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.
Living during the mid-Eocene, about 43 million years ago, in a shallow sea-covered region that is now part of Egypt‘s Western Desert, Phiomicetus was an early protocetid – an amphibious foot-powered swimmer, at a transitional point in the evolution of whales from deer-like terrestrial animals to fully aquatic screaming torpedoes.
About 3m long (~10′), it had large jaw muscles and sharp teeth with wear patterns that suggest it was a raptorial hunter grabbing and snapping at prey with powerful bites. It would have probably tackled fairly big prey compared to other protocetids, hunting things like large fish, turtles, and even smaller whales in an ecological role similar to that of modern orcas.
Along with the distantly-related long-snouted Rayanistes it’s one of the earliest known whales from Africa, giving us further glimpses at a time period when early cetaceans were first dispersing out from the South Asian subcontinent via the ancient Tethys Sea.
Discovered in the Mazon Creek fossil beds in Illinois, USA, this species dates to the late Carboniferous period around 310 million years ago. A single near-complete specimen about 5cm long (~2″) preserves impressions of the body outline and numerous tiny scales, giving us a pretty good idea of what it looked like in life.
Joermungandr had a long streamlined tubular body with small limbs and a short tapering tail, and a stubby snout with fused bones heavily reinforcing its skull. Along with microscopic ridges on its body scales that resemble the dirt-repelling scales of some modern reptiles, this combination of features suggest it was a headfirst burrower that wriggled its way through soil with snakelike motions.
(This was originally supposed to be a final-day-of-#Spectember bonus post, but it got much longer than I expected so it’s a few days late.)
To finish off this year’s diversion into speculative evolution, instead of pulling from my still-rather-long list of unused submissions I’m doing something a little different – trying to give an idea of how I go through the actual process of designing a speculative species.
It was on the cover of the old edition of After Man I first discovered as a kid in the local library, it immediately caught my attention, and as a result it’s always been one of my favorite species from the book.
But some of its anatomy doesn’t really hold up.
I really really Do Not Like the “official” redesign that replaced the original art in the 2018 reprint. It’s shrinkwrapped.
I just think it’s neat.
Reedstilt in both original flavor and 2018 revamp style.
It’s September, the Cambrian series has been delayed until later this year, so instead let’s get speculative – it’s time for the return of #Spectember! I can’t manage daily content this time around, but I still have plenty of submitted concepts left over from last time.
So let’s get started with some marsupials suggested by someone crediting themselves only as Bruno Drundridge:
But I’m not talking about the dubious claims of non-avian dinosaur fossils found in places they shouldn’t be. This is about something else entirely: an unassuming little bird known as Qinornis paleocenica.
Living in Northwest China during the mid-Paleocene, about 61 million years ago, Qinornis was roughly pigeon-sized at around 30cm long (12″). It’s known only from a few bones from its legs and feet, but those bones are unusual enough to hint that it might have been something very special.
Uniquely for a Cenozoic bird, some of its foot bones weren’t fully fused together. This sort of incomplete fusion is seen in both juvenile modern birds and in adults of non-avian ornithurine birds from the Cretaceous – and the Qinornis specimen seems to have come from an adult animal.
If it was fully grown with unfused feet, then that would suggest it was actually part of a “relic” lineage living 5 million years after the mass extinction, surviving for quite some time longer than previously thought.
Remarkably similar-looking gliding reptiles have appeared multipledifferenttimes over the group’s evolutionary history, including the modern Draco – and despite being unrelated to each other almost all of them have achieved this in the exact same way, supporting their wing membranes on extremely elongated rib bones.
These early members of the neodiapsid lineage were the very first vertebrates known to have experimented with gliding, all the way back in the late Permian period 260-252 million years ago. And while they superficially resembled all the later rib-gliders, their wings were actually something never seen before or since in a gliding reptile.
Basically, these animals were the closest that Earth life ever came to legitimately evolving a dragon.
Coelurosauravus elivensis here was a weigeltisaurid living in what is now Madagascar, which at the time was part of southern Pangaea. About 40cm long (1’4″), its body was adapted for a life climbing and gliding around in the treetops, with pneumatized air spaces lightening its bones and long slender limbs similar to those of modern tree-climbing lizards.
Its large wings were formed from around 30 pairs of long hollow rod-shaped bones extending out from the sides of its belly. These flexible structures could furl and unfurl with a motion like a foldable fan, and are thought to have been highly modified from osteoderms in the skin, creating an entirely new part of its skeleton.
Towards the front of the wing the rods were arranged in several closely-packed “bundles”, and one specimen of Coelurosauravus preserves an impression of what seems to be the outline of the wing membrane’s leading edge – showing a stiffened pointed shape resembling the alula of a bird wing, which may have served a similar aerodynamic stabilization function.
From fig 2 in Schaumberg, G. et al (2007). New information on the anatomy of the Late Permian gliding reptile Coelurosauravus. Paläontologische Zeitschrift 81, 160–173. https://doi.org/10.1007/BF02988390
But aside from the wings, the most striking feature of weigeltisaurids were their heads. Their skulls featured large crest-like frills resembling those of chameleons and ceratopsid dinosaurs, and their edges were adorned with prominent bumps and spikes. These were probably used for visual display and might have been a sexually dimorphic feature, with males having larger spikier crests than females. The crests may also have anchored large powerful jaw muscles, giving weigeltisaurids a wider gape and faster bite speed, helping them to snap up their fast-moving insect prey.
