Vespersaurus

For around 50 years some very unusual dinosaur tracks have been found in ancient desert sediments in South America: strange footprints showing the impression of only a single toe, a walking style never before seen in any reptiles.

And recently a fossil of what might be the track maker has actually been found.

Named Vespersaurus paranaensis, this new species lived during the Late Cretaceous of Brazil (~90 mya) and was a member of the noasaurid family of theropods, closely related to the weird-jawed Masiakasaurus from Madagascar.

Measuring about 1.5m long (~5′), Vespersaurus was fairly lightly built with legs proportioned for running – and its feet were absolutely unique. Although it had the standard three main toes of a theropod, it bore its weight entirely on the middle toe and held the other digits off the ground. The two raised toes on each foot also had large knife-like claws which may have been used during hunting, vaguely similar to the sickle claws on the feet of dromaeosaurs. But unlike dromaeosaurs these claws weren’t highly curved or pointed, suggesting Vespersaurus used more of a scratching and slashing technique rather than the raptors’ puncture-and-restraint strategy.

Much like ancient horses, it may have developed its single-toed stance as an adaptation for more efficient fast running, possibly to avoid larger predators or to chase down small fast-moving prey like hopping desert mammals.

The known one-toed fossil footprints are actually slightly older than the Vespersaurus fossil, and similar tracks in Argentina have been found dating back to the Late Jurassic (~150mya), so there may have been a long lineage of “one-toed” desert-dwelling noasaurids in South America that haven’t been found yet.

Glowing Dinosaurs

Many modern birds are capable of seeing into the ultraviolet regions of the electromagnetic spectrum, and some of their non-avian dinosaur ancestors might have had the same sort of vision. And much like their living relatives, that means various parts of their bodies and plumage may also have been UV-reflective and UV-fluorescent.

So here’s a Velociraptor with some speculative UV coloration – although this is just what it would look like to human eyes under a blacklight. What it would actually look like to a creature that can see extra colors is impossible to depict on a screen designed for trichromatic vision!

Island Weirdness #08 – Balaur bondoc

When Balaur was described in 2010 it was initially thought to be a dromaesaurid closely related to Asian forms like Velociraptor. With its particularly stocky legs built for strength rather than speed, two-fingered hands, and two large sickle claws on each foot, it was interpreted as a weird highly specialized predator terrorizing the other Hațeg Island species at the end of the Cretaceous. Although only 1.8m long (5’10”), it was hypothesized to have taken down prey much larger than itself with powerful slashing kicks.

But later analyses cast doubt on this interpretation.

A lot of the anatomical features of Balaur’s skeleton were odd for a dromaeosaurid, but matched those of avialans – a group of close evolutionary “cousins” to the dromaeosaurids, containing Archaeopteryx and the common ancestors of all modern birds. And, by 2015, multiple studies had confirmed Balaur wasn’t really a “raptor” but instead a little further along on the bird lineage.

So now our picture of this dinosaur is very different: a chunky-bodied island bird, grown large and secondarily flightless sort of like a Cretaceous equivalent to the dodo. Its double sickle claws were probably adaptations for climbing and perching in trees, and based on similar avialans it was likely a herbivore rather than a hypercarnivore.

Qianzhousaurus

Qianzhousaurus sinensis, a tyrannosaur from the Late Cretaceous of southern China (~72-66 mya). Measuring about 9m long (29′6″) it had an unusually long and slender snout for a tyrannosaur, leading to its nickname of “Pinocchio rex”.

The only other known long-snouted tyrannosaur was the closely related Alioramus from Mongolia – but since only juveniles of that genus have been found so far, it’s also possible that Qianzhousaurus was actually just a fully-grown species of Alioramus.

Erlikosaurus

Erlikosaurus andrewsi, a therizinosaur from the Late Cretaceous of Mongolia (~90 mya).

Named after Erlik, the Turko-Mongolian god of death, it’s only known from partial remains – but it was the first therizinosaur ever found with a preserved skull, helping to fill in some of our knowledge of these oddball dinosaurs’ anatomy.

It was closely related to Therizinosaurus, but was only about half the size, estimated to have measured around 4-5m long (13′-16’4″). It would have had a toothless beak at the front of its jaws, an adaption for a herbivorous diet, along with long claws on its hands and a coat of fluffy down-like feathers. I’ve also given it some longer quill-like feathers here, similar to those known in Beipiaosaurus.

Australovenator

Australovenator wintonensis, a megaraptoran dinosaur from the Late Cretaceous of Queensland, Australia (~100-94 mya). It was a medium-sized member of the group, about 6m long (19′8″), and despite only being known from a partial skeleton it’s still one the best-known megaraptorans – and also the most complete predatory dinosaur from Australia.

Megaraptorans were a group of fairly large theropod dinosaurs, currently known from Australia, South America, and Japan (and maybe Egypt). Their relationships to other theropod groups are rather uncertain, with different studies placing them as neovenatorids, tyrannosaurids, or most recently as an early branch of the coelurosaurs.

They had very lightly-built bodies, with bird-like bones full of weight-reducing air spaces, proportionally small heads with long slender snouts, and leg bones adapted for running. But their most distinctive feature was their hands, featuring massively enlarged claws on the first and second fingers, with the third finger being much smaller and somewhat vestigial-looking. While some other theropods like allosaurids and spinosaurids also had big hand claws, megaraptorans’ almost tyrannosaurid-like mostly-two-fingered arrangement is rather odd.

Their arms and fingers were much more flexible than those of most other non-avian dinosaurs, allowing them to reach out, grab onto prey with those claws, and then pull it in close to their bodies, restraining it in a sort of death-hug while their relatively weak jaws finished it off.

A distinctive injury to the second toe of Australovenator also suggests these dinosaurs may have been able to deliver powerful kicks like modern cassowaries.

Halszkaraptor

Halszkaraptor escuilliei, a dromaeosaurid (“raptor”) dinosaur from the Late Cretaceous of Mongolia (~75-71 mya). It’s known from a single near-complete skeleton and would have been about the size of a modern mallard duck, around 60cm long (2′).

It had some very odd features for a raptor, with many small sharp backwards-pointing teeth, crocodile-like sensory pits on its snout, a long flexible neck, small flipper-like arms, a relatively short tail, and a more upright body posture than its other relatives. All these traits together suggest it may have been semi-aquatic, which is a pretty big deal since the only other group of non-avian dinosaurs known to have developed adaptations for life in the water were the spinosaurids.

The fossil was originally illegally excavated by fossil poachers and was owned by private collectors for several years, but it has now been returned to science and is due to be repatriated to Mongolia. With its odd anatomy and the exact origin of the specimen being unknown, there’s some skepticism about whether Halszkaraptor represents a genuine animal or an elaborate fake chimera – but synchrotron scans of the fossil and its similarity to previously-discovered more fragmentary short-armed raptors like Mahakala suggest that it is real, and it really is that weird.

Mirischia

Mirischia asymmetrica, a theropod dinosaur from the Early Cretaceous of Brazil (~112-99 mya). Although known only from its hips and a few other partial bones, these pieces were so well-preserved that it was given a genus name that translates to “wonderful pelvis”.

In life it would have been about 2m long (6′6″), but since the known fossil represents a subadult its full-grown size may have been a little bit larger. It was probably a member of the compsognathids, closely related to Compsognathus and Aristosuchus – which would make it the only representative of that family currently known from the Americas.

The ischium bones of Mirischia’s pelvis were oddly asymmetrical, hence the species name ‘asymmetrica’, with one side featuring a hole and the other side only having a notch in the same position. The fossil specimen also had thin-walled bird-like bones, and soft-tissue impressions of intestines and a posterior air sac.

Utahraptor

Utahraptor ostrommaysorum lived during the Early Cretaceous (~130-124 mya) in Utah, USA, and was the largest known dromaeosaurid. Reaching lengths of around 6m long (20′), it’s often compared in size to the fictional raptors of Jurassic Park.

Recent discoveries show it had some weird proportions compared to its relatives – a thick stocky body, chunky legs, smaller arms, a shorter and more flexible tail, and a large deep skull with an oddly curved lower jaw.

But we still don’t know very much about it… yet.

There’s a huge slab of rock full of Utahraptor fossils just waiting to be extracted and studied. There are at least six raptors in there ranging from babies to adults, hinting at the presence of a family group or even pack hunting behavior, and potentially other animals and new discoveries too – but the main roadblock for this project is lack of funding.

The paleontologists involved have turned to crowdfunding to attempt to raise enough money for essential equipment and the services of a professional fossil preparator, but they’re still only at about 10% of their goal.

So this first week of April is #UtahraptorWeek in the paleontology community, raising awareness of this fascinating giant raptor and how close we are to finding out so much more about it. Spread the word, and if you’re able to please consider helping out the Utahraptor Project on GoFundMe.

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.