & Schoch, R. 2012. Comparative cranial osteology and feeding mechanics of two Late Jurassic macrophagous metriorhynchids from Europe. Programme and Abstracts, SVPCA, 60th Annual Symposium on Vertebrate Palaeontology and Comparative Anatomy. 22.

Thursday 16 August 2012

Palaeontologist rises

It has been nearly a year since my last post. Too long. When I started this blog I was at the peak of my game in terms of PhD research etc. The long and short of it is I spread myself too thin and paid the price. One of the sacrifices I had to make was cutting out my bloging. But now, with over 22 views this month, 2 alone today, despite 11 months of stagnation I feel I owe the blogosphere something, if only a little.

First: I would like to plug my fellow PhD research students' new blog Ancient Anglers, they will be on my side bar from now on. They are not time specific, they just like the kind of dead fish you can't cook. However, Luke's research stream keeps him in the Silurian and Chris will be studying Late Jurassic fish. This is all worth looking at if you're wondering how monstrous fish can be, what the animals of MM ate, or indeed what ate the animals of MM.

Second: Pterosaur teeth. Wow they were pretty diverse weren't they?! We've seen that with Pterodaustro and I do believe I promised a three parter. Now, I've had the second part written up and on my desktop for about as long as I have not posted for... You see, I have not been lazy, just reluctant. The three parter shall be no more. Not to say that you won't hear plenty about teeth and diet. In fact, there might be a MM/Ancient Anglers collaboration to come on this topic.

...So what is going on in the world of palaeontology? Well, it's conference season. It's the time of year when academics stop what they're doing, relax, hang out, get drunk and somewhere in the middle tell everyone else what they have found out this year. These events are where the latest research is presented in its rawest form and where new ideas and collaborations are formed. Therefore, for active researchers this is pretty important. Personally, this year I will be attending only one conference...SVPCA Oxford. This is an important one, it's the biggest vertebrate palaeontology gathering in the UK, perhaps Europe and this year it's in the birth place of modern palaeontology and my home town. So I will be doing a post on the results of that in a month's time and in the meantime I will try and exaggerate how important Oxford is to palaeontology.

The Birthplace of Modern Palaeontology

Arguably, Oxford is the birthplace of modern palaeontology. It was the dinosaurs that sparked the Victorian imagination, leading to the golden age of palaeontology. The first dinosaur ever recorded was of course "scrotum humanum" a therepod dinosaur from the Middle Jurassic of Oxfordshire. A petition was made to the board of the ICZN to give Megalosaurus priority as a name, but it was overturned on the basis that the name scrotum was not erected (*sniggers*) properly by Richard Brookes (1763), nor was the material diagnostic. So the first ever illustrated piece of dinosaur material is now referred only as Megalosaurus cf. More material turned up in Stonesfield, Oxfordshire in the early 19th Century. It was then, with the advice of comparative anatomist Georges Cuvier that William Buckland published the material as Megalosaurus Conyberi, which was not used (Nomen Oblitum) in favour of the later binomial Megalosaurus bucklandii. It was due to the discovery and description of this animal as a giant lizard that Richard Owen, founder of the Natural History Museum, maimer of Mantell and overlord of the Empire's palaeontology coined the term dinosaur.

So, Megalosaurus was now tied up in academic interests in Oxford, London and Paris and it is what the Dinosauria is based upon. But what has happened to it since? Richard Owen also placed Cetiosaurus from Oxfordshire, along with Iguanadon, not from Oxfordshire into Dinosauria. Modern cladistic analyses have placed Megalosaurus in the clade Spinosauroidea, in Megalosauridae, within a further clade, Megalosaurinae, sister group to the Eustreptospondylinae. By the way, Eustreptospondylus is also from Oxfordshire.

This isn't to say that since those first discoveries were the end of palaeontology in Oxford. Since then there have been pterosaurs, crocodiles, fish, mammals and other dinosaurs discovered in what is colloquially termed the Stonesfield slate. A section of Bathonian and possibly Bajocian oolites, sands, silts and limestones. Oxford was a very different place 170 million years ago. The sands and silts show that there was land very near by, if indeed drops in sea level didn't  expose land in this area full stop. The silts are thought to indicate a huge river, similar to the amazon in fact, and often turns up bits of Cetiosaurus and other goodies. The oolite indicates a high energy shallow environment, like the mangroves and long shallow beaches seen in the modern Bahamas. As mentioned before, the interesting stuff comes out of the river deposits and as the name - Stonesfiled slate - would suggest, out of the slatey oolite layers.

There has been very little work done on this material for a very long time, but recently myself and a team from UoP (Including Ancient Anglers) plus Dave Hone of Archosaur Musings went to some exposure. The locality cannot be exposed due to illegal digging that appears to be on going. If it was a case of some fancy scraps being removed there would not be a problem, but we found evidence of some articulated material, which rubs salt in the wound created by the fact that members of the general public are digging in a place protected for its geology under the rules of Natural England's SSSI. That aside, we left from the visit having found some crinoids, brachiopods, mollusks, as well as a couple of isolated crocodile teeth on oolite slabs and a chunk of bone. See Dave's Archosaur Musings post!
Crocodile tooth in situe. Steneosaurus cf.
Crocodile tooth preped out and glued. Steneosaurus cf.
Bivalve mollusk with colour banding.

Rhynchonellid brachiopod
 Tooth indet. (possible Teleosaurus)
Dinosaur bone, found by Dave Hone

So, all in all Oxford is a great place for palaeontologists. Not only is there some amazing stuff in its history and the museum's drawers, there is also some great stuff in the ground. But I must ask the ambitious amateurs out there to leave it alone, or report your finds to the Oxford University Museum of Natural History. Exposure and finds are so rare now that the brick pits and slating works have closed that all vertebrate material found in Oxfordshire is important to science.