Island Weirdness #06 – Zalmoxes robustus

Hațeg Island was home to quite a few unique species right at the end of the Cretaceous, so we’ll be focusing on it for a few more days.

Zalmoxes robusutus was a member of the rhabdodontids, a group of herbivorous ornithopod dinosaurs related to well-known names like Iguanodon, Tenontosaurus, and the hadrosaurs.

It had a chunkier build than its closest relatives, with a deep skull, a large beak, and a rotund body. Like other rhabdodontids it would have had powerful jaw muscles and ridged cheek teeth specialized for scissoring, adaptations for cutting up particularly tough plant matter.

It was also quite small, about 2.4m long (7’10”), although since the largest known fossils represent subadults this may not have been its full size. A second species in the same genus (Zalmoxes shqiperorum) lived on the same island and was actually slightly bigger, suggesting that Z. robustus represented a minor case of insular dwarfism.

Island Weirdness #05 – Magyarosaurus dacus

At the very end of the Cretaceous period, between about 72 and 66 million years ago, tectonic uplift from the start of the formation of the Alps created an island in the area corresponding to modern-day Romania.

Known as Hațeg Island, after the region where fossils of the native species were found, it was similar in size to Hispaniola and was surrounded by deeper waters than most of the other European archipelago islands.

Magyarosaurus here was was a titanosaur living on this island, and was one of the smallest known of all sauropod dinosaurs at just 6m long (19’8″). Much of that length would have been in its neck and tail, and its body was only actually about the size of a horse.

Like some other titanosaurs it had bony osteoderm armor along its back, although since only one isolated piece has been found the exact arrangement isn’t known.

Discovered by Franz Nopsca (the gay Transylvanian baron-paleobiologist-spy), in the early 1900s, it was one of the first dinosaurs proposed as an example of insular dwarfism. Later researchers disagreed with this hypothesis, suggesting instead that the Magyarosaurus fossils were just juveniles – and it wasn’t until 2010 that studies of bone microstructure proved that these miniature sauropods really were fully grown adults.

Island Weirdness #02 – Europasaurus holgeri

Sauropod dinosaurs are mainly known for being enormous, and so even some of the smallest members of the group were actually quite large compared to modern animals.

Europasaurus was an early brachiosaurid that lived during the Late Jurassic, about 154 million years ago, on a small island in the Lower Saxony region of northwestern Germany. It was an example of insular dwarfism in a sauropod, only growing to around 6.2m in length (~20′) – less than half the size of some of its other relatives.

A layer of rock just above the deposit of Europasaurus fossils also gives us a clue about their eventual fate. Footprints of large carnivorous theropods – bigger than the mini-sauropods themselves – suggest that at some point the sea level dropped and predators from the mainland were able to reach the island.

Since there were no large predators on the island before then,the small Europasaurus had no defenses against these new giant invaders. They very likely were literally eaten into extinction.

Island Weirdness #01

Islands are natural sites for evolutionary experiments. Their isolation and limited resources put a lot of selective pressure on their native species, often resulting in spectacular and unique adaptations. Big animals become small, small animals become big, and ecological niches can end up being filled in unexpected ways.

From the dodo becoming the first well-known example of human-caused extinction, to Darwin’s Galápagos finches being influential in the development of the theory of natural selection, to famous-but-endangered living examples like the kiwi and marine iguana, island species are fascinating and often fragile examples of how diverse life can get even in restricted conditions.

In fact, this theme ended up containing so many species I wanted to feature that I can’t possibly fit them all into just a single month. So, for the first time, a theme is going to need two months – with part 1 happening right now, and part 2 coming later this summer.


Thecodontosaurus antiquus

For much of the Mesozoic Europe was an archipelago of islands in a shallow tropical sea. During the Late Triassic, about 205-201 million years ago, some of the paleo-islands in this region existed around southern Wales and South West England, near the city of Bristol.

Thecodontosaurus was actually one of the first non-avian dinosaurs ever named by modern science, discovered in the mid 1830s – several years before the term “dinosaur” was even created to classify the “great ancient lizards”.

It was an early member of the herbivorous sauropodomorphs, the group that would eventually include the largest ever land animals. But unlike its enormous later cousins it was short-necked and bipedal, and was particularly small compared to other contemporary “prosauropods”, measuring only about 2m long (6′6″). This would make it one of the oldest known examples of insular dwarfism.

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.

Zby

Zby atlanticus, a sauropod dinosaur from the Late Jurassic of Portugal (~156-151 mya). While its genus name might look like a keyboard smash, it was actually named after the Russian-French paleontologist Georges Zbyszewski, who spent much of his career studying Portuguese fossils.

(As for how to pronounce it, according to the original paper it’s “zee-bee”.)

It was a close relative of Turiasaurus, the largest dinosaur currently known from Europe – and although Zby itself wasn’t quite so enormous it was still pretty big, probably measuring somewhere around 15-19m long (49′2″-62′4″).

In fact, all the sauropods known from Late Jurassic Portugal seem to have grown to very large adult sizes. The complete lack of medium or small forms suggests that other types of herbivorous dinosaurs may have dominated the region’s lower-browsing niches at the time.

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.

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.

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.)