Nix Illustration – Page 14 – Paleontology and science illustration, and feathering ALL the dinosaurs

It Came From The Wastebasket #19: The Pterrible Fate Of Ptychopariida

The Ptychopariida were some of the earliest known trilobites, first appearing in the early Cambrian about 521 million years ago and surviving until the end of the Ordovician about 444 million years ago. They included some of the most numerous and common trilobite species, and were probably ancestral to multiple other major lineages – including the very last trilobites at the end of the Permian – making them incredibly important in understanding the overall evolution of trilobites as a whole.

…But this group is also one of the biggest wastebaskets in paleontology.

First established in the early 20^th century, the ptychopariids seemed to have some fairly good defining characteristics based on their facial sutures, large thoraxes, and relatively small pygidia. But the group quickly became a dumping ground for a massive amount of Cambrian trilobites, eventually containing numerous different families, hundreds of genera, and many more individual species.

Actually figuring out their internal evolutionary relationships also turned out to be extremely difficult – so much so that some paleontologists working on them just gave up trying and arranged the genera names alphabetically instead!

Even cladistic studies from the 1970s onward struggled to make sense of these highly “problematic” trilobites, and any larger-scale analysis was a daunting task due to how huge and diverse the ptychopariid wastebasket had become over the years. Worse, some of the anatomical features the group had been based around were starting to look more like the result of a lot of convergent evolution across multiple lineages than any actual shared ancestry.

Efforts were still made at breaking up the mess, however, with better-understood sub-groups like the Proetida, Harpida, Asaphida, Trinucleida, and Olenida being gradually split off into their own separate orders over the course of the last few decades.

An illustration of Ptychoparia, an extinct trilobite from the Cambrian period. It has a large semicircular head with a pair of antennae, small eyes, and a bulbous "forehead" region. Its body has 13 segements, and its "tail" is small and shaped like a blunted triangle. — *Ptychoparia striata*

But even by the early 2010s what remained of the Ptychopariida was still paraphyletic at best, more of an “evolutionary grade” of early trilobites than a single lineage, with most of its constituent families also rather poorly defined. There was even a proposal to abandon the group entirely, stating that “it serves no scientific purpose” and that its orphaned contents should be considered “order uncertain” until their actual relationships can be untangled.

Today the “ptychopariids” are in dire need of a full revision – since they were the ancestors of many other major groups they’re still crucial for understanding early trilobite evolution. There may be a salvageable single lineage somewhere in the remains of this wastebasket, even if it’s restricted to just close relatives of the genus Ptychoparia, but until somebody tackles them properly they’re stuck in taxonomic limbo with their name only being used in a loose sense.

It Came From The Wastebasket #18: Lots And Lots of Lepidotes

Lepidotes was a ray-finned fish that lived during the Mesozoic, found in both freshwater and shallow marine environments. It was a member of the ginglymodian fish lineage, related to modern gars, and along with distinctive thick enamelled scales on its body it was also one of the earliest types of fish able to protrude its jaws for suction feeding.

First discovered in Jurassic-aged fossil deposits in Europe in the 1830s, this genus was quickly turned into a notorious wastebasket taxon for any similar-looking fossil fish. Over time dozens of different Lepidotes species were named, many of them rather dubious, from locations all around the world and spanning a time period of over 100 million years.

Lepidotes gigas

But despite Lepidotes being a wastebasket for almost two centuries, it wasn’t until surprisingly recently that any real progress began to be made on cleaning it all up.

In the early 2010s a large-scale review of ginglymodian relationships found that many “Lepidotes” species were either invalid or polyphyletic, belonging in completely different genera or families. True Lepidotes were restricted down to just the original type species Lepidotes gigas and a few of its closest relatives, all from the early Jurassic of Europe, while some other forms were moved into the newer genera Scheenstia and Callipurbeckia. Since then some other “Lepidotes” have also been reclassified, creating new names like Macrosemimimus, Occitanichthys, and Quasimodichthys.

There’s still work needing to be done on untangling all these Lepidotes-like fish – Scheenstia might actually now represent several different lineages, for example – but at least Lepidotes itself is now in a much better situation than it was just a couple of decades ago.

It Came From The Wastebasket #17: Getting Ornithomimus In Order

The ostrich-like “bird-mimic” dinosaur Ornithomimus was named in 1890, based on some hand and foot bones from Late Cretaceous-aged fossil beds in Colorado, USA.

The first ornithomimid known to science, it was initially thought to be a ornithopod, but then a few years later more fossil material revealed it was actually a theropod – and then it spent some time classified as a “megalosaur” before ornithomimids were finally recognized as being coelurosaurs in the early 20^th century.

And for nearly a century after its discovery it was treated as a wastebasket taxon for any similar-looking fossil material from North America and Asia, with around 17 different species named within the genus. One of these was split off into Struthiomimus in 1917, but it wasn’t until much later that the rest began to get sorted out.

A review of known Ornithomimus fossils in the early 1970s renamed a couple more species into the new genera Archaeornithomimus and Dromiceiomimus, and dismissed most of the remaining species as dubious or invalid. Just two valid species now remained: the original Ornithomimus velox from Colorado, and Ornithomimus edmontonicus from Alberta, Canada.

An illustration of Ornithomimus, an extinct feathered dinosaur. It has a a small beaked head atop a long slender neck, two wing-like arms with three clawed fingers, long ostrich-like legs, and a counterbalancing tail with longer feathers towards the tip. — *Ornithomimus edmontonicus*

Since then opinions have gone back and forth about some of the other Ornithomimus species. For a while Dromiceiomimus was merged back into Ornithomimus, but more recently it’s been found to have distinct limb proportions and was probably actually a separate genus after all. Another species that’s usually considered to be part of Struthiomimus is also sometimes instead classified as an Ornithomimus instead.

Really all of the North American ornithomimids are in need of a modern taxonomic revision – especially since Ornithomimus edmontonicus shows enough anatomical variation that it might actually represent a species complex of multiple very similar forms, which might get split apart in the future if anyone can figure out how to reliably distinguish them.

It Came From The Wastebasket #16: Catopsalis Catastrophe

The rodent-like multituberculates were a major lineage of mammals that were only distantly related to modern marsupials and placentals. They originated around the time of the mid-Jurassic (~168 million years ago), survived through the end-Cretaceous mass extinction, and went on to become one of the most diverse and successful types of mammal in the Paleocene. After that point they began to decline, and after anw over-130-million-year-long run they went extinct* in the early Oligocene (~33 million years ago).

(* Except, possibly, in South America, where an enigmatic fossil known as Patagonia peregrina may represent a multi surviving as recently as about 18 million years ago in the early Miocene.)

First discovered in North America in the 1880s, Catopsalis foliatus was part of a group of multituberculates called taeniolabidoids. These multis got significantly larger than the rest of their kind – averaging beaver-sized but with some species getting up to at least capybara-sized – and were some of the first mammals to evolve into relatively big herbivores after the extinction of the non-avian dinosaurs.

An illustration of Catopsalis, an extinct multituberculate mammal. It resembles a rodent, with a whiskery nose, large eyes, small rounded ears, short clawed legs with spurs on its ankles, and a long tufted tail. Its colored mostly brown with pale spotted markings along its sides. — *Catopsalis foliatus*

Catopsalis was named based on a partial jawbone and a few teeth, and over the next century or so various other similar-looking fossils from both North America and Asia were added into the genus as additional species. Eventually Catopsalis contained eight different species, ranging over about 10 million years from the late Cretaceous to the early Eocene – not especially big compared to some other wastebaskets we’ve looked at this month, but it was still a problem, muddying up attempts to understand the actual evolutionary relationships and biogeography of the taeniolabidoids.

Cladistic studies in the 1980s showed that Catopsalis was paraphyletic, made up of at least five separate lineages, and a few of them were subsequently renamed and reclassified. The Cretaceous Asian forms became Djadochtatherium and Catopsbaatar, and are now considered to be part of a different lineage of multis known as djadochtatherioids, while one of the remaining North American species then became Valenopsalis.

…But a couple of other new Catopsalis species have also been named in the meantime (one as recently as 2018), so there are still seven different species that need sorting out in this particular wastebasket.

It Came From The Wastebasket #15: Rauisuchian Revolution

Pseudosuchians, or “croc-line archosaurs”, are one of the two major lineages of archosaur reptiles, alongside the avemetatarsalians (pterosaurs and dinosaurs). Although today they’re represented only by crocodilians, they were especially successful and diverse back in the Triassic – and it was only after a mass extinction took out most of them that the dinosaurs were able to rise to prominence for the rest of the Mesozoic Era.

A grouping of pseudosuchians traditionally known as “rauisuchians” had upright limbs in a distinctive “pillar-erect” hip arrangement. Many of these croc-relatives were large quadrupedal predators, but others developed bipedal theropod-like postures, with some so remarkably convergent that they were initially misidentified as ornithomimosaurs.

The first rauisuchians were discovered in the 1930s, represented only by fragmentary remains, and while they were initially recognized as being pseudosuchians their exact evolutionary relationships within that group were poorly understood for a long time. Over the next several decades they were classified with aetosaurs (early armored pseudosuchians), then ornithosuchids (even earlier pseudosuchians), and then erythrosuchids (not even pseudosuchians but an earlier type of archosauriform).

More complete fossil discoveries and better cladistic analysis methods in the 1980s led to them being classified as being very closely related to crocodylomorphs, with three main lineages recognized: the prestosuchids, the rauisuchids, and the poposauroids.

An illustration of three different "rauisuchians", extinct relatives of modern crocodiles. At the top is Prestosuchus, a quadrupedal reptile with a boxy theropod-dinosaur-like head, platigrade bear-like legs, and a long tapering tail. It's colored yellow-brown with lighter underbelly and cat-like darker spots-and-stripes. In the middle of Postosuchus, a bipedal reptile that convergently resembles a tyrannosaur, with a boxy head, small arms, plantigrade legs, and a long counterbalancing tail. it's colored brown on top and white underneath, with irregular splotches of black and white across its body. At the bottom is Effigia, a bipedal reptile that convergently resembles a featherless ornithomimosaur, with a beaked bird-like head, a long neck, small arms, bird-like legs, and a counterbalancing tail. It's dark-colored with faint reddish and yellowish stripes and a paler underside. — The “prestosuchid” *Prestosuchus chiniquensis*, the rauisuchid *Postosuchus kirkpatricki*, & the poposauroid *Effigia okeeffeae* (not to scale)

But even by the end of the 20^th century “Rauisuchia” had never actually gotten a formal definition, and it had very much become a wastebasket taxon for a variety of paracrocodylomorph pseudosuchians that didn’t easily fit into any other major lineages.

In the 2000s renewed interest in rauisuchians’ anatomy and evolutionary relationships led to increasing recognition that they weren’t even a single defined group, with various species instead falling into different points along an “evolutionary grade“. The poposauroids and rauisuchids still seem to be distinct lineages, but the “prestosuchids” were found to be polyphyletic, with some forming a grade between the other two “rauisuchid” groups and others turning out to not even be paracrocodylomorphs.

A cladogram showing the classification of poposauroids, Prestosuchus, and rauisuchids within the group Pseudosuchia. They're shown as three separate lineages branching off between aetosaurs and the ancestors of modern crocodilians. A bracket marking indicates that all three traditionally used to be classified as "rauisuchians".

And although the taxonomic concept of “Rauisuchia” as a distinct group has now been abandoned, the term “rauisuchians” does still remain in common use as an informal name for these animals – probably because it’s much more concise than saying “non-crocodylomorph paracrocodylomorphs”.

It Came From The Wastebasket #14: The Protorthoptera Puzzle

Protorthoptera was a group of fossil insects created in the early 20^th century to categorize “primitive” neopterans – some of the earliest insects to have evolved the ability to fold their wings down over their backs. Known mostly from just fossilized forewings, they first appeared around 320 million years ago in the late Carboniferous, and after heavy losses during the Great Dying mass extinction they eventually disappeared in the mid-Triassic about 240 million years ago.

And this group was a massive wastebasket taxon.

As early as the mid-20^th century the protorthopterans were recognized as being a general taxonomic dumping ground, containing a mixture of early members of multiple different “orthopteroid” insect lineages. But invertebrate paleontologists at the time considered this collection of “primitive” insects to lack enough distinctive features to confidently separate them out from each other, and so the highly paraphyletic grouping continued to be used well into the 1990s.

An illustration of Ctenoptilus elongatus, an extinct insect. It has long thin antennae, a small grasshopper-like head, six legs each ending in two small claws, a cylindrical abdomen, and two pairs of large wings folded over its back. It's colored red, tan, and dark brown, with striped markings on its wings. — *Ctenoptilus elongatus*

But in the early 2000s this situation finally changed. Proper cladistic analysis of protorthopteran fossils identified defining features of the wing vein patterns, and many species were reclassified into various lineages within the Archaeorthoptera – which includes modern grasshoppers, crickets, and locusts along with several closely related fossil groups like the titanopterans and caloneurodeans.

“Protorthoptera” is still sometimes used in a loose sense for fossil neopteran insects that still can’t be confidently classified anywhere else, so the wastebasket isn’t entirely cleared here.

And there are some alternate classification systems (mainly proposed by Russian paleontologists) that instead consider many protorthopterans to be notopterans closely related to modern ice-crawlers, and place others as part of other modern neopteran lineages such as webspinners and true bugs.

Hopefully better fossil discoveries and future studies will eventually help clear things up, and give us a better overall picture of the evolution of these insects.

It Came From The Wastebasket #13: Certifying Cetiosaurus

Discovered in England in the early 1840s, Cetiosaurus was one of the first sauropod dinosaurs known to science – although its scrappy remains were initially mistaken for a massive crocodile-like marine reptile, hence its name meaning “whale lizard”.

It wasn’t even identified as being some sort of dinosaur until a couple of decades later, and then in the 1870s discoveries of much more complete sauropods like Brontosaurus and Diplodocus in North America led to it finally being recognized as a similar long-necked form.

Like some other early dinosaur discoveries it quickly became a wastebasket taxon, with vaguely-similar fragmentary fossils found in England, France, Switzerland, and Morocco all being lumped under its name. By the end of the 20^th century nearly 20 different Cetiosaurus species had been created, most of them highly dubious and based on poor fossil material without any distinctive anatomical features.

An illustration of Cetiosaurus, a sauropod dinosaur. It has a small head atop a long neck, a chunky four-legged body with mitten-like forefeet and three-clawed hindfeet, and a long tapering tail. It's colored pale teal with darker red-brown stripes and a lighter underside, with brighter yellow-green towards its head. There are also speculative red quill-like structures on its throat, cheeks, neck, and tail tip. — *Cetiosaurus oxoniensis*

It wasn’t until the early 2000s that the mess was finally cleaned up. A major revision and redescription of Cetiosaurus determined that just one species was actually valid: Cetiosaurus oxoniensis from the mid-Jurassic of England, known from fairly complete remains and dating to about 170 million years ago.

But this did create a new problem – it meant that the original type species Cetiosaurus medius wasn’t actually based on anything distinctive. So, much like what happened with Iguanodon, the type species was officially changed to Cetiosaurus oxoniensis in 2014, ensuring that this historically significant genus was defined by decent fossil material rather than by dubious fragments.

It Came From The Wastebasket #12: Coelurosaur Confusion

Historically Coelurosauria was the counterpart to the Carnosauria, with both of them representing two major lineages of theropod dinosaurs.

Created as a group in the early 20^th century, coelurosaurs quickly became a dumping ground for all small-bodied theropods – including coelophysoids, compsognathids, ornithomimids, oviraptorosaurs, dromaeosaurids, and troodontids– and for a while this wastebasket taxon also included the large-bodied ceratosaurids and tyrannosauroids, before they were moved over into the carnosaurs.

But during the 1960s and 1970s this arrangement began to break down. A better understanding of groups like dromaeosaurs revealed a confusing mixture of traditional “carnosaur” and “coelurosaur” anatomical features, and paleontologists struggled to figure out where these sorts of theropods actually fit in.

The development of cladistic methods from the 1970s onwards led to efforts to clean up the coelurosaur wastebasket, trying to figure out a more accurate version of these animals’ evolutionary relationships. After briefly collapsing Coelurosauria down to just coelophysoids and “coelurids“, the growing recognition of modern birds as living theropod dinosaurs eventually resulted in the group being properly redefined in the 1980s as “birds, and all theropods closer related to them than to carnosaurs“.

An illustration showing four examples of coelurosaurs, theropod dinosaurs closely related to birds. One the left is Citipati, a bird-like feathery oviraptorosaur that has a cassowary-like crest on its head, a short beak, a long neck, feathered wings, long slender legs, and a short tail with a feather fan at the end. It's mostly colored black and white, with bright blue and yellow face markings and small eyespots on its wing and tail feathers. At the top is Albertosaurus, a tyrannosaur with short bony crests above its eyes, tiny two-fingered hands, long bird-like legs, and a long thick counterbalancing tail. It's colored with a blotchy striped pattern of yellow, red, and dark brown, with bright blue on the crests over its eyes. On the right is Yi, a small bird-like scansoriopterygid with a fluffy feathery coat, four long tail feathers, and large membranous wings supported by a bony extension from its wrist that make it look like a dino-bat or a wyvern. It's colored brownish-grey with a yellow snout and striped markings on its neck, wings, and tail feathers. At the bottom is Sinosauropteryx, a compsognathid with a typical theropod body plan – triangular head, S-shaped neck, three-clawed hands, bird-like legs, and a long tail – but it's covered in fluffy feathers which are especially bushy on its tail. it's colored ginger-and-white, with a black raccoon-like mask marking over its eyes and a stripey tail. — Clockwise from the left (not to scale): *Citipati osmolskae*, *Albertosaurus sarcophagus*, *Yi qi*, *Sinosauropteryx prima*

The coelophysoids were finally removed entirely, reclassified as a much earlier branch of theropods – but quite a few of the other groups from earlier concepts of Coelurosauria survived this reshuffling, with the compsognathids, ornithomimids, oviraptorosaurs, dromaeosaurs, and troodontids all proving themselves to have really been closely related the whole time. Meanwhile the tyrannosauroids were brought back in, along with the therizinosaurs, alvarezsauroids, and a whole bunch of paravian and avialan lineages.

(Megaraptorans might belong somewhere in the coelurosaurs, too – possibly being tyrannosauroids – but their classification is currently being disputed.)

It Came From The Wastebasket #11: A Cetothere Change

Cetotheres were a group of small baleen whales, one of three major lineages of these cetaceans alongside the rorquals and the right whales. They first appeared in the fossil record in the mid-Miocene, about 14 million years ago (but are estimated to have actually originated 10-15 million years earlier), and disappeared during the Pleistocene about 2 million years ago.

First recognized in the mid-19^th century, for a long time the cetotheres were used as a wastebasket for all fossil baleen whales that didn’t clearly fit into any modern whale families. By the start of the 21^st century nearly 30 different genera representing numerous different species were all lumped into the group – and the genus Cetotherium was another wastebasket in itself with at least 12 assigned species, many of which were based on fragmentary or dubious remains.

An illustration of Ciuciulea, an extinct cetothere baleen whale. It looks similar to modern rorquals, with a streamlined and relatively slender body, but lacking the typical throat grooves of that type of whale. Its jaws are long and narrow, with a paired blowhole at the top of its head and small eyes set near the corners of its mouth. It also has fairly small flippers, a dorsal fin set about two-thirds of the way down its back, and a horizontal tail fluke. It's coloration is countershaded, mostly grey on top and white underneath. — *Ciuciulea davidi*

This was finally cleaned up in the 2000s, when a revision of the cetotheres cut the group down to just 6 genera. Since then a handful of additional new genera and species have been named, and while a few polyphyletic Cetotherium species may still need tidying up the cetotheres have overall gone from being a total taxonomic mess to actually being one of the best studied groups of fossil baleen whales.

Their exact evolutionary relationships with each other are still in flux, but the most surprising discovery from the improved understanding of these ancient whales is that they might not be extinct after all.

A set of three screenshots from the animated movie "Ice Age: Dawn of the Dinosaurs". The first image shows the two opossum characters Crash and Eddie asking, "Were you killed?!" The second image shows the weasel buck looking away and replying, "Sadly, yes…" The third image shows Buck leaning closer and adding "but I lived!" Buck's face has been photoshopped into that of a Cetotherium whale in both shots.

A study in the early 2010s suggested that the pygmy right whale may actually be a living cetothere. This classification was initially controversial, but further discoveries of fossil relatives of this enigmatic modern whale and comparisons of their distinctive inner ear anatomy have provided stronger evidence for an evolutionary link.

At this point it seems fairly likely that the pygmy right whale really is either the last surviving representative of the cetothere lineage, or at least is a very close evolutionary “cousin” (a “cetotherioid”) closer related to them than to any other modern baleen whales.

It Came From The Wastebasket #10: Struggling With Stegoceras

First described and named in the early 1900s, Stegoceras validum was a dog-sized small pachycephalosaur that lived in Alberta, Canada, during the Late Cretaceous (~77-74 million years ago).

Initially just known from its skull domes, it was one of the first pachycephalosaurs to be discovered and was very poorly understood until more complete remains were found in the 1920s. Then it spent a couple of decades being mixed up with Troodon due to similarities in tooth shape, until the discovery of Pachycephalosaurus led to pachycephalosaurs finally being recognized as a distinct group of ornithischian dinosaurs in the 1940s.

An illustration of Stegoceras, an extinct pachycephalosaur. It's a small bipedal dinosaur with tiny arms, bird-like legs, a speculative coat of fluffy protofeathers over most of its body, and a long tapering tail with speculative bristly quills. It has a large bony dome on its forehead, rimmed with short spikes, and a short snout with a stubby beak. It's mainly colored white and grey, with brighter red and yellow markings on its face and red towards the tip of its tail. — *Stegoceras validum*

For much of the 20^th century Stegoceras was treated as a wastebasket taxon for any small-to-mid-sized North American (and one Asian) pachycephalosaur, and multiple different species were named based on what were often rather dubious fragmentary fossils. But towards the start of the 21^st century this mess did start getting cleaned up, merging some dubious species into the original Stegoceras validum, and moving others to separate genera like Sphaerotholus, Colepiocephale, Hanssuesia, and Sinocephale.

By the early 2000s just the Canadian Stegoceras validum remained – but then in 2011 the new species Stegoceras novomexicanum was named based on specimens from New Mexico, USA. The validity of this second species has been debated, since the fossils are juveniles and might instead belong to Stegoceras validum or another genus like Sphaerotholus, but if it is some sort of Stegoceras then it significantly re-extends the known geographic range of this little pachycephalosaur.