The truly strange looking animal above is Falcarius utahensis. It's an early, omnivorous member of the theropod clade known as therizinosaurs. Not only does it look weird, it's also a bit different from other skeletals you may have seen on the web. Join me after the break for a bit of a discussion about Falcarius, and the challenges I faced with this reconstruction.

I should warn you, this won't be a tutorial on how I make my skeletal reconstructions. That would certainly be a fun series, but it would require quite a lot of time to do properly, so for now it'll have to wait. But there are still several points worthy of discussion.

First off, the animal was discovered in a bone bed of disarticulated individuals. The good news is that most of the individual elements are known, but the down side is the bones aren't all from the same sized animals. That means that cross-scaling is needed to restore the skeleton, but even that presents a challenge; the usual method of cross-scaling involves double-checking the results against the proportions of close relatives. Alas, in this case the fossil record for the base of the therizinosaur family tree isn't well known, and what is known makes it clear that Falcarius has very different proportions than it's closest known relative: Beipiaosaurus.

(Image copyright Greg Paul)

When the original description of Falcarius was published in 2005, it came with the skeletal drawing at left. Obviously I don't agree with those proportions now, but at the time it had been done when fewer bones had been excavated, prepared, and described in detail, so Greg Paul had to try and scale them based on a smaller amount of material to compare with.

In fact, given the difficulty of restoring the proportions I intentionally avoided doing a Falcarius skeletal reconstruction for several years. I might have avoided it all together, but towards the end of my tenure at the WDC we mounted a cast of Falcarius that Gaston Design produced. Working on that skeleton I was able to not only measure and photograph all of the elements, but spend time looking at how the individual elements were matched up. Some parts of the cast's vertebral column are from different sized individuals (an unavoidable consequence of trying to piece together a skeleton from several different individuals). In other cases, vertebrae I had assumed to be from different sized animals were in fact crushed.

In addition to the hands-on data, Lindsay Zanno had been hard at work publishing more detailed information on Falcarius (this is actually notable, as not all researchers are as timely with getting more detailed descriptions of a new animal into print).

As the information piled up I felt that a skeletal was possible to be done. I still didn't tackle it though, as there were plenty of "low-hanging fruit" skeletals that could be done from less-challenging animals.

As luck would have it, I ended up being asked to produce a skeletal of Falcarius for a display in the new Utah Museum of Natural History building (side note: the new UMNH building just opened, and houses one of the most impressive natural history displays in North America, go see it!).

Since I was working with the UMNH, I got valuable input from several of the researchers who worked on the specimens. They were able to provide additional information - I won't go into the nitty-gritty of it (although you may if you would like), but I wanted to point out that the end result was quite a surprise to me. And little is more satisfying than when you are really surprised at the end of a skeletal reconstruction.

Resulting skeletal in hand, you can compare it to the most recent studies of the therizinosaur family tree, as well as the excellent research being done by Lindsay Zanno and Peter Makovicky on the origin of plant-eating in theropod dinosaurs, and Falcarius starts to tell an interesting tail about the order in which therizinosaur traits appeared.

Falcarius appears to already be specialized for browsing for high forage. Given the lack of an enlarged gut for fermentation it probably preferred to seek out higher-quality plant matter, like fruiting bodies or seeds. The partially upright stance appears concurrently with a widening of the passage through the pelvis (not visible in side view) allowing move guts into that area, causing the center of gravity to sit further back despite the elongation of the neck.

The large hand claws (from which the authors derived the name "sickle-cutter") may have allowed Falcarius to pick up small prey, but they also may have served as defense for a fairly slow animal with small teeth. The first toe is low and long enough to start interacting with the ground, perhaps to provide balance and stability when browsing high. All of these features would be carried to extremes in advanced therizinosaurs, but they seem to already be playing the same (albeit incipient) functional roles in Falcarius.

So with Falcarius we have an animal that at first glance appears inexplicably strange, but when viewed through the lens of where it was coming from (long-bodied small-headed meat eaters) and where it ends up (the upright, pot-bellied therizinosaurs) the combination of traits start to make a lot of sense.

Isn't science grand?

References:

Kirkland, J. I., Zanno, L. E., Sampson, S. D., Clark, J. M. & DeBlieux, D. D., 2005. A primitive therizinosauroid dinosaur from the Early Cretaceous of Utah. Nature, v435, pp 84-87.

Zanno, L. E. 2006. The pectoral girdle and forelimb of the primitive therizinosauroid Falcarius utahensis (Theropoda, Maniraptora): Analyzing evolutionary trends withing Therizinosauroidea. Journal of Vertebrate Paleontology, v26 n3, pp 636-650.

Zanno, L. E. 2010. Osteology of Falcarius utahensis (Dinosauria: Theropoda): characterizing the anatomy of basal therizinosaurs. Zoological Journal of the Linnean Society. v158, pp 196-230.

Zanno, L. E. & Makovicky, P. J., 2011. Herbivorous ecomorphology and specialization patterns in theropod dinosaur evolution. Proceedings of the National Academy of Sciences. v108 m1, pp 232-237.

In 1999 Jeff Wilson and Matt Carrano published an excellent paper addressing the phenomena of "wide-gauge" sauropod trackways. For years researchers had been working to explain why sauropod trackways seemed to come in two very different flavors - some of them were very closely spaced...so much so that they would actually overlap on the midline of the track. Other sauropod tracks seemed to show animals walking with their feet spread much further apart.

What were paleontologists to make of this?

One explanation was that the trackways were made by the same type of sauropods that were engaging in different behaviors. In other words, perhaps sometimes a sauropod would walk with its legs close in, while at other times it would use a wide-gauge stance.

Wilson & Carrano proposed that instead the trackways were made by sauropods with different skeletal adaptations. They mustered quite a few lines of evidence, but perhaps the best was that there was a group of sauropods - titanosaurs - that in fact had a much wider pelvis than other sauropods. The paper created a framework for later workers to use when attempting to correlate track makers with fossilized trackways, and is generally a towering success.

But I did want to take issue with one figure of the paper - one that pops up repeatedly at SVP. It is figure 5, demonstrating their interpretation of hing leg stance:

That's Camarasaurus on the left and Opisthocoelicaudia on the right. The clever reader may have already surmised from the title of this post that I think the animal on the right has its legs spread too far apart. But I have a larger issue: both animals have their legs spread much too far apart.

Remember that narrow-gauged trackways actually have their feet fall so close together that they frequently overlap along the midline. There's no way even sauropod "A" could make those tracks in the stance as figured. And this is why I'm bringing this up, because animals generally don't walk around with their legs acting as perfectly vertical beams. If you spend time watching large animals walk away from you, you'd see something like this:

(Elephant image from here, rhino image from here.)

People also move like this, with our vertical limbs generally sloping in toward the midline when we walk or run. There are probably several reasons for this (including mechanical efficiency) but for our purposes here let's just setting on the fact that it happens. Large, straight-limbed graviportal animals tend to walk with the limbs angled inward, not down (and certainly not angled out).

And the trackways also demonstrate this. If you place place sauropods over the actual trackways in question, you end up with a stance more like this:

In this case I've put a diplodocid (Supersaurus) on the left, while the animal on the right is scaled to the pelvic dimensions of Opisthocoelicaudia as seen in the original paper. Both animals have the hind legs mostly vertical but gently sloping inward.

This is not to say that sauropods never adopted a pose with their legs spread out a bit; Wilson & Carrano point out that titanosaurs have adaptations that may have allowed them to evert their hind limbs more effectively. They suggest that titanosaurs may have done so when rearing up, or during other activities that require greater stability.

I don't take issue with that, and those sorts of differences in the legs and pelvis may make it possible to tease out further behavioral differences between sauropod groups. But when walking around in their day to day lives both the footprints and modern analogs make a strong case that the limbs should be vertical, and if anything sloping in towards the midline rather than spread away from it.

Reference:

Wilson, J. A, & Carrano, M. T. 1999. Titanosaurs and the origin of "wide-gauge" trackways: a biomechanical and systematic perspective on sauropod locomotion. Paleobiology, 25(2), pp. 252-267.