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Head-Butting, Face-Biting, and Tail-Whacking: Dinosaur Intra-Species Combat

The image of Nature “red in tooth and claw” is a compelling vision which appeals to the popular imagination. Time and again, paleo-art illustrations depict dinosaurs and other prehistoric animals actively engaged in fighting, hunting, and killing. It’s a well-known fact that violence sells, and it’s also a well-known fact that the animal kingdom can sometimes be very brutal. But was the Mesozoic world really a landscape of perpetual violence and bloodshed with animals constantly engaged in the savage business of survival?

Most naturalists, biologists, and animal behaviorists today would say “probably not”. Animals do not engage in a perpetual brawl-fest with each other. Even so, animals do have violent interactions, not only among different species (inter-species combat), but also within the same species (intra-species combat). The dinosaurs were no exception to this, and we have many pieces of evidence that individuals within certain dinosaur species engaged in violent behavior towards each other.

Before I get into the particulars of the paleontological evidence, it’s important to establish some ground rules as to the sort of intra-species combat that animals engage in today, and what the dinosaurs likely engaged in during the past. Physical combat between individuals or at least physical harm inflicted by one individual upon another is typically rooted in either social or environmental causes. Animals hurt each other for a variety of reasons, but seldom is it done purely for the hell of it – only people do that. Social reasons for intra-species combat include violence associated with mating and with mate selection. Bighorn sheep rival males cranially collide with each other until one contestant or another gives up. Other individuals within numerous animal species fight each other in order to assert their right to mate. Mating-based violence can also include some very rough love – some males within certain shark species will actually bite the females in order to assert their power over the female. Speaking of this, asserting dominance is also one of the main causes for intra-species violence, regardless of whether or not mating is involved. This involves dominance within a hierarchy system, such as a lion pride or a wolf pack. Other reasons for intra-species combat are environmental, and are usually tied to the availability of food and other resources. Territorial defense in a strong motivator in this behavior, and this is strongly tied to yet another reason, which is competition of food.

Now that we have established some of the motivating factors behind why modern animals hurt each other, let’s examine the sort of intra-species combat that dinosaurs would have engaged in. For instance, many animals will kick either out of aggression, self-defense, or purely to express annoyance. One dinosaur that possibly engaged in combative kicking was the late Cretaceous ornithopod Parksosaurus. This small speedy herbivore possessed unusually long scythe-like claws on its feet. One may hypothesize that Parksosaurus engaged in kicking contests like in cockfights, or like the modern-day Australian cassowary bird. Then again, Parksosaurus could have also used these long claws for better traction when running, like the cleats on a runner’s shoes, or could have used them like digging tools to scratch into the dirt to search for food or water.

Of course, when people imagine kicking dinosaurs, the first thing that likely pops into their minds are the “raptor” dinosaurs, such as Deinonychus, Velociraptor, and Troodon. Did raptor dinosaurs, with their killing claws, do the same? The large hook-shaped toe claws were certainly used for a specific function, either ripping prey open or pinning it to the ground. I can easily imagine two bird-like raptors squabbling with each other and kicking out with their feet, like a pair of roosters, but this is purely speculative as there is no hard evidence for raptors engaging in kicking each other.

Acheroraptor. © Jason R. Abdale. July 16, 2014.

Years ago, it was proposed that another meat-eater, the late Jurassic carnivore Ceratosaurus, could momentarily balance itself on its thick tail like a kangaroo and kick out. However, this idea has since been disproven. In order for this kicking behavior to work, the tail has to be very thick and muscular and at the same time be very flexible. Ceratosaurus’ tail was deep, but thin in cross-section, more like a crocodile’s tail than a kangaroo’s. Furthermore, it only had limited up-down flexibility. For the most part, the tail was held stiff for balance, and its range of flexibility was largely confined to side-to-side motion, not up-and-down.

Ceratosaurus. © Jason R. Abdale. April 23, 2012.

Ceratosaurus is famous for having a prominent horn on the end of its nose, hence its name. However, the horn was very thin and blade-like in form, and was certainly used for display rather than offensive action. However, there were dinosaurs and other animals in the past that likely used their heads as weapons. “Head-butting”, when animals engage in combat by using their heads as hammers, possibly occurred in earlier animals, such as the dinocephalians of the Permian Period. They had thick flattened skulls, and either pressed and shoved against one another or might have collided cranium against cranium. The dinosaurs which are most associated with head-butting are the marginocephalians, “the wide skulls”, the group that includes pachycephalosaurs and ceratopsians. At first glance, their skulls seem to have been specially designed for head-on physical combat. The eponymous Pachycephalosaurus had a rounded skull that was a solid foot thick, and many scientists have automatically assumed that such skulls were used in head-butting contests, like with modern-day bighorn sheep. A recent study by the University of Wisconsin has found that 20% of pachycephalosaur skulls exhibit head trauma, suggesting with some certainty that the pachycephalosaurs did indeed engage in head-butting behavior.

Pachycephalosaurus. © Jason R. Abdale. October 19, 2013.

But what about the other members of the marginocephalians? The ceratopsians, “the horned faces”, which include the likes of Triceratops and Styracosaurus, have also been assumed to have been highly combative animals, with their spikes, horns, and frills. In recent years, the idea of these horned behemoths duking it out with each other or impaling predators on their sharpened horns has come under intense criticism. Many of their frills are dominated by wide holes which served to lighten the weight but also made them practically useless for protection. Some scientists think that the frills and horns were primarily there for display and species recognition, and their use in defense was only an afterthought.

Chasmosaurus. © Jason R. Abdale. March 31, 2016.

As you’ve probably seen by now, most of the animals which have physical features that can be used in combat are herbivores. Why? Because they sometimes have to physically fight in order to stay alive and avoid being eaten by carnivores. Aside from teeth and claws, the meat-eating theropod dinosaurs don’t seem to have much in the way of special features that would be involved in fighting, not just eating. Ceratosaurus’ nasal horn was too thin and flimsy for attacking something, and so too were the eyebrow horns of its larger contemporary Allosaurus. However, another carnivore did possess eyebrow horns which very well might have been used in fighting – Carnotaurus, one of my personal favorites. Ever since its discovery in the 1970s, paleontologists and paleo-artists have imagined this dinosaurian toro engaged in head-butting clashes with other members of its kind. However, based upon the build of the skull, it seems more likely that it was engaged in cranial “shoving matches”, in which both competitors would press their skulls against one another (hence the Velcro-like arrangement of bumps and nodules on the top of their heads in between the horns) and proceed to push and shove in a demonstration of pure muscular strength until one side or another decided that their opponent was too strong, and retreated.

While predators might not necessarily have physically struck each other with their skulls, they could have used their heads in another way that is far more common among carnivorous animals of all sorts today – face-biting. Face-biting is a way to assert dominance among individuals, especially in communal or pack-hunting societies. Several modern carnivorous animals, such as lions, foxes, and wolves, engage in this behavior. The infamous creature known as “Jane”, who might be either a Nanotyrannus or a juvenile Tyrannosaurus (to this day, nobody is exactly sure), has evidence of face-biting. Since many animals today who engage in face biting do so in order to assert their position of dominance in a pack society, this could be further evidence that this animal was itself a pack hunter, at least as a juvenile. At least one specimen of a juvenile Daspletosaurus also has evidence of face-biting. Sue the T. rex possesses marks on the jaw which were previously thought to have been the result of bites, but were later proven to have actually been caused by a bone infection.

Predators aren’t the only animals today that engage in face-biting, so there may have been herbivorous dinosaurs that engaged in the same behavior. The most likely candidate for this is the small African herbivore Heterodontosaurus. The tusks on this creature could have been wielded in actual biting, or they could have been used for fang-bearing contests like modern baboons. Many animals bear their fangs or canines when aggressive, and Heterodontosaurus possibly did this to intimidate rivals and scare off predators. Another animal that can be compared with Heterodontosaurus is the musk deer. However, their long saber-like canine teeth are grown for display, not combat. Musk deer grow huge teeth instead of growing antlers in order to over-awe rival males and to impress females.

Another possibility for serious dinosaur fights was among the sauropods. With their massive builds, any hit, no matter how light, likely would have caused some kind of damage. One modern long-necked animal that uses its body in sheer brute force is the giraffe – a rather placid-looking animal, but don’t make it angry. During the mating season, male giraffe will proceed to whack each other, swinging their long stiffened necks around like baseball bats, with the short stumpy horns on the tops of their heads inflicting some serious pounds-per-square-inch. Some sauropods, like Apatosaurus, had very massive thick necks in proportion with their body size. This leads some to speculate that Apatosaurus and its ilk used their bruiser builds to inflict bruises on others.

But what about the opposite end of a sauropod? For many of them, the tail was just as long, or longer, than the neck. Tails can be effective weapons. Crocodilians and monitor lizards engage in tail whacking as a way to ward off threats. Many sauropods had thick tails, but others, like Diplodocus, have very long thin tails, and some believe that these long whip-like tails were indeed used like whips. A sharp crack across the side would make any Allosaurus wary. Of course, there are dinosaurs that almost certainly used their tails specifically for combat: the stegosaurs and the ankylosaurs. Evidence has been found for injuries inflicted by these animals upon predators, but I’m not certain if any evidence exists for stegosaur spikes or ankylosaur clubs being used upon members of their own kind. However, I can’t imagine it NOT happening.

Well, if you don’t have any biological weaponry on your side, like fangs, horns, spikes, clubs, or whatever, then raw physical force is your go-to option. There is evidence that predator species tangled with prey. The famous fossil find of a Velociraptor and a Protoceratops perpetually locked in a mutual mortal combat proves this. But this is likely an example of an attack-gone-wrong. Did dinosaurs of the same species physically grab onto and grapple with each other? Did dinosaurs wrestle, the way that some lizard species do today? Monitor lizards are a prime example of this, when two males will attack each other by essentially doing reptilian ju jitsu. Did dinosaurs wrestle? I’m not sure, but I’m leaning towards no, especially for the larger ones. Many small dinosaurs had thin delicate bones that could be easily broken, and many of the larger dinosaurs simply did not have the arm dexterity to do rough-and-tumble wrestling maneuvers the way that you see monitor lizards doing today. Furthermore, with their large size, being body-slammed to the ground would have done a lot of damage. As they say, the bigger they are, the harder they fall. Many dinosaurs show signs of physical trauma, including broken bones. Many led a very brutal life, with some skeletons being covered with injuries. For those reasons, I would say that most dinosaurs wanted to avoid intense physical combat.

Sometimes, the violence goes to its absolute extreme, and animals deliberately kill each other. Like intra-species fighting, intra-species killing has several motivating factors, both environmental and social. Animals kill each other to either reduce or totally eliminate competition over limited resources. Animals will also kill rivals to increase their own chances for mating, as well as killing the offspring of rivals to increase their own offspring’s chances for survival. As an example, new male lions that take over an existing pride will often kill all of the pride’s cubs in order to completely eliminate the legacy of the preceding male leader.

The most extreme form of intra-species combat is killing followed by cannibalism. Although it is largely taken for granted that prehistoric carnivorous animals ate their own kind under certain circumstances, there is little evidence to support this hypothesis. Some animals will kill and eat the young of other individuals in order to improve the chances of survival for their own young. Others may kill and eat their own kind out of starvation. Still others, like alligators, may view other members of their own kind as a legitimate food source, no different than any other prey item, and actively hunt, kill, and eat each other.

For a long time, it was believed with the firmest dogmatic conviction that the late Triassic dinosaur Coelophysis practiced cannibalism. However, this long-held belief has come into question upon closer examination of the famous Ghost Ranch specimens. It now appears that many of the bones which were previously believed to be inside the ribcages of others were actually lying underneath the ribcages. Furthermore, some of the bones previously identified as juvenile specimens have recently been re-identified as belonging to other reptile species. For the record, I am not stating that Coelophysis never engaged in cannibalism. I am stating that the evidence for cannibalism in this species is not as clear-cut as once believed and needs to be taken with a certain degree of doubt. If the study of paleontology has taught me anything, it’s that there is no such thing as dogma.

Coelophysis. © Jason R. Abdale. April 26, 2015.

Although there’s questionable evidence for cannibalism in Coelophysis, there is more compelling evidence in another dinosaur from the opposite end of the Mesozoic spectrum – Majungasaurus, an abelisaurid from Madagascar who lived at the very end of the Cretaceous Period. In 2007, scientists published findings that tooth marks discovered on some Majungasaurus bones matched the teeth in Majungasaurus’ jaws. So far, this is the only conclusive proof that a theropod species killed and/or ate the flesh of its own kind.

I would like to say one thing, though: just because there’s evidence that an animal was cannibalized, that doesn’t necessarily mean that this individual was killed by the animal feeding off of it. As said before, scavengers will sometimes eat the dead bodies of their own kind. To them, meat is meat, no matter where it comes from. Others will not usually eat their own kind, but will do it if they’re desperate enough and cannot find other sources of food. As an example, most humans who have engaged in cannibalism do it out of necessity, not out of habit.

Anyway, that’s my take on intra-species combat amongst dinosaurs. Hope you enjoyed it.

Ornitholestes with feathers

Greetings all. Every child with a rough grasp of what life was like in Late Jurassic North America probably knows the Morrison Formation’s main characters. If such a child were to be asked to name the meat-eaters from that formation, the name Ornitholestes would definitely pop up, likely somewhere around third or fourth place.

Ornitholestes was a 6-foot long coelurosaurid theropod dinosaur that lived in western North America during the late Jurassic Period, 155-145 MYA. It is commonly depicted scampering about in the forest, or along the edge or the forest, or sneakily hiding in the shadows out of sight of the larger predators. With the likes of Allosaurus and Torvosaurus stomping around, it’s easy to see why paleo-artists have relegated little Ornitholestes to a bit-part on the Jurassic stage.

But I like to think that Ornitholestes‘ part was much bigger in the never-ending drama of Mesozoic life. Let’s look at its body. I’ve already stated that it was 6 feet long and was therefore about 2 feet tall – large enough to bite you on the knee. It likely weighed a hundred pounds or a smidge less than that – certainly not more. Its skull is worth looking at. Contrary to what has been commonly portrayed, it DID NOT have a little Ceratosaurus-like crest on the end of its nose. That mistake was made when a dislocated bone was mis-identified as a nasal crest. The skull was thin and deep, like a battle axe, and based upon its structure and that of its neck, it likley had a very strong bite. The teeth are small, but they are rather thick in cross-section. A powerful bite and thick teeth? This makes Ornitholestes sound like a precursor to the tyrannosaurs, and no wonder, because the tyrannosaurs are, in fact, highly-evolved coelurosaurs – the same group that Ornitholestes belonged too. The eye sockets on this baby were huge, so it is likely that Ornitholestes was a nocturnal hunter. As for its body, it was a bit on the muscular stocky side, so it was physically strong. It was equipped with long arms ending in three hook-like claws on each hand, and it had a long tail. We can also be fairly sure that Ornitholestes had a coat of thin whispy fur-like feathers on its body since other coelurosaurids that were more primitive and more advanced that Ornitholestes had feathers.

So what can we determine? It was strong for its size, its jaws could crack through eggshells and small bones, it could run, and it could grapple. In short, Ornitholestes was the hyena of the Jurassic savannah.

Hyenas are nothing to laugh at (I’m sorry, that was bad). Hyenas have a reputation for being scavengers, likely because they are commonly seen picking at the leftovers of the lions’ dinner, and because their jaws are the strongest jaws pound-for-pound of any meat-eating animal on the African plains – good for cracking hrough thick bones of carcasses. But in reality, hyenas are effective hunters as well. They are pack hunters, like lions or wolves, and it’s not unusual to see a gaggle of them, panting and bare-teethed, running down a zebra or a wildebeest.

Was Ornitholestes the same way? Unfortunately, fossils rarely provide evidence for animal behavior. The fact that Ornitholestes fossils are so rare doesn’t help matters. But I dare say that these carnivorous critters were a serious threat to dinosaur mothers who had eggs to protect, they likely did significant danage to hatchlings, they preyed upon smaller animals like thick-boned mammals, and asuredly were seen scavenging carcasses leftover by other larger meat-eating dinosaurs.

A while back, I drew a picture of Ornitholestes and posted it to this blog. However, it was an “old school” picture portraying Ornitholestes covered in scales. I have recently made an updated version, and I’m posting that image below.


In addition to the feathers, I’ve also slightly altered the shape of the skull to be a little more accurate. I always try to improve my work, and I dare say that a few years from now after my skills have improved further, I’ll make a drawing of this guy that’s even better than the one you see here.

Keep your pencils sharp, people.

Dryptosaurus: A possible North American megaraptorid? – part 2

In January, I published a post in which I hypothesized that Dryptosaurus, a Late Cretaceous theropod found in Eastern North America, was misidentified. For the longest time, Dryptosaurus was believed to be a tyrannosaur, possibly a rather primitive one. However, with discoveries made within the past two decades, I came to question this taken-for-granted identification.

The megaraptorids are a weird bunch, since nobody knows for certain where exactly they fit. When the type species Megaraptor was found in Argentina by the paleontologist Fernando Novas, it was believed to be a giant dromaeosaur – hence the “raptor” name – measuring at least 25 feet long, which would have made it the largest raptor ever discovered up to that point.

Then in 2010, a study conducted by Benson, Carrano, and Brusatte claimed that the megaraptorids were more related to the allosaurs than the dromaeosaurs. Specifically, the study stated that the megaraptorids were very closely related to Neovenator. It certainly helped when a complete arm was discovered, which showed that the 15-inch long killing claw didn’t come from the foot, but actually came from the hand, similar to Baryonyx.

In 2012, Fernando Novas conducted his own study of Megaraptor and its relatives. He and his colleagues said that while Neovenator and the carcharodontosaurids were close relatives of each other, and that both belonged within the superfamily Allosauroidea, he also stated that Megaraptor and its ilk did not belong in this group. Instead, he stated that the megaraptorids were actually coelurosaurs, and were more closely related to the tyrannosaurs.

In 2014, more evidence to back up a connection between the megaraptorids and the tyrannosaurs came to light when a juvenile Megaraptor was described by J. D. Porfiri, Fernando Novas, and others. Porfiri even placed Eotyrannus, long thought to be a primitive tyrannosaur, as a member of Megaraptora. Because of this, the megaraptorids are thought of by some to be either close relatives of the tyrannosaurs or possibly even an offshoot of the tyrannosaur family.

As a result of learning all of this, I began to wonder if Dryptosaurus was actually a member of Megaraptora, and I published a post saying as much. However, Chase Brownstein, a paleontologist specializing in eastern North American dinosaurs who works at the Stamford Museum, and who I have been in contact with on a fairly regular basis, immediately challenged my hypothesis. He stated that while Dryptosaurus might have had some features that made it visibly look like a megaraptorid, the animal itself was not a member of the megaraptorid family. He put these physical similarities down to convergent evolution – when two different kinds of animals evolve in such a way that they look similar to each other. Convergent evolution is most often brought about by environmental conditions, which infers that both Dryptosaurus and the megaraptorids lived in similar environments, had similar lifestyles, or both.

I recently discovered that my hypothesis was not unique. An internet search showed that at least by 2014, other people had been looking at Drytposaurus with questioning eyes and were wondering if it was actually a megaraptorid. Damn, this happens all the time. Every time that I think I’ve come up with a new idea, it turns out that some has already thought of it before. Oh well.

While my assessment of Dryptosaurus as a megaraptorid may or may not be correct – we’ll never know the real answer until more Dryptosaurus specimens are found and analyzed – I feel that my drawing of Dryptosaurus is nevertheless accurate. A phylogenic analysis conducted in 2013 placed Dryptosaurus between Raptorex (which, according to some, is actually a misidentified juvenile Tarbosaurus) and Alectrosaurus. Both Raptorex and Alectrosaurus had similarly-shaped skulls, so I gave my rendition of Dryptosaurus a skull that was very similar to these two species. I gave it the massive thumb claws that are seen on the holotype specimen. I also gave my creation a mane of fibrous feathers, since many primitive three-fingered tyrannosaurs are known to have had feathers covering some or most of their bodies.

Figure 1. Skull of Alectrosaurus. Illustration by Tracy Ford (I think). http://www.paleofile.com/Dinosaurs/Theropods/Alectrosaurus.asp.


Figure 2. Skeleton of Raptorex. Photo by Kumiko (September 24, 2011). https://commons.wikimedia.org/wiki/File:Raptorex_vs_Psittacosaurus.jpg.



Figure 3. My own drawing of Dryptosaurus.


Tyrannosaurus rex with scales

Tyrannosaurus full body with scales

Behold my masterpiece.

This is the fifth T. rex drawing that I’ve posted to this blog, and it is the hardest drawing that I have ever had to make. Every individual scale was done by hand, one by one. This drawing took me months to finish. To give you a better idea about the utterly insane amount of detail, the actual drawing of the dinosaur itself from the tip of its nose to the tip of its tail measures precisely 24 inches. Most of the drawn scales measure at only one millimeter in diameter.

As you can see, it is done in the same pose as my previous two full-body T. rex drawings, but I made some noteable improvements:

  1. Slightly changing the shape of the skull – my original one looked a little too much like Tarbosaurus rather than Tyrannosaurus.
  2. Not making the face as shrink-wrapped as the original head drawing was.
  3. Making the neck more detailed and fuller.
  4. Changing the position of the hands to be more anatomically corect.
  5. Making its body fatter – the original was too skinny.
  6. Making the tail thicker and fatter to properly counter-balace the now-heavier front half of the body.
  7. Changing the shape of the feet.

This drawing was made on several sheets of 8.5 x 11 printer paper, with just an ordinary No. 2 pencil…and a whole lot of patience.

Requests for articles and artwork

A while back, I asked you, the reader, if you had any requests for articles and artwork that you would like me to do, but I received no reply. However, I recently looked at the search terms that come up on this blog’s administration page. Most of the terms concern subjects that I’ve already written about or illustrated, but there were a few others on subjects that I haven’t touched yet, or have only just alluded to. Terms which showed up frequently were (in order of frequency):

  • Alamosaurus (12)
  • Caenagnathus / Chirostenotes (9)
  • Pterosaurs (8)
  • Liopleurodon (7)
  • Mosasaurs (6)
  • Dakotaraptor (5)
  • Velociraptor (in color) (5)
  • Suchomimus (4)
  • Carnotaurus (3)
  • Oviraptor (3)


Others caught my interest as potential future art or writing projects, including:

  • Abelisaur
  • Allosaurus courting
  • Allosaurus head
  • Allosaurus walking
  • Australovenator
  • Deinonychus
  • Dinosaurs of Texas
  • Dracorex head
  • Elasmosaurus
  • Iguanodon head
  • Neovenator
  • Pachycephalosaurus keeping shelter
  • Styracosaurus
  • Triceratops eating
  • Tyrannosaurus juvenile
  • Lacrimal horns on dinosaurs
  • Mesozoic turtles
  • What dinosaurs lived on Long Island?

The last three sound like interesting research projects. Anyway, based upon what I have seen, I think that I can gauge what you would like me to do. So, I’m treating these statistics pretty much like a to-do schedule. Right now, I’m really hammering on a super-detailed drawing of a full-body T. rex, which I hope to have finished within one or two weeks, and then put up here for you to admire and comment on. After that, I’ll focus on the items on these two lists – the “frequency list” will take priority. I’m happy to say that some of these terms are on things that I’ve had in the back of my mind for a while, so this will give me the impetus to do them. Take care everybody, and keep your pencils sharp.

Dryptosaurus: A possible North American megaraptorid?

This is an idea that I’ve had knocking around in my head for a while. A recent post by fellow paleo-blogger Chase (who has a special interest in eastern North American Mesozoic life) on Dryptosaurus has spurred me to action in terms of writing a short article as well as doing some much delayed artwork.

For those of you who are too lazy to read Chase’s excellent article about this animal, Dryptosaurus was a medium-sized theropod dinosaur, approximately 20-25 feet long which lived in eastern North America during the late Cretaceous Period. Unfortunately, our total knowledge of this dinosaur is known from only a few fragmentary remains, including a hand claw that seems way too big in proportion with the rest of this animal’s body.

For as far back as I can remember, Dryptosaurus was classified as a tyrannosaur. But recently, I have my doubts about this classification. Even very primitive tyrannosaurs such as Guanlong and Proceratosaurus don’t have some of the anatomical features that Dryptosaurus appears to possess.

My curiosity centered around that claw. It didn’t look like a tyrannosaur claw – to me, it looked more like an allosaur claw. An unusually large hand claw also reminded me of another animal – Megaraptor, from South America. Originally, this was thought to be a gigantic dromaeosaur, but then it was hypothesized to be more closely related to the allosauroids, like Neovenator, Giganotosaurus, and Carcharodontosaurus. The allosaur-like claw would make this classification a good fit. Then I saw a picture of the skeletal remains of Australovenator, a megaraptorid that was discovered in (you guessed it) Australia. I immediately noticed similarities in the hand and body structure between Australovenator and Dryptosaurus.

  • Massive thumb claws in comparison with the other finger claws.
  • Short muscular arms and huge hands
  • Slender lower jaws with small closely-packed hook-shaped teeth.

What I find really interesting is that in 2012, a hypothesis was put forward by Fernando Novas and other paleontologists that the megaraptorids might actually be extremely primitive members of the tyrannosaur family. In 2014, fragments from a juvenile Megaraptor were discovered, including part of the upper jaw. The structure of the juvenile Megaraptor’s maxilla was very similar to the structure of the dentary from Australovenator. That year, Juan Porfiri re-iterated Novas’ hypothesis that the megaraptorids might be primitive tyrannosaurs.

So, with all of that being said, I hypothesize that Dryptosaurus was a member of Megaraptora, which would make it the first of its kind found within North America.

How did Dryptosaurus feed? The large hook-shaped claws and the small hook-shaped closely-packed teeth seem to indicate that Dryptosaurus and other megaraptorids were fish-eaters. The fossils of Dryptosaurus were discovered in the New Egypt Formation and the Navesink Formation, the later of which is known for both dinosaur fossils as well as fossilized shells. Also, Australovenator was found in deposits that indicate a swampy still wetlands environment, full of bivalves, fish, and turtles. The fact that this megaraptorid was found in a water-rich environment full of aquatic life leads me to suspect that Dryptosaurus might have had a similar lifestyle.

To conclude this short article, I have a drawing of the enigmatic Dryptosaurus portrayed as a megaraptorid rather than as a typical often-illustrated tyrannosaurid. Who knows – maybe my less-than-scholarly idea about Dryptosaurus being a fish-eating megaraptorid will prove out to be right. Only time and the discovery of more specimens will tell.


Keep your pencils (and minds) sharp, everybody.



Torvosaurus tanneri (“Nathan E. Tanner’s savage lizard”) was one of the largest theropod dinosaurs in the Morrison Formation. It measured 35 feet long, the same size as Allosaurus. However, Torvosaurus came from a more primitive line of theropods, the megalosaurs. As such, it retained some more primitive features compared to more advanced theropods living at that time like Allosaurus, and was probably less intelligent than Allosaurus (although not by much, apparently, since Allosaurus wasn’t exactly the brightest bulb either, according to studies of Allosaurus’ brain).

Torvosaurus and Allosaurus may have lived in the same location at the same time, but Allosaurus was clearly the most numerous theropod in the Morrison Formation. Very few remains of its competitor have been found. The first fossils of this animal were discovered in Colorado in 1971, and the species was officially named and described in 1979. Another species, T. gurneyi, was found in Portugal’s Lourinhã Formation, also dated to the late Jurassic. Although known from incomplete remains, it’s evident that the European species has a more boxy rectangular skull than its North American counterpart.

Torvosaurus and Allosaurus had the same length, but they possessed different physical proportions. These anatomical differences no doubt drove these two species to develop different hunting styles. It seems that Torvosaurus was a Jurassic analog for a tyrannosaur, since it had an unusually large head and unusually small arms in proportion to its body. Its body was long and shallow, whereas the body of Allosaurus was short and deep – good for a large heart and lungs, indicating an active lifestyle. Torvosaurus’ neck was short and muscular, while Allosaurus’ neck was longer and more sinuous. Torvosaurus had short arms and small hands (but unusually large thumb claws), while Allosaurus had longer arms, huge hands, and absolutely huge claws – obviously used for grabbing and ripping things. Torvosaurus seems to be rather front heavy (good for physically slamming it’s jaws onto prey) while the weight on Allosaurus appears to be more evenly distributed. Allosaurus also had an unusually long tail in proportion with its body – a definite feature of an agile runner. Therefore, it seems that Torvosaurus was primarily a short-distance chase ambush hunter who relied upon its jaws to do most of the work. By contrast, Allosaurus was a very active energetic predator who was capable of impressive speed and quick turns.

This drawing took a long time, as you can assume from its high amount of detail. Every individual scale was drawn one by one. To give you a better appreciation of the time to draw this, in real life this drawing frome nose-tip to tail-tip is only 21 inches long – 1/20 scale, as most of my prehistoric drawings are. Medium was No. 2 pencil on copy paper, along with some touch-up on my computer to fix the places where the two pieces of paper were joined together.

Keep your pencils sharp, everybody.