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The Ichnology of Jurassic Park

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All paleontologists remember their first time. Mine was in 1993, during a hot, steamy summer in Atlanta, Georgia. I had just spent the previous month camping in wilderness areas of Wyoming, so coming back to a big city with all of its urban temptations meant I was weak and susceptible to seeking out unusual sources of pleasure. Although I was not quite ready to be taken for such an exhilarating ride, it was an experience I’d never forget. Afterwards, once I had recovered enough to be able think about it, I wanted to do it again.

I am, of course, talking about seeing the film Jurassic Park on a movie screen. Sure, this movie has been around long enough (20 years) that nearly every paleontologist has also watched it on a TV, computer, or mobile device. But there is something about seeing dinosaurs – which, let’s face it, are most famous for their size – shown big. The initial glimpse of a Brachiosaurus munching on the tops of tall trees, a herd of Paralophosaurus ringing a glistening lake, an ill Triceratops dwarfing its human caretakers, the grand entrance of the Tyrannosaurus: all of these “actors” were meant to be seen large, and fill us with awe. It worked. Plot, acting, and science aside, Jurassic Park was, and probably still is, the best movie made for conveying what it would feel like for us humans, separated by a minimum of 65 million years, to see real, living dinosaurs.

“It’s, it’s a dinosaur.” That pretty much said it all in 1993, and still does. But what traces were being made by this Brachiosaurus as it strolled through its all-you-can-eat salad bar, known to you and me as a “landscape”? Please read on.

In 1993, though, I did not have an appreciation for some of the smaller details included in this film, and how my research specialty of ichnology – the study of traces, like tracks, burrows, and nests – was reflected throughout it. What dinosaur traces were included in the movie, and how were these traces used to serve or advance the plot? I also wondered how 20 years of field experience and scholarly research in ichnology might have changed my perceptions of it since that first viewing.

So with the re-release of Jurassic Park in 3-D last week, I decided it was time to view it from an ichnological perspective and share these thoughts with others. After all, my next book, Dinosaurs Without Bones (Pegasus Press), is about dinosaur trace fossils, and written for a popular audience. Also, in between the movie’s first release and now, I wrote two editions of a college textbook on dinosaurs (Introduction to the Study of Dinosaurs). Thus I went to the theater well justified in watching Jurassic Park once more, to see for myself how dinosaur traces were portrayed in the most well-loved of all dinosaur movies. And oh yes, for the fun.

For the sake of simplicity, I’ve divided these traces into two categories: those viewers could directly observe in the film, and others that could be inferred from the dinosaurs’ behaviors. Wherever possible, I also connect traces shown in the movie to research done on dinosaur trace fossils during the last 20 years, giving a broad sense of how far dinosaur ichnology has progressed since 1993.

(Ichnologist’s note: Even though all of the live dinosaurs in the movie were set in the 1990s, the study of their modern traces still qualifies as neoichnology. In contrast, any reference I make to actual dinosaur trace fossils is paleoichnology. Just so you know.)

Dinosaur Traces in Jurassic Park

• Velociraptor hatchling traces. Jurassic Park shows two different but complementary examples of hatchling traces for “Velociraptor.” (I will call this dinosaur Velociraptor throughout this post, but as most dino-philes know, the director, Steven Spielberg, scaled up the Late Cretaceous Velociraptor to maximize its frightfulness. Hence it is actually more like the Early Cretaceous Deinonychus or Utahraptor.)

One is an egg-emergence trace, which is the hole left in an eggshell where a dinosaur broke out of its egg. In this scene, a cooing Velociraptor hatchling pokes its cute little nose out of its egg. (This nose, if everything worked out for it, would some day would be warmed by fresh human viscera.) We first witness this tracemaking in the Jurassic Park laboratory toward the start of the film, the same day most of the protagonists arrive on the island (Isla Nublar). As far as I know, such trace fossils have not been interpreted from the fossil record, or if they have, they have not been referred to as trace fossils: which they should be.

The next day, after dinosaur paleontologist Alan Grant and his two companions – Lex and Tim Murphy – were sufficiently terrified (and enthralled) by various dinosaur encounters out in the park, they come across a Velociraptor nest. The nest has about 15-20 broken eggs, and the fracture patterns of the eggshells provide clear evidence of hatching. But these traces also had tiny, two-toed tracks leading away from them. The tracks, with two toes studded by digital pads, were typical for deinonychosaurs. However, unlike nearly every theropod track I’ve seen, these tracks lacked claw marks at their ends. (Tsk, tsk, says this nitpicking ichnologist.)

Baby-Velociraptor-Traces-JPAw, look at the cute little Velociraptor tracks and hatched eggs. Don’t these traces just make you want to say, “Who’s the cutest little predator in the world?” Still from Jurassic Park (1993), taken from www.anyclip.com.

Even though these tracks were flashed on the screen for only a few seconds, what’s really cool is how they convey three important pieces of information. One is that the Velociraptor chicks hatched after the torrential rainstorm of the previous night, and thus only mere hours before our wandering heroes saw their traces. Second, the tracks demonstrate that the hatchlings were not altricial, but ready to move and leave the nest immediately, presumably without parental care. Third, Dr. Grant realizes that these successfully fertilized and hatched eggs mean the “female-only” genetic fail-safe plan for the dinosaurs just got disproved. In other words, these traces mattered.

One point about that nest: as far as I could tell from, this Velociraptor mother did not make a rimmed structure to protect the eggs, such as those made by another Late Cretaceous theropod, Troodon, or Late Cretaceous sauropods in Argentina. Instead, the eggs were laid out in the open, like some ground-nesting shorebirds might do. In contrast, the Jurassic Park sequels featured Velociraptor nests that were much more overt as traces, such as a rimmed nest seen in Jurassic Park III.

Troodon-Rim-NestPartially preserved rimmed nest structure of Troodon, a Late Cretaceous theropod that lived in what we now call Montana. The rim has eroded quite a bit since its discovery in the mid-1990s; the Troodon egg clutch was in the area of the foreground before its extraction. (Photograph by Anthony Martin; scale in centimeters.)

• Triceratops feces. “That is one big pile of sh*t,” observes Dr. Ian Malcolm, the “chaotician” (mathematician) who supplies both pessimism and comic relief throughout the movie. In this scene, where the main protagonists attend to an under-the-weather Triceratops, two impressive piles of fecal material inspire Dr. Ellie Satler, a paleobotanist, to figure out whether or not the ceratopsian had eaten any toxic plants.

Somehow I suspect this scene was meant as a metaphor for what most paleontologists have to do in their day jobs in order to do any paleontology at all.

Still, when added together, this amount of still-moist waste was far too voluminous to have been from one or two depositional events: I mean, this dinosaur was sick, but not that much. As a result, park personnel must have been responsible for making these dung heaps from several days worthy of Triceratops contributions. (Strictly speaking, then, these heaps were composite traces.) If so, this would have been a rather unenviable job, but maybe they were better paid than Dennis Nedry, the disgruntled computer programmer who later provided ample fodder for Dilophosaurus.

Unfortunately, fossil Triceratops feces (coprolites) are thus far unknown from the geologic record. What is exciting, though, is that several excellent studies have been done by Dr. Karen Chin on Late Cretaceous hadrosaur coprolites. These coprolites, like the fictionalized Triceratops feces, contain lots of plant material, telling us much about what these hadrosaurs ate 75 million years ago. They also tell us what ate the feces or grazed on them, which were dung beetles and snails, respectively. (Indeed, I now wonder if Isla Nubar had a severe shortage of dung beetles, which might explain how those Triceratops feces got piled higher and deeper.)

Two-Medicine-CoproliteDinosaur coprolite – probably from a large hadrosaur, such as Maisaura – and filled with wood fragments, accompanied by special bonus trace fossils: dung beetle burrows! Specimen from the Two Medicine Formation (Late Cretaceous, Montana) as part of a Museum of the Rockies traveling exhibit at Fernbank Museum of Natural History. (Photograph by Anthony Martin, taken in 2001 and scanned from a 35-mm slide; scale in centimeters.)

• Tyrannosaurus tracks. Probably the most memorable scene in Jurassic Park is the grand entrance of the Tyrannosaurus, whose approach is first detected by “impact tremors” transmitted in cups of water on the dashboard of a jeep. Following this first bout of terror and the arrival of Ellie Sattler and big-game hunter Robert Muldoon, Malcolm, convalescing in the back of a jeep, looks down at a three-toed Tyrannosaurus track. The track, filled with water from the rain, communicates a warning as it vibrates from the footfalls of the approaching giant theropod. This repeats the previous image of the trembling water in the cup, but is made doubly dreadful by happening in a freshly made footprint of the same animal causing the tremors.

So what was by far the most exciting moment in the movie for me, ichnologically speaking? The Tyrannosaurus making a track, in which mud pushes up and out to the sides of its right foot, observed at 2:38 in the following video clip. Just watch:

This was already a great scene for all of its action, suspense, and lawyer eating. But check out that track-making!

Only a few fossil tracks have been attributed to Tyrannosaurus or other tyrannosaurids, mostly for being the right size (really big) and geologic age (Late Cretaceous). One was discovered in New Mexico in 1983, but wasn’t reported in a scientific journal until the year after Jurassic Park came out. More than a decade passed before another was found in Montana in 2007 and reported in 2008. Tragically, both were isolated tracks, and a Tyrannosaurus trackway, with two or more consecutive steps, has not yet been found. If so, it would make for a pretty darned nice find. So please do let the world know if you find one.

Large-Theropod-Track-CretaceousA large and well-preserved three-toed theropod track from the Early Cretaceous Glen Rose Formation of Texas, made about 95 million years ago. Although this track was more likely made by Acrocanthosaurus, rather than Tyrannosaurus rex, you can be assured that this theropod, like all living things, was a distant relative of T. rex. (Photograph taken by Anthony Martin; scale in centimeters.)

• Velociraptor tracks (adults). These tracks, shown only for a few seconds, are outside of the Velociraptor enclosure after the power was shut down. Muldoon, accompanied by Sattler, spots the footprints, and he wordlessly identifies them. (His expression also tells the audience that Sattler and he are going to be in deeper doo-doo than the Triceratops piles.) The twisted and broken bars of the enclosure provide additional traces affirming the conclusion that these ‘raptors are on the loose. All of these traces are shown only minutes before Muldoon utters his meme-inspiring last words, “Clever girl.”

Tracking-Velociraptors-JPUh oh: Velociraptor tracks, and these don’t look like they’re from hatchlings. Good thing Muldoon is a big-game hunter, who’s skilled at tracking and predicting Velociraptor behavior based on their tracks. But too bad his hypothesis was falsified in such an unpleasant way, but I suppose he could have picked kinder reviewers. Still from Jurassic Park (1993), taken from www.anyclip.com.

Deinonychosaur-Track-UtahHere’s what a real deinonychosaur track looks like. This one, from the Early Cretaceous of Utah, is a right foot impression, and is just slightly smaller than the adult tracks depicted in Jurassic Park. Notice the digits are thinner and end with sharp clawmarks, too. (Photograph by Anthony Martin; scale in centimeters.)

• Bioerosion of fossil dinosaur bones by modern dinosaurs. Toward the end of the film, the main human heroes – Grant, Sattler, Murphy, and Murphy (which sounds like a law firm, but we know how T. rex feels about those) – are confronted by a Velociraptor pack in the Jurassic Park visitor center. During their attempts to flee the ‘raptors, both species end up disarticulating and breaking some of the mounted dinosaur skeletons in the atrium of the visitor center. Their actions were thus a form of bioerosion, in which the fractured dinosaur bones are traces of their activities. Alternatively, the bones may have been artificial casts, in which case their breakage would have constituted bioerosion of modern substrates.

This bioerosion is made more complicated when the Tyrannosaurus rex (who everyone agrees is the ultimate protangonist of the movie) enters the atrium and, among other antics, smashes a skeleton of itself with a recently crunched Velociraptor. As a result, the jumbled assemblage of bones at the end is attributable to three separate, interacting tracemakers: four humans (two adult, two juvenile), two Velociraptors (both adults), and one Tyrannosaurus (adult). What should be noted, though, is that if the Velociraptor was already dead when flung by the Tyrannosaurus, then the broken skeleton is a trace of the Tyrannosaurus, not the Velociraptor. In other words, the Velociraptor body was just being used as a tool.

Bioerosion in action, as a result of Velociraptor and human interactions. Also, at 2:45: T. rex smash!

Dinosaur Trace-Making Behaviors in Jurassic Park

• Brachiosaurus tracks, browsing traces. When Drs. Grant and Sattler experience their first jaw-dropping glimpse of a Brachiosaurus, they watch it rear up on its hind feet, and come down hard on front feet. Considering that a Brachiosaurus this size might have weighed at least 30 tonnes, it surely would have left deep tracks in both the front and rear from the increased stresses imparted by these actions. Also, its cropping the tops of trees would have caused some easily visible gaps in the canopies of forests on Isla Nubar.

• Theropod toothmarks. Part of the fun of Jurassic Park was indulging in our worst nightmares about these non-avian theropods frequently sampling human flesh. Assuming that the theropod teeth in each instance penetrated skin and muscle and contacted bone, toothmarks would have included the following: (1) Tyrannosaurus toothmarks on goat, human, and Velociraptor bones; and (2) Velociraptor and Dilophosaurus toothmarks on human bones.

• Triceratops resting trace. When the paleontologists and others visit the ailing Triceratops, it was lying on its right side. I couldn’t help but think that if Triceratops or any other large ceratopsian dinosaur ever reclined like that, and in the right type of sediment, it would have left a gorgeous body impression. This scene also reminded me of bison traces I’ve seen in Yellowstone National Park, in which bisons roll onto their sides for a dust bath, leaving outlines of their bodies. Did dinosaurs – especially the feathered ones – ever take dust baths, and leave similar body impressions? We don’t know yet, but such trace fossils are something to look for.

• Dinosaur stampede. One of the most astonishing computer-generated effects of Jurassic Park, and one that was especially effective in 3-D, was of a dinosaur stampede. In this scene, a flock of Gallimus run toward and around Grant, Murphy, and Murphy, just before the ambush-hunting Tyrannosaurus rex slaughters one of them (the Gallimus, that is). I’ve written about this scene before, connecting it to a dinosaur tracksite in Queensland, Australia that has more than 3,000 tracks preserved. Although the site was originally interpreted as the only evidence of a dinosaur stampede, the tracks were recently reinterpreted as swim tracks. I’ll write about this topic at length in my upcoming book, so for now, I ain’t saying nothing more.

Run away, run away!

• Tyrannosaurus drag mark. After the Tyrannosaurus rex decides that a measly goat was just an appetizer and begins seeking out the nearest available mammals for nomming purposes, at some point it overturns and begins pushing an SUV, which still has Lex and Tim Murphy trapped underneath it. Its flipping the SUV with its head certainly would have left a substantial mark on the muddy ground, a trace that then would have been connected to a semi-circular dragmark (clockwise oriented), and with tracks directly adjacent to these traces. Her tracks also may have been deeper in their fronts because of her head being down as she pushed, reflecting a shift in her weight distribution. However, I should again remind everyone that just like with the dead Velociraptor used for bioerosion by this same T. rex later in the film, the SUV is not making the trace. It is only a tool being used by the tyrannosaur, which is the real tracemaker.

• Tyrannosaurus running trackway – This pulse-quickening chase scene, in which the T. rex pursues a jeep driven by Muldoon and with Malcolm and Sattler as passengers, very likely would have caused a wonderful sequence of tracks. These tracks would have shown increasing stride lengths from a standing start to full-speed run, and each successive track would have registered external and internal structures consistent with this acceleration. Even better, the tracks would have cross-cut the jeep tire-tracks at some points, demonstrating to a later observer that the tyrannosaur was very likely following the jeep. (The demolition of a low-hanging tree branch by the T. rex during the chase also counts as some bioerosion along the way.) Some convincing studies have been done since showing that an adult Tyrannosaurus could not have moved as fast as the one in Jurassic Park, but it still could have caught most running humans. And just to repeat what I said earlier, it’d be really nice for someone to find a T. rex trackway, which would give us more direct evidence of how these massive theropods moved.

• Velociraptor scratch marks and other traces. This time, while watching the harrowing and claustrophobic scene in which a pair of Velociraptors hunt the Murphy siblings in a kitchen, I started thinking about the traces they might have left. Did their claws leave scratch marks on the door handles and kitchen counters? Did they indent the steel counters when they jumped up on these surfaces? A broken window is also shown as a trace of their smashing through glass once they became frustrated with a locked door.

OK, enough of the fanciful ichnology. What about other dinosaurs and their traces? Well, it turns out that Jurassic Park saved the real, living dinosaurs for the very end of the movie. These were five brown pelicans (Pelecanus occidentalis), flying in formation as Grant, Sattler, and their companions leave Isla Nubar in a helicopter. For Grant, this is a poignant moment, as he is likely reflecting on how dinosaurs were still with us today as birds. With that thought, I will say “amen,” and add that dinosaur traces – tracks, nests, feces, bite marks, and all – are still here with us, too, and don’t require special glasses to see them in three dimensions. Thanks for that reminder, Jurassic Park.

Pelican-Tracks-SapeloWant to see some modern dinosaur traces? Here are tracks of a brown pelican, made in wet sand while it was loafing on a beach at low tide on Sapelo Island, Georgia. To see more modern dinosaur traces, just go outside, and you’ll find them wherever birds are found. (Photograph by Anthony Martin; scale in centimeters.)

Further Reading

Chiappe, L.M., Schmitt, J.G., Jackson, F., Dingus, L., and Grellet-Tinner, G. 2004. Nest structure for sauropods: sedimentary criteria for recognition of dinosaur nesting traces. Palaios, 19: 89–95.

Chin, K. 2007. The paleobiological implications of herbivorous dinosaur coprolites from the Upper Cretaceous Two Medicine Formation of Montana: why eat wood? Palaios, 22: 554-566.

Chin, K., and Gill, B.D. 1996. Dinosaurs, dung beetles, and conifers: participants in a Cretaceous food web. Palaios, 11: 280-285.

Elbroch, M., and Marks, E. 2001. Bird Tracks and Sign of North America. Stackpole Books, Mechanicsburg, Pennsylvania.

Erickson, G. M., Van Kirk, S. D., Su, J., Levenston, M. E., Caler, W. E., & Carter, D. R. 1996. Bite force estimation for Tyrannosaurus rex from tooth-marked bones. Nature, 382: 706–708.

Gignac, P.M., Makovicky, P.J., Erickson, G.M., and Walsh, R.P. 2010. A description of Deinonychus antirrhopus bite marks and estimates of bite force using tooth indentation simulations. Journal of Vertebrate Paleontology, 30: 1169-1177.

Hutchinson, J.R., and Garcia, M. 2002. Tyrannosaurus was not a fast runner. Nature, 415: 1018-1021.

Jacobsen, A.R. 1998. Feeding behaviour of carnivorous dinosaurs as determined by tooth marks on dinosaur bones. Historical Biology, 13: 17-26.

Lockley, M.G., and Hunt, A.P. 1994. A track of the giant theropod dinosaur Tyrannosaurus from close to the Cretaceous/Tertiary Boundary, northern New Mexico. Ichnos, 3: 213-218.

Manning, P.L., Ott, C., and Falkingham, P.L. 2008. A probable tyrannosaurid track from the Hell Creek Formation (Upper Cretaceous), Montana, United States. Palaios, 23: 645-647.

Martin, A.J. 2013. Life Traces of the Georgia Coast: Revealing the Unseen Lives of Plants and Animals. Indiana University Press, Bloomington, Indiana: 692 p.

Romilio, A., and Salisbury, S.W. 2011. A reassessment of large theropod dinosaur tracks from the mid-Cretaceous (late Albian–Cenomanian) Winton Formation of Lark Quarry, central-western Queensland, Australia: a case for mistaken identity. Cretaceous Research, 32: 135-142.

Romilio, A., Tucker, R., Salisbury, S. 2013. Reevaluation of the Lake Quarry dinosaur tracksite (late Albian-Cenomanian Winton Formation, central-western Queensland, Australia): no longer a stampede? Journal of Vertebrate Paleontology. 33: 1, 102-120.

Sellers, W.I., and Manning, P.L. (July 2007). Estimating dinosaur maximum running speeds using evolutionary robotics. Proceedings of the Royal Society of London, B, 274: 2711-2716.

Thulborn, R.A., and Wade, M., 1979. Dinosaur stampede in the Cretaceous of Queensland. Lethaia, 12: 275-279.

Varricchio, D.J., Jackson, F. and Trueman, C.N. 1999. A nesting trace with eggs for the Cretaceous theropod dinosaur Troodon formosus. Journal of Vertebrate Paleontology, 19: 91-100.

 

Tracking Wild Turkeys on the Georgia Coast

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Of the many traditions associated with the celebration of Thanksgiving in the U.S., the most commonly mentioned one is the ritual consumption of an avian theropod, Meleagris gallopavo, simply known by most people as “turkey.” The majority of turkeys that people will eat this Thursday, and for much of the week afterwards, are domestically raised. Yet these birds are all descended from wild turkeys native to North America. This is in contrast to chickens (Gallus gallus), which are descended from an Asian species, and various European mammals, such as cattle, pigs, sheep, and goats (Bos taurus, Sus scrofa, Ovis aries, and Capra aegagrus, respectively).

Trackway of a wild turkey (Meleagris gallopavo) crossing a coastal dune on Cumberland Island, Georgia. Notice how this one, which was likely a big male (“tom”), was meandering between clumps of vegetation and staying in slightly lower areas, its behavior influenced by the landscape. Scale = 20 cm (8 in). (Photograph by Anthony Martin.)

American schoolchildren are also sometimes taught that one of the founding fathers of the United States, Benjamin Franklin, even suggested that the wild turkey should be elevated to the status of the national bird, in favor of the bald eagle (Haliaeetus leucocephalus). With an admiring (although I suspect somewhat facetious) tone, he said:

“He [the turkey] is besides, though a little vain & silly, a Bird of Courage, and would not hesitate to attack a Grenadier of the British Guards who should presume to invade his Farm Yard with a red Coat on.”

There are eight of us, and only one of you. Do you really want to mess with us? (Photograph by Anthony Martin, taken on Cumberland Island, Georgia.)

Unfortunately, because I live in the metropolitan Atlanta area, I never see turkeys other than the dead packaged ones in grocery stores. Nonetheless, one of the ways I experience turkeys as wild, living animals is to visit the Georgia barrier islands, and the best way for me to learn about wild turkey behavior is to track them. This is also great fun for me as a paleontologist, as their tracks remind me of those made by small theropod dinosaurs from the Mesozoic Era. And of course, as most schoolchildren can tell you, birds are dinosaurs, which they will state much more confidently than anything they might know about Benjamin Franklin.

Compared to most birds, turkeys are relatively easy to track. Their footprints are about 9.5-13 cm (3.7-5 in) long and slightly wider than long, with three long but thick, padded toes in front and one shorter one in the back, pointing rearward. In between these digits is a roundish impression, imparted by a metatarsal. This is a trait of an incumbent foot, in which a metatarsal registers behind digit III because the rear part of that toe is raised off the ground. The short toe is digit I, equivalent to our big toe, but not so big in this bird. Despite the reduction of this toe, its presence shows that turkeys probably descended from tree-dwelling species, as this toe was used for grasping branches. Clawmarks normally show on the ends of each toe impression, and when a turkey is walking slowly, it drags the claw on its middle toe (digit III), thus making a nicely defined linear groove.

Wild turkey tracks made while it was walking slowly up a gentle dune slope, dragging the claw on the middle digit of its right foot, making a long groove. Also notice the bounding tracks of a southern toad (traveling lower right –> upper left), cross-cutting the turkey tracks. (Photograph by Anthony Martin, taken on Cumberland Island.)

A normal walking pace (right foot –> left foot, left foot –> right foot) for a turkey is anywhere from 15-40 cm (6-16 in), and its stride (right foot –> right foot, left foot –> left foot) is about twice that, or 30-80 cm (12-32 in), depending on the age and size of the turkey. Their trackways show surprisingly narrow straddles for such wide-bodied birds, only 1.5 times more than track widths. This is because they walk almost as if on a tightrope, with angles between each step approaching 180°; so they still make a diagonal pattern, but nearly define a straight line. However, turkeys meander, stop, or change direction often enough to make things interesting when tracking them. Their flocking behavior also means their tracks commonly overlap with one another or cluster, making it tough to pick out the trackways of individual turkeys. However, in such flocks, the dominant male’s tracks are noticeably larger than those of the females or younger turkeys, so these can be picked out and help with sorting who’s who.

Turkey trackway in which it walked across the wind-rippled surface of a coastal dune on Cumberland Island, meandering while moseying. Same photo scale as before. (Photograph by Anthony Martin.)

An abrupt right turn recorded by a turkey’s tracks. Check out that beautiful metatarsal  impression in the second track from the right, and how the claw dragmark in the thrid track from the right points in the direction of the next track. (Photograph by Anthony Martin.)

One of the more remarkable points about these Georgia barrier-island turkeys, though, is how their tracks belie their stereotyped image as forest-only birds. Although they do spend much of their time in the forest, I’ve tracked turkeys through broad swaths of coastal dunes, and sometimes they will stop just short of primary dunes at the beach. So however difficult it might be to think about these birds as marginal-marine vertebrates, their tracks overlap the same places with ghost-crab burrows and shorebird tracks. Geologists and paleontologists take note: this exemplifies the considerable overlap between terrestrial and marginal-marine tracemakers that can happen in coastal environments. This also happened with dinosaurs that strolled onto tidal flats or otherwise passed through marginal-marine ecosystems.

Turkey tracks heading toward the beach, with the open ocean visible just beyond. Is this close enough to consider turkeys as marginal-marine tracemakers? (Photograph by Anthony Martin.)

Do these turkeys also have an impact on the dunes themselves? Yes, although these effects vary, from trackways disrupting wind ripples to more overt changes to the landscape. For instance, one of the most interesting effects I’ve seen is where they’ve caused small avalanches of sand downslope on dune faces. Interestingly, this same sort of phenomenon was also documented for Early Jurassic dinosaurs that walked across dry sand dunes, which caused grainflows that cascaded downhill with each step onto the sand.

Grainflow structure (arrow), a small avalanche caused by a turkey walking down a dune face. (Photograph by Anthony Martin.)

Close-up of grainflow structure (right) connected to turkey tracks, which become better defined once the turkey reached a more level surface. (Photograph by Anthony Martin, taken on Cumberland Island.)

What other traces do turkeys make? A lot, although I’ve only seen their tracks. Other traces include dust baths, feces, and nests. Dust baths, in which turkeys douse themselves with dry sediment to suffocate skin parasites, must be awesome structures. These are described as 50 cm (20 in) wide, 5-15 (1-3 in) deep, semi-circular depressions, and feather impressions show up in those made in finer-grained sediments. Although such structures would have poor preservation potential in the fossil record, I hold out hope that if paleontologists start looking more at modern examples, they are more likely to find a fossil dust bath, whether in Mesozoic or Cenozoic rocks.

Turkey feces, like most droppings from birds, have white caps on one end, but are unusual in that these can tell you the gender of their depositor. Male turkeys tend to make curled cylinders that are about 1 cm wide and as much as 8 cm long (0.4 X 3 in), whereas females make more globular (not gobbular) droppings that are about 1 cm (0.4 in) wide. These distinctive shapes are a result of their having different digestive systems. Turkeys are herbivores, so their scat normally includes plant material, but don’t be surprised to see insects parts in them, too. Still think about how exciting it would be to find a grouping of same-diameter cylindrical and rounded coprolites in the same Mesozoic deposit, yet filled with the same digested material, hinting at gender differences (sexual dimorphism) in the same species of dinosaur maker.

Turkeys normally make nests on the ground by scratching out slight depressions with their feet, but evidently this is a flexible behavior. On at least one of the Georgia barrier islands (Ossabaw), these birds have been documented as building nests in trees. Although this practice seems very odd for a large, ground-dwelling bird, it is an effective strategy against feral hogs, which tend to eat turkey eggs, as well as eggs of nearly every other species of bird or reptile, for that matter. Just to extend this idea to the geologic past, ground nests are documented for several species of dinosaurs, but tree nests are unknown, let alone whether species of ground-nesting dinosaurs were also capable of nesting in trees.

As everyone should know from their favorite WKRP episode, domestic turkeys can’t fly. But wild turkeys can, and use this ability to get into the branches of live oaks (arrow), high above their predators, or even curious ichnologists. (Photograph by Anthony Martin, taken on Cumberland Island.)

So whether or not you have tryptophan-fueled dreams while dozing later this week, keep in mind not just the evolutionary heritage of your dinosaurian meal, but also what their traces tell us about this history. Moreover, it is an understanding aided by these magnificent and behaviorally complex birds on the Georgia barrier islands. For this alone, we should be thankful.

Paleontologist Barbie, tracking wild turkeys on the Georgia coast to learn more about how these tracemakers can be used as modern analogs for dinosaur behavior and traces, and once again demonstrating why she is the honey badger of paleontologists. (Yes, photograph by me, and taken on Cumberland Island. P.S. Happy Thanksgiving!)

Further Reading

Dickson,J.G. (editor). 1992. Wild Turkeys: Biology and Management. Stackpole Books, Mechanicsburg, Pennsylvania: 463 p.

Elbroch, M., and Marks, E. 2001. Bird Tracks and Sign of North America. Stackpole Books, Mechanicsburg, Pennsylvania: 456 p.

Fletcher, W.O., and Parker, W.A. 1994. Tree nesting by wild turkeys on Ossabaw Island, Georgia. The Wilson Bulletin, 106: 562.

Loope, D.B. 2006. Dry-season tracks in dinosaur-triggered grainflows. Palaios, 21: 132-142.

Into the Dragon’s Lair: Alligator Burrows as Traces

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American alligators (Alligator mississippiensis) tend to provoke strong feelings in people, but the one I encounter the most often is awe, followed closely by fear. Both emotions are certainly justifiable, considering how alligators are not only the largest reptiles living on the Georgia barrier islands, but also are the top predators in both freshwater and salt-water ecosystems in and around those islands. I’ve even encountered them often enough in maritime forests of the islands to regard them as imposing predators in those ecosystems, too.

Time for a relaxing stroll through the maritime forest to revel in its majestic live oaks, languid Spanish moss, and ever-so-green saw palmettos. Say, does that log over there look a little odd to you? (Photo by Anthony Martin, taken on St. Catherines Island.)

But what many people may not know about these Georgia alligators is that they burrow. I’m still a little murky on exactly how they burrow, but they do, and the tunnels of alligators, large and small, are woven throughout the interiors of many Georgia barrier islands. Earlier this week, I was on one of those islands – St. Catherines – having started a survey of alligator burrow locations, sizes, and ecological settings.

Entrance to an alligator burrow in a former freshwater marsh, now dry, yet the burrow is filled with water. How did water get into the burrow, and how does such traces help alligators to survive and thrive? Please read on. (Photograph by Anthony Martin and taken on St. Catherines Island, Georgia.)

In this project, I’m working cooperatively (as opposed to antagonistically) with a colleague of mine at Emory University, Michael Page, as well as Sheldon Skaggs and Robert (Kelly) Vance of Georgia Southern University. As loyal readers may recall, Sheldon and Kelly worked with me on a study of gopher tortoise burrows, also done on St. Catherines Island, in which we combined field descriptions of the burrows with imaging provided by ground-penetrating radar (also known by its acronym, GPR). Hence this project represents “Phase 2” in our study of large reptile burrows there, which we expect will result in at least two peer-reviewed papers and several presentations at professional meetings later this year.

Why is a paleontologist (that would be me) looking at alligator burrows? Well, I’m very interested in how these modern burrows might help us to recognize and properly interpret similar fossil burrows. Considering that alligators and tortoises have lineages that stretch back into the Mesozoic Era, it’s exciting to think that through observations we make of their descendants, we could be witnessing evolutionary echoes of those legacies today.

Indeed, for many people, alligators evoke thoughts of those most famous of Mesozoic denizens – dinosaurs – an allusion that is not so farfetched, and not just because alligators are huge, scaly, and carnivorous. Alligators are also crocodilians, and crocodilians and dinosaurs (including birds) are archosaurs, having shared a common ancestor early in the Mesozoic. However, alligators are an evolutionarily distinct group of crocodilians that likely split from other crocodilians in the Late Jurassic or Early Cretaceous Period, an interpretation based on both fossils and calculated rates of molecular change in their lineages.

Archosaur relatives, reunited on the Georgia coast: great egrets (Ardea alba), which are modern dinosaurs, nesting above American alligators (Alligator mississippiensis), which only remind us of dinosaurs, but shared a common ancestor with them in the Mesozoic Era. (Photograph by Anthony Martin, taken on St. Catherines Island, Georgia.)

Along these lines, I was a coauthor on a paper that documented the only known burrowing dinosaur – Oryctodromeus cubicularis – from mid-Cretaceous rocks in Montana. In this discovery, we had bones of an adult and two half-grown juveniles in a burrow-like structure that matched the size of the adult. I also interpreted similar structures in Cretaceous rocks of Victoria, Australia as the oldest known dinosaur burrows. Sadly, these structures contained no bones, which of course make their interpretation as trace fossils more contentious. Nonetheless, I otherwise pointed out why such burrows would have been likely for small dinosaurs, especially in Australia, which was near the South Pole during the Cretaceous. At least a few of these reasons I gave in the published paper about these structures were inspired by what was known about alligator burrows.

Natural sandstone cast of the burrow of the small ornithopod dinosaur, Oryctodromeus cubicularis, found in Late Cretaceous rocks of western Montana; scale = 15 cm (6 in). (Photograph by Anthony Martin, taken in Montana, USA.)

Enigmatic structure in Early Cretaceous rocks of Victoria, Australia, interpreted as a small dinosaur burrow. It was nearly identical in size (about 2 meters long) and form (gently dipping and spiraling tunnel) to the Montana dinosaur burrow. (Photograph by Anthony Martin, taken in Victoria, Australia.)

What are the purposes of modern alligator burrows? Here are four to think about:

• Dens for Raising Young Alligators – Many of these burrows, like the burrow interpreted for the dinosaur Oryctodromeus, serve as dens for raising young. In such instances, these burrows are occupied by big momma ‘gators, who use them for keeping their newly hatched (and potentially vulnerable) offspring safe from other predators.

Two days ago, Michael and I experienced this behavioral trait in a memorable way while we documented burrow locations. As we walked along the edge of an old canal cutting through the forest, baby alligators, alarmed by our presence, began emitting high-pitched grunts. This then provoked a large alligator – their presumed mother – to enter the water. Her reaction effectively discouraged us from approaching the babies; indeed, we promptly increased our distance from them. (Our mommas didn’t raise no dumb kids.) So although we were hampered in finding out the exact location of this mother’s den, it was likely very close to where we first heard the grunting babies. I have also seen mother alligators on St. Catherines Island usher their little ones through a submerged den entrance, quickly followed by the mother turning around in the burrow and standing guard at the front door.

Oh, what an adorable little baby alligator! What’s that? You say your mother is a little over-protective? Oh. I see. I think I’ll be leaving now… (Photograph by Anthony Martin, taken on St. Catherines Island.)

• Temperature Regulation – Sometimes large male alligators live by themselves in these burrows, like some sort of saurian bachelor pad. For male alligators on their own, these structures are important for maintaining equitable temperatures for these animals. Alligators, like other poikilothermic (“cold-blooded”) vertebrates, depend on their surrounding environments for controlling their body temperatures. Even south Georgia undergoes freezing conditions during the winter, and of course summers there can get brutally hot. Burrows neatly solve both problems, as these “indoor” environments, like caves, provide comfortable year-round living in a space that is neither too cold nor too hot, but just right. The burrowing ability of alligators thus makes them better adapted to colder climates than other crocodilians, such as the American crocodile (Crocodylus acutus), which does not make dwelling burrows and is restricted in the U.S. to the southern part of Florida.

• Protection against Fires – Burrows protect their occupants against a common environmental hazard in the southeastern U.S., fire. This is an advantage of alligator burrows that I did not appreciate until only a few days ago while in the field on St. Catherines. Yesterday, the island manager (and long-time resident) of St. Catherines, Royce Hayes, took us to a spot where last July a fire raged through a mixed maritime forest-freshwater wetland that also has numerous alligator burrows. The day after the fire ended, he saw two pairs of alligator tracks in the ash, meaning that these animals survived the fire by seeking shelter, and further reported that at least one of these trackways led from a burrow. The idea that these burrows can keep alligators safe from fires makes sense, similar to how gopher tortoises can live long lives in fire-dominated long-leaf pine ecosystems.

An area in the southern part of St. Catherines Island, scorched by a fire last July, that is also a freshwater wetland inhabited by alligators with burrows. The burrow entrances are all under water right now, which would work out fine for their alligator occupants if another fire went through there tomorrow. (Photograph by Anthony Martin, taken on St. Catherines Island.)

• Protection against Droughts – Burrows also probably help alligators keep their skins moist during droughts. Because these burrows often intersect the local water table, alligators might continue to use them as homes even when the accompany surface-water body has dried up. We saw several examples of such burrows during the past few days, some of which were occupied by alligators, even though their adjacent water bodies were nearly dry.

For example, yesterday Michael and I, while scouting a few low-lying areas for either occupied or abandoned dens, saw a small alligator – only about a meter (3.3 ft) long – in a dry ditch cutting through the middle of a pine forest. Curious about where alligator’s burrow might be, we approached it to see where it would go. It ran into a partially buried drainage pipe under a sandy road, a handy temporary refuge from potentially threatening bipeds. Seeing no other opening on that side of the road, we then checked the other side of the road, and were pleasantly surprised to find a burrow entrance with standing water in it. This small alligator had made the best of its perilously dry conditions by digging down to water below the ground surface.

Alligator burrow (right) on the edge of a former water body. Notice how water is pooling in the front of the burrow, showing how it intersects the local water table. The entrance also had fresh alligator tracks and tail dragmarks at this entrance, showing that it was still occupied despite the lack of water outside of it. (Photograph by Anthony Martin, taken on Cumberland Island, Georgia.)

Alligator burrows (left foreground and middle background) in a maritime forest, also not associated with a wetland but marking the former location of one. Although the one to the left was unoccupied when we looked at it, it had standing water just below its entrance. This meant an alligator could have hung out in this burrow for a while after the wetland dried up, and it may have just recently departed. Also, once these burrows are high and dry, bones strewn about in front of them also add a delicious sense of dread. Here, Michael Page points at a deer pelvis, minus the rest of the deer. (Photograph by Anthony Martin, taken on St. Catherines Island, Georgia.)

What is especially interesting about the American alligator is how the only other species of modern alligator, A. sinensis in China, is also a fabulous burrower, digging long tunnels there too, which they use for similar purposes. This behavioral trait in two closely related but now geographically distant species implies a shared evolutionary heritage, in which burrowing provided an adaptive advantage for their ancestors.

Thus like many research problems in science, we won’t really know much more about alligator burrows until we gather information about them, test some of the questions and other ideas that emerge from our study, and otherwise do more in-depth (pun intended) research. Nonetheless, our all-too-short trip to St. Catherines Island this week gave us a good start in our ambitions to apply a comprehensive approach to studying alligator burrows. Through a combination of ground-penetrating radar, geographic information systems, geology, and old-fashioned (but time-tested) field observations, we are confident that by the end of our study, we will have a better understanding of how burrows have helped alligators adapt to their environments since the Mesozoic.

Juvenile alligators just outside two over-sized burrows, made and used by previous generations of older and much larger alligators. How might such burrows get preserved in the fossil record? How might we know whether these burrows were reused by younger members of the same species? Or, would we even recognize these as fossil burrows in the first place? All good questions, and all hopefully answerable by studying modern alligator burrows on the Georgia barrier islands. (Photograph by Anthony Martin, taken on Sapelo Island, Georgia.)

Further Reading

Erickson, G.M., et al. 2012. Insights into the ecology and evolutionary success of crocodilians revealed through bite-force and tooth-pressure experimentation. PLoS One, 7(3): doi:10.1371/journal.pone.0031781.

Martin, A.J. 2009. Dinosaur burrows in the Otway Group (Albian) of Victoria, Australia and their relation to Cretaceous polar environments. Cretaceous Research, 30: 1223-1237.

Martin, A.J., Skaggs, S., Vance, R.K., and Greco, V. 2011. Ground-penetrating radar investigation of gopher-tortoise burrows: refining the characterization of modern vertebrate burrows and associated commensal traces. Geological Society of America Abstracts with Programs, 43(5): 381.

St. John, J.A., et al., 2012. Sequencing three crocodilian genomes to illuminate the evolution of archosaurs and amniotes. Genome Biology, 13: 415.

Varricchio, D.J., Martin, A. J., and Katsura, Y. 2007. First trace and body fossil evidence of a burrowing, denning dinosaur. Proceedings of the Royal Society of London B, 274: 1361-1368.

Waters, D.G. 2008. Crocodlians. In Jensen, J.B., Camp, C.D., Gibbons, W., and Elliott, M.J. (editors), Amphibians and Reptiles of Georgia. University of Georgia Press, Athens, Georgia: 271-274.

Acknowledgements: Much appreciation is extended to the St. Catherines Island Foundation, which supported our use of their facilities and vehicles on St. Catherines this week, and Royce Hayes, who enthusiastically shared his extensive knowledge of alligator burrows. I also would like to thank my present colleagues and future co-authors – Michael Page, Sheldon Skaggs, and Kelly Vance – for their valued contributions to this ongoing research: we make a great team. Lastly, I’m grateful to my wife Ruth Schowalter for her assistance both in the field and at home. She’s stared down many an alligator burrow with me on multiple islands of the Georgia coast, which says something about her spousal support for this ongoing research.

Of Sandhill-Crane Footprints and Dinosaurs Down Under

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Last week, while in Athens, Georgia, I found myself musing about footprints from the barrier islands of Georgia and the Cretaceous rocks of Australia, despite their separation by half a world and more than 100 million years. These seemingly random thoughts came to me during a visit to the Department of Geology at the University of Georgia to give a lecture in their departmental seminar series.

It was a pleasure speaking at the geology department for many reasons, but perhaps the most gratifying was how it was also a homecoming. I had worked on my Ph.D. there in the late 1980’s, and in 1988-1989 had taught introductory-geology classes in the very same lecture hall where I gave my presentation. Several of my former professors, who were junior faculty then, are still there and now comprise a distinguished senior faculty. So seeing them there now, their smiling faces in the audience along with the latest generation of undergraduate and graduate students, generated all sorts of warm-and-fuzzy feelings.

But enough about the present: let’s go back about 100 million years to the Cretaceous Period, which was the subject of my talk. I had actually asked to speak about the modern Georgia barrier islands and their traces: you know, the main theme of this blog and my upcoming book of the same title (Life Traces of the Georgia Coast, just in case you need reminding). Nonetheless, my host and valued friend, paleontologist Dr. Sally Walker, figured that a summary of my latest research on the Cretaceous trace fossils of Victoria, Australia would bring in a wider audience, especially if I used the magical word “dinosaur” in the title (which I did).

For my talk at the UGA Department of Geology, I could have talked about this place – St. Catherines Island, Georgia – and it’s modern traces. After all, it’s only about a four-hour drive and short boat ride from Athens, Georgia.

But instead I talked about this place – coastal Victoria, Australia – and its trace fossils from more than 100 million years ago. Which wasn’t such a bad thing.

In retrospect, she was right, and I thoroughly enjoyed putting together an informative and (I thought) entertaining presentation that shared highlights of fossil discoveries from that part of Australia during the past five years. For the benefit of the students in the audience, basic geology was woven throughout the talk, as I included facets of sedimentology, stratigraphy, geochemistry, paleobotany, paleoclimatology, plate tectonics, evolution, history of science, field methods, and oh yes, dinosaurs. (If you are interested in hearing more about the science and personal experiences behind these recent findings in Australia, these are related in another blog of mine written previous to this one, The Great Cretaceous Walk.)

So how do the barrier islands of the Georgia coast and their animal traces relate to the Cretaceous of Australia? I mentioned the main reason briefly in my talk, but will elaborate more here: I likely owed one of my most important fossil discoveries in Australia to track-imprinted memories gained from field work on the Georgia coast. The fossil find, which happened in June 2010, was of about two dozen thin-toed theropod dinosaur tracks in Cretaceous rocks along the Victoria coast. These tracks represent the best assemblage of dinosaur tracks found thus far in southern Australia, and the largest collection of polar-dinosaur tracks in the Southern Hemisphere. Moreover, some of these tracks just happened to be about the same size and forms of footprints made by sandhill cranes (Grus canadensis).

Comparison between the footprint of a sandhill crane (Grus canadensis), made in moist sand next to a freshwater pond, St. Catherines Island, Georgia (top), and a footprint made by a theropod dinosaur about 105 million years ago on a river floodplain, Victoria, Australia (bottom). Notice the resemblance?

Sandhill cranes do not normally live on the Georgia barrier islands, and nearly all of them simply fly over or stop briefly during their annual migrations from south of Georgia to the Great Plains, or vice versa. However, at least a few have settled on St. Catherines Island, the same place on the Georgia coast where I recently studied gopher tortoise burrows. According to Jen Hilburn, the island ornithologist, some of these cranes found life so comfortable on the island that they stayed. This turned out to be fortunate for me, as I became familiar with their tracks after repeated visits to St. Catherines. Even though these tall, beautiful, and majestic birds restrict themselves to just one island year-round, St. Catherines is big enough to hold a wide variety of habitats and substrates, so I have seen their tracks in salt marshes, next to fresh-water ponds, and along dusty roads throughout the entire length of the island.

Who are you calling a “dinosaur”? A sandhill crane on St. Catherines Island graciously poses for its portrait, helping this ichnologist get a better idea of what an anatomically similar tracemaker might have looked like more than 100 million years ago.

Sandhill-crane trackway on the sandy substrate of a high salt marsh, St. Catherines Island, Georgia. In this environment, its tracks are accompanied by fiddler-crab burrows and feeding pellets, as well as the tracks and dig marks of raccoons hunting the fiddler crabs. Scale (toward the top of the photo) in centimeters.

So to make a long story short, while walking along the Victoria coast last year, I also carried with me mental picture of these tracks in Georgia. These images, I am sure, contributed to my stopping to look at a rock surface that held faint but nearly identical impressions made by dinosaurian feet on the once-soft sediments of a river floodplain. This is how ichnology is supposed to work, and it did.

A comparison between sandhill-crane tracks on the Georgia barrier islands and those of Cretaceous dinosaurs in Australia is actually not as far-fetched as one might think at first. For one, we now know that birds are dinosaurs, evolutionarily speaking. This formerly vague hypothesis is now a certainty, and is based on an ever-improving fossil record of feathered theropod dinosaurs, as well as studies from modern biology that show genetic and developmental affinities between modern birds and theropods. Even so, this idea is not new, either. For example, evolutionary biologist Thomas Huxley (1825-1895), friend and noted proponent of Charles Darwin, readily connected Archaeopteryx, the Late Jurassic bird (or dinosaur, depending on evolutionary perspective) with theropod dinosaurs.

Preceding Huxley, though, was one of the first scientists to formally apply ichnology to fossilized dinosaur tracks, Edward Hitchcock (1793-1864). Hitchcock interpreted the abundant dinosaur tracks of the Connecticut River Valley – many made by theropods – as those of large, flightless birds that lived before humans. Although he never made the evolutionary connection between dinosaurs and birds, his hypothesis reflected anatomical similarities between their feet.

A close-up look at sandhill crane feet while it takes a step. Notice the left foot has a little toe facing backwards, but off the ground. This is the equivalent of our “big toe,” also known as digit I, and it rarely registers in their tracks unless a crane walks in soft mud or sand. Instead, you will see impressions of the other three toes with clawmarks, and the middle toe normally makes the deepest mark.

Theropod dinosaurs, like many modern birds, mostly made three-toed tracks, a condition also called tridactyl. Although theropod tracks are occasionally confused with similar tracks made by ornithopod dinosaurs, they have the following traits: (1) three prominent, forward-facing digit impressions; (2) a footprint that is longer than wide; (3) angles of less than 90° between the outermost digits; and (4) well-defined clawmarks. One of the many changes that happened to bird feet as they evolved from non-avian theropods was the dropping of and rearward projection of their first digit (equivalent to our big toe). This condition was a great adaptation for grasping branches in trees and otherwise getting around off the ground. Bird tracks from the Cretaceous Period also tend to be wider than long, a function of the angles between the outermost toes becoming greater than 90°, and most of these also show the impression of a backward-pointing toe. Sandhill-crane footprint made in firm sand of a high salt marsh, St. Catherines Island, Georgia. Like many bird tracks, this one is wider than it is long, which is unlike most theropod dinosaur tracks. Still, these are very similar to tracks made by certain types of thin-toed theropod dinosaurs during the Cretaceous Period. Scale in centimeters.

Much later in their evolutionary history, though, some lineages of birds became either flightless or otherwise spent more time on the ground than in the trees, such as wading birds and shorebirds. These circumstances resulted in their first digit becoming reduced or absent, or vestigial. Violá, the tridactyl theropod-dinosaur footprint came back in style, so to speak, and now dinosaur ichnologists regularly study the tracks and behaviors of birds with such feet to better understand how their theropod relatives may have moved during the Mesozoic Era.

Comparison of a track made by a greater rhea (Rhea americana, right), which is a large flightless bird native to Argentina, to that of an equivalent-sized theropod dinosaur track (right). Both tracks have three forward-facing digits ending with sharp clawmarks and are longer than wide. Scale = 15 cm (6 in). The dinosaur track is a replica of an Early Jurassic theropod (from about 200 million years ago) from the western U.S. Photograph of the rhea track is by Anthony Martin, and of the dinosaur-track replica is by Ty Butler of Tylight™. Scale in the photo to the left = 15 cm (6 in).

Thus while writing the research paper on the dinosaur tracks, I kept in mind the comparison between sandhill-crane footprints in Georgia and the Australian dinosaur tracks. I also recalled how paleontologists had previously measured theropod skeletons – feet and rear limbs, specifically – and proposed a relationship between foot length and probable hip height.

Based on these studies, you can take a theropod track, multiply it by 4.0, and you get the approximate hip height of its trackmaker. When I applied this calculation to the Australian tracks, their hip heights ranged from about 25 to 60 centimeters (10-23 inches). The smallest of these dinosaurs I imagined as chicken-sized; perhaps these were juveniles of the larger ones. But what might be living today that would compare to the largest of the trackmakers? Immediately I thought of herons, but then it struck me that sandhill cranes provided a more apt analogy.

So I think you know where this is going. Adult sandhill-crane tracks are about 12 centimeters (4.7 inches) long, so if you apply the same formula for theropod-dinosaur tracks to them, their hip heights should be 48 centimeters (19 inches). Would this relationship also hold up on a modern dinosaur, such as a sandhill crane?

Just to satisfy my curiosity, I wrote to Jen Hilburn (St. Catherines Island) and asked her to do me a little favor: could she measure the hip height of a living, adult sandhill crane for me? Fortunately, Jen carried out my unusual request (she said it was not easy, so I definitely owe her), and she wrote back with an answer: 58 centimeters (22 inches). This wasn’t a perfect fit with regard to the footprint formula, but it certainly worked for the size of the Australian dinosaurs I had in mind as trackmakers. Based on my study of the Australian tracks, they were made by small ornithomimids, which likewise made thin-toed tridactyl tracks.

After thanking Jen, I delighted in explaining how her measurement of a Georgia-island-dwelling sandhill crane related to a dinosaur-track discovery on the other side of the world. Furthermore, in the Emory University press release that accompanied the publication of the dinosaur-track discovery in August 2011, the reporter (Carol Clark) used my analogy of the trackmakers as “…theropods ranging in size from a chicken to a large crane.”

Sandhill crane walking down a sand pile next to a fresh-water pond and maritime forest on St. Catherines Island, Georgia, and leaving lovely tracks for an ichnologist to study and keep in mind while tracking non-avian theropod dinosaurs.

Artist conception of Struthiomimus, a Late Cretaceous non-avian theropod dinosaur from western North America. Although not a perfect fit, the tracks of cranes and other similarly sized birds can be compared to those of ornithomimid dinosaurs to better discern the presence and behaviors of these dinosaurs. Artwork by Nobu Tamura and from Wikipedia Commons.

What other modern traces from the Georgia coast will contribute to our better understanding the fossil record? Time will tell, and I hope some day to again share those thoughts at my former home – the Department of Geology at the University of Georgia – with friends, students, and colleagues, new and old.

Further Reading

Elbroch, M., and Marks, E. 2001. Bird Tracks and Sign: A Guide to North American Species. Stackpole Books, Mechanicsburg, PA: 456 p.

Forsberg, M. 2005. On Ancient Wings: The Sandhill Cranes of North America. Michael Foreberg Photography: 168 p.

Henderson, D.M. 2003. Footprints, trackways, and hip heights of bipedal dinosaurs: testing hip height predictions with computer models. Ichnos, 10: 99–114.

Johnsgard, P.A. 2011. Sandhill and Whooping Cranes: Ancient Voices over America’s Wetlands. University of Nebraska Press, Lincoln, NB: 184 p.

Lockley, M.G. 1991. Tracking Dinosaurs: A New Look at an Ancient World. Cambridge University Press, Cambridge, UK: 264 p.

Martin, A.J., Anthony J., Rich, T.H., Hall, M., Vickers-Rich, P., and Gonzalo Vazquez-Prokopec. 2011. A polar dinosaur-track assemblage from the Eumeralla Formation (Albian), Victoria, Australia. Alcheringa: An Australiasian Journal of Palaeontology, article online August 9, 2011. DOI: 10.1080/03115518.2011.597564