Category: paleoart

Lisowicia

Dicynodonts were a group of herbivorous animals with toothless beaks and protruding tusks, part of the synapsid lineage and much closer related to mammals than to reptiles. They were some of the most successful and widespread land vertebrates from the Late Permian to the Middle Triassic, with one genus even briefly taking over the world in the aftermath of the End-Permian mass extinction event.

And it turns out some of them got very big.

Fossils of a surprisingly large dicynodont were first reported in 2008, but it wasn’t until just recently (in late 2018) that this giant creature was finally given an official name – Lisowicia bojani.

Close in size to a modern elephant, at around 2.6m tall (8′6″) and 4.5m long (14′9″), it was by far the largest known example of its kind to have ever lived. And while most other dicynodonts had upright hindlimbs and sprawling forelimbs, Lisowicia seems to have developed a fully upright posture much more similar to that of quadrupedal dinosaurs and modern mammals.

It was also one of the very last of its kind, living during the Late Triassic of Poland, about 208 million years ago (although there was a possible later survivor in Australia). This was around the same time that early sauropod dinosaurs were likewise first starting to experiment with gigantism, suggesting that both groups were convergently evolving to exploit newly-available ecological niches.

Enaliarctos

Enaliarctos mealsi, an early seal from the Late Oligocene and Early Miocene of California, USA (~23-20 mya).

Measuring about 1.5m long (5′), it was a transitional form between modern seals and their more otter-like ancestors. It was well-adapted for swimming with a flexible spine and flipper-like limbs, but unlike most modern pinnipeds it probably used both its front and hind flippers for propulsion.

Its teeth also still resembled those of terrestrial carnivores, with slicing carnassials at the back of its jaws. This suggests that it had to drag larger prey items back to shore in order to tear them apart and eat them, similar to the behavior of modern otters.

Ocepechelon

Ocepechelon bouyai, a sea turtle from the late Cretaceous of Morocco (~70-66 mya). Closely related to the modern leatherback turtle and the pug-nosed Alienochelys, it’s only known from a single 70cm-long skull (2′4″) – and while its body proportions aren’t known for certain it was probably very big, possibly up to 4m long (13′).

Unlike any other known turtle it had a unique narrow tube-shaped snout. This is thought to be an adaptation for suction feeding, vacuuming up tiny fish, squid, and jellyfish in a similar manner to modern pipefish or beaked whales.

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.

Grendelius

Grendelius mordax, an ichthyosaur from the Late Jurassic of England (~155-150 mya).

Named after the monster Grendel from the epic poem Beowulf, this 4m long (~13′) marine reptile had a big robust skull with large teeth, proportionally short flippers, and smaller eyes than some of its other relatives. It also had an unusual bony “hump” on its snout above its nostrils.

(About 20 years ago Grendelius was reassigned into Brachypterygius on the basis of the two not being distinct enough from each other to justify having separate genus names – but a more recent study suggests that that they actually were different after all, and the name may be valid again.)

Diplacodon gigan

Diplacodon gigan, a brontothere from the Early Eocene of Wyoming, USA (~46-42 mya). Standing around 2.1m tall at the shoulder (~7′) it was named after the kaiju Gigan for its relatively large size – not quite as big as some later brontotheres, but still about 20% larger than other known species of Diplacodon.

It had a pair of blunt bony projections on its snout which would have been covered with skin in life, similar to the ossicones of modern giraffids, with males having larger “horns” than females.

Despite looking very similar to rhinos, brontotheres were actually much more closely related to horses, with the resemblance being a result of convergent evolution for the same sort of big-tanky-herbivore ecological niche.

Vaderlimulus

Vaderlimulus tricki, a horseshoe crab from the Early Triassic of Idaho, USA (~251-247 mya). Named for its resemblance to the shape of Darth Vader’s helmet, it’s the earliest known Mesozoic horseshoe crab from North America and was closely related to another oddly-shaped form from Australia.

It was much smaller than its modern relatives, only about 10cm long (4″), and probably lived in a brackish estuary environment where seawater and freshwater met.

Paludidraco

Paludidraco multidentatus from the Late Triassic of Spain (~237-227 mya).

This 3m long (9′10″) animal was a member of the nothosaurs, a group of semi-aquatic seal-like marine reptiles that were closely related to plesiosaurs (and both were also evolutionary cousins to modern turtles).

It had long slender jaws full of numerous tiny teeth, creating an interlocking comb that was probably used for filter feeding – scooping up mouthfuls of fine-grained sediment from the seafloor and filtering out small invertebrates or soft plant matter.

The bones of its skeleton were also highly thickened and dense, a condition known as pachyostosis that provided ballast to weigh it down in the water. This would have made it a slow and unmaneuverable swimmer, but a very energy-efficient one, using its natural neutral buoyancy to hover or walk along the seabed.

It was essentially a reptilian manatee, filling a similar sort of ecological niche.

Litovoi

Litovoi tholocephalos, a multituberculate mammal from the Late Cretaceous of Romania (~70-66 mya). Living on what was at the time the large offshore Hațeg Island, this rat-sized animal (about 25cm /10″ long) was part of a lineage of insectivorous multis called the kogaionids, with the same sort of red-colored enamel on its teeth as other species like Barbatodon.

Its brain was surprisingly tiny proportional to its size – one of the smallest known brain-to-body ratios of any mammal, and more similar to those of non-mammalian cynodonts – but it also seems have been highly specialized for processing sensory input, with relatively enormous regions associated with smell, eyesight, balance, and motor control. The olfactory bulbs of its brain were so enlarged, in fact, that they caused its skull to bulge out into an unusually dome-shaped forehead.

Its reduced brain size may have been due to limited food availability on its isolated island home. Brains are very metabolically expensive organs, and some other extinct island mammals like hippos, hominids, and goats are also known to have evolved smaller brain sizes. Modern shrews even seasonally shrink their own brains during winter for similar energy-saving reasons.

Caelestiventus

Caelestiventus hanseni, a pterosaur from the Late Triassic of Utah, USA. Living about 208-210 million years ago, it was very closely related to Dimorphodon – but unlike its younger coastal-dwelling relative it instead lived in a desert environment made up of a massive sand dune sea with occasional interdunal lakes.

It’s the earliest known example of a desert pterosaur, over 60 million years older than other examples, suggesting that even fairly early in their evolutionary history these flying animals had already adapted to a much wider range of habitats than previously thought.

Although only known from a partial skull and a single wing bone, it was probably one of the largest Triassic pterosaurs with a wingspan of over 1.5m (4′11″). It had a “keel” on its lower jaw that may have supported a soft-tissue crest or a pelican-like throat pouch, and there were several different types of teeth in its mouth – large pointed fangs at the front, “leaf-shaped” blades further back in its upper jaw, and numerous much smaller teeth along its lower jaw.

The skull roof also preserved the impression of Caelestiventus’ brain shape, showing that it had very well-developed vision but a poor sense of smell.