Hello everybody. A month ago, I posted that I would be keeping myself busy this summer by cranking out lots of artwork. When will I learn to NEVER make plans, because whenever I do, something always happens to ruin them, and sure enough, that’s happened once again. Life has a habit of getting in the way of my life. Several things have come up all at once that are altering my life situation, and they must be addressed right away. These will not be quick fixes, but will instead take months or even an entire year to address. As such, I will not have any time for art or writing articles on this website.
So, for the time being, it’s goodbye. I hope you understand.
Hi everyone. I know that the next artwork on my to-do schedule is an Allosaurus’ head, but it’s taking a while to collect the info on this, and I wanted to put something on here in the meantime. So, here’s a quick drawing that I made of a little-known Morrison Formation theropod named Coelurus. Note the unusually long metatarsal bones. This guy was likely a swift runner. I imagine him as a combination between a secretary bird, roadrunner, and cheetah.
There are two images here. The first is an uncolored pencil drawing, and the second is a colored drawing that I made using Prismacolor colored pencils. I don’t like coloring my drawings because it tends to wash out the detail. Black and white is more my “thing”.
Hi everybody. Here is my latest Hell Creek paleo-art. Say hello to Dakotaraptor steini, a large dromaeosaurid raptor that lived in South Dakota at the end of the Cretaceous Period. How large? We don’t have an exact measurement because this animal is known only from partial remains. However, enough was recovered to give a ballpark estimate that the creature measured somewhere around 15 to 20 feet long. Not as big as Utahraptor, but still pretty impressive.
This drawing was made with No. 2 pencil, Crayola and Prismacolor colored pencils, a black felt-tipped marker, and A LOT of touch up work on the computer in order to make the scanned image as bold and vivid as it is in real life.
During the 1940s, the front half of a fossilized skull was discovered in China. It was named and described as Lukousaurus yini in 1948. Lukousaurus lived during the early Jurassic Period, approximately 195 million years ago (MYA). Based upon the size of its remains, which consist only of the front half of its skull, it may have been six to eight feet long.
Some may cite Lukousaurus for it’s old age, but what grabbed my attention was when I read that the teeth had serrations only on the back edge. I have been told that this is a feature that is only found in the carnivorous dinosaurs commonly called “raptors”, more properly known as Deinonychosauria. This clade is divided into two families: Dromaeosauridae and Troodontidae. All dromaeosaurids have teeth which are serrated only along the posterior (back) edge, and some troodontids have this feature as well.
Although all raptor dinosaurs are found during the Cretaceous Period, paleontologists have hypothesized for years, based upon phylogenic analysis, that the ancestor of the raptors appeared millions of years earlier during the Jurassic Period. It may well be that Lukousaurus is that ancestor. Could it be that Lukousaurus is the oldest-known “raptor”?
Evidence to back up this claim is a bit thin. For starters, we’re not even sure if Lukousaurus was a dinosaur; it’s been proposed that it might, in fact, be a crocodilian. But let’s assume for the time being that it is a dinosaur. Is there any evidence which suggests that Lukousaurus might be a member of Deinonychosauria, or perhaps a close relative?
The first piece of evidence to support the hypothesis that Lukousaurus is a very primitive raptor is its age. Paleontologists have speculated that raptors appeared during the Jurassic Period, specifically either the early or middle Jurassic. The reason why is because birds are believed to have been descended from raptors, and the oldest-known birds come from the late Jurassic – therefore, raptors must have appeared a little earlier. Lukousaurus comes from the early Jurassic.
The second bit of evidence is geographic location. Raptors are believed to have originated in Asia and then spread elsewhere. Lukousaurus comes from China, specifically the Lower Lufeng Formation in Yunnan Province, China. It would have shared the landscape with the prosauropods Gyposaurus, Lufengosaurus, and Yunnanosaurus. it would have also lived alongside the early carnosaur Sinosaurus and the ornithischian Tatisaurus (we’re not sure if it was an ornithopod or an early thyreophoran; it might have looked similar to Scutellosaurus).
The third piece of evidence, which I have already mentioned before, is tooth structure. Lukousaurus’ teeth are very thin and blade-like, and are sharply recurved backwards. What is especially noteworthy is that the teeth have serrations only on the posterior edge – a feature found only in raptors.
This brings about the fourth piece of evidence, although this is subject to intense debate – taxonomy. It has been hypothesized that Lukousaurus was a coelurosaur, and the coelurosaurs were the ancestors of Maniraptora. This clade includes the ornithomimids, the therizinosaurs, the oviraptorosaurs, and the raptors. However, due to the incredibly fragmentary nature of Lukousaurus – it is, after all, known only from one fragmentary snout – its phylogenic position is uncertain. Yes, it has been classified as a coelurosaur, but it has also been classified as a ceratosaur, and even as a crocodilian. So, using taxonomy as evidence is incorrect; it’s more likely an opinion rather than evidence.
Lukousaurus might be an early raptor, but personally, I think it is an advanced coelurosaur which shows the beginning of raptor-like traits. This would make Lukousaurus a borderline coelurosaur-maniraptoran. Until more material from this particular species is uncovered, any assertions made as to which clade this creature belongs to will always be tinged with uncertainty.
Below is a drawing of the partial skull made by Tracy Ford.
- Lessem, Don; Glut, Donald F. The Dinosaur Society Dinosaur Encyclopedia. New York: Random House, Inc., 1993.
- Padian, Kevin, ed. The Beginning of the Age of Dinosaurs: Faunal Change Across the Triassic-Jurassic Boundary. Cambridge: Cambridge University Press, 1988.
- The Theropod Database. “Lukousaurus in Nesbitt’s matrix”, by Mickey Mortimer (May 7, 2011). http://theropoddatabase.blogspot.com/2011/05/lukousaurus-in-nesbitts-matrix.html. Accessed on December 24, 2013.
- Dinosaur Mailing List. “What is Lukousaurus?”, by Mickey Mortimer (September 4, 2000). http://dml.cmnh.org/2000Sep/msg00086.html. Accessed on December 24, 2013.
- The Bite Stuff. “Troodontid Teeth – WP#6”, by Jaime A. Headden (June 6, 2010). http://qilong.wordpress.com/2010/06/06/weekly-picture-6-troodontid-teeth/. Accessed on December 24, 2013.
Now that the manuscript for my history book on the ancient history of the Balkans is finished, I have some time to work on my art, which I have been neglecting for months. A while back, I wrote a post saying that I had a “to-do list” of various subjects that I wanted to address either in artwork or articles based upon items that have appeared in your searches of my website, but that was some time ago, and a lot has changed since then. Even so, I have kept this list in my mind, and I have been working on tackling the various items on it. Projects that I’ve completed so far are Alamosaurus, Ornithomimus, a Jurassic pliosaur, and – my latest post – Caenagnathus (which might be the same animal as Chirostenotes).
Now it’s time to move on to other things. A lot of you have been looking for stuff related to Dakotaraptor. Alright, that’s my next project, and I’ve already started work on it. Hopefully, it will be finished by the end of the month. It’s still very much in the pre-production research phase.
But what about what comes afterwards? Well, I’ve got several projects lined up. Here is a “top ten” schedule of what I’ll be doing, based upon what you have been looking for:
- Dakotaraptor (work has already begun on this).
- Allosaurus head (6 searches).
- Re-doing my full-body Allosaurus drawing, for the sixth time (a LOT of you have been looking for Allosaurus-related stuff on this website; 81 searches).
- Re-doing my Troodon drawing. The drawing that I posted to this website years ago is pathetically inaccurate, and needs to be re-done. (53 searches).
- Velociraptor (23 searches).
- Prehistoric sharks (10 searches).
- Prehistoric fish (7 searches).
- Carnotaurus. This guy’s one of my personal favorites, and I’m really looking forward to doing a full-body rendition of him (7 searches).
- Mosasaur (7 searches).
- Pterosaur (7 searches).
During the early 1920s, Charles W. Gilmore, a paleontologist from the Smithsonian Institute in Washington, DC, was prospecting for fossils in Alberta, Canada. While on this trip, he would discover several new species of dinosaurs, including a strange creature known only from a pair of incomplete hands. These hands had long slender fingers, which was highly unusual for theropods known at the time. He officially named and described them as Chirostenotes pergracilis in 1924.
Chirostenotes was originally believed to be a member of the family Elmisauridae. This is an enigmatic group of dinosaurs, whose members consist of only one genus, Elmisaurus. This animal lived in Mongolia during the late Cretaceous Period about 80 MYA, and the only evidence that we have of its existence is one incomplete foot and a hand found in 1970. Scientists recognized that the hands of Chirostenotes and Elmisaurus looked similar, and so Chirostenotes was placed into that family. By 1990, Elmisauridae was recognized as an invalid family name, and it was discarded.
Chirostenotes is now classified as a member of the family Caenagnathidae, named after the genus Caenagnathus, which might actually be the same animal as Chirostenotes (as early as 1990, scientists suspected that these two might actually be the same animal). The canaegnathids were a group of bird-like theropod dinosaurs who belonged to a much larger group called the oviraptorosaurs, who are well-known from Asia. Their presence in North America only adds further proof to a faunal exchange between Asia and North America. Caenagnathids are distinguished from oviraptorids by their feet, which look more like those of the ornithomimids, more commonly-known as “ostrich dinosaurs”. This suggests that the oviraptorosaurs evolved from the ornithomimids. According to current phylogenic analysis, the ornithomimids are more primitive than the oviraptorosaurs, so this hypothesis might be plausible.
Because Caenagnathus and Chirostenotes are known from incomplete specimens, nobody can make up their minds as to whether or not they’re two separate genera or if they’re the same animal. Some paleontologists firmly believe the former, while others firmly believe the latter. Because of their incompleteness, we are also not 100% sure what the animal looked like. It’s reasonably certain that it bore a strong resemblance to Oviraptor, Citipati, or Anzu, but any recreation of what the entire animal looked like is guesswork. During the 80s and 90s, there were a wide range of images crafted by various paleoartists which took a stab at what the whole animal would look like if it were fleshed out. Ever since the discovery of Anzu, which is both the largest and most well-known caenagnathid, the diversity of images has largely disappeared. Now, modern depictions of both Caenagnathus and Chirostenotes, if you can find them, are really nothing more than clone copies of Anzu, which I disagree with not only as a paleontology buff, but also as an artist.
Below is my own rendition of what I think Caenagnathus, or possibly Chirostenotes, or both, would have looked like. Since no complete skull of either species has been found, the design for the head is based upon a hypothetical skull drawing made by Tracy Ford. My drawing was made on printer paper with No. 2 pencil, Crayola and Prismacolor colored pencils, and a black felt-tiped marker. Since my scanner has a tendency to wash out a lot of the detailing, I had to do a bit of touching-up on my computer to replicate how the image looks in real life. Hope you enjoy, and keep your pencils sharp.
The Hell Creek Formation of the north-central United States is famous for its dinosaur fossils, notably those of Tyrannosaurus, Triceratops, and others whose names are well-known to children and adults. However, this fossilized environment was home to more than just dinosaurs. The Hell Creek Formation was home to a wide range of fish, amphibians, reptiles, and mammals. One of the animals that called this landscape home during the late Cretaceous was Habrosaurus.
Despite its name, Habrosaurus was not a dinosaur, and it wasn’t even a reptile. It was, in fact, an amphibian, and a large one at that. Habrosaurus dilatus was a three-foot long siren, a type of salamander that bears more of a resemblance to an eel than the lizard-like forms that we associate slamanders with. Unlike most salamanders, sirens are fully-aquatic amphibians that retain gills throughout their whole lives, unlike other amphibian species that possess gills only in the early development stages of their lives. Sirens also possess small rudimentary lungs, and are able to breath air. There are four species of sirens that are alive today, and all of them are found within North America. Depending upon the species, they can have one to three gill slits on each side of the head. They have completely lost their hind limbs, and their front limbs have shrunk considerably, with three or four short stubby fingers on each hand. Sirens have tiny eyes and no eyelids, and possess a long tail reminiscent of an eel or a sea snake – ideal for swimming. Sirens prefer to live in slow-moving or static bodies of water with lots of underwater vegetation and muddy bottoms. They might occasionally come onto land during the night if the ground is wet or if it’s raining.
Habrosaurus is, to date, the oldest-known siren genus. So far, there are two species known: H. prodilatus, which was found in Alberta, Canada in rocks dating to the Campanian Phase (83-70 MYA) of the late Cretaceous, and H. dilatus, which is much more widespread in the western United States, being found in Montana and Wyoming (with more specimens being found in Wyoming) and dating to the Maastrichtian Stage (70-65 MYA) of the late Cretaceous, as well as being found in the early Paleocene Epoch of the Tertiary Period. This means that H. dilatus was one of several species to survive the K-T Extinction, if only for a short while. It may be possible that H. dilatus is simply the evolved form of H. prodilatus.
Habrosaurus dilatus was named by the eminent paleontologist Charles W. Gilmore in 1928. To my knowledge, six specimens have been found of this animal, and all of them have been found in stream channel deposits. The presense of this type of animal, as well as its impressive size of three feet in length, indicates the presence of large bodies of fresh water, such as slow-moving rivers or ponds. However, the possibility of a dry year was ever-present, and for a fully-aquatic or mostly-aquatic animal like Habrosaurus, that could spell doom. During dry periods or droughts, modern-day sirens are able to dig burrows into the mud and encase themselves in a cocoon, like a lungfish, and Habrosaurus might have adopted the same strategy.
Habrosaurus had rows of blunt teeth arranged in the roof of its upper jaw, which indiates that these jaws were designed for crushing rather than grabbing. Presumably, it fed upon tiny mollusks and arthropods, such as snails and shrimp. Modern-day sirens feed mainly upon worms, aquatic snails, shrimp, and occasionally algae. Like fish, sirens possess lateral lines to find prey by indicating differences in water pressure and underwater vibrations.
An appropriate modern-day analog for the three-foot long Habrosaurus dilatus is the Greater Siren (Siren lacertina), which also grows to three feet long and is the largest siren species in the world today.
Below is a simple drawing of a Habrosaurus that I made with a felt-tipped marker. This style is a considerable departure from my usual style of highly-detailed pencil drawings, but I wanted to do some artistic experimenting.
Years earlier, I posted a picture of a Late Jurassic pliosaur known as Megalneusaurus. The illustration that I put up was based heavily on a skeletal drawing of Liopleurodon, it had hardly any detailing, and the skull was shockingly shrink-wrapped. Not my best work. You can see that post here.
I’m happy to say that I have recently done a revised drawing of this 25-foot long marine reptile, and I think that it’s a substantial improvement over the earlier illustration.
Below is the original drawing that I made of Megalneusaurus back in 2013.
This drawing was made with No. 2 and No. 3 pencils on roll paper, with some touch-up tweaking on my computer. The animal, from the tip of its nose to the tip of its tail, measures fifteen inches long (1/20 scale). As for the fish, they’re just generic fish, I suppose. I tried to find images of fish fossils from the Sundance Sea, but I couldn’t find anything worthwhile.
Hope you enjoy it. Please like and comment.
Hello all. I’ve recently finished an important writing project that I’ve been laboring upon for months. Now that it’s finished, I have a little breathing room to do art, and this is what I’ve done so far. I decided to do an updated version of an old illustration that I had made of an Ornithomimus. While the general color scheme was what I had in mind, I was never truly happy with the end-product. This latest version is much more in line with what I was imagining the “Bird Mimic” would look like.
Here is the “before” picture, made in 2013.
And here is the “after”, made today.
You’ll notice several differences right away, the most noteable of them being the re-shaping of its wing feathers. While Ornithomimus, or perhaps ornithomimids in general, had pennaceous feathers, I don’t think that they had primaries, because those would have been attached onto the wrist and the hand. This would have been difficult for ornithomimids because, unlike “raptor” dinosaurs (dromaeosaurids and troodontids), ornithomimids could not flex their hands backwards. I also increased the size of its tail feathers, made the neck thicker, changed the shape of the skull so that it was more anatomically accurate, and added Secretary Bird-style feathers to the back of its head. So much for form. In terms of color, I made it more vibrant, with deeper richer yellows and oranges and a lot more black patches. I changed the color of its bare skin from pink to a mixture of tan and black. I made its beak black, I changed its eye from yellow to blood red, and gave it black feet.
I can definitely see this character rushing about on the plains of the Hell Creek Formation. This shows that artists should never be stagnant. They must always strive to improve their work, and in so doing, improve their skill.
This drawing was made on computer printer paper with a No. 2 pencil, Prismacolor colored pencils, markers, and a black felt-tiped pen. The size of the drawing, from the tip of its nose to the tip of its tail feathers, measures 10.75 inches long, which is almost 1/12 scale, as the real animal possibly measured 12 feet long with its neck and tail fully stretched out.
Keep your pencils sharp.
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 giraffes 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.
In conclusion, animals will hurt each other and kill each other for a variety of reasons, not only between species but also within species. Competition for mates, competition for food and territory, and establishing your position within the social hierarchy are all seen within the modern animal kingdom, and it’s highly likely that dinosaurs did the same.