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.