Cartorhynchus: helping ichthyosaurs crawl back into the mainstream.

Over the last 12 months or so, I’ve been researching ichthyosaurs for my masters project, and since then, I’ve been working on publishing my results. As such, I’ve learnt a fair bit of ichthyosaur palaeobiology and systematics. I’m no expert, but at this early stage in my academic career, I can say that at the moment, ichthyosaurs (specifically ichthyosaur endocranial anatomy) are my ‘specialisation(s)’, perhaps even making me an ichthyo-sir (heh). To this end, Motani et al.’s recent publication in Nature was massive news for ichthyosaur palaeobiologists. And that’s why it’s got its own little blog post.

What’s all the fuss about then? This year (2014) marked the anniversary of the 200 years since the first appearance of ichthyosaurs in scientific literature, and ichthyosaurs are closely associated with palaeontological celebrities, both historical (Mary Anning) and rather more recent (Alfred Romer). In those 200 years, we’ve learnt a lot about ichthyosaurs, and whilst they’re not ‘some kind of fish-lizard’, they are diapsid reptiles that were some of the first tetrapods to evolve a thunniform (fish/tuna-like) bodyplan, which aided them in their marine adventures. We know what colour some of them were thanks to melanosomes (Lindgren et al. 2014), we also know that they gave birth to live young, like mammals and some sharks do. We have exceptional fossils of ichthyosaurs actually giving birth, and others with amazing detailed and undisturbed soft tissue outlines. However despite all these amazing discoveries, we still don’t know a whole lot about two major aspects of ichthyosaur palaeobiology: their precise biomechanical function (we can’t create fancy 3D digital models due to the lack of 3D specimens, most ichthyosaur remains are mostly pancake-flat, even the really awesome ones) and perhaps more importantly, how they place in wider diapsid phylogeny.

The miracle of ichthyosaur birth, over 200 million years-ago. Very cool.

The miracle of ichthyosaur birth, over 200 million years-ago. Very cool.

Now before I go any further, it might be a good idea to explain what I mean by diapsid. Diapsida is a group of organisms (more specifically tetrapods) that have two temporal fenestrae (holes) in each side of their heads. Now this is a pretty large group, including archosaurs (dinosaurs, birds and crocs), lizards, snakes and tuataras. So whilst we have some vague idea where ichthyosaurs lie within this pretty large evolutionary tree, we’re not entirely sure. Why? Well because we don’t have transitionary fossils, ichthyosaurs previously (before Motani et al. 2014) appeared in the fossil record as highly adapted marine reptiles, well suited to the marine environment (remember, they look like fishes). So without any hint of which precise group of terrestrial organisms they evolved from, the topic of where ichthyosaurs came from is highly debated. So much in fact that in 2006, a very prominent ichthyosaur worker, Michael Maisch declared that the placement of ichthyosaurs within Diapsida was “…impossible…” (Maisch et al. 2006) without more basal specimens.

The internal phylogeny of ichthyosaurs isn’t a much better state either, with tree topologies changing at every opportunity of the last 10 years or so, threatening to change again when new systematic methods are applied. This again is largely due to the lack of well preserved three-dimensional specimens. But it’s not all doom and gloom, amazingly preserved specimens like those used in Lindgren et al. 2014 have shown us the colour of these ancient fish-dolphins (joke name, please don’t take it seriously), and Fischer et al. 2013’s discovery of Malawania has helped, to some degree, solve the internal phylogeny of at least neoichthyosaurs and ophthalmosaurs (ichthyosaurs from the Jurassic onwards). And obviously, my work on ichthyosaur endocranial and neuroanatomy from an exceptionally three-dimensionally preserved specimen will be hopefully  well received (more on that in the coming months). So it’s not all doom and gloom. But still, ichthyosaurs aren’t exactly the Brangelina of the palaeontological scene, no sir, those celebrity couples occupying all the headlines are dinosaur discoveries such as Deinocheirus and Dreadnoughtus, and the number of ichthyosaur workers isn’t exactly huge.

To my shocked delight, on the afternoon of the 5th of November, 2014 I stumbled upon a fresh new ichthyosauriform, in a Nature paper. Good heavens! Could it be true? Well, of course, other wise I’d have spent the last hour typing madly about ichthyosaurs for no apparent reason. Catorhynchus lenticarpus (‘shortened snout’, ‘flexible wrist’) is a weird, small beast. At first glance, you’d be forgiven for thinking that Catorhynchus wasn’t even a ichthyosaur at all. Well, technically, it isn’t an ichthyosaur at all, it’s an ichthyosauriform.  Catorhynchus comes from the Lower Triassic, approximately 248 million years-ago, and whilst some would call it an ‘ichthyosaur’, the Ichthyosauria (essentially all of the things your properly allowed to call ‘ichthyosaurs’) didn’t occur until later on in the Triassic. So, what the hell is Catorhynchus? Simple, it’s an ichthyosauriform, an ichthyosaur-looking creature which is more closely related to Ichthyosaurus communis than to a hupesuchian? Wait, what the hell are hupehsuchians, and what do they have to do with anything?

Hupehsuchians, think ichthyosaurs but a little more 'vacant' looking.

Hupehsuchians, think ichthyosaurs but a little more ‘vacant’ looking.

Good question. Hupehsuchians are a weird bunch of marine reptiles, who you’d be very much forgiven for calling ichthyosaurs, because well, they look quite a lot like ichthyosaurs. This simple fact has led many researchers to state that ichthyopterygians and hupehsuchians were related, however, there’s been little evidence to really cement this (just because two organisms look the same/have similar features, doesn’t mean they’re closely related. For example birds and bats both have wings, but they evolved powered flight independently and convergent to each other). As I’ve previously said, this is due to the lack of really primitive fossil ‘ichthyosaurs’ as well as our fairly poor understanding of where ichthyosaurs fit relative to other diapsids. However, Catorhynchus has given us a glimmer of hope, enabling us to, for the first time, really start to understand how ichthyosaurs first came about. Now, thanks to Catorhynchus, we think that ichthyosauromorphs (which now includes hupehsuchians) originated in China in the Earliest Triassic, which was a warm tropical archipelago ‘back in the day’. This is interesting, as we know that other groups of marine reptiles, such as sauropterygians (plesiosaurs, pliosaurs et al.) may have also originated in this area at the same time, so Earliest Triassic China may have provided very good conditions to harbour the evolution of many marine reptiles.

Phylogeny of ichthyosauromorphs, modified from Motani et al. 2014.

Phylogeny of ichthyosauromorphs, modified from Motani et al. 2014.

Don’t worry, I’ll stop teasing you now, I’ll actually talk about the fossil for a bit. With a host of unusual features such as really short snout, large flippers and a short body length (the shortest of all ichthyosauromorphs, estimated at a tiny 40 cm) and a really deep lower jaw, Catorhynchus is a weird beast. Yet, despite all these abnormalities, it looks like an ichthyosaur, I mean look at those big eyes! However, it also looks like a juvenile ichthyosaur. For me, and other ichthyosaur workers I’ve spoken to, this is the main reason why people of sceptical about drawing so many big conclusions from Catorhynchus. However, other people (untrustworthy creator of reptileevolution.com) have said that it certainly can’t be an ichthyosaur, and has to be an ‘ichthyosaur-mimic’, because yeah, if it has loads of scientifically diagnostic features of an ichthyosaur the most obvious answer is that it wants you to think it’s an ichthyosaur, just to troll the scientific community, and then years later scream ‘psyche!’ to everyone, you know, because fossils love to mess with us, the jerks.

Catorhynchus fossil from Motani et al. 2014. E represents a  newborn Chaohusaurus, for comparison.

Catorhynchus fossil from Motani et al. 2014. E represents a newborn Chaohusaurus, for comparison.

ANYWAY. I think it’s worth pointing out that it realistically might turn out to be a juvenile, even though Motani et al. do present some evidence that it’s a fully grown adult, for example the forefins of Catorhynchus are almost as long as its skull, a feature found exclusively in adult individuals. However, it’s also worth mentioning that even despite this, Motani et al. don’t completely dismiss the possibility of this specimen being a juvenile. Essentially, I feel it’s best to take this discovery with a pinch of salt until we find a few more specimens of Catorhynchus. Despite this uncertainty, we can be fairly sure that Catorhynchus may have been amphibious. Yeah, that’s right, amphibious and NOT an amphibian. Other articles have said that Catorhynchus is an amphibian, this is incorrect, as Amphibia form their only little group of organisms, which ichthyosauromorphs aren’t part of! However, Catorhynchus is amphibious, i.e. it shares its time between land and water. How do we know this? Well from the fossil, Motani observed that the carpus may have allowed the flipper to bend in a way much like the flippers can bend in seals, and since seals have flippers for limited terrestrial locomotion, it seems likely that this was also the case for the flippers of Catorhynchus. Motani also presents a case for suction feeding in Catorhynchus, which brings the contentious debate of whether other ichthyosaurs fed via suction feeding back to the table.

To summarise Motani and friends have presented the world with a new ichthyosauromorph which, if verified with further specimens, will help us to really start to understand how ichthyosaurs (and perhaps marine reptiles more widely) first evolved, as well as to understand the place of ichthyosauromorphs within Diapsida. And since it was published in Nature, it might turn a few heads, perhaps persuading more people to join the very small field of ichthyosaur of palaeobiology. As always let us know what you think, comment below or Tweet us (or indeed, even Facebook us).

Not only was it amphibious, Catorhynchus was also the most miserable of all the ichthyosauromorphs.

Not only was it amphibious, Catorhynchus was also the most miserable of all the ichthyosauromorphs.

Deinocheirus: why beer-bellies are bad-ass and the importance of being weird

Today started out as a fairly normal day. I overslept thanks to marathonning House late into the night/morning (note: not due to working late/early on my publication, oops), I dragged myself out of bed and into the office. I then, still half-asleep checked Twitter (the morning ritual was well underway) and then suddenly, I displayed both ends of the NedryGrant excitement chart (patent pending) simultaneously. Deinocheirus. It was DeinocheirusDEINO-RUDDY-CHEIRUS! At the moment, I’m in an office full of volcanologists, so no-one understood my excitement (in fact most thought I had some form of disposition, I mean I was practically frothing at the mouth with excitement). I immediately texted Richard and all my other palaeontological friends/colleagues with two words: DEINOCHEIRUS PUBLISHED.

My face on the morning of the 22nd October 2014. (I even laughed like a Dilophosaurus).

Story time

So why was I so stupidly excited? Well, I’m glad you asked. To explain this excitement, our tale begins in 1965. It was July, and the Polish-Mongolian Palaeontological Expedition had stumbled upon a ‘monster’ find. Forelimbs and a shoulder girdle 2.4 metres long belonging to a 70 million-year-old dinosaur with surely the largest forearms of a bipedal animal ever. However, that was all they found. What in the Seven Hells was this magnificent beast? Surely these the arms of some superpredator, akin to Allosaurus or perhaps a mega-Velociraptor? Deinocheirus mirificus was (‘unusual horrible hand’) was ‘born’. For seven-years, this was the most likely explanation. In this time, palaeontologists and members of the public alike went wild with fantastical recontructions of this new and wacky beast, some even going as far as noting that the arms were used much like those of a giant sloth. Alas, in 1972 John Ostrom (the guy responsible for revolutionising the way we think about dinosaurs in relation to birds in the 60s) noted that the bones in the forearm of Deinocheirus appeared similar to those found in the ornithomimosaurs, a group of secondarily-herbiverous theropod dinosaurs very similar to modern ostriches. This agreed with the sentiments of the team that initially discovered Deinocheirus, so it was settled, the beast was in fact an ornithomimosaur. Mystery solved. Right?

Dem Claws.

Dem Claws.

Unfortunately not. Fast forward a little over 40 years later to October 2013, and we still hadn’t found any more remains of the all-too mysterious Deinocheirus. That was all to change. At the SVP 2013 Symposium (one of the biggest annual events in palaeontology) there were hushed, exciting whisperings of new Deinocheirus material (apparently, I couldn’t afford to go). And then, a speaker emerged and confirmed it, Deinocheirus was back, the mystery was apparently solved. New material had been discovered and we now had a 95% complete skeleton to work with. However, this wasn’t fully shown at SVP, and the entire palaeontological community had to wait with baited breath until the work was published. One of the greatest mysteries of 20th and 21st century dinosaur palaeontology had been solved, but we had to wait. It was agonising. Personally, I grew up enthralled with the mystery of Deinocheirus as did many palaeontologists, both young and old, so to be kept in the dark like this was painful.

The Big Reveal

Fast forward again, exactly (pretty much) to a year later. Late October 2014. A dreary-eyed, 20-something-year-old palaeo grad-student is almost hyperventilating over an image he found on Twitter. Ladies and gentlemen, Deinocheirus has landed. And bloody hell if it isn’t the weirdest thing we’ve ever seen.

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The Beer-Bellied weirdo in all it’s glory. Deinocheirus mirificus.

Mystery Solved

Standing almost as tall as T. rex, and weighing in at a hefty 6 tonnes Deinocheirus is the biggest ornithomimosaur to dateSo it was big, no biggie right (heh)? Wrong, in addition to it’s monstrous size it’s also (and I might have already said this) bloody weird. With a really deep lower jaw, no teeth, huge forearms, relatively small hindlimbs, a big old “beer belly” (the best description of dinosaur’s anatomy ever, thanks Tom Holtz!) and tall neural spines (similar to those seen in SpinosaurusDeinocheirus sure is different to the ‘typical’ ornithomimosaurian body plan of Galimimus, with long legs and many other features that suggested it was a fast runner. Quite the opposite, Deinocheirus was a big, sluggish brute with a huge appetite. After 50 years, the mystery of Deinocheirus seems to be solved then, it’s a incredibly odd looking, slow moving, bulky, T. rex sized, beer-bellied behemoth. Myth busted, right?

Skeletal reconstruction of Deinocheirus mirificus. Modified from Lee et al. 2014.

Skeletal reconstruction of Deinocheirus mirificus. Modified from Lee et al. 2014.

Again, wrong. These new specimens are that good that we can already begin to hypothesise how Deinocheirus actually lived out it’s seemingly odd, slow lifestyle. Deinocheirus was discovered in the Nemegt Formation, a deposit which is 70 Million years-old (Late Cretaceous), and was an ecosystem similar to that of the Okavango delta today. First off, over 1400 gastroliths were present, probably used to aid in digestion of food, (mainly plants) making up for the lack of teeth. The morphology of it’s jaws and its broad bill (similar to those found in hadrosaurs and ducks) suggest that certain muscles associated with biting were small, meaning that Deinocheirus probably ate soft (and possibly water-dwelling) plants. But there wasn’t just some stones in that big beer belly, no sir! Evidence of a half-eaten fish was found as well, indicating that Deinocheirus was no means a fussy eater, and probably a ‘megaomnivore’ eating pretty much anything it could get it could swallow. This seems to fit well, especially when you consider Deinocheirus’ place in the Nemegt ecosystem, as generalist ‘all you can eat’ type deal (finally, a dinosaur I can relate to) it wouldn’t be in such harsh competition with the other herbiverous dinosaurs in the area that mostly ate plant matter from trees. However, not only do you need to outcompete you friendly neighborhood herbivores to keep on truckin’ in a Cretaceous world, you also need to be not eaten yourself. The main threat in the Nemegt ecosystem was probably the 12 metre long, 5 ton tyrannosaur, Tarbosaurus. However, Deinocheirus seemingly has an answer to everything by sacrificing speed for bulk and size, it was probably too big (and bloody hell, those claws) for Tarbosaurus to safely take on.

Deinocheirus_fin_colcorr_lres

Deinocheirus in situ. Image credit: Andrey Atuchin.

We also know a few more tricks that Deinocheirus had up its exceedingly large sleeves. Remember those Spinosaurus-like neural spines? They were probably there to support the bulky beer belly, similar to an “asymmetrical cable-stayed bridge“. It also had broadended tip-toes (pedal unguals, to be technical), allowing it not to sink when wading into wetter areas. And those claws? No longer used as lethal disembowlers, but for digging/plant gathering. So Deinocheirus seemingly was perfectly adapted to life on the braided, meandering rivers of the Nemegt ecosystem, unafraid of pesky Tarbosaurus, perfectly content to munch away until its heart (and beer belly) was content, and then waddling to the next patch of river to devour (and P.S Deinocheirus didn’t half walk funny).

And the moral of the story is…

By now, you’ve probably found literally hundreds of grammatical and spelling errors, due to the fact that I’ve been excitedly vomiting words onto my laptop in wave after wave of dino-induced mania. Yes it’s weird, and yes I love it because it’s pretty much me in dinosaur form, but why is this important? You’ll probably see this on IFLS (I F***ing Love Science) in a summary post, with ‘weird fat dinosaur discovered’ alongside ‘cure for cancer found’ and ‘artificial intelligence finally sorted’, making palaeontology, yet again look like the stupid and childish sibling of all the other sciences (e.g. “dino with big nose discovered”, unfortunately not a joke). But this is more than just some crazy guys with beards and stetsons finding a random pile of bones and shouting eureka until Nature finally publishes their work. Oh no. This, as well as many other finds over the last year shows us just how extreme dinosaurs can get. In the past 12 months, we’ve had a new, now with more swimming (TM) Spinosaurus recontruction, Dreadnoughtus, possibly the largest dinosaur ever, as well as long-snouted and pygmy tyrannosaurs. Not to mention feathered ornithischians (R). Dinosaurs have often been regarded as evolutionary extremes, and we’re only now beginning to understand just how these extreme animals lived and evolved.This understanding allows us to further understand evolution works, and how organisms can evolve in various environments and under different conditions.Not only is Deinocheirus a weird and wonderful beast, but when we look at it as a living, breathing animal, rather than a poster-child for all things weird and wonderful, we can begin to further understand  the evolutionary processes involved in theropods, a group which would garner the evolution of an incredibly diverse and successful group of animals, the birds. Deinocheirus exemplifies that palaeontologists, by investigating extremely adapted animals, such as dinosaurs, can further the understanding of the the process of evolution, one of the most important processes on Earth, and just how far it can go, and what wonderfully strange creatures it can help to explain.

So there you have it. Deinocheirus. It sure is a good day to be a palaeontologist.

Taxon of the Week: Postosuchus

In this week’s TotW, Ryan takes us through the posto child of the ‘rauisuchians’, Postosuchus.

When someone mentions the Mesozoic, you instantly think about dinosaurs. Admit it, it’s fine, there’s no judgement on this blog. You also will predominately think about dinosaurs from the Jurassic and the Cretaceous, with good old T. rex and co. (allosaurs, carcharodontosaurs, spinosaurs etc.) ruling the roost at the top of the food chain, whilst sauropod behemoths (amongst other ridiculously sized herbivores) wandering about in herds etc. etc. However, the Triassic (seemingly the Cretaceous and Jurassic’s ugly sister) is often forgotten about. Yes, we don’t have things which are outrageously large or ridiculously bipedal (or do we..?), but in the Triassic, crurotarsans (crocodile-line archosaurs) were having a bit of a field day.

awesomesozoic

The image that immediately springs to mind as soon as you mention ‘Jurassic’ or ‘Cretaceous’. Clearly.

Here on TDS, we think the Triassic (as well as plenty other eras, not just the Jurassic and Cretaceous) is pretty awesome too. The Triassic was a time of recovery, the Permian-Triassic mass extinction event had been and gone (and almost taken all of life on Earth with it). Dinosaurs were just starting out, and sitting on top of the food chain was, you guessed it, Postosuchus. If you look at the skull of Postosuchus kirkpatricki below, look carefully. Back in the 1980s famous palaeontologists thought Postosuchus (along with Poposaurus) could be a tyrannosaur ancestor. You can see where they’re coming from. Postosuchus was first discovered in 1922, and for 60 odd years after that, people didn’t really know what to make of it. First reports penned it as a Coelophysis, 20 years later, other finds were thought to belong to a new phytosaur. It wasn’t up until 1985 that the holotype, a well preserved skull and some postcranial remains, of Postosuchus kirkpatricki was formally announced. 

BronzePostosuchus

Totally not a dinosaur. No seriously.

Weighing in at almost 300kg, at reaching almost 4m when fully grown, Postosuchus was one (if not the) largest predator in the Triassic. With good long distance vision, a decent sense of smell, and a possible Jacobson’s organ, and oh, not to mention, over 7cm dagger-like teeth, this killing machine well may have taken down a fair few aetosaurs in it’s time (not a small feat). So fairly fearsome, but not as impressive as the theropods that were to come later in the Mesozoic, surely? Well, again, no.

tumblr_m3zd8iT4YA1rrpn3bo1_500

These coelophysoids clearly came to the wrong neighbourhood.

What makes Postosuchus (and many other ‘rauisuchians‘) so interesting are its hindlimbs. One of the major dinosaurian innovations was the erect hindlimb posture, enabling more efficient locomotion. In the Triassic, descendants of crocodiles (who now have the ‘sprawling’ hindlimb posture) such as Postosuchus had a go at this hindlimb arrangement (evolutionary speaking). Whilst debated, many palaeontologists view Postosuchus (amongst other Triassic crurotarsans) as being bipeds (or at the very least facultative bipeds). So that means Postosuchus could use it’s forelimbs to kill things as well as it’s terrifyingly huge mouth (like bears do). To summarise, Postosuchus is a nightmare-inducing, killer croc-bear from back in time. It also raises the question (to be investigated by a future blog post on TDS, hopefully) of why exactly did dinosaurs survive through to the Jurassic, and rauisuchians go extinct, and why did crurotarsans go back to being solely quadrupedal?

biobeast-sm

Killer croc-bear from back in time. (Thank you internet).

Told you the Triassic was awesome. (Also, more to come on the locomotory strategies of Triassic crurotarsans to come, right after I finish my final 4th year exams…).

Bonus picture (because it’s cool and reasonably accurate, although not as accurate as the previous picture):

Postosuchus_mural

There’s no escape from the Post(o) Man (not actually a man).

References

  • Case, E. C. (1922). “New reptiles and Stegocephalians from the Upper Triassic of western Texas”. Carnegie Institution of Washington Publication 321: 1–84.
  • Case, E. C. (1932). “On the caudal region of Coelophysis sp. and on some new or little known forms from the Upper Triassic of western Texas”. University of Michigan Museum of Paleontology Contributions 4 (3): 81–91.
  • Case, E. C. (1943). “A new form of Phytosaur pelvis”. American Journal of Science 241 (3): 201–203. doi:10.2475/ajs.241.3.201.
  • Chatterjee, S. (1985). “Postosuchus, a new Thecodontian reptile from the Triassic of Texas and the origin of Tyrannosaurs”. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences 309 (1139): 395–460. doi:10.1098/rstb.1985.0092.
  • Drymala, S. & Bader, K. (2012). Assessing predator-prey interactions through the identification of bite marks on an aetosaur (Pseudosuchia) osteoderm from the Upper Triassic (Norian) Chinle Formation in Petrified Forest National Park (Arizona, USA). Journal of Vertebrate Palaeontology, Program and Abstracts 2012, p89.

What’s New(s): 6/01/2014 incl.; Naked Dinosaurs, Saudi Arabian dinosaurs and Ichthyosaur storms.

Christmas is a time of rest, festive cheer, spending time with loved ones and (probably most importantly) food.       This is seemingly not the case for academics. Firstly, Richard and I have been busy revising for our January finals, so whilst we’ve tried to give you a few juicy morsels over to tide you over the festive season, we’ve not really had chance to bring you the latest news. Coupled with this is that over this year’s festive period there’s been a lot of palaeontology going on. Holiday, what holiday?

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PhD Comics, get used to laughing (and crying) along to them as a postgrad.

So here is a What’s News(s) bumper edition, with 5 of the biggest news stories in palaeontology over the festive period. This week, we’ve got Saudi Arabian dinosaurs, naked dinosaurs, ichthyosaurs, body-size trends in evolution and some Hungarian palaeoneurobiology! Since we don’t want to spam you, we might start evolving our What’s New(s) sections so they are weekly, rather than as-and-when the news comes out (unless it’s really cool).

The first Saudi Arabian dinosaurs. Like has been previously stated, new dinosaur finds aren’t rare occurrences. They happen roughly every 1.5 weeks. Big deal right. Wrong (again). Benjamin Kear’s team have discovered a few caudal vertebrae and some teeth from Saudi Arabia, from the Maastrichtian (75 Ma, ish), and have confidently identified the vertebrae to be from a titanosaur, and the teeth to be from an abelisaurid. The confidence of these groupings is the first time that fossils the Arabian peninsula have been able to be classified as dinosaurian without contention. It also stretches the palaeogeographical ranges of titanosaurs and abelisaurids to the northern margin of Gondwana, whilst showing us (with just one find) that dinosaur ecology in this area may have been quite diverse in the mid-late Cretaceous. The papers also open access (over here on PloS One).

saudidinos

A-C: vertebra of a titanosaur from Saudi Arabia; D-F: tooth of a abelisaurid (again from Saudi Arabia). From Kear et al. (2013).

Naked dinosaurs a common sight during the Mesozoic. For a pretty ‘young’ blog, we’ve already mentioned naked dinosaurs (ooo err!) twice. That says a lot about Richard and I. Moving swiftly on… Since the discovery of the feathered Sinosauropteryx in 1996 (and a plethora of other feathered Chinese dinosaurs since) has caused a bit of frenzy. So much so, that even the Jurassic Park conceded, and created this monstrosity (they’ve now de-conceded, and have yet again ignored feathered dinosaurs). Since 1996, palaeontologists have endeavoured to find just how far back feathers go in the dinosaur lineage. Up until the early 2000s, we thought we had it covered, and that feathers were ancestral to theropods (with discoveries such as Dilong paradoxus, a feathered tyrannosaur sparking fierce debate over whether good old T. rex  had a majestic feathered coat). Yet, as always, it only takes one discovery to turn everything upside down. Pscittacosaurus was that discovery. Pscittacosaurus is a ceratopsian (basal relative to the frilled dinosaur celebrity Triceratops), but with some proto-feathers. Crazy times.

bakker deino

Richard’s favourite naked dinosaur, Deinonychus (which probably wasn’t naked at all).

Paul Barrett then set about to try and solve just where the feathered dinosaur bus stopped. He and his team looked at all of the dinosaur skin impressions found to date, looking for any sign of feathers (or similar structures) and then considered the data is a evolutionary context. He concluded that despite Pscittacosaurus, most ornithischians (ceratopsians, ornithopods, pachycephalosaurs and thyreophorans) and sauropods would have had scales. With the majority of dinosaurian clades having scales rather than feathers, Barrett tentatively concluded (at SVP 2013, in sunny Los Angeles) that scales were probably the ancestral condition in dinosaurs.  But by now we know that all it takes is one feathered dinosaurs from the Triassic (or even the early Jurassic) to upheave this study.

The I(chthyosaur) of the Storm. Quick bit of local (for British palaeontologists  anyhow) news for everyone. After heavy storms (no, seriously, before any Americans/Canadians/anywhere with ‘proper weather’ complain) a 1.5 m long partial ichthyosaur skeleton has been revealed at the base of a cliff in Dorset, and is being restored by the Jurassic Coast Heritage organisation. Three ichthyosaurs have been revealed in similar ways after storms in the past year along the Jurassic Coast. So remember kids, 80mp/h winds and floods aren’t all bad.

Ichthyosaur_hharder

That’s right, icthyosaurs can fly. And then they become storms. True story (Not actually true).

Growing fields: body-size trends throughout the fossil record. Whilst by no means is the study of body-size trends through evolutionary history a new field, but Mark Bell has just published a brilliant, relatively short and Open Access (whoop!) introduction to body-size trends in the fossil record. The article really does make you feel rather small (literally). It also goes through some long established rules on body-size evolution (e.g Cope’s rule), whilst also noting some nice examples of giganticism and dwarfism in the fossil record. Finally, he also states that new computer simulations/software maybe able to help us to further understand these trends in the future.

Bell_gigantism_Figure-1

Where’s Wally, PhyloPic edition. (From Bell 2013 and PhyloPic).

The very Hung-a-ry dinosaur brain. This gem of palaeontological news really does show how fieldwork and digital analysis can produce fantastic results. A new find of a partial skull of Hungarosaurus (from, you guessed it, Hungary) has enabled Hungarian palaeontologists to made a cast of the endocranial cavity, allowing them to analyse the braincase of this European anklyosaur. Initial results suggest that the cerebellum (area of the brain associated with motor control) is larger in volume than other ankylosaurs. This may well mean that Hungarosaurus was better able to run than other anklyosaurs (well known for not being the fastest of starters…).

hungarybrain

Endocast of Hungarosaurus. cbl=cerebellum (roughly circled, from Osi et al. 2013)

References:

Kear BP, Rich TH, Vickers-Rich P, Ali MA, Al-Mufarreh YA, et al. (2013) First Dinosaurs from Saudi Arabia. PLoS ONE 8(12): e84041. doi:10.1371/journal.pone.0084041

Mayr, G., Peters, D. S., Plodowski, G. & Vogel, O. Naturwissenschaften 89, 361–365 (2002)

Zheng, X.-T., You, H.-L., Xu, X. & Dong, Z.-M. Nature 458, 333–336 (2009).

http://www.nature.com/news/feathers-were-the-exception-rather-than-the-rule-for-dinosaurs-1.14379

http://www.bbc.co.uk/news/uk-england-dorset-25548426

http://www.palaeontologyonline.com/articles/2014/trends-body-size-evolution-fossil-record-growing-field/

Ősi, Attila, Pereda Suberbiola, Xabier, and Földes, Tamás. 2014. Partial skull and endocranial cast of the ankylosaurian dinosaur Hungarosaurus from the Late Cretaceous of Hungary: implications for locomotion, Palaeontologia Electronica Vol. 17, Issue 1; 1A; 18p;
palaeo-electronica.org/content/2014/612-skull-of-hungarosaurus

What’s New(s): Acheroraptor.

‘Whats New(s)’ is our new (poorly titled) news and views-esque section, where we keep you up-to-date on the latest findings in palaeontology, as well as explaining some key ideas behind them. For TDS first ever What’s New(s) we’ve got the exciting discovery of Acheroraptor! It also represents the first post on TDS with actual content (and dinosaurs). Huzzah!

New dinosaur fossils are being found all year round. No big deal, right? Wrong. Quite a lot of these new fossils fall under 3 very interesting categories:

  1. Crazy looking (a technical term).
  2. Exceptional preservation (and a shameless Bristol Palaeo plug).
  3. Macroevolutionary importance.
acheroraptor_fossil

Maxilla (top) and dentary (bottom) of Acheroraptor (with non-isolated teeth).

Acheroraptor falls into number 3. Not only does it have one of the best names ever, Acheroraptor temertyorum (literally meaning ‘Underworld thief’), but it’s one of the first major fossils (previously all we had was just isolated teeth) of dromaeosaurs (velociraptors and their close relatives) from North America in the Late Cretaceous. I say ‘major fossils’ but it’s still only 2 bones in the skull, a full maxilla and an almost complete dentary. Oh, and some non-isolated teeth. Nonetheless, the little blighter is (apparently, according to a wonderful reconstruction by Danielle Dufault) a cutie!

archeroraptor

As ‘underworld thieves’ go, this ones adorable.

So why is it important? Palaeontologists reconstruct evolutionary relationships by looking at how morphological features vary between different species. So, the more complete the fossil record is for a species, the more features you can compare, and the more confidence you can have when inferring the evolutionary relationship. So, going from a few isolated teeth, to a couple of (relatively) whopping great big skull bones is a fantastic leap! So, Acheroraptor has (despite being ‘American‘) been found to be more closely related to Asian dromaeosaurs, such as Velociraptor mongoliensis. This means that there was more faunal interchange between ‘America’ and ‘Asia’ back in the Late Cretaceous.

Cool right?

References

Evans, D. C., Larson, D. W. and Currie, P. J. (2013) A new dromaeosaurid (Dinosauria: Theropoda) with Asian affinities from the latest Cretaceous of North America, Naturwissenschaften, 100(11), 1041-1049