Unsolved Paleo Mysteries Month #18 – The Biggest Beefy Boys

In 1878, during the Bone Wars of American paleontology, Edward Drinker Cope published a description of a partial sauropod vertebra and femur from the Late Jurassic of Colorado (~150 mya). He classified it as a new species of the diplodocoid genus Amphicoelias (which he had named earlier that same year), designating it as Amphicoelias fragillimus in reference to the bone’s poor condition and incredibly fragile structure.

But what set this fragmentary find apart was its sheer size. The partial back vertebra measured around 1.5m tall (5′), with estimates of its full height anywhere up to 2.7m (8′10″) – twice the size of the same bone in Diplodocus, and far larger than anything else known.

Obviously its very difficult to accurately estimate the full body size of an animal from a single broken bone, but plenty of attempts have been made anyway, producing lengths of up to 60m (197′). For comparison, the largest living animal the blue whale reaches lengths of around 33m (108′).

Around the time of Cope’s death in 1897, his massive fossil collection was sent to the American Museum of Natural History, and the A. fragillimus vertebra was entered into their catalog

Only to vanish, never to be seen again.

Multiple searches through the collection have found no trace of it, and there’s speculation that at some point the fragile bone may have crumbled entirely into pieces and been thrown away. No other material of A. fragillimus has ever been found in the ~140 years since its description, despite searches of the area where it was originally discovered, leading to claims of the entire specimen being a hoax – suggestions that Cope exaggerated or typoed his measurements in his rush to outdo his rival Othniel Charles Marsh.

Without that paleontological holy grail of finding the lost fossil or a new specimen, we just don’t know how big that bone truly was, or whether A. fragillimus was a living kaiju or a much more “normal-sized” sauropod. There’s even been some speculation of it being proportioned more like a rebbachisaur, with tall “sailback” vertebrae.

Except

In a surprise plot twist, there is another.

An absolutely enormous neck vertebra hints at the existence of other gigantic mega-sauropods. We still don’t have enough remains to know what the heck was going on with these animals – how did they even manage to get so huge? were they rare individuals who lived long enough to grow into “super-adults”? – but the prospect of perhaps one day finally validating A. fragillimus’ enormous size is exciting.


My version of Amphicoelias fragillimus here works out to about 50m long (164′), although it might be closer to 60m long with a more horizontal neck posture. Its proportions are mainly based on a mixture of Diplodocus, Supersaurus, and Barosaurus, with slightly taller neural spines raising its back profile a bit and some big fat deposits thickening up its tail.

Unsolved Paleo Mysteries Month #16 – Strange Snoots 2: Oddball Ornithischians

Those extinct horses weren’t the only ancient creatures with unexplained noses. Some dinosaurs had equally weird things going on with their snouts – and while hadrosaurs’ big honkin’ snoots are fairly well-known, there were other ornithischians with their own bizarre nasal anatomy.


An illustration of the skull of an extinct horned dinosaur, showing the unusually large nasal cavity. Below is a reconstruction of the dinosaur's head in life.
Triceratops horridus skull and head reconstruction

Many ceratopsids had an enormous nasal opening forming a giant bony “window” through their snout, with the chasmosaurines like the famous Triceratops having additional bony projections and hollowed regions within these holes. They probably supported some huge elaborate cartilage structures in life, but what they were for is still a mystery. They may have helped with heat dissipation or moisture conservation, aided sound production, provided a highly sensitive sense of smell, housed a vomeronasal organ, held part of an air-filled pneumatic system… or, getting more speculative, possibly even some sort of inflatable nasal display structure.


An illustration of the skull of an extinct armored dinosaur, showing the multiple holes inside the nasal cavity. Below is a reconstruction of the dinosaur's head in life.
Minotaurasaurus ramachandrani skull and head reconstruction

Some ankylosaurids, meanwhile, went with multiple holes instead. Minotaurasaurus here had two additional openings around its nostrils, and Pinacosaurus could have up to five – the purpose of which is unknown. Many ankylosaurs also had forward-facing nostrils (a rare trait in archosaurs) and incredibly complex looping airways through their skulls. These may have allowed for mammal-like “air conditioning”, regulating the heat and moisture content of each breath, or perhaps enhanced their sense of smell or served some sort of resonance chamber function. Or, again, maybe even nose balloons.

Also floofy ankylosaur because I can.

Unsolved Paleo Mysteries Month #13 – The Case of the Absent Archaeopteryx

One of the most famous of all fossil organisms, and a classic example of a transitional form, Archaeopteryx is currently known from 12 body fossil specimens.

Except one of them is missing.

The Maxberg specimen was part of the private collection of Eduard Opitsch, the owner of the Bavarian quarry where it was originally discovered in 1956. Despite being partially disintegrated, and missing its head and tail, it was still an immensely important discovery – at the time, it was only the third recognized Archaeopteryx ever found.

After briefly attempting to sell the new Archaeopteryx, Opitsch eventually allowed it to be held at the local Maxberg Museum. In 1974 he permitted casts to be made from it – but then suddenly removed it from public display and refused all further requests to access or study it.

(This may have been a reaction to the 1973 announcement of the more complete Eichstätt specimen. Opitsch, who was described as having “a difficult personality”, became increasingly defensive about the fossil, seeming to feel this new discovery was getting more attention and was deliberately devaluing his own.)

From then on the Maxberg specimen was lost to science.

When Opitsch died in 1991 his heir attempted to locate the fossil – it was rumored to be kept under his bed – but it was nowhere to be found. There’s some speculation that he was buried with it, literally taking his prized Archaeopteryx to the grave as a final act of spite. Another possibility is that it was stolen and sold in secret, perhaps to this day hidden away in a wealthy owner’s private collection.

It’s been missing for over 25 years, but there’s still lingering hope that the missing Maxberg specimen will one day resurface.

For now, though, all we have left are a few casts, photographs, and x-rays.

Unsolved Paleo Mysteries Month #04 – Who’s That Theropod?

In the early 1970s an opalized dinosaur leg bone in a South Australian gem shop came to the attention of paleontologist Neville Pledge. The specimen’s owner allowed it to be borrowed and studied, and it was eventually named as Kakuru kujaniKakuru after the Rainbow Serpent of Australian Aboriginal mythology, and kujani after a variant spelling of the Guyani, the local indigenous people. Later the fossil was auctioned off to another private owner and lost to science for nearly 30 years, until finally being acquired by the South Australian Museum in 2004.

But all we really know about Kakuru is that it was some sort of theropod dinosaur. The 33cm (1′) tibia probably belonged to an animal up to about 2m long (6′6″), living during the Early Cretaceous (~125-112 mya), but any placement in a specific group is almost impossible. Based on particular features of the bone – such as a tall and narrow astragalar process – it’s been proposed to be either an oviraptorosaur or an abelisaur. But more recent examinations have concluded the bone’s preservation is too poor for those features to be confidently identified, and consider Kakuru to be a basal coelurosaur or even just a dubious name for an indeterminate theropod.

It’s all a bit of a mess, really, and more and better material is needed to clear up this mysterious dinosaur’s identity.

I’ve restored Kakuru here in three different ways, to illustrate just how varied the interpretations are – on the left, an early oviraptorosaur; in the middle, a generic coelurosaur; and on the right, an abelisaur.

(Yes, the abelisaur is fluffy. South Australia was within the Antarctic Circle during the Early Cretaceous, and while the climate there wasn’t as cold as it is today it was still chilly enough for some floofy insulation to be useful.)

Bathornis

Bathornis grallator, a flightless bird about 75cm tall (2′6″) from the Late Eocene and Early Oligocene of Midwestern USA (~37-34 mya).

It was originally mistaken for a long-legged vulture (under the name Neocathartes) when first discovered in the 1940s, but later studies have shown it was actually one of the smaller members of the bathornithids – close cousins of the more well-known South American “terror birds”, successfully occupying terrestrial predator niches alongside large carnivorous mammals.

Brachytrachelopan

Aaand we’re back to normal updates with a fully working computer again!

Let’s properly start off this year’s art pieces with a particularly weird sauropod dinosaur. This is Brachytrachelopan, known from Argentina at the very end of the Jurassic (~152-145 mya).

A member of the dicraeosaurids, it was a close relative of the spiky-necked Amargasaurus and was roughly the same size at about 10m long (32′9″) – but it also had the shortest neck of any known sauropod, suggesting it was specialized for a completely different diet. It may have been a sort of “iguanodont-mimic”, adapted to a low browsing niche, since actual iguanodonts were absent from its ecosystem.

I’ve given this one a little bit of speculative bristly fuzz, because I can. While all currently known sauropod skin impressions show scales, we don’t have full-body coverage and fuzz was almost certainly present in their ancestors – and both types of integument can also exist on the same animal in the same places.

Also I just like the idea of sauropods with manes and beards.