Saturday, September 10, 2022

Euhelopus



Type Species: Euhelopus zdanskyi
Classification: Dinosauria – Saurischia – Sauropoda - Gravisauria - Eusauropoda - Neosauropoda – Macronaria – Titanosauriformes – Somphospondyli – Euhelopodidae
Time Period: Early Cretaceous
Location: China
Diet: Herbivore

The Chinese sauropod Euhelopus was the first Chinese dinosaur to be scientifically studied in 1923. It is the namesake for the family group of Euhelopopidae, all of which are found in East Asia. Euhelopus had longer forelegs than hindlegs, and it is one of the few sauropods found with a relatively complete skull. Euhelopus was a large-sized macronarian sauropod, weighing in between 17-22 tons and reaching up to 49 feet in length. 

Nqwebasaurus



Type Species: Nqwebasaurus thwazi
Classification: Dinosauria – Saurischia – Theropoda – Tetanurae – Coelurosauria – Tyrannoraptora – Maniraptoromorpha – Ornithomimosauria
Time Period: Early Cretaceous
Location: South Africa  
Diet: Herbivore or Omnivore


The African dinosaur Nqwebasaurus – whose full name means ‘fast runner of the Kirkwood district’ – lived during the earliest stage of the Early Cretaceous. This is the only named coelurosaur discovered in Africa, and it shows that coelurosaurian dinosaurs lived in Gondwana 50 million years earlier than previously thought. 

This ornithomimosaur was small, only about a foot high and three feet in length. Its long, three-fingered hands had a partially opposable thumb and a recurved claw. Unlike most theropods – but in keeping with some other ornithomimosaurs – its first and second digits were recurved while the third claw was not. Ornithomimosaurs ran the gauntlet of dietary styles, and Nqwebasaurus was likely an herbivore, as it lacked serrations on its maxillary teeth and used gastroliths to assist in pulverizing its food. Skeptics point out that some predators use gastroliths – particularly those that eat fish and invertebrates; thus Nqwebasaurus may have been an omnivore.  Nqwebasaurus also had fewer teeth than most other theropods; ornithomimosaurs ran the gauntlet of teeth types, with some having few teeth, others having lots of teeth, and even some, like Gallimimus, who had no teeth but a keratinous bill! Some scientists speculate that Nqwebasaurus was partially feathered or had a feather coat for insulation; this reasoning is based on its relationship to other feathered dinosaurs.

Saturday, October 16, 2021

Xuanhuaceratops

Type Species
: Xuanhuaceratops niei
Classification: Dinosauria – Ornithischia – Marginocephalia – Ceratopsia – Chaoyangsauridae 
Time Period: Late Jurassic 
Location: China
Diet: Herbivore

Xuanhuaceratops was a small, bipedal herbivore that scurried among the thick forests of Late Jurassic China, dodging predators by hiding in thick undergrowth and running speedily away on two legs. It’s known from four fragmentary skeletons, hinting at a family group. Though it looks alien compared to the later and famous ceratopsians of the Cretaceous Period, Xuanhuaceratops had already developed the classic sharp, cropping beak of the ceratopsians and had the beginnings of the neck frill that would become a trademark of Cretaceous ceratopsians. 

Chaoyangsaurus

Type Species
: Chaoyangsaurus youngi
Classification: Dinosauria – Ornithischia – Marginocephalia – Ceratopsia – Chaoyangsauridae 
Time Period: Late Jurassic 
Location: China
Diet: Herbivore

While little remains for this small herbivorous dinosaur have been discovered, those remains indicate that it was an early ceratopsian. Chaoyangsaurus was a small, bipedal herbivore whose lineage lies along the lay-lines that would eventually spawn one of the most dominant dinosaurs of the Cretaceous, the ceratopsians. Chaoyangsaurus is the namesake of the group that includes the earliest ceratopsians, such as Hulianceratops, Yinlong, and Xuanhuaceratops. All are from the Late Jurassic China, and they inform us that the ceratopsian lineage began there before radiating throughout the entire world during the Cretaceous Period. 

Friday, October 15, 2021

Chilesaurus

Type Species
: Chilesaurus diegosuarezi
Classification: Dinosauria 
Time Period: Late Jurassic 
Location: South America 
Diet: Herbivore

Chilesaurus is an oddball of a dinosaur. Reaching ten and a half feet in length, it had spatula-shaped, elongated teeth that obliquely pointed forward, a design perfect for eating plants. Its herbivorous lifestyle is also attested by its backward-pointing pubic bone, which made room for a large gut. Its hind limb wasn’t well adapted for running, and its broad feet had a weight-bearing front toe. It had strong arms with a large claw that could be extended outwards, just as is seen in the sauropodomorphs. All this to say, it looks like a cross between a theropod and an ornithischian, and no one really knows where to place it in the dinosaur family tree. 

Those who argue for a theropod lineage point out that it’s not uncommon – although it’s certainly not usual – for theropods to adapt herbivorous lifestyles. We see this with the therizinosaurs, who became herbivorous, and with the ornithomimosaurs, who became omnivorous. Perhaps Chilesaurus is simply a theropod that went vegan. Others, however, consider the mixture of traits between theropods and ornithischians as evidence that we’ve got the dinosaur family tree all wrong. The current cladogram, which subdivides Dinosauria into the lizard-hipped Saurischians and the bird-hipped Ornithischians, wasn’t the only cladogram proposed; another was proposed by Thomas Huxley in 1869 (and revived by some scientists in 2017). Huxley argued that Dinosauria should be subdivided into Saurischia and Ornithoscelida. In his proposal, Saurischia contained all the sauropodomorphs, and Ornithoscelida contained the theropods and the ornithischians. In Huxley’s scheme, theropods are more closely related to ornithischians than to the sauropodomorphs. Proponents of his view point to Chilesaurus as evidence that his thesis is not only justifiable but correct, and that Chilesaurus, despite its relatively late appearance in the fossil record, is evidence of a ‘vestigial’ family line that eventually gave rise to both ornithischians and theropods. 

Kentrosaurus



Type Species
: Kentrosaurus aethiopicus
Classification: Dinosauria – Ornithischia – Thyreophora – Stegosauria – Stegosauridae
Time Period: Late Jurassic 
Location: Africa
Diet: Herbivore

The African stegosaur Kentrosaurus was closely related to Stegosaurus though it was half its size, clocking in at around fifteen feet in length. Kentrosaurus had a small, elongated head with a beak that it used to sever tough plant material to be digested in its barrel-like gut. Its skin was covered in bony osteoderms, and it had small plates on its neck. These small plates were dwarfed by the plates that ran along its back in a series of fifteen rows. These plates were elongated with a thickened section in the middle, as if they were modified spines, and they were probably covered in horn. These plates gradually merged into spikes on the hip and tail. The longest spikes were on the end of its tail, and it would’ve used its thagomizer as a defensive weapon. It also had a long spike on each shoulder. Because the thigh bones come in two different types, it’s likely that males and females differed in their stoutness (a case of sexual dimorphism). 

Kentrosaurus is considered a low-browsing herbivore, and it likely roamed the thick conifer forests of northern Africa’s inland woodlands and may have even browsed on foliage in the less-lush coastal regions. If it ate while on all fours, it could reach up to five and a half feet off the ground; if it was capable of rearing back on its hind legs to eat, it could access food up to eleven feet off the ground. As a low-browser, it would’ve shared its niche with the iguanodont Dysalotosaurus, leaving the higher foliage to macronarian sauropods such as Giraffatitan. 

Kentrosaurus shared its environment with predators such as Elaphrosaurus, Allosaurus, and Veterupristisaurus. The former was too small to pose any real threat, but Allosaurus and Veterupristisaurus were a different story. The forty-foot-long Veterupristisaurus was the top predator in its environment, and it’s likely that Kentrosaurus would’ve faced-off with this predator on numerous occasions, and those plates and spikes would’ve come in good use. Scientists estimate that it could swing its tail up to speeds of 30 miles per hour, and continuous rapid swings wouldn’t only discourage attacks but could deal massive damage as the spikes ripped open its attackers’ skin, punctured its soft tissues, and broke ribs or facial bones. Repeated blows could even fracture the sturdy limb bones of the stoutest predator. With its ability to pivot quickly round on its hind legs, it would be adept at keeping its spikes pointed towards the attacker. If Kentrosaurus were a herding animal, the family group may have ‘circled-the-wagons’ with their tail spikes facing out to ward off curious predators. Such a wall of spikes would be virtually impenetrable and would likely be enough to discourage even a pack of hungry Allosaurus. Some scientists speculate that a lone Kentrosaurus, when under attack, might have charged backwards, using its tail spines like a spear, much in the manner of modern porcupines. 

Ostafrikasaurus

Type Species
: Ostafrikasaurus crassiserratus
Classification: Dinosauria - Saurischia - Theropoda - Carnosauria – Megalosauroidea – Megalosauria – Spinosauridae – Baryonychinae
Time Period: Late Jurassic 
Location: Africa
Diet: Carnivore

Ostafrikasaurus is known only by a single tooth, and yet that lone tooth changed a theropod lineage forever. The single took, discovered in the Tendaguru Formation of Tanzania, is different from those of most theropods and more aligned with the unique teeth of the spinosaurs. Because all other spinosaurs date from the Cretaceous Period, the presence of a spinosaur tooth in the Tendaguru Formation pushed their genesis back into the Late Jurassic. Whereas most theropods have recurved, blade-like teeth with serrations for cutting through meat, spinosaur teeth were straighter, more conical, and had few if any serrations. Ostafrikasaurus’ teeth had a few serrations, indicating that these serrations were lost as the spinosaur family evolved. This may be because spinosaurs embraced a pescetarian (fish-hunting) lifestyle: conical, spear-like teeth are seen in modern fish-hunting gharials, as their design lends them to piercing and maintaining grip on slippery aquatic prey that can be swallowed whole rather than torn apart. The estimated 28-foot-long Ostafrikasaurus likely hunted in the coastal environments of northern Africa, hunting fish and even snagging the occasional pterosaur or two. Though its skull hasn’t been found, it’s likely that it had the crocodile-like snouts of its descendants. However, given its early placement in the spinosaurid family, it may have resembled non-spinosaurid theropods, as well. Until more remains are found, we can only speculate as to what it looked like fleshed-out. 

The spinosaurs are divided into two subfamilies: Baryonychinae and Spinosaurinae. Baryonchines have slightly curved, finely-serrated teeth with more oval cross-sections, whereas spinosaurines have straight, fluted teeth with reduced or absent serrations. Given the fact that Ostafrikasaurus’ teeth are more in line with the former, it’s been placed with the baryonychines and likely represents a primitive form of that subfamily. 

Giraffatitan



Type Species
: Giraffatitan brancai
Classification: Dinosauria – Saurischia – Sauropoda - Gravisauria - Eusauropoda - Neosauropoda – Macronaria – Titanosauriformes – Brachiosauridae
Time Period: Late Jurassic 
Location: Africa
Diet: Herbivore

Giraffatitan
was originally thought to be a species of Brachiosaurus but has since been given freedom to stand on its own. It was one of the largest sauropods of the Late Jurassic, averaging between 72 and 74 feet in length but capable of reaching up to 85 feet snout-to-tail. Its neck, held vertical, reached up to forty feet in length. It had a giraffe-like build (hence its name) with long forelimbs and a long neck. It had chisel-like ‘spatulate’ teeth and the first three toes on its hind feet were clawed. Its distinctive high-crested skull was once thought to be characteristic of the brachiosaurids, to which Giraffatitan originally belonged; however, it’s possible that many brachiosaurs didn’t have this feature, since this feature is known only from African specimens now assigned to Giraffatitan – all this to say that the classic portrayal of Brachiosaurus may actually not represent Brachiosaurus at all, at least as far as the skull design goes. Like other sauropods, Giraffatitan had a sacral enlargement above the hip; scientists of an earlier age thought this housed a ‘second brain,’ given that sauropods had pretty small brains to begin with, but it’s know believed to be the location of glycogen bodies. Giraffatitan likely roamed the sweeping conifer forests of the Tendaguru Formation, avoiding the coastal environments of brackish coastal lakes, ponds, and pools where vegetation would be harder to come by. 

Giraffatitan’s
nostrils were once thought to be located on the top of its head, lending earlier scientists to speculate that it was a water-dweller, snorkeling in the burgeoning North Atlantic. However, studies have shown that the water pressure placed on the rib cage would make it extremely difficult for a submerged Giraffatitan to breathe; extended time submerged would undoubtedly lead to drowning. Studies of the skull in 2001 suggested that while the nasal openings in the skull were above the eyes, this didn’t mean that the nostrils wouldn’t emerge at the tip of the snout. In this case, Giraffatitan’s tall ‘crests’ may have housed a fleshy resonating chamber. 

Australodocus



Type Species: Australodocus bohetii
Classification: Dinosauria – Saurischia – Sauropoda - Gravisauria - Eusauropoda - Neosauropoda – Macronaria – Titanosauriformes – Somphospondyli 
Time Period: Late Jurassic 
Location: Africa
Diet: Herbivore

The 56-foot-long and 8800-pound sauropod Australodocus was originally classified as a diplodocid but has since been reclassified as an early titanosauriform, making it more closely related to Brachiosaurus than Diplodocus. Australodocus is currently considered one of the first specimens of the somphospondyls, a sauropod lineage that would give birth in the Cretaceous to the larger-than-life armored titanosaur sauropods. This ‘large-nosed’ macronarian roamed the dense conifer forests of Africa’s Tendaguru Formation, separated to the south of North America by the widening strip of water that would eventually become the Atlantic Ocean. While the Morrison Formation in North America was dominated by diplodocids, the Tendaguru Formation was dominated by macronarians, likely as a result of the different environments. The Morrison was a savannah-like floodplain cut by lakes and rivers that were forested on the peripheries; the Tendaguru, however, was more densely-packed with thick conifer forests. The low-lying foliage of the Morrison was perfect eating for low-browsing diplodocids whereas macronarians with vertically-oriented necks did better with the plentiful trees of the Tendaguru. 

Saurophaganax

Type Species
: Saurophaganax maximus
Classification: Dinosauria – Saurischia – Theropoda - Carnosauria – Allosauroidea – Allosauria – Allosauridae
Time Period: Late Jurassic 
Location: North America 
Diet: Carnivore

Saurophaganax was the largest predator of the Morrison Formation, reaching lengths up to 46 feet snout-to-tail, making it twice as large as its more common and contemporary cousin Allosaurus (because of the similarity between these two theropods, some scientists argue that Saurophaganax is actually a larger species of Allosaurus, but those making these claims are currently in the minority). As the chief hunter of Late Jurassic North America, it’s not surprising that its remains have been scant: the larger the predator, and the greater its competition in the environment, the less prevalent it is. Saurophaganax had lots of predatory competition, principally from the smaller (but still large) Allosaurus and Torvosaurus. Saurophaganax likely hunted large sauropods such as Diplodocus and Brachiosaurus; it may have hunted in groups, like many of its contemporaries, but there’s currently no evidence for this. Some scientists believe that it may even have hunted other theropods, as there have been discoveries of Allosaurus bones with teeth marks matching the size of those belonging to Saurophaganax (it’s noteworthy that these same-sized teeth marks have also been found on the remains of the ankylosaur Mymoorapelta). Because of its large size, some paleontologists argue that Saurophaganax would’ve been slow-moving and would’ve leaned more towards scavenging than hunting. This, too, would explain the presence of its teeth marks on the Allosaurus bones. Given its size, it may have relied on smaller predators taking down prey and then moving in to take over the kill-site; even the mighty Allosaurus would think twice before defending its kill against a predator twice its size. 

a Saurophaganax takes a break from being Top Dog

Stokesosaurus



Type Species
: Stokesosaurus clevelandi
Classification: Dinosauria – Saurischia – Theropoda – Tetanurae – Coelurosauria – Tyrannosauroidea – Pantyrannosauria - Stokesosauridae
Time Period: Late Jurassic 
Location: North America 
Diet: Carnivore

Stokesosaurus was a medium-sized theropod from the Late Jurassic Morrison Formation of North America. By the Cretaceous Period, tyrannosaurs would be becoming larger-than-life despite austere beginnings in the Jurassic. Stokesosaurus represents the gradual increase of size among the tyrannosaur lineage; while the earliest tyrannosaurs emerged in the Middle Jurassic small and lithe, as the Jurassic progressed they were growing larger. Stokesosaurus graduated from a small-sized predator to a medium-sized one, clocking in at ten to thirteen feet in length. A fleet-footed predator, this tyrannosaur likely hunted Morrison ornithopods such as Camptosaurus and Dryosaurus, perhaps even wrangling with an occasional stegosaur. The larger predators of its environment, such as Allosaurus and Torvosaurus, likely preyed on the much-larger sauropods. 

Fruitadens

Type Species
: Fruitadens haagarorum
Classification: Dinosauria - Ornithischia - Heterodontosauridae
Time Period: Late Jurassic 
Location: North America 
Diet: Omnivore

The heterodontosaur Fruitadens is the smallest known heterodontosaur. It’s known from partial skulls and skeletons from at least four individuals of differing biological ages; the presence of these skeletons in the same locale indicate that this heterodontosaur may have travelled in family packs. Young adults grew to around 26 to 30 inches in length and weighed between a pound and a half. Fruitadens had relatively short arms and long feet and shins. The lower jaws had an enlarged canine-like tooth which corresponded to a gap in the upper jaw. Fruitadens also had a small peg-like tooth in front of its canine-like tooth. It had replacement teeth present in the jaws, a unique find among other heterodontosaurs. Its hind limb bones were hollow like those of small theropod dinosaurs. 

Paleontologists believe Fruitadens was an omnivore, and it lived in an environment rich with food for the plucking. It likely prowled the many riverbeds and streams of the savannah-like Morrison Formation, feeding on plant material in addition to snails, clams, crayfish, and insects. Being on the smaller size, it would’ve been wary of running across crocodylomorphs. While large theropod dinosaurs such as Allosaurus, Ceratosaurus, and Torvosaurus lived in the same environment, Fruitadens would’ve likely evaded these predators by running into heavy thickets or hiding in the gallery forests spreading out from rivers and lakes. 

Barosaurus

Type Species
: Barosaurus lentus
Classification: Dinosauria – Saurischia – Sauropoda – Gravisauria - Eusauropoda - Neosauropoda - Diplodocoidea – Flagellicaudata – Diplodocidae
Time Period: Late Jurassic
Location: North America
Diet: Herbivore


The North American Barosaurus was one of the largest sauropods of the savannah-like Morrison Formation during the Tithonian Stage of the Late Jurassic. While most individuals were already larger-than-life, clocking in at 82-89 feet in length and weighing between twelve and twenty tons, at least one specimen may have reached up to 157 feet in length with a 49-foot neck. Barosaurus was closely related to the more popular Diplodocus, though it had some significant differences: it had a longer neck, a shorter tail, and its skeleton was less robust than its contemporaneous cousin. Additionally, Barosaurus’ cervical vertebrae were designed in such a way that it had a lot of side-to-side flexibility at the cost of up-and-down flexibility. This indicates it ate by sweeping its neck in crescent-shaped arcs over the low foliage, which would’ve been a perfect feeding method for the savannah-like conditions of the Morrison Formation. While its neck and skull have not been recovered, it’s assumed that, due to its close relationship with Diplodocus, Barosaurus had a whip-like tail and a skull with an elongated, sloping snout with peg-like teeth.

Saturday, April 24, 2021

Alcovasaurus



Type Species
: Alcovasaurus longispinus
Classification: Dinosauria – Ornithischia – Thyreophora – Stegosauria – Stegosauridae – Dacentrurinae
Time Period: Late Jurassic
Location: North America
Diet: Herbivore

The North American stegosaur Alcovasaurus grew up to eighteen feet in length; this medium-sized stegosaur would’ve been a low browser in prehistoric North America. Its main enemies would’ve included the theropods Allosaurus, Torvosaurus, and perhaps Ceratosaurus. Much of Alcovasaurus’ anatomy is unknown, but because what we do know is similar to the African Kentrosaurus, most reconstructions make it similar to its African contemporary. Alcovasaurus was originally identified as a species of Stegosaurus. This classification was questioned, however, due to five significant anatomical differences, not least its long dermal spikes. Alcovasaurus had two tail spike pairs as its thagomizer that were slender and elongated and ninety percent of the thighbone length. Some scientists argued that these larger spike pairs weren’t indicative of a different species but of sexual dimorphism used for display; perhaps, the argument went, male stegosaurs had flashier thagomizers. Other scientists argued that this stegosaur was less closely related to Stegosaurus and had more affinity with the African Kentrosaurus. Serious studies of this dispute were hampered when the type specimen was damaged by water after a pipe burst at the University of Wyoming; studies couldn’t continue until more specimens were recovered. Recently those scientists who argued for Alcovasaurus being a different genera won out, and Alcovasaurus is now differentiated from its contemporary Stegosaurus.

Friday, January 22, 2021

Archaeopteryx



Type Species: Archaeopteryx lithographica
Classification: Dinosauria – Saurischia – Theropoda – Coelurosauria – Maniraptora – Paraves – Avialae – Archaeopterygidae
Time Period: Late Jurassic 
Location: Europe 
Diet: Carnivore

Archaeopteryx’s name means ‘Ancient Wing/Feather’, and for a long time it was thought to be the oldest known member of the Avialae (‘birds’), at least until earlier specimens were unearthed in China as far back as the Middle Jurassic. This Late Jurassic paravian lived among the cycad- and conifer-dotted wooded islands of prehistoric Germany, mingling with small lizards, pterosaurs, other paravians, and small theropods such as Compsognathus. Multiple specimens have been uncovered in what’s known as Solnhofen Lagoon, which during the Late Jurassic was interspersed with dozens of small islands. Archaeopteryx was similar in size to a Eurasian magpie, though larger individuals could reach the size of a raven. The largest species grew to about one and a half feet in length and would’ve weighed just over two pounds. Though originally considered to be the first bird, many paleontologists decry this statement, for Archaeopteryx had more in common with non-avian theropods – particularly dromaeosaurs and troodontids – than with birds. Just for beginners, it had toothy jaws, three clawed fingers on each hand, a lony bony tail, and hyper-extendable ‘killing claws’ on its feet. Though it had feathers, these are a shared morphology between birds and many different theropod classes. Because it’s morphologically closer to non-avian dinosaurs than modern birds, many have considered it a ‘transitional fossil’ between non-avian dinosaurs and avian dinosaurs and their modern-day descendants. Ironically, this ‘transitional fossil’ appears millions of years after more advanced paravians such as Serikornis and Anchiornis.

Archaeopteryx’s
feathers were similar in structure to modern-day bird feathers. Its feathers were asymmetrical and showed the same structure as modern birds’ flight feathers: vanes given stability by a barb-barbule-barbicel arrangement. The tail feathers, too, were assymetrical with firm vanes. Its thumb didn’t yet bear a separately movable tuft of stiff feathers. Serious studies of Archaeopteryx feathers have been done one specimen dubbed ‘the Berlin specimen’. In this species, its legs had ‘trousers’ of well-developed feathers that are firm and capable of supporting flight. Pennaceous feathers ran along its back; these were asymmetrical and firm, though not as stiff as the flight-related feathers; thus these were similar to the contour feathers of the body plumage of modern birds. Aside from these feathers, the rest of the Berlin specimen was covered in a type of ‘proto-down’ similar to that found in the Early Cretaceous Sinosauropteryx. This ‘proto-down’ was decomposed and fluffy, and it may even have resembled fur in real life (though the fact that it wasn’t fur would be clear up-close under a microscope). This ‘proto-down’ went as far as the lower neck. In all species, the upper neck and head are clear of feathers. This is explained in one of two ways: either Archaeopteryx simply lacked feathers or proto-down on the upper neck and head, or this is an artifact of preservation. In the latter scenario, Archaeopteryx indeed had feathers (or, more likely, proto-down) on its upper neck and head, but these features were lost in death. Scientists believe most Archaeopteryx specimens became embedded in anoxic sediment after drifting for quite some time on their backs in the sea; in these anoxic waters, their corpses wouldn’t be scavenged, for marine life would be limited to smaller organisms that can survive such oxygen-depleted waters. While drifting on the waves, the head, neck, and tail bent downwards, with the body floating atop. They began to rot before they sank under the waves, resulting in loosening tendons and muscles resulting in the infamous ‘death pose.’ The skin, already softened by decay and by underwater friction, wouldn’t be able to keep hold of feathers or proto-down. Before the corpse settled to the seabed, those parts underwater – the neck, head, and tail – would begin to lose their feathers. The more firmly attached body feathers would’ve remained intact by the time the corpse settled on the seabed to be covered with sediment and fossilized for our enjoyment. 

Scientists have used electron microscopy and energy-dispersive X-ray analysis to detect the structure of the melanosomes of one of Archaeopteryx’s wing feathers and compared them with those of over eighty modern bird species; the conclusion was that Archaeopteryx’s original feather color was black with heavier pigmentation in the distal tip. In 2013 another study was done that indicated that Archaeopteryx’s flight feathers had complex light- and dark-colored plumage with heavier pigmentation in the distal tips and outer vanes. This type of coloration is consistent with many modern birds in which black melanosomes have structural properties that strengthen feathers for flight. This leads, of course, to the ultimate question: ‘Was Archaeopteryx capable of powered flight?’ Some scientists doubt that it could fly on its own, insisting that it was a ‘glider’ who would climb high into a tree, launch off, and glide to another tree or to the ground. Others argue that it was indeed capable of flight, though its flight mechanisms would’ve differed from those seen in modern birds. That it was capable of some sort of flight is undisputed. The fact that its feathers are asymmetrical hints at flight, for flightless birds tend to have symmetrical feathers; however, some flightless birds have asymmetrical feathers similar to those of Archaeopteryx. However, the degree of asymmetry in this dinosaur’s feathers more closely resemble those of slow-flying birds than flightless ones. If Archaeopteryx was capable of flight, it would’ve been more ungainly than what we’re used to; for instance, recent studies of flight feather barb geometry reveal that modern birds possess a larger barb angle in the feather’s trailing vane, and Archaeopteryx, lacking this large barb angle, would’ve been a weaker flier. Furthermore, the lack of a bony breastbone upon which flight muscles could attach also testifies to weak flying capabilities; detractors from this conclusion speculate that its strong flight muscles may have attached to the thick, boomerang-shaped wishbone, the plate-like coracoids, or even to a cartilaginous sternum. However, even if it had strongly-anchored flight muscles, its shoulder anatomy made it unable to lift its wings above its back, a requirement for the upstroke used by modern flying birds. However, it may have utilized a downstroke for powered flight. If it were capable of powered flight, its power would’ve been hindered by its large wings, which would’ve resulted in a low stall speed and reduced turning radius. The short, rounded shape of the wings would’ve increased drag, but scientists point out that it would’ve also improved its ability to fly through cluttered environments dense with trees and brush. Such heightened aerial mobility would’ve been improved by its hind wings on its legs. 

While much of the debate over Archaeopteryx’s flying ability (or lack thereof) revolves around its feather and anatomical structure, in 2004 some scientists took a different approach, asking themselves, ‘Did Archaeopteryx have a brain suited for flying?’ By analyzing a detailed CT scan of the braincase of an Archaeopteryx, the scientists found that its brain was proportionately much larger than those of most dinosaurs. The regions associated with vision took up nearly a third of the braincase, and other well-developed areas included hearing and muscle coordination. These are all factors seen in modern birds and necessary for aerial locomotion. The scientists also examined the inner ear and discovered that it more closely resembled the ears of modern birds than those of non-avian dinosaurs. Archaeopteryx had a cerebrum-to-brain-volume ratio 78% on the way to modern birds from the condition of non-coelurosaurian dinosaurs such as Allosaurus, which had a crocodile-like brain and inner ears. All this together suggests that Archaeopteryx had the keen sense of hearing, balance, spatial perception, and coordination needed to fly. The studies of Archaeopteryx’s braincase were revolutionary in the debate over its place in the sky, and in 2014 a team of dedicated scientists reported that their consensus was that Archaeopteryx was indeed capable of powered flight, but in a manner distinct and different from that of modern birds. Its modern equivalents would be pheasants and other burst flyers. 

If we were to step back in time to the Late Jurassic Period in Germany, we would find ourselves in the Solnhofen Lagoon among scattered low-lying, semi-arid, sub-tropical islands. The vegetation of these islands consisted of low-lying shrubs and cycads; interestingly, the islands of this lagoon seem to have lacked conifers. Few trunks have been found in the sediments, and tree pollen is absent. It was in this environment that Archaeopteryx lived, and it was a prime environment for a pheasant-like burst-flying hunter. It most likely hunted small prey, seizing it with its jaws if it was small enough, or with its claws if it was larger.  

Sciurumimus



Type Species: Sciurumimus albersdoerferi
Classification: Dinosauria - Saurischia - Theropoda - Carnosauria - Megalosauroidea
Time Period: Late Jurassic 
Location: Europe 
Diet: Carnivore

The small bipedal theropod Scuirumimus lived among the large islands and archipelagos of prehistoric France and Germany. During the Late Jurassic, much of modern western Europe was submerged by the Oxford Sea and shallow sea armlets of the Tethys Sea that were ringed with coral reefs. Emerging from this vast spider-web network of waterways were dry, forested islands cut by streams and lagoons. These islands catered to smaller terrestrial organisms: lizards, mammals, and a number of small-fry dinosaurs, Scuirumimus among them. This theropod lived alongside the compsognathids Compsognathus and Juravenator, as well as a number of paravians, such as Ostromia, Wellnhoferia, Alcmonavis, and of course the infamous Archaeopteryx.

Sciurumimus’ name means ‘Squirrel-mimic’ for its tail’s resemblance to that of the modern tree squirrel. It’s known from a single juvenile specimen, so its adult length is unknown. While classified as a megalosaurid, this classification is hotly debated. The single specimen was preserved with traces of feather-like filaments. The specimen’s body proportions – the short forelimbs, the lack of fusion in the skeleton, as well as the fact that its skull is 156% the length of the femur – indicate that it was a juvenile and perhaps as young as a hatchling. 


Juravenator



Type Species: Juravenator starki 
Classification: Dinosauria – Saurischia – Theropoda – Tetanurae – Coelurosauria – Tyrannoraptora – Compsognathidae   
Time Period: Late Jurassic 
Location: Europe 
Diet: Carnivore

The small bipedal theropod Juravenator lived among the large islands and archipelagos of prehistoric France and Germany. During the Late Jurassic, much of modern western Europe was submerged by the Oxford Sea and shallow sea armlets of the Tethys Sea that were ringed with coral reefs. Emerging from this vast spider-web network of waterways were dry, forested islands cut by streams and lagoons. These islands catered to smaller terrestrial organisms: lizards, mammals, and a number of small-fry dinosaurs, Juravenator among them. This theropod lived alongside its larger cousin Compsognathus, the squirrel-like theropod Sciurumimus, and a number of paravians, such as Ostromia, Wellnhoferia, Alcmonavis, and of course the infamous Archaeopteryx. Juravenator is known from a single juvenile specimen that was twenty-nine inches head-to-tail. This fleet-footed hunter likely preyed on lizards, mammals, and insects. The scleral rings of Juravenator resemble those of nocturnal birds, suggesting that it was a night-time hunter (but some believe these scleral rings are due to the fact that it was a juvenile and that adults would’ve been daytime hunters). A patch of Juravenator’s skin shows dinosaur scales as well as traces of proto-feathers. 

Compsognathus



Type Species: Compsognathus longipes
Classification: Dinosauria – Saurischia – Theropoda – Tetanurae – Coelurosauria – Tyrannoraptora – Compsognathidae   
Time Period: Late Jurassic 
Location: Europe 
Diet: Carnivore

The small bipedal theropod Compsognathus lived among the large islands and archipelagos of prehistoric France and Germany. During the Late Jurassic, much of modern western Europe was submerged by the Oxford Sea and shallow sea armlets of the Tethys Sea that were ringed with coral reefs. Emerging from this vast spider-web network of waterways were dry, forested islands cut by streams and lagoons. These islands catered to smaller terrestrial organisms: lizards, mammals, and a number of small-fry dinosaurs, Compsognathus among them. This theropod lived alongside its smaller cousin Juravenator, the squirrel-like theropod Sciurumimus, and a number of paravians, such as Ostromia, Wellnhoferia, Alcmonavis, and of course the infamous Archaeopteryx. Compsognathus itself may have island-hopped all the way down to Portugal, for teeth that may belong to this dinosaur have been found in the Lourinha Formation. 

Compsognathus is known from two nearly complete specimens, one from France and one from Germany. The French specimen was forty-nine inches long, and the German specimen was 35 inches long. This lithe theropod likely weighed as little as seven pounds full grown. Compsognathus had long hind legs and a long tail, which it used for balance while running; some scientists have postulated that it could reach speeds up to forty miles per hour. Its forelimbs were smaller than its hindlimbs, and each hand bore two large clawed digits and a third, smaller digit that may have been non-functional. Their delicate skulls were long and narrow with tapered snouts. Its eyes were large in proportion to the skull, indicating that it was a visually-oriented predator that relied more on sight than smell for hunting. Its long neck enabled it to move its head side-to-side without moving its body, helping it spy out prey; and the long neck would’ve come in handy when plunging its head into the undergrowth to root out hiding prey. This dinosaur was designed for catching small and fast-moving prey like lizards that would’ve scurried into the undergrowth as soon as they were seen. Compsognathus’ speed is attested by a proportionately small humerus when compared to the lower legs, a trademark of a fast runner. It balanced itself on its toes rather than the flat of its foot, another design appropriate for speed; this digitigrade stance meant that the main foot bones extended the length of the leg and thus increased its stride. Its tail, held erect off the ground, would’ve served as a balancing aid as it chased prey through the wooded islands of prehistoric western Europe. Its small, sharp teeth were suited for a diet of small vertebrates and perhaps even insects. Its frontmost teeth were unserrated, but those farther back in the jaw were flattened and recurved. The specimens we have preserve part of its diet: in the French specimen, the remains of unidentified lizards and sphenodonts (lizard-like reptiles) are found in its thoracic cavity; in the German specimen, the articulated remains of a full lizard are in plain view. These lizard remains were originally thought to belong to an embryonic Compsognathus, which would’ve rewritten the book on dinosaur reproduction, but further research showed that it belonged to a Bavarisaurus lizard. This lizard was fast and agile, which meant that Compsognathus would’ve also needed to be fast and agile in order to hunt it. Compsognathus may also have preyed on small mammals, as its close Early Cretaceous relative Sinosauropteryx has been discovered with the remains of small mammals in its stomach. 

Some artistic renditions depict Compsognathus with feathers while others do not; this is because the presence of feathers or feather-like features on this theropod is hotly debated. While some of Compsognathus’ relatives have been preserved with the remains of simple feathers covering the body like fur, this isn’t the case with Compsognathus. Archaeopteryx, found in the same sediments as Compsognathus, is preserved with plenty of feathers, which means that the environment was suitable for feather preservation. A patch of fossilized skin from the tail and hind-limb of its close relative Juravenator show mainly scales, though there is some indication that simple feathers were present in some areas. There are thus three possibilities when it comes to Compsognathus: it may have been featherless, it may have had partial feathers such as may be the case with Juravenator, or it may have been fully feathered like its more distant cousins. The jury is out until more evidence comes in. 

a Compsognathus perches atop a dead juvenile dwarf sauropod

Miragaia



Type Species: Miragaia longicollum
Classification: Dinosauria – Ornithischia – Thyreophora – Stegosauria – Stegosauridae – Dacentrurinae
Time Period: Late Jurassic 
Location: Europe 
Diet: Herbivore

The stegosaur Miragaia was closely related to its contemporary cousin Dacentrurus. Miragaia could grow eighteen to twenty feet in length and would clock in at around two tons. Paired triangular plates ran down the midline of its neck; these plates were asymmetrical with a convex outer side and a concave inner side. They were obtuse but lightly hooked at the front. A long, narrow, and straight spike has been preserved; some paleontologists believe this was a shoulder-spike seen in some stegosaurs, but others believe it was part of the tail. Miragaia’s tail anatomy isn’t known, but it’s usually reconstructed with a four-spiked thagomizer like that seen in its near relatives. Because Miragaia’s front limbs were almost as high as the rear limbs, its overall posture was more horizontally level to the ground than what we find in most other stegosaurs, whose bodies slope down to the ground so that their heads were better situated for low browsing.

Miragaia is noteworthy for its elongated neck, which was built by seventeen vertebrae. It had the longest neck of any known stegosaur, and most scientists believe this represents the pinnacle of a trend toward longer necks in stegosaurs. Thyreophorans – the dinosaur clade to which stegosaurs belong – originally had nine neck vertebrae, and one of the most basal stegosaurs, the Chinese Huayangosaurus of the Middle Jurassic, had nine, as well. While more advanced stegosaurs such as Stegosaurus had twelve or thirteen vertebrae, Miragaia outdoes them – and it even outdoes most sauropods of its time. Only a few Chinese sauropods – such as Euhelopus, Mamenchisaurus, and Omeisaurus – had as many neck vertebrae as Miragaia; most sauropods of the Late Jurassic had only twelve to fifteen widely-spaced vertebrae. Scientists have come up with two explanations for Miragaia’s elongated neck. The first holds that it developed due to sexual selection: if longer-necked stegosaurs of this species were seen as more attractive, then it makes sense that necks would get longer over time. Another theory, and one which is more likely, is that the long neck developed as an aide to niche partitioning. Miragaia lived alongside the obviously low-browsing Dacentrurus (and Stegosaurus may have even ocean-hopped to reside in Portugal); because of this, these two species would be in direct confrontation. Niche partitioners coexist by eating different foods, and it may be that Miragaia evolved as a medium-browser, able to reach foods inaccessible to other stegosaurs. Its limb structure, which indicates a shift away from a low-browsing stance, supports this theory for the origin of Miragaia’s long neck. 

Lusotitan



Type Species: Lusotitan atalaiensis
Classification: Dinosauria – Saurischia – Sauropoda - Gravisauria - Eusauropoda - Neosauropoda – Macronaria – Titanosauriformes – Brachiosauridae
Time Period: Late Jurassic 
Location: Europe 
Diet: Herbivore

The Late Jurassic sauropod Lusotitan lived in prehistoric Portugal as part of Portugal’s Lourinha Formation, which resembled North America’s Morrison Formation and which emerged as a result of the genesis of the Atlantic Ocean. This brachiosaurid was related to the North American Brachiosaurus, and it grew up to seventy to eighty feet in length. Lusotitan walked on four pillar-like legs; its front legs were longer than its back legs, so that its body sloped downwards towards its short tail. Some scientists believe it could rear back on its hind legs to reach super high foliage, though some believe it kept its four legs on the ground at all times. Lusotitan’s neck reached vertical rather than horizontal like diplodocids. This gave it a feeding advantage: whereas most of its sauropod contemporaries were low-browsing diplodocids, Lusotitan could browse foliage up to fifty feet off the ground to feed on high conifers and ginkgoes. It undoubtedly practiced niche partitioning alongside the low-browsing diplodocid Dinheirosaurus. As part of the Lourinha Formation, it also lived alongside large predators such as Allosaurus and Torvosaurus, stegosaurs such as Dacentrurus and Miragaia, the early ankylosaur Dracopelta, and numerous early ornithopods.