archosaur – Nix Illustration

Rhacheosaurus

Metriorhynchids were a group of fully marine crocodyliforms known from the mid-Jurassic to the early Cretaceous of Europe and the Americas. They were the most aquatic-adapted of all known archosaurs, with streamlined bodies, smooth scaleless skin, small front flippers, larger hind flippers, and shark-like tail flukes. They may also have been endothermic, and might even have given live birth at sea rather than laying eggs.

Rhacheosaurus gracilis here was a metriorhynchid that lived in warm shallow waters around what is now Germany during the late Jurassic, about 150 million years ago. Around 1.5m long (~5′), its long narrow snout lined with delicate pointed teeth suggests it fed on small soft-bodied prey, a niche partitioning specialization that allowed it to coexist with several other metriorhynchid species in the same habitat.

Unlike most other marine reptiles metriorhynchids didn’t have particularly retracted nostrils, which may have had a limiting effect on their efficiency as sustained swimmers since higher-set nostrils make it much easier to breathe without having to lift the whole head above the surface. The lack of such an adaptation in this group may be due to their ancestors having a single nasal opening formed entirely within the premaxilla bones at the tip of the snout, uniquely limiting how far it could easily shift backwards – other marine reptiles had nostrils bound by the edges of multiple different bones, giving them much more flexibility to move the openings around.

(By the early Cretaceous a close relative of Rhacheosaurus did actually evolve nostrils bound by both the premaxilla and the maxilla, and appeared to have started more significant retraction, but unfortunately this only happened shortly before the group’s extinction.)

Metriorhynchids also had well-developed salt glands in front of their eyes, but the large sinuses that accommodated these glands may have made their skulls ill-suited to deep diving, being more susceptible to serious damage from pressure changes and restricting their swimming to near-surface waters only.

Preserved skin impressions in some metriorhynchid fossils show several unusual “irregularities”, including curl shapes, small bumps, and cratering. It’s unknown what exactly caused these marks, but they may represent scarring from external parasites such as lampreys and barnacles.

Wukongopterus

Wukongopterus lii was a pterosaur that lived during the mid-to-late Jurassic, about 164 million years ago, in what is now northeastern China. It was fairly small, with a wingspan of around 70cm (~2’4″), and showed a mixture of anatomical features in-between the long-tailed short-headed ‘rhamphorhynchoids‘ and the short-tailed long-headed pterodactyloids.

Its long jaws were lined with tiny pointed conical teeth, suggesting it was adapted for primarily feeding on insects. It also had a very slight overbite, with the first two pairs of teeth in its upper jaw protruding almost vertically over the end of its lower jaw.

As a fully mature adult it would have had a low bony crest on its head that probably supported a larger cartilaginous structure – similar to other known wukongopterids – although the exact size and shape is unknown since the one confirmed specimen of Wukongopterus is missing that particular part of its skull. Another fossil nicknamed “Ian” may represent a second individual of this species, showing a different crest arrangement further forward on its snout, so I’ve made two different versions of today’s image to reflect that possibility.

Lewisuchus

Last week I mentioned the one oddball dinosauriform that had crocodilian-like osteoderm armor, so let’s take a look at that one too.

Lewisuchus admixtus lived in what is now northwest Argentina during the late Triassic, around 236-234 million years ago. About 1m long (3’3″), it was an early member of the silesaurids – a group of dinosauriforms that weren’t quite dinosaurs themselves, but were very closely related to the earliest true dinosaurs.

(They’ve also been proposed as instead being early ornithisichians, but we’re not getting into that today.)

Much like its later silesaurid relatives Lewisuchus had a long neck and slender limbs, and was probably mainly quadrupedal, possibly with the ability to briefly run bipedally to escape from threats. Its serrated teeth suggest it was carnivorous, likely feeding on both smaller vertebrates and the abundant insects found in the same fossil beds.

Uniquely for an early dinosauriform it also had a single row of bony osteoderms running along its spine. Although it lived at close to the same time as the similarly-armored Mambachiton their last common ancestor was at least 10 million years earlier, and no other early dinosaur precursors with osteoderms are currently known – so this was probably a case of Lewisuchus independently re-evolving the same sort of feature.

Mambachiton

Mambachiton fiandohana lived during the mid-Triassic, about 237 million years ago, in what is now Madagascar – which at the time wasn’t yet an island, still being connected to both east Africa and India as part of southern Pangaea.

It represents the earliest known branch of the avemetatarsalians, or “bird-line archosaurs”, a major group of the archosaur reptiles that also includes pterosaurs and dinosaurs/birds.

It’s only known from a few fragments but it was probably around 2m long (~6’6″), and would have been a carnivorous lizard-like animal with a long neck and semi-erect quadrupedal limb posture.

Unexpectedly for a bird-line archosaur it also had a staggered double row of bony osteoderms along its back, suggesting that the very earliest avemetatarsalians had some crocodilian-like armor. This seem to have very quickly been lost, though – there’s no sign of osteoderms in the next branches to split off after Mambachiton, the aphanosaurs and pterosauromorphs – and although they occur again later in one dinosauriform and various non-avian dinosaurs, this appears to be multiple cases of independent re-evolution rather than retaining the original ancestral trait.

Spectember/Spectober 2023 #08: Various Filter-Feeders

Admantus asked for a “freshwater baleen whale”:

A shaded sketch of a speculative freshwater baleen whale. It has a very wide duck-like snout with whisker-like bristles, short baleen inside its mouth, very small reduced eyes, and broad paddle-like flippers.

Rostrorutellum admantusi is descended from small cetotheres that became isolated in a large inland body of water (similar to the modern Caspian Sea), eventually becoming landlocked and gradually reducing in salinity towards fully freshwater.

Highly dwarfed in size, just 2-3m long (~6’6″-9’10”), they’re slow swimmers with broad duck-like snouts that are used to scoop up mouthfuls of sediment and strain out their invertebrate prey in a similar feeding style to gray whales.

Due to the murkiness of the water, and the lack of large predators in their environment, they have poor eyesight and instead use sensory bristles and electroreceptors around their snouts to navigate and detect prey.

And an anonymous submission requested a “whale-like filter-feeding marine crocodile”:

A shaded sketch of a speculative filter-feeding crocodile. It has spatula-like jaws lined with many delicate closely-spaced needle-like teeth, flipper-like limbs, and a long paddle-like tail.

Sestrosuchus aigialus is a 6m long (~20′) crocodilian closely related to the modern American crocodile, living in warm shallow coastal waters.

It’s adapted for an almost fully aquatic lifestyle convergently similar to the ancient thalattosuchians, swimming with undulations of its long tail and steering with flipper-like limbs. But unlike other crocs it’s specialized for filter-feeding, with numerous delicate needle-like teeth in its jaws that interlock to sieve out small fish and planktonic invertebrates from the water.

A couple more suggestions also asked for “fully aquatic pinnipeds” and “future crabeater seal evolution”:

A shaded sketch of a speculative filter-feeding fully aquatic crabeater seal. It has four wing-like flippers, a streamlined body, and elongated jaws with many lobed teeth used to sieve krill.

Euphausiolethrus volucer is a fully aquatic descendant of the crabeater seal. About 5m long (~16’4″), it occupies the ecological niche of a small baleen whale in the krill-abundant Antarctic waters that lack most actual baleen whales.

Its jaws contain numerous finely-lobed teeth that are used to strain krill from the water, and it utilizes all four of its wing-like flippers to swim in an “underwater flight” motion similar to that of plesiosaurs.

Highly social, it tends to congregate in pods that cooperate to herd swarms of krill for easier feeding.

Strange Symmetries #12: Pterosaur Crossing

Rhamphorhynchus muensteri was one of the first pterosaurs known to science, and its snaggletoothed snout and long vaned tail have become classic features of many fictional “pterodactyls”. But despite its prevalence in pop culture depictions, it actually seems to have been quite a highly specialized pterosaur compared to its closest relatives – and a few specimens also seem to have an unusual little bit of asymmetry going on.

Living during the Late Jurassic, about 150-145 million years ago, around the warm shallow seas of what is now southeast Germany, Rhamphorynchus had a a wingspan of up to at least 1.8m (~6′), with larger fragmentary fossils suggesting a maximum of around 3m (~9’10”).

It had proportionally long wings, splaying intermeshing needle-like teeth, and a toothless beak at the tip of its jaws. The lower beak hooked strongly upwards, while the upper seems to have varied from upwards-curving to straight to downward-curving in different individuals – and some of these arrangements mean the keratinous beak tips must have crossed when the jaws closed, twisting to each side to asymmetrically pass each other similarly to modern crossbill birds.

Several specimens have been found with fish and cephalopod remains preserved in their guts, and along with the pointy intermeshing teeth this indicates Rhamphorhynchus was probably mainly piscivorous, occupying a similar ecological role to modern seabirds.

The different shapes of the toothless jaw tips may suggest there were several distinct populations of this pterosaur species exploiting slightly different food sources to each other, and the crossing beaks may have been an adaptation to pry the soft parts out of hard-shelled prey.

Natovenator

Halszkaraptorines were a group of small dromaeosaurids known only from the Late Cretaceous of Mongolia. They were odd little raptors with flattened snouts, long necks, and flipper-like arms – features that suggest they were specialized for swimming, making them the second known lineage of semi-aquatic non-avian dinosaurs after the spinosaurids.

This “duck-raptor” interpretation has been a little controversial since it was first proposed in 2017, but we’ve just gotten some more evidence for it in the form of an entirely new halszkaraptorine.

Natovenator polydontus lived in what is now the Gobi Desert in southern Mongolia, around 72 million years ago. The size of a small duck, about 45cm long (18″), it had jaws full of many needle-like teeth, a long flexible goose-like neck, and a streamlined body with a wide flattened ribcage convergently shaped like those of modern diving birds.

Although it had long strong legs, these don’t show much in the way of aquatic specializations and would have been used more for walking and running on land. Instead it may have used its flipper-like arms to propel itself through the water, like modern penguins or auks.

It probably had a lifestyle similar to modern mergansers, swimming and diving in lakes and rivers, and preying on fish, amphibians, and aquatic invertebrates.

Spectember 2022 #01: Arboreal Ornithopod

Despite some minor delays, it’s time once again for #Spectember – when I dive back into the big pile of speculative evolution concepts that you all submitted to me in 2020, and try to get through a few more of the backlog.

(…There’s still over 50 of them left. This is going to take a while.)

So today’s concept comes from an anonymous submitter, who requested an arboreal ornithopod dinosaur:

Jakapil

The thyreophorans were heavily armored ornithischian dinosaurs, with their most famous representatives being the stegosaurs and the ankylosaurs. Earlier members of the group were all small bipedal animals covered in rows of prickly osteoderms, and until now these “primitive” forms were known only from the early-to-mid Jurassic, around 200-165 million years ago.

But now the recent discovery of Jakapil kaniukura is suggesting a lineage of early thyreophorans actually survived for much much longer than previously thought – all the way into the Late Cretaceous, about 97-94 million years ago.

Just 1.5m long (5′), Jakapil lived in what is now southern Argentina, in an ancient desert with a braided river system. It was bipedal, with a short beak, small arms, and a body bristling with spiky armor, and its unusually deep lower jaw and heavily worn teeth indicate it fed on rather tough vegetation that required a lot of chewing to process.

It’s currently only known from somewhat fragmentary remains, so reconstructions of its full appearance are rather speculative and there’s already been some dispute about whether Jakapil actually was a thyreophoran. One proposal is that it shared a lot of anatomical features with early ceratopsians instead, which if true would make it an incredibly weird armored ceratopsian, and also the first definitive member of that group from South America. But the ceratopsian-like features could also just be due to convergent evolution – and a Jakapil-like dinosaur might actually help explain the only other known dubious South American “ceratopsian” Notoceratops, and the similarly-disputed Australian Serendipaceratops.

But whatever it was – late-surviving basal thyreophoran, southern armored ceratopsian, or even a previously unknown lineage of ornithishcians entirely new to science – it’s an exciting and unexpected discovery.

Amargasaurus

Amargasaurus cazaui was a sauropod dinosaur with a very distinctive-looking skeleton, sporting a double row of long bony spines along its neck and back. It lived in what is now Argentina during the Early Cretaceous, about 129-122 million years ago, and was fairly small compared to many other sauropods, reaching about 10m in length (~33′) with a proportionally short neck compared to its body size.

And despite being known from fairly complete skeletal remains there’s still a lot we don’t know about this dinosaur – especially what was actually going on with those vertebral spines. While it’s sometimes been depicted with skin sails over the spines, for the last couple of decades the general opinion has trended towards them being more likely to have been covered by spiky keratinous horn-like sheaths.

But recently that’s been brought back into question. A detailed study of the microscopic bone structure of Amargasaurus‘ spines shows no evidence for keratin attachment and instead found textures associated with skin coverings, along with an extensive web of ligaments connecting the spines to each other along each row.

So maybe it had big flashy sails after all!