This species was originally named back in 2015, but at the time the only known specimens were missing their heads. It was assumed that its skull would have looked similar to those of other hupehsuchians… but now new fossils have been found, and it seems to have actually been much much weirder!
Eretmorhipis’ head was surprisingly tiny in proportion to its body – sort of like a marine version of Cotylorhynchus – and its shape convergently resembled the modern platypus, with a wide “duck bill” and very small eyes. It may have hunted for food along the seafloor in a similar manner to the platypus, using either a highly sensitive sense of touch or possibly even electroreception to locate small invertebrates like worms and shrimp.
It also had much larger bony osteoderms than its other known hupehsuchian relatives, forming a distinctive protruding spiky ridge down its back. At about 85cm in length (2′9″) it was one of the largest marine animals around at the time, so this structure probably wasn’t needed for defense – but as with other hupehsuchians its actual function is still unknown.
Living in Texas, USA, during the Late Triassic, about 229-226 million years ago, Triopticus was a type of archosauriform reptile (a “cousin” to crocodiles, pterosaurs, and dinosaurs). Classifying it any more specifically than that is rather difficult since it’s only known from a single partial skull.
It had five large bony bosses on its head that convergently resembled the domes of pachycephalosaurs, suggesting it may have engaged in similar headbutting or flank-butting behavior. At the back of its skull there was also a distinctive deep pit that looked like a “third eye socket”, inspiring it its name – although this feature probably wasn’t actually a parietal eye, instead just being the result of the way several of the bosses came together at that point.
The rest of its appearance is unknown, and this reconstruction is rather speculative as a result. But based on other archosauriformes it was likely to have been a small semi-sprawling quadruped, possibly around 80cm in length (2′7″).
About 4cm long (1.6″), it had a wormlike body covered in spicules (tiny spines) which suggests it was a member of the aplacophoran molluscs – but it also had a row of seven larger shells along its back resembling those of chitons.
Modern aplacophorans are all shell-less and were traditionally thought to be a very early branch of the mollusc lineage that retained a “primitive” ancestral body plan. More recently, however, a combination of genetic evidence and fossil discoveries of animals like Kulindroplax have revealed that they’re actually close relatives of the chitons and instead lost their shells much more recently during the course of their evolution.
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.
Measuring around 60cm long (2′), it had a pair of large forward-facing horn-like spikes at the front of its shell – the function of which isn’t clear, but they may have been useful for defense if it was incapable of fully retracting its head into its shell.
This year I’ve been lucky enough to have some of my work featured in several PBS Eons videos – and I even recently got the opportunity to do some custom images for them! Since I didn’t show any of these off at the time, here they are now:
Nicknamed “Santa Claws”, Sanctacaris uncata was a marine arthropod from the Middle Cambrian (~505 mya) Burgess Shale deposits of Canada. Its exact evolutionary relationships are unclear, but it’s thought to have been very closely related to or part of an early branch of the chelicerates – the lineage that includes modern arachnids and horseshoe crabs.
Measuring up to about 9cm long (3.5″), it had forward-facing eyes and five pairs of grasping appendages on the underside of its head, adaptations that suggest it was an active predator convergently similar to anomalocaridids. It probably swam around grabbing onto whatever small prey items it could catch, trapping them in its “limb basket” while it ate them.
Peltephilus ferox, an armadillo from the Early Miocene of Argentina (~17-16 mya) that was similar in size to a large dog, probably around 1.5m long (5′). It had less solid armor than its modern relatives, with its bony osteoderms being arranged more like chain mail, loosely connected to each other and slightly overlapping, creating a much more flexible body covering.
Its most unusual features were the horns on its snout, convergently resembling the later horned gophers of North America. But unlike other mammals Peltephilus‘ horns were actually modified plates of its face armor, enlarged pointed osteoderms that were only connected to its skull by soft tissue membranes – meaning that after death they tended to fall off, and the exact number and position of them is still a little uncertain.
Its unusually broad snout and large teeth were originally interpreted as evidence of it being an active carnivore, but more recent studies of its anatomy have suggested that it was much more likely to have been a herbivorous or omnivorous digger, mainly feeding on underground plant matter like roots and tubers.
Living during the Early Jurassic (~183-179 mya) in the shallow seas that covered most of Europe at the time, Stenopterygius was an average-sized ichthyosaur growing up to about 4m in length (13′). A fossil found in Germany has some incredibly good soft-tissue preservation, showing smooth flexible scaleless skin, a layer of insulating blubber very convergently similar to that found in cetaceans, and even evidence of countershaded coloration.
While the confirmation of blubber is amazing, and gives further evidence that ichthyosaurs were warm-blooded, the color preservation might actually be even more interesting. The skin pigmentation is preserved in enough fine detail for branched melanophores to be visible under a microscope – a type of cell associated with the ability to change color. So there’s a possibility that ichthyosaurs could actively darken or lighten their color patterns, for purposes such as better camouflage, UV protection, or temperature regulation.
Although it looked very shark-like it was actually much more closely related to modern chimaeras, and its most distinctive feature was the forward-pointing “unicorn horn” spine just behind its head – a sexually dimorphic structure formed from a highly modified dorsal fin, found only on mature males.
The spine’s function is unknown for certain, but it may have been a sort of clasper involved in courtship and mating, since one fossil seems to preserve a female in the act of biting onto it. Some of its close relatives like Damocles and Stethacanthus also had similarly weird dorsal fins, so whatever these fish were actually doing with these structures it must have been a fairly successful strategy.
Falcatus lived out in the open ocean, with proportionally big eyes giving it good vision in deep dark water, and its large symmetrical tail fin suggests it was a fast maneuverable swimmer that actively chased after small prey. Numerous fossils have been found together, which may also indicate schooling behavior.
Although definite fossils of falcatids are only known from the Carboniferous, recently there’s been some possible evidence of them surviving for much much longer. A few isolated fossil teeth from Europe suggest that some of these fish may have persisted for at least another 180 million years into the Early Cretaceous, living in isolated deep water refugia environments in a similar situation to the modern coelacanth – making them fossils of what would have been “living fossils” at the time!