Compsognathus

First discovered in the 1850s, Compsognathus longipes was the first theropod dinosaur known from a fairly complete skeleton, and also the smallest known non-avian dinosaur for over 130 years.

(A second specimen was also, briefly, the “first” aquatic non-avian dinosaur, but that’s another story.)

Living in what is now Europe during the late Jurassic, about 150 million years ago, it was a lightly built animal with long legs and a long tail, growing to around 1.2m long (~4′). Its hands seem to have had only two functional fingers, with the third being vestigial and possibly not even having a claw.

Skin impressions from about a third of the way along its tail show small bumpy scales – but since other compsognathids like Sinosauropteryx are known to have been covered in fur-like feathers, this likely means that just that particular region of Compsognathus’ body wasn’t fluffy.

Some of Compsognathus‘ diet is known for certain, since preserved gut contents show it fed on smaller vertebrates like lizards and rhynchocephalians. The remains of a lizard in the stomach of one specimen were even identified as belonging to a previously-unknown species, Schoenesmahl dyspepsia, with the dismembered nature of the skeleton suggesting Compsognathus tore its prey into bite-sized chunks in a similar manner to modern predatory birds.

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Heterohyus

Apatemyids were a group of unique early placental mammals that lived during the first half of the Cenozoic, known from North America, Europe, and Asia. Due to their specialized anatomy their evolutionary relationships are rather murky (they were traditionally part of the convoluted mess that was “Insectivora”), but currently they’re thought to be a very early offshoot of the Euarchontoglires, the branch of placentals that includes modern rodents, lagomorphs, treeshrews, colugos, and primates.

Living in what is now western Europe during the mid-Eocene, around 47 million years ago, Heterohyus nanus was a small apatemyid about 30cm long (~12″) – although just over half of that length was made up of its tail.

Like other apatemyids it had a proportionally big boxy head, with large forward-pointing rodent-like incisors in its lower jaw and hooked “can-opener-shaped” incisors in its upper jaw.

Example of an apatemyid skull from the closely related American genus Sinclairella.
From Samuels, Joshua X. “The first records of Sinclairella (Apatemyidae) from the Pacific Northwest, USA.” PaleoBios 38.1 (2021). https://doi.org/10.5070/P9381053299

The rest of its body was rather slender, and fossils with soft tissue preservation from the Messel Pit in Germany show that it had a bushy tuft of longer fur at the end of its long tail.

But the most distinctive feature of apatemyids like Heterohyus were their fingers, with highly elongated second and third digits resembling those of modern striped possums and aye-ayes. This suggests they had a similar sort of woodpecker-like ecological role, climbing around in trees using their teeth to tear into bark and expose wood-boring insect holes, then probing around with their long fingers to extract their prey.

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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.

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Aureia

Aureia rerehua was a toothed whale that lived during the late Oligocene and early Miocene, around 23-22 million years ago, in shallow coastal waters covering most of what is now Aotearoa New Zealand.

It was closely related to the waipatiids – a group traditionally classified as platanistoids (the South Asian river dolphin lineage), but more recently proposed as instead representing a separate earlier branch of the toothed whale evolutionary tree.

About 2m long (~6’6″), Aureia had distinctive tusk-like teeth that splayed outwards from its snout, interlocking when its mouth was closed. Along with a flexible neck and its fairly delicately-built skull and jaws, this suggests it was specialized for catching small prey in a “fish trap” of teeth, a unique feeding strategy for a toothed whale.

Along with different feeding specializations in other close relatives like Nihohae, Aureia shows us how multiple species of these ancient Aotearoan cetaceans were able to coexist in the same place and time by diversifying into different novel ecological niches.

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Gaiasia

Gaiasia jennyae was a tetrapodomorph – an amphibian-like relative of early tetrapods – that lived about 280 million years ago during the early Permian in what is now Namibia.

Although it’s only known from incomplete skull and vertebral column material it probably looked quite similar to the colosteids, a closely-related group of tetrapodomorphs with elongated bodies and small limbs. If it had the same sort of body proportions as these relatives it would have been huge, the largest known stem-tetrapod at potentially around 4m long (~13′).

It had a wide flat head with a short boxy snout, and large interlocking fangs on the roof of its mouth and at the front of its lower jaw. It would have been fully aquatic and probably not a particularly fast swimmer, instead likely being an ambush predator using suction from rapidly opening its jaws to pull prey into its mouth before clamping down with its fangs.

It’s also notable for living considerably later than most other stem-tetrapods, and in an unexpected part of the world. While its close relatives are all known from the tropics of the Carboniferous, Gaiasia was in a location that was much closer to the South Pole during the early Permian (~55° S), inhabiting an immense freshwater lake in a rift valley with a cold-temperate climate.

Its presence in this habitat may suggest that other stem-tetrapod lineages survived and thrived in high latitudes for much longer than previously thought, while the true tetrapods were all diversifying nearer the equator – or it might represent a Paleozoic equivalent of Koolasuchus, an isolated straggler lurking in a cold refugium.

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Lokiceratops

Lokiceratops rangiformis was a ceratopsian dinosaur that lived during the Late Cretaceous (~78 million years ago) in what is now Montana, USA. Estimated at about 6.7m long (~22ft), it was one of the largest known members of the centrosaurine branch of the ceratopsians.

It had a unique arrangement of ornamentation on its skull, with no nose horn, two long brow horns, and a pair of huge asymmetrical curving blade-like spikes on the top of its square frill – some of the largest known frill spikes of any ceratopsian.

It lived in a swampy environment near the shore of the Western Interior Seaway, in an area that seems to have had an unusually high diversity of ceratopsians – along with Lokiceratops there were three other centrosaurines (Medusaceratops, Albertaceratops, and Wendiceratops), and one chasmosaurine (Judiceratops).

(There’s also a possibility that it might not actually be a unique species. We know some other ceratopsians’ faces changed quite drastically as they aged, so Lokiceratops could instead represent a fully mature individual of Medusaceratops.)

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Tachypleus syriacus

Tachypleus syriacus was a horseshoe crab from the late Cretaceous (~100-95 million years ago) of what is now Lebanon.

Closely related to modern tri-spine horseshoe crabs, it displayed a similar level of sexual dimorphism. Females grew to at least 25cm long (~10″), with rounded front edges to their carapaces and shorter rear spines, while males were around 30% smaller with a scalloped shape to the front of their carapaces.

One recently described female specimen also preserves distinctive nodules around the rim of its carapace, which may represent some sort of sensory structure.

This particular specimen is also unique for preserving a coprolite in the process of being expelled from the horseshoe crab’s body – that’s right, it died while pooping.

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Xenerodiops

Xenerodiops mycter was an unusual heron from the Oligocene (~30 million years ago) of what is now Egypt.

Known only from a partial skull and an arm bone, it’s estimated to have stood around 70cm tall (~2’4″) and was probably fairly similar in overall appearance to modern night herons. Its beak was powerfully built and had a distinctive downwards curve, shaped more like some types of stork than other herons – suggesting it may have had a convergently stork-like lifestyle, slowly walking through its marshy habitat probing around for prey and snapping up whatever its beak came into contact with.

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Palaeoplethodon

There are no salamanders living in the Caribbean today, but one tiny fossil shows that this wasn’t always the case.

Palaeoplethodon hispaniolae was discovered in a chunk of amber from the Dominican Republic on the island of Hispaniola. The exact age of this type of amber is uncertain, but it most likely dates to the early-to-mid Miocene, about 20-15 million years ago.

The only known specimen is a hatchling, just under 2cm long (0.8″). It’s unclear what its full adult size could have been, but based on its modern relatives it may have grown to anywhere between 4.5cm and 20cm long (~2-8″).

Its strongly webbed hands and feet suggest it was very closely related to modern tropical climbing salamanders – but Palaeoplethodon had a unique webbing arrangement, with its feet relatively elongated and its hands fully fused into small rounded pads.

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Pachydectes

Modern mammals are the only living representatives of the synapsids, but back during the Permian there were numerous other evolutionary branches – first the pelycosaurs, and later their descendant the therapsids.

Some of the first non-mammalian therapsids were the biarmosuchians, mid-sized carnivores with a more upright posture than their pelycosaur ancestors. They had large canine teeth in their jaws and powerful bites, and some of them also developed elaborate ornamentation on their skulls, with various bony bumps and crests adorning their faces.

Pachydectes elsi was a 1.5m long (~5′) biarmosuchian living in what is now South Africa during the late Permian, about 265 million years ago. Bone texture indicates its head ornamentation was covered by either tough thickened skin or a keratinous sheath, and the large bulbous bosses on the sides of its snout had a particularly rich blood supply, suggesting these structures could have been continuously growing throughout its entire life.

But despite how well-protected it looked, Pachydectes’ skull was actually relatively fragile and wouldn’t have been able to withstand the impact forces of using its headgear for fighting or defense. Instead it may have been mostly used for visual display – and the blood supply to the snout bosses might even have given it the ability to “blush” them if they had a soft-tissue covering.

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