archosauromorpha – Nix Illustration

Akidostropheus

Akidostropheus oligos was a small tanystropheid archosauromorph reptile that lived during the late Triassic, about 223-218 million years ago, in what is now Arizona, USA.

Only a few tiny isolated vertebrae have been discovered, so its full size and appearance isn’t known – making any reconstruction rather speculative – but it was probably around 30cm long (~12″). Like other tanystropheids it would have been a long-necked lizard-like animal, and may have had a similar build to the closely-related Tanytrachelos.

But despite the scarcity of material the few known vertebrae are unique among archosauromorphs, bearing elongated spikes with a surface texture that suggests they were covered with keratinous sheaths. The spikes were conical, sharp, and hooked on the neck and upper back, but became more flattened, straighter, and blade-like on the lower back and tail.

These structures were probably defensive in nature, especially considering that there’s direct fossil evidence for predators targeting the long necks of tanystropheids and decaptiating them.

Akidostropheus lived in a tropical floodplain environment around a meandering river system, but without more and better fossils it’s impossible to tell what its ecology was. Tanystropheids were a strange and diverse bunch, with both terrestrial and aquatic lifestyles, bipedal runners, and possibly even bizarre leg-gliders, so this spiky little Triassic weirdo could have been doing almost anything.

Mirasaura

Back in 1939, fossil collector Louis Grauvogel discovered a couple of reptile fossils in Middle Triassic-aged deposits (~247 million years old) in eastern France. A large preserved structure was noted above the animal’s back, but for many years it was interpreted as an unrelated fish fin, insect wing, or plant frond.

It was only when the State Museum of Natural History Stuttgart acquired the specimens in 2019 that they were recognized as representing something very special: a long-sought-after relative of the bizarre and enigmatic Longisquama!

Mirasaura grauvogeli grew to around 30cm long (~1′) and was, if anything, even stranger than its relative. It had humped shoulders, grasping limbs, and a bird-like head with large forward-facing eyes and a long pointed snout that was toothless at the front, probably used to probe for small invertebrates in cracks and crevices.

But most strikingly it had up to 20 tall structures overlapping along its back to form a sail-like crest. Although they were superficially feather-like in shape with preserved melanosomes that resemble those of birds, structurally they weren’t feathers at all – but they also weren’t modified scales. Instead these appear to have been an entirely novel type of skin appendage, made up of continuous sheets with a midline shaft and a corrugated texture.

The crest was probably used for visual display, and 80 additional fossils of isolated crest structures suggest they were regularly shed and regrown.

Along with Longisquama, Mirasaura appears to have been an early member of the drepanosaur lineage – a group of wonderfully weird tamandua-like reptiles whose evolutionary relationships are still disputed, with different studies currently recovering them as either a unique early offshoot of the diapsids or as archosauromorphs.

(Interestingly, a specimen of Drepanosaurus reportedly preserves some soft tissue on its back that may also be one of these strange new crest structures. Drepanosaurs just keep on getting weirder and weirder and I love them.)

Unguinychus

Drepanosaurs were a weird little group of tree-climbing Triassic reptiles with prehensile claw-tipped tails, chameleon-like bodies, humped backs, grasping feet, long necks, and somewhat bird-like skulls that may have been tipped with toothless beaks in some species.

Recently some of them have been recognized as also having adaptations for digging and ripping into insect nests, similar to modern anteaters, with highly specialized forelimb bones and a massively enlarged hoked claw on each hand.

And now we have another one of these digging drepanosaurs: Unguinychus onyx, whose name delightfully translates to “claw claw claw”!

Living in what is now New Mexico, USA during the late Triassic, around 215-208 million years ago, Unguinychus is only known from its enlarged hand claws but was probably similar in size to some of its close relatives, likely around 40cm long (~1’4″).

Based on skin impressions from the early drepanosaur Kyrgyzsaurus it also would have been covered in small scales, possibly with a skin crest and a chameleon-like throat sac.

Drepanosaurs’ evolutionary relationships are rather unclear, with various studies classifying them as an early branch of diapsid reptiles, as close relatives of the gliding kuehneosaurids, or as protorosaurian archosauromorphs. But recently another idea has been proposed, instead placing them slightly further up the archosauromorph evolutionary tree in the allokotosaur lineage close to trilophosaurids – and notably making them very closely related to fellow Triassic bird-headed weirdo Teraterpeton.

Dinocephalosaurus

Dinocephalosaurus orientalis was a fully aquatic protorosaur reptile living in what is now southwest China during the mid-Triassic, about 244 million years ago.

Up to 6m long (~19’8″), it had a long serpentine body with paddle-like limbs and an especially elongated neck – but despite the superficial similarities to its semi-aquatic cousin Tanystropheus, Dinocephalosaurus’ long neck appears to have been independently evolved.

Much like the similarly-shaped elasmosaurs, its neck may have had a “stealth” function, allowing it to bring its jaws closer to targets before the rest of its body was visible, then using side-to-side snapping bites to catch its prey in its interlocking “fish-trap” teeth.

A preserved well-developed embryo inside one specimen also suggests that Dinocephalosaurus gave birth to live young, making it one of only two archosauromorph lineages known to have ever evolved this reproductive strategy.

Tropidosuchus

Proterochampsids were a group of Triassic archosauriformes, closely related to the true archosaurs (crocodilians, pterosaurs, and dinosaurs/birds).

Known only from South America between about 242 and 205 million years ago, these reptiles’ heads were wide at the back but very narrow along the snout, often with prominent bony bumps and ridges on their skulls, and they had less osteoderm armor on their bodies than other archosauriformes.

They’ve traditionally been interpreted as very crocodile-like and semi-aquatic, but their long slender limbs and presence in rather arid paleoenvironments suggest they may have been more terrestrial fast-running predators.

Tropidosuchus romeri here lived about 235 million years ago in what is now Argentina. It was one of the smaller proterochampsids, only about 50cm long (1’8″), with just a single row of osteoderms along its back, and had larger and lower-set eyes compared to its relatives.

CT scans of its braincase indicate it had a particularly good sense of smell, and it may have relied mainly on scent to locate prey.

Retro vs Modern #06: Plesiosaurus dolichodeirus

Plesiosaurs were first recognized as a distinct group of fossil animals in the early 1820s, only a few years after ichthyosaurs. Initially they were perceived as being closer in form to reptiles in the “chain of being” than the more fish-like ichthyosaurs were, and so the group’s scientific name ended up reflecting that early interpretation – “plesiosaur” roughly translates to “near to reptiles”.

The first named species of plesiosaur was Plesiosaurus dolichodeirus, based on a near-complete skeleton discovered by Mary Anning that revealed the strange long-necked proportions of these animals for the first time.

1830s-1850s

Early reconstructions of plesiosaurs in the 1830s compared them to “a snake threaded through a turtle”, giving them highly sinuous necks and a turtle-like body. Much like ichthyosaurs they were assumed to be amphibious, using their flippers to crawl up onto the shore like a sea turtle.

The 1850s Crystal Palace plesiosaur statues show a variant of this design with smooth skin textures and fairly flexible reptilian bodies, with powerful shoulders and flipper postures that give them an overall almost seal-like appearance.

1860s-1990s

From the 1860s onwards a more upright S-shaped neck pose became the most common depiction of plesiosaurs. The writhing snake-like necks persisted in some reconstructions of the extremely long-necked elasmosaurids, but the overall design for these animals that caught hold for the next century was an egg-shaped body with oar-like flippers and a swan-like neck – a body plan that would end up so influential in pop culture that it was incorporated into modern lake monster folklore, with the Loch Ness Monster being the most famous example.

During this period plesiosaurs were often portrayed as floating or swimming at the water’s surface, rowing along with their flippers and using their long necks to snatch up prey. They were generally assumed to still haul out turtle-style to lay their eggs on the shore, although it wasn’t clear how the very largest species would have been able to support their own weight.

2020s

Since the 1990s a boom of new plesiosaur species and biomechanical studies have brought a lot of changes to our understanding of these marine reptiles.

Their necks are now considered to have been less flexible, capable only of more gentle curving, and were probably much thicker and more streamlined with the body than previously depicted. Rather than oar-like rowing all four of their flippers were probably used in more of an “underwater flying” vertical motion similar to modern sea turtles – which is pretty fitting, considering that their closest living relatives are now thought to actually be turtles.

They gave live birth and were probably warm-blooded, with a thick layer of insulating blubbery fat and a teardrop-shaped body outline. Their skin texture was smooth, but one exceptionally well-preserved specimen shows a covering of tiny thin millimeter-sized scales that wouldn’t have been visible in life except in extreme closeup.

We now know Plesiosaurus itself was a fairly small species, around 3.5m long (~11’6″), with a broad body and a short thick tail that probably had a rudder-like fin – usually assumed to be vertically-oriented, but possibly horizontal instead. It lived during the Early Jurassic, about 201-183 million years ago, in the shallow tropical sea that covered what is now southern England, and had a rather small head compared to other plesiosaurs, with its eyes facing upwards and to the sides.

It had sharp needle-like teeth that would have been used to catch soft-bodied aquatic prey like fish and cephalopods. It’s not known whether it had extensive fleshy lips, croc-like snaggletoothed jaws, or something in-between, so the facial soft tissue on this particular reconstruction is rather speculative.

Spinosuchus

Allokotosaurs were a group of mostly-herbivorous archosauromorph reptiles, distantly related to the ancestors of crocodiles, pterosaurs, and dinosaurs. They lived across Eurasia, Africa, and North America during the mid-to-late Triassic period, and their lineage included some weird and diverse forms – such as the bull-horned Shringasaurus, the long-beaked Teraterpeton, and possibly also the gliding kuehneosaurids.

Spinosuchus caseanus here was yet another one of these Triassic allokotosaurian weirdos, part of the trilophosaurid family and closely related to Trilophosaurus and Teraterpeton.

Living about 221-212 million years ago in what is now northwest Texas, USA, Spinosuchus was around 2.2m long (~7’2″) and had distinctive elongated neural spines along the vertebrae of its back and the base of its tail, forming a “high back” or short “sail”. Since it’s only known from a partial spinal column the rest of its anatomy isn’t known for certain, but it probably had body proportions similar to its close relative Trilophosaurus, with sprawling limbs and a short-snouted beaked head adapted for herbivory.

Like many other fossil “sailbacked” animals the exact function of Spinosuchus’ elongated vertebrae is unclear, but the structure may have been used for visual display. I’ve depicted it here with a speculative frill of colorful elongated scales, along with a flashy dewlap.

Styxosaurus

Styxosaurus snowii here was one of the largest known elasmosaurids, named after the mythological river separating the worlds of the living and the dead.

Reaching around 11m long (36′), with half of that being entirely neck, it lived during the late Cretaceous period about 83-80 million years ago in what is now the American Midwest – a region that at the time was submerged under a large inland sea.

With pointy interlocking teeth in its proportionally tiny head, Styxosaurus would have fed on slippery aquatic animals like fish and cephalopods, possibly using its long neck to get up close to its targets while the bulk of its body remained out of sight in dark murky waters. Large numbers of gastroliths found in the stomach regions of some specimens would have been used to grind up the hard parts of prey items after they were swallowed whole.

Seeleyosaurus

Seeleyosaurus guilelmiimperatoris here was a smallish plesiosaur (about 3.5m long / 11’6″) found in Germany during the early Jurassic, about 182 million years ago.

And back in the 1890s, a specimen of this species was discovered with soft tissue impressions showing a diamond-shaped tail fin.

But despite us knowing about plesiosaur tail flukes for such a long time, they’re surprisingly under-represented in reconstructions, never seeming to have become associated with the popular image of these animals in the same way that early pterosaur’s tail vanes did. It doesn’t help that no other direct impressions of plesiosaur tail fins have ever been found, or that the Seeleyosaurus specimen’s soft tissue got painted over at some point in the mid-1900s, making it incredibly difficult to study without causing further damage.

(Perhaps modern non-invasive scanning techniques could be able to see under the paintjob, but as far as I’m aware nobody’s tried that yet.)

These tail fins are usually assumed to have been vertically oriented like those of other aquatic reptiles, moving side-to-side and acting like a rudder. However, there’s also a hypothesis that their fins might have actually been horizontal more like those of modern cetaceans and sirenians, based on several anatomical quirks – such as their tail regions being very wide and flat at the base, and the vertebrae at the tip being unusually pygostyle-like, very different from the way the tail bones of vertically-finned reptiles look.

Silesaurus

Silesaurus opolensis here was a type of dinosauriform – a reptile very closely related to the ancestors of true dinosaurs, but not quite actually a dinosaur itself.

Living in Poland during the Late Triassic (~230 million years ago), it was a quadrupedal animal roughly the size of a large modern dog, about 50cm tall at the shoulder (1’8″) and 2m long (6’6″). The front of its lower jaw was toothless and covered with a keratinous beak, and there may have been a corresponding much smaller beak at the very tip of its upper jaw, too.

It was originally thought to be a herbivore, but coprolites full of insect remains suggest it was probably more of an omnivore, possibly foraging by pecking in a convergently similar manner to its distant bird cousins.

In fact, one of those pieces of Silesaurus poop was recently found to preserve a new species of tiny beetle in incredible detail.