Friday phalanges: Megaraptor vs. Saurophaganax
April 19, 2013
Up top there is a commercially obtained cast sculpture of a thumb claw of Megaraptor. Down below is an unpainted urethane cast of one of my favorite inanimate objects in the universe: OMNH 780, a thumb claw of Saurophaganax. I dunno how much of the Megaraptor claw is real [none, it turns out, but it's based on a true story]; certainly the cast is faithful enough to record some tool-marks in the rugose part near the base. But I know how much of OMNH 780 is legit, and that is all of it. I would have put in a photo of the actual specimen but irritatingly I forgot to take any during my recent visit, and I didn’t have the Megaraptor claw back then anyway. Hopefully I’ll get back to the OMNH this summer, and then it is ON.
The kaiju-loving fanboys of CarnivoraForum undoubtedly want to know how these two compare. Well, much to my disappointment, the Megaraptor claw is a shade longer (28.7 cm max straight-line distance) than the Saurophaganax claw (26.3 cm). But the Saurophaganax claw is about twice as thick and way more robust, and the flexor tubercle which anchored the tendon that powered the claw’s movement is friggin’ immense. It’s like pitting an NBA forward against an NFL linebacker: one is a little taller, but the other one will pound you like a tent stake.
If anyone’s wondering, these claws are both waaay shorter than those of Therizinosaurus (half a meter and up), which still holds the longest-claws-of-anything-ever title. The problem for fans of excessive violence is that Therizinosaurus probably wasn’t doing terribly exciting things with its claws–grooming its feathers, making veggie kabobs, and scratching its ample behind, most likely.
The same was not true for Saurophaganax, which the unbelievers call Allosaurus maximus, a red-blooded all American murder machine with a triple PhD in kicking your ass. When it wasn’t drinking camptosaur blood straight from the jugular, it was eating mud-mired diplodocids butt first while they were still alive. And what about those rumors that Saurophaganax was completely feathered in $100 bills, or that it was the direct linear ancestor of Charles Bronson and Steven McQueen? It’s probably too soon to say, since I just made them up, but I’ll bet your mind is blown nonetheless.
How dangerous was Saurophaganax? Let me put it this way: it’s still dangerous. Thanks to the high concentration of heavy elements in Morrison dinosaur bones, you’re supposed to air out the specimen cabinets before you start working so the radon can escape. Otherwise you might breathe in freakin’ radioactive gas and get cancer (in contrast to some “facts” in the previous paragraph, this is actually true). That’s right, Saurophaganax can kill you, just by lying around in a drawer. After 145 million years, it’s still reaping souls for Hades. By god, that’s giving them what for!
In short, the thumb claw of Saurophaganax is the most impressive instrument of dinosaurian destruction I’ve yet laid eyes on. If you want to see it in context, check out the mounted skeleton at the Oklahoma Museum of Natural History in Norman.
Night at the Museum: LACM’s Camp Dino
April 8, 2013
Last night London and I spent the night in the Natural History Museum of Los Angeles County (LACM), as part of the Camp Dino overnight adventure. So we got lots of time to roam the exhibit halls when they were–very atypically–almost empty. Above are the museum’s mounted Triceratops–or one of them, anyway–and mounted cast of the Mamenchisaurus hochuanensis holotype, presented in glorious not-stygian-darkness (if you went through the old dino hall, pre-renovation, you know what I mean).
We got there early and had time to roam around the museum grounds in Exposition Park. The darned-near-life-size bronze dinos out front are a minor LA landmark.
The rose garden was already closed, but we walked by anyway, and caught this rainbow in the big fountain.
After we checked in we had a little time to roam the museum on our own. I’ve been meaning to blog about how much I love the renovated dinosaur halls. The bases are cleverly designed to prohibit people touching the skeletons without putting railings or more than minimal glass in the way, and you can walk all the way around the mounted skeletons and look down on them from the mezzanine–none of that People’s Gloriously Efficient Cattle Chute of Compulsory Dinosaur Appreciation business. Signage is discreet and informative, and so are the handful of interactive gizmos. London and I spent a few minutes using a big touch-screen with a slider that controlled continental drift from the Triassic to the present–a nice example of using technology to add value to an exhibit without taking away from the real stuff that’s on display. There are even a few places to sit and just take it all in. That’s pretty much everything I want in a dinosaur hall.
Also, check out the jumbotron on the left in the above photo. It was running a (blessedly) narration-free video on how fossils are found, collected, prepared, mounted, and studied, on about a five-minute loop. Lots of pretty pictures. Including this next one.
There are a couple of levels of perspective distortion going on here, both in the original photo and in my photo of that photo projected on the jumbotron. Still, I feel confident positing that that is one goldurned big ilium. I’m not going to claim it’s the biggest bone I’ve ever seen–that rarely ends well–but sheesh, it’s gotta be pretty freakin’ big. And apparently a brachiosaurid, or close to it. Never mind, it’s almost certainly an upside-down Triceratops skull. Thanks to Adam Yates for the catch. I will now diminish, and go into the West.
Triceratops, Styracosaurus, and Einiosaurus–collect the whole set!
Of course, the centerpiece of the second dinosaur hall–and how great is it that there are two!?–is the T. rex trio: baby, juvenile (out of frame to the right), and subadult. Yes, subadult: the “big” one is not as big as the really big rexes, and from the second floor you can see unfused neural arches in some of the caudal vertebrae (many thanks to Ashley Fragomeni for pointing those out to me on a previous visit).
Awwwww! C’mere, little fella!
Still, this ain’t Vulgar Overstudied Theropod Picture of the Week. Here are some sweet pneumatic diplodocid caudals in the big wall o’ fossils (visible behind Mamenchisaurus in the overhead photo above). The greenish color is legit–in the Dino Lab on the second floor, they’re prepping a bunch of sauropod elements that look like they were carved out of jade.
Sudden violent topic shift, the reason for which will be become clear shortly: London and I have been sculpting weapons of mass predation in our spare time. In some of the photos you may be able to see his necklace, which has a shark tooth he sculpted himself. Here are a couple of allosaur claws I made–more on those another time.
The point is, enthusiasm for DIY fossils is running very high at Casa Wedel, so London’s favorite activity of the evening was molding and casting. Everyone got to make a press mold using a small theropod tooth, a trilobite, or a Velociraptor claw. Most of the kids I overheard opted for the tooth, but London went straight for the claw.
Ready for plaster! Everyone got to pick up their cast at breakfast this morning, with instructions to let them cure until this evening. All went well, so I’ll spare you a photo of this same shape in reverse.
We were split into three tribes of maybe 30-40 people each, and each tribe bedded down in a different hall. The T. rex and Raptor tribes got the North American wildlife halls, but our Triceratops tribe got the African wildlife hall, which as a place to sleep is about 900 times cooler. Someone had already claimed the lions when we got there, so London picked hyenas as our totem animals.
Lights out was at 10:30 PM, and the lights came back on at 7:00 this morning. Breakfast was out from 7:15 to 8:00, and then we had the museum to ourselves until the public came in at 9:30. So I got a lot of uncluttered photos of stuff I don’t usually get to photograph, like this ammonite. Everyone should have one of these.
London’s favorite dino in the museum is Carnotaurus. It’s sufficiently weird that I can respect that choice.
Not that there’s anything wrong with the old standards, especially when they’re presented as cleanly and innovatively as they are here.
Finally, the LACM has a no tripod policy, and if they see you trying to carry one in they will make you take it back to your car. At least during normal business hours. But no one searched my backpack when we went in last night, and I put that sucker to some good use. Including getting my first non-bigfoot picture of the cast Argentinosaurus dorsal. It was a little deja-vu-ey after just spending so much time with the giant Oklahoma Apatosaurus–elements of the two animals really are very comparable in size.
If you’re in the LA area and interested in spending a night at the museum–or at the tar pits!–check out the “Overnight Adventures” page on the museum’s website. Cost is $50 per person for members or $55 for non-members, and worth every penny IMHO. It’s one of those things I wish we’d done years ago.
Hyperossified megafrogs of the Oxford University Museum of Natural History
September 25, 2012
Another extraordinary specimen from the wonderful Oxford University Museum of Natural History: the skeleton of a goliath frog Conraua goliath, the largest extant anuran, which comfortably exceeds 30 cm and 3 kg in life:
As noted by sometime SV-POW!sketeer Darren Naish over on Tetrapod Zoology, frogs have stupidly weird skeletons — surely the most derived of any tetrapod, despite their lowly, early diverging “amphibian” status. Rather than describe all the oddities myself, I’ll just quote Darren’s article:
Anurans have (at most) nine presacral vertebrae, and some have as few as five; ribs are either highly reduced or absent; the radius and ulna are fused (forming the radioulna); the bones of the pectoral girdle are highly reduced and complimented by an assortment of new weird bits; the pelvis consists of a rod-like central unit (the urostyle) surrounded by two super-long, shaft-like ilia; and in their (generally) elongate hindlimbs, the tibia and fibula are fused (forming the tibiofibula) while the ankle bones are elongated to form a long ‘extra’ limb segment.
That’s a pretty astonishing list; and, sure enough, frog skeletons weird me out every time I see them. (Of all the dead animals I’d like to get hold of in decent condition, to extract the bones from, frogs miss the top of the list only to bats, crocs and turtles. And maybe raptors.)
This particular species of frog has another skeletal oddity that caught my eye:
As you can see, the humerus is perforated: there is a distinct foramen running down it just behind the anterior edge. Is the anterior bar a partially detached deltopectoral crest? Or is it a completely novel ossification that has become partially fused to the humerus?
For what it’s worth, this feature doesn’t seem to be consistently present in goliath frogs. A bit of googling shows that it’s present in this skeleton, but not in this one from Bone Clones. The humerus of the latter does have a distinctly protruding deltopectoral crest, but it lacks the perforation. So I guess that is evidence against the Novel Ossification hypothesis.
Does anyone know more about this odd feature? Does it develop through ontogeny? Is it found in other frogs? What is its mechanical significance?
Hoatzins lie (and so do parrots)
September 20, 2012
Back when we were at Cambridge for the 2010 SVPCA, we saw taxidermied and skeletonised hoatzins, and were struck that the cervical skeleton was so very much longer than the neck as it appears in life — because necks lie. At Oxford last week for the 2012 SVPCA, we saw a similar pair of hoatzin mounts (one adult, one juvenile) that clarified the situation:
And here is juvenile in side-view:
As you can see, it’s folding its neck way down out of the way, so that externally it appears much shorter. (And comparing with the Cambridge specimen, you can see that the neck skeleton is proportionally much longer than this in adult.)
Why does it do this? I have no idea.
But I do know it’s not unique to hoatzins. Another nice illustration of how misleading birds’ necks are when viewed in a live animal is this parrot (probably Amazona ochrocephala) in the Natuurhistorisch Museum of Rotterdam (from this Love in the Time of Chasmosaurs post):
One thing that’s not clear to me is how much of the neck the bird can extend in life. If the parrot wants to uncoil all that spare cervical skeleton to reach upwards or forwards, can it? Will the soft tissue envelope allow it? My guess is not, otherwise you’d surely see them doing it. But then … why is all that neck in there at all?
Plateosaurus sacra of the AMNH
August 15, 2012
We’ve shown a lot of sauropod sacra around here lately (for example here, here, and here), so here’s a little look back down the tree.
You haven’t heard from me much lately because I’ve been busy teaching anatomy. Still, I get to help people dissect for a living, so I can’t complain.
Further bulletins as events warrant.
Turtle laminae of the Yale Peabody Museum
June 23, 2012
Here’s a cool skeleton of the South American pleurodire Podocnemis in the Yale Peabody Museum.
What’s that you’re hiding in your neck, Podocnemis?
Laminae! Here’s a closeup:
The laminae run from the transverse processes to the prezygapophyses and the centrum, which I reckon makes them analogues of the PRDLs and ACDLs of sauropods.
As long as I’m posting on Peabody turtles, here’s Archelon. It’s not bad, if you’re into that sort of thing. Which Mike clearly ain’t, but for a good reason, which will be revealed soon.
For more info on vertebral laminae in extant non-dinosaurs, see this post and the lower left paragraph on page 212 of this paper.
Eyelashes of the Harvard Museum of Natural History
June 19, 2012
Secretary bird:
Matt pointed out to me something that in retrospect is obvious, though I’d never thought about it before: the eyelashes of birds are not homologous with ours, since mammals’ eyelashes are modified hairs and birds don’t have hair. Instead, their lashes are modified feathers. It would be interesting to see both kinds of eyelash under a microscope and compare.
It certainly looks as though these “feathers” are simple unbranched filaments — much like the earliest protofeathers found on so many of those wacky Chinese raptors. I wonder how closely they resemble the ancestral state?
Sperm whales of the Harvard Museum of Natural History
June 17, 2012
Check this baby out:
I know, I know what you’re thinking. “Enough with the vulgar overexposed skull of this beast, Taylor”, you cry: “Show us its zygapophyses!”
But of course.
This is from the anterior part of the tail, in right lateral view: the vertebrae that you see here are the third to seventh of those that carry chevrons.
The hot news here is of course that sperm whales go to all the bother of developing zygapophyses, right up at the top of their neural arches, down in a region of the body where they don’t come close to articulating and are of no conceivable use.
Anyone know why? Care to hazard a guess?
For previous adventures in the Harvard Museum of Natural History, see here (monotremes) and here (bird eggs).
Bird eggs of the Harvard Museum of Natural History
June 12, 2012
More from my flying visit to the Harvard Museum of Natural History. I found this exhibition of bird eggs very striking. In particular, it was shocking how much bigger the elephant-bird egg is than that of the ostrich.
From smallest to largest, the eggs are those of:
- Ruby-throated Hummingbird Archilochus colubris
- Common Redpoll Carduelis flammea
- House Finch Carpodacus mexicanus
- Eastern Screech Own Megascops asio
- Thick-billed Parrot Rhynchopsitta pachyrhyncho
- Red-necked Grebe Podiceps grisegeno
- Magnificent Frigatebird Fregata magnificens
- Red-tailed Hawk Buteo jamaicensis
- Cackling Goose Branta hutchinsii
- Bald Eagle Haliaeetus leucocephalus
- Tundra Swan Cygnus columbianus
- Wandering Albatross Diomedeo exulans
- Ostrich Struthio camelus
- Elephant bird Aepyornis sp.
As always, click through for full resolution.






































