Showing posts with label ceratopsid. Show all posts
Showing posts with label ceratopsid. Show all posts

Wednesday, 25 March 2015

Tyrannosaurus and Triceratops - friends at last?

Tyrannosaurus and Triceratops, not locked in mortal combat. Something must be wrong.  Cretaceous interspecies adoption concept, mimicking similar behaviours seen in modern mammals and birds, by Chidumebi Browne. Prints are available here.
Is there a more iconic palaeontological scene than Tyrannosaurus facing down Triceratops? The artistic association of these taxa has existed since at least 1906 when the very first, highly influential restoration of Tyrannosaurus (by Charles Knight, of course) pictured these animals alongside each other (Glut 2008). This idea flowed into aspects the first dinosaur movies - The Ghost of Slumber Mountain (1918) and The Lost World (1925) (unsurprisingly, given how much these films are indebted to Knight) - and, by 1928, the year Knight completed the famous Field Museum mural of Tyrannosaurus and Triceratops, their adversarial relationship was truly cemented. Book illustrations, TV shows and films have so perpetually shown encounters between these species that it's difficult to think of a new angle on this scene. At least, that's what I thought until being contacted by Chidumebi Browne, who asked me about working up a second Tyrannosaurus picture for him, this time co-starring Triceratops. Instead of combat however, he wondered about likelihood of a juvenile Triceratops being 'adopted' by the tyrant, as some animals make the headlines for doing so today (see below). Clearly I liked the idea enough to carry out the commission (I try to avoid things I feel are too unreasonable), but is this pure speculation, playing on gaps in our knowledge, or is there something credible to this idea? Could Triceratops and Tyrannosaurus, after more than a century of conflict, learn to be friends?

The literature on animal adoption is vast, with something like 270 species of mammal and bird known to adopt juveniles of their own species (via kidnapping, accidental inheritance or other means - Riedman 1982; Avital et al. 1998). Interspecific adoption is far rarer however, and most records pertain to animals housed in zoos or wildlife park. These adoptions can work both ways: juveniles can 'recruit' surrogate parents as readily as parents adopt surrogate offspring (for instance, the bond between Owen, a young hippo, and Mzee, a century-old giant Aldabran tortoise, seems to mostly reflect efforts of the hippo). There is relatively little documentation of interspecies adoption in wild animals, however. The example everyone knows is the Kenyan lioness Kamunyak, who has become something of a sensation for her habit of adopting young oryx. She adopted at least six calves before she was last sighted in 2004, defending them from others - including predators, humans seeking to intervene, and oyrx mothers - as if they were her own cubs. At least one species of monkey, as well as wading, raptorial and passerine birds have also adopted and reared the juveniles of other species (Izar et al. 2006; Literak and Mraz 2011; Oswald et al. 2013). Brood parasitism - the offloading of parental duties to other species - clearly exploits this behaviour (Riedman 1982), and famously occurs in cuckoos, certain ducks and geese, cowbirds, fish and bees.

The significance and evolutionary purpose of these interspecific relationships remains mysterious in many cases. Of course, the internet is awash with suggestions that these species have become 'friends', typically accompanied by heavily-edited video footage showing two different species at their squeeful snugglywugilinest. If they feature predators engaging in joyful play or nurturing behaviour with usual prey species, all the better. According to those sagest of human beings - internet commenters - these examples of natural harmony show us - spiteful, war-making human beings - to be the real animals. Truly, we are awful.

In the real world, the causes of these relationships are considerably less fluffy. The fact that most interspecies adoptions develop in captivity is not surprising, likely resulting from the close quarters contact between individuals and the deficient of conspecifics. Desires for parents, mates or group behaviours in some animals may be so strong in some species that they become blinded to the clear differences between themselves and the only other individuals they know. It's difficult to know whether these examples provide good models for interspecific adoption in natural circumstances.

Pictured: trouble in the neighbourhood.
The rarity of wild cases of interspecies adoption makes it hard to draw any firm conclusions about its adaptive significance, if it even has any (Izar et al. 2006). Although juvenile animals may receive some benefit from being adopted (especially if the alternative is not having parents at all), most biologists consider interspecific adoption a mistake - 'misdirected parenting' from confused adults. For some instances of bird adoption, this might reflect the similar appearance of chicks within certain lineages: adults simply can't tell them apart (Oswald et al. 2013). The circumstances surrounding some 'adoptions' are truly bizarre, where adoptees are ex-prey items which have become surrogate offspring. This has certainly happened with sea eagles where, having brought local buzzard chicks back to their own nest, presumably to eat, they started rearing them instead (Literak and Mraz 2011). It is assumed that the appearance of a raptor chick in their nest overrode any feeding impulses of these eagles, and they successfully reared several buzzards in this fashion (Literak and Mraz 2011). The idea that these parenting 'misfires' reflect recognition errors is supported by at least one instance where Caspian terns, rearing Ring-billed gulls, dropped their degree of parenting as juveniles outgrew resemblance to typical tern offspring (Oswald et al. 2013).

It is less easy to explain adoption across taxonomic and ecological boundaries so wide that even passing resemblance is unlikely. It must be said here that peer reviewed literature on these cases is hard to find, at least in my experience, so much of what is reported online is found in documentaries and news stories - not the most ideal venues for discussing complex, unusual animal behaviour (this is not a sleight against the experts featured in such outlets, just that these things are highly-edited and narrative-hungry, which often leads to embellishment and distortion of facts). As an example of how highly selective these reports can be, some stories of lions 'adopting' prey animals result from 45 minutes of observation, receiving justified scepticism from biologists. 45 minutes of coexistence does not equal a clear case of adoption, especially in species renowned for toying with easily overpowered prey.

Where these cases carry more reliability - such as the widely verified case of Kamunyak and her oryx calves - behavioural factors remain unclear. It seems unlikely that a lioness would visually confuse an oryx calf was her own, except for the possibility that her eyesight was very poor. I see explanations that possible recent, traumatic loss of her (genetic) offspring as premature on the available evidence, most likely spurred on by a desire to project human values into a simplified narrative. The fact that Kamunyak ended up eating the starved carcass of one of her adoptees, and became a serial adoptee suggests her condition might be more complex and deeper-seated than a response to one recent event. Moreover, if cub death is the catalyst for this behaviour, would it not be more common in other lions? As far as I'm aware, cub death is a pretty frequent occurrence. It also strikes me that lots of medical conditions - head trauma, brain tumours, organ malfunction leading to hormone imbalances, even certain diseases - can drastically alter animal behaviour. As far as I'm aware, no assessment of Kamunyak's health was made before she disappeared. I wonder if an illness of some kind is a more parsimonious explanation of Kamunyak's condition than complex, psychological trauma.

Let's bring all this back to Chidumebi's concept: could extinct dinosaurs have engaged in inter-species adoption, especially species as different as Triceratops and Tyrannosaurus? We certainly know that modern animals can establish these weird relationships even between animals as different as large predators and tiny prey. We also know that dinosaurs are capable of inter-species adoption, because modern birds engage in this behaviour. On these analogies, a Tyrannosaurus adopting a Triceratops is not too far fetched. We might assume that their morphological distinctions are so great that the tyrant is not misidentifying the ceratopsid for offspring of its own, and thus must be a 'behaviourally abnormal' tyrannosaur: a Cretaceous Kamunyak, if you like. The background tyrants are meant to be behaviourally 'normal', and have sighted the Triceratops calf - I expect, as is reported for many of Kamunyak's adoptions, that the Triceratops infant would not last long.

So... is this the first picture of an obviously slightly unhinged tyrannosaur?
This exercise is hampered ultimately by a lack of knowledge about the parentage of fossil dinosaurs however, and particularly that of tyrannosaurs. Despite the relative wealth of knowledge on tyrant dinosaur palaeobiology (they are extremely well studied compared to other fossil groups), we still know very little, if anything, about tyrannosaur parental behaviour. Parenting is so varied among reptiles and birds that even phylogenetic brackets are of questionable use here. Strong parental instincts seem like a prerequisite for interspecific adoption, and the evidence is equivocal for such instincts in Tyrannosaurus. Until we know more about this, the likelihood of the scene above remains questionable. Of course, that doesn't mean the image composition is without merit: there are scenarios where predators and baby prey individuals coexist peacefully, such as when adult prey animals have run off and juveniles, being slower, have hidden instead. Indeed, such scenarios likely explain some hastily dubbed predator-prey 'adoptions' reported in the media. At least that provides a partial answer to our question, then: could Tyrannosaurus and baby Triceratops get along? Probably - at least until the former got hungry.

References

  • Avital, E., Jablonka, E., & Lachmann, M. (1998). Adopting adoption. Animal Behaviour, 55(6), 1451-1459.
  • Glut, D. (2008). Tyrannosaurus rex: a century of celebrity. In: Larson, P. and Carpenter, K. (eds) Tyrannosaurus rex, the tyrant king. Indiana University Press. 398-427
  • Izar, P., Verderane, M. P., Visalberghi, E., Ottoni, E. B., Gomes De Oliveira, M., Shirley, J., & Fragaszy, D. (2006). Cross‐genus adoption of a marmoset (Callithrix jacchus) by wild capuchin monkeys (Cebus libidinosus): case report. American Journal of Primatology, 68(7), 692-700.
  • Literak I, & Mraz J. (2011). Adoptions of young Common Buzzards in White-tailed Sea Eagle nests. The Wilson Journal of Ornithology 123(1), 174-176.
  • Oswald, S. A., Wails, C. N., Morey, B. E., & Arnold, J. M. (2013). Caspian Terns (Hydroprogne caspia) Fledge a Ring-billed Gull (Larus delawarensis) Chick: Successful Waterbird Adoption Across Taxonomic Families. Waterbirds, 36(3), 385-389.
  • Riedman, M. L. (1982). The evolution of alloparental care and adoption in mammals and birds. Quarterly Review of Biology, 405-435.

Friday, 7 November 2014

Prints, custom palaeoart, and antisocial Triceratops

Hey now - look at this: there's a way to buy high-quality prints of my artwork, and it's dead simple. Drop me an email at wittonprints@gmail.com with your requirements, pay off the invoice, and wait for your prints to arrive - hopefully within a week or so of order confirmation. Prices, sizes and all are discussed over here. Added 02/2015: visit my print store!

To celebrate this occasion, I'm also offering a limited number of über-cheap palaeoart commissions for private clients:


Yep - your own palaeoartwork, a print and delivery for just £100, which is a stupidly cheap price for original artwork. Full details (including a few important conditions) are here (edit 02/2015: not any more!). As you may expect, I can't sustain working at that price for long. For that reason, there's only five of these deals being offered, and at time of writing, three of these deals have been taken. If you want in, don't delay. Don't despair if you miss this deal but would still like your own commission: drop me a line and we might be able to work something out.

Finally, because things have been a bit quiet about here for the last month or so, here's something to fill the void: a monochrome bristly Triceratops horridus, the dromaeosaur Acheroraptor temertyorum, and an interaction inspired by the wise, yellow philosophy of The Simpsons.

"...and like people, some [animals] are just jerks."

Apologies for yet another short post. Coming soon (when I'm allowed to publish them): Mammaliaformes! Heaps of pterosaurs! Deinonychus! Diminutive tyrannosaurines! And perhaps other subjects too!

Thursday, 10 January 2013

Skin-deep: the 'One Skin Fits All' approach to integument reconstruction in palaeoart

The snowy, chilly plains of Maastrichtian Alaska, where Pachyrhinosaurus perotorum roamed. But were they scaly like other ceratopsids, or covered in protofeathers, as shown here?
So... no pressure here, then. I innocently replaced my festive Facebook profile picture with some detail from the painting above last Sunday (07/01/13) and quickly found a storm (well, gusty conditions) of discussion, 'likings' and shares, with several folks mentioning their anticipation of this post to see what all the fuss is about. The Facebook responses have been interesting and mixed: nods of approval, some head-slapping 'why didn't I think of that', a revelation that Tom Hopp already did this last year and, perhaps more predictably, scepticism from a number of individuals who consider the whole concept very silly indeed. In short, there seems to be a certain amount of expectation in the air about this image, and I wouldn't be surprised if some virtual beer bottles are hurled at me across the Internet should this explanation not prove convincing. Here's hoping I've done my homework properly, then.

The painting in question shows a family of the Alaskan centrosaurine Pachyrhinosaurus perotorum, a species notable for its existence in rather chilly, latest Cretaceous climates at palaeolatitudes of 80-90°. It differs from other pictures of this species by having its Muskox Quotient upped by 500%, replacing the scaly hides of more traditional Pachyrhinosaurus reconstructions with a blanket of fuzz analogous to the fuzzy, unkempt feathers of modern ratites. Fuzzy polar dinosaurs are not unusual in palaeoart nowadays and they result in animals that look immediately more at home in icy, subfreezing climates than their scaly brethren. This image, however, directly contradicts what most folks will say we know about horned dinosaur integument. Some comments on Facebook have already wheeled this argument out: known ceratopsian integuments were predominately scaly, so the concept of a shaggy pachyrhinosaur is nonsense, right? Well, I'm going to argue here that it's not, or at least not a concept that is easily dismissed. Before we go any further, it's worth stressing that I'm not presenting this image as the new 'standard' for Pachyrhinosaurus perotorum: I don't know of any new evidence that confirms the shaggy hides shown here, be it soft-tissue remains of ceratopsids or a new interpretation of dinosaur evolution that suggests super-fuzzy ornithischians were common. Nor, for that matter, do I have the heads up on research indicating that latest Cretaceous Alaskan palaeoclimates were much lower than expected. Instead, across four points, I'm going to argue that, based on what we know of dinosaur evolution, the responses of modern animals to their environments, and - importantly - the vast gulf of unknown data regarding dinosaur appearance, that this concept is as plausible as our scaly variants and, in some respects, may be more plausible. On the way, I'm going to suggest that, as with some other considerations in palaeoart, we may be too conservative when it comes to depicting animal integuments, because we focus too much on their evolutionary relationships without considering their likely adaptations to habitats and lifestyles. Hmm... this is all starting to sound very All Yesterdays, isn't it? That's not a coincidence.

1) Ornithischians were fuzzy, and some were probably fuzzier than others.
First up, the least controversial pin in this case. Thanks to Tianyulong and the early ceratopsian Psittacosaurus, we know that ornithischians were covered in more than just scales, the former being covered in filamentous structures akin to early feathers and the latter possessing long quills (Mayr et al. 2002; Zheng et al. 2009) Accordingly, it's now fairly fashionable, and by no means unreasonable, to restore even large ceratopsids with at least a smattering of quills across their bodies like those seen on Psittacosaurus, reflecting a relict integument from an earlier phase of their evolutionary history. It naturally follows that we should expect some taxa to have been more densely adorned with filaments and quills than others, just as fur and feathers are of variable densities in modern species. Accordingly, while a shaggy pachyrhinosaur is certainly at the 'extreme' end of our predictions for an ornithischian integument, it does not directly contradict anything we know regarding dinosaur evolution. Ceratopsids probably had the appropriate genetic blueprints to produce a shaggy animal, so long as the right conditions promoted its expression. There is a question of how appropriate it is to cover a ceratopsid in shaggy integumentary structures however, in light of preserved skin impressions of other ceratopsids. How likely is it that any horned dinosaurs were fuzzy?


Fossil integument of Chasmosaurus belli. From Sternberg 1925.
2) Is the extrapolation of preserved integuments to other species that reliable, really?
Skin impressions and the remains of other integumentary structures are Holy Grails to palaeoartists, and we use them extensively in restoring extinct animals. Through phylogenetic bracketing, or use of their basic phylogenetic proxy when less data is available, we stretch these remains over entire clades so that the known integument of one species becomes the norm for an entire group - what I'll call 'One Skin Fits All' approach. Thus, because we have scaly skin impressions for three ceratopsids - Centrosaurus, Triceratops and Chasmosaurus (see image, above, of the latter. From Sternberg 1925), it's assumed that scales were common to the entire clade. There's nothing necessarily wrong with this assessment and, one may argue, it's the most parsimonious way to interpret this data. A stick in the mud, however, is that another dataset, the diversity of integuments in modern animals, suggests that integuments can vary wildly within groups, and that we could be vastly underestimating the integumentary variation in extinct animals.

Consider the different varieties of fluff, fur, feathers, hair, bristles and other fuzzes in a group of modern animals and then think how a future palaeoartist would reconstruct all varieties of that group if they only had access to only one or two examples of integument. Perhaps all reconstructions of bovids would have woolly coats like those of sheep, or, conversely, the sparse, almost naked skin like a water buffalo? We may deck all primates out in the long capes of colobus monkeys, all pigs with boar-like fur, or cover every inch of birds with feathers. We know such approaches are wrong because these groups demonstrably show variation in the distribution, length and structure of their varying integuments, and yet we maintain a One Skin Fits All' approach to fossil clades. We can't even play the 'extremely close relationship card' in this game as the likes of woolly mammoths, and the fuzzy Sumatran and woolly rhinos, show vastly different integuments to their closest, naked relatives.

One could counter this point by arguing that the relative abundance of scaly remains in certain dinosaur lineages suggest that most, if not all members of that clan were scaly. Perhaps, but we should consider both the sample sizes here and the taphonomic window through which fossils are passed to the modern day. We have, at best, skin impressions from a handful of species compared to the group diversity, so statistical support for the 'One Skin Fits All' approach is low. Moreover, which types of skin are more likely to be preserved? Taphonomic observations on modern animals suggest that fur and feathers are easily removed from carcasses by biological or physical processes, so their preservation potential in ancient animals is low outside of fossil Lagerstätten. Is it a coincidence that the only skin impressions we find outside of Lagerstätten are scaly, leathery hides? I don't have the answer to that question, but it's worth chewing over.

With all this in mind, I wonder if applying the fossil integuments of one species to all its relatives, even close ones, is a questionable practise. I'm not saying that skin impressions are useless and that we should pay them no attention, but we should remember that they only highlight possibilities and perhaps some degree of probability for integumentary structures in a related species. They may well also have no bearing whatsoever on the appearance of their relatives. We're dealing with a great amount of unknown data when reconstructing ancient integuments, and we know how complex this issue is through modern species. When applying this thought to horned dinosaurs, we can say that the scaly skin impressions we have for a few species demonstrate that some bore scales, but we cannot rule out the possibility that others were covered in entirely different structures, like the quills and fuzz that seem deeply rooted in dinosaur ancestry. It does seem likely that many centrosaurines heads, including Pachyrhinosaurus, bore heavily keratinised scales and pads (Hieronymus et al. 2009), but, of course, this doesn't tell us much about the rest of the body. The majority of skin in Pachyrhinosaurus could be scaly, fuzzy, or anywhere inbetween. Without skin impressions to directly tell us the integument of specific species, there's no way to be sure. We need to be careful that we do not afflict ourselves with palaeoartistic phyloblindness here, by only considering these animals as denizens of cladograms and evolutionary hypotheses. Phylogenies may tell us what is possible for integument reconstructions, but other factors may help us decide is more probable.

3) Phylogeny is far from the only factor controlling integument, and can be readily overruled
It's funny to think that, for all the time we spend looking at the phylogenies of extinct animals, we're often missing much about the raw power that drove their evolution: adaptation. This is probably because we're lacking so much anatomical detail in their fossils that their responses to even broad environmental changes are largely undetectable, so understanding why they change through time is not always as certain as how. Nevertheless, we can be sure that different environments drove modification to the anatomy of extinct lineages on small and large scales, and integuments were likely to be one of the most affected tissues. Animal integuments are critical interfaces between body and environment, and have to be appropriately adapted for given habitats. This is a readily observable phenomenon in modern animals, because their integuments reflect all sorts of environmental factors including sun exposure, temperature, local vegetation types, water availability, parasite prevalence, and their local predators. Presumably, this is why such variation in integument exists in even closely related species. But we frequently reconstruct fossil species as if they all live in the same place. Sedimentological and isotope data reveals that closely related ancient species sometimes lived in starkly contrasting settings, but because we frequently take the 'One Skin Fits All' approach, our animals look very similar, irrespective of the requirements of their habitats.

Hot Fuzz: a reference to the condensing breath of the animal, the controversial concept depicted here, or just an excuse for a bad pun? Whatever: it's an excuse to link to this clip from Hot Fuzz: Best. Granny. Kick. Ever.
Behaviour may also have an effect on integument. Sun-shy, non-aggressive and cursorial animals may well bear thinner integuments than slower, frequently exposed or bad-tempered species, for instance. Morphology, too, will have an influence, with larger animals having lessened needs for insulation or being capable of carrying heavier, armoured hides. These are all things palaeoartists should be considering when reconstructing extinct animals: they should look adapted to the lifestyles we predict for them, rather than being based on phylogenetic hypotheses alone. Perhaps some desert-living dinosaurs had elephant-like, deeply wrinkled skin to help heat dissipation, while smaller desert-dwellers had extremely short feathers, or none at all, to prevent overheating. Maybe large theropods had heavy scales on their faces to defend themselves during bouts of head biting. We don't know for sure, but we can be certain that these species had to be appropriately adapted for wherever and however they lived. In short, we need to be wary reconstructing our ancient species by cladogram alone, and realise that integuments, and soft-tissue anatomies in general, should reflect a combination of phylogenetic data and possible adaptations to habitats and lifestyles. This, undoubtedly, involves some of the 'informed speculation' that has been discussed so much with All Yesterdays, but the results are more consistent with our knowledge of modern animals and evolution generally, and arguably producing a more convincing look into the ancient world ('convincing' is the right word here: I'm not sure we're ever going to get 'accurate' results in this game). In fact, after mulling this over for some time, I find the typical and conservative, 'One Skin Fits All' approach much harder to defend than the more open minded, environmentally-influenced reconstructions argued for here.

Bringing this back to our fuzzy pachyrhinosaurs, we again have to question the how applicable the currently available ceratopsid skin impressions are to this Alaskan species. The scaly hides of Chasmosaurus, Centrosaurus and Triceratops represent animals living in more southerly regions than Pachyrhinosaurus, which were at least temperate to subtropical in climate. The former two taxa also lived somewhat before Pachyrhinosaurus, when global temperatures were, on average, a little warmer. These sub-arctic coastal plains encountered by Pachyrhinosaurus perotorum, by contrast, were much cooler, and sometimes genuinely cold. Accordingly, the selection pressures on integument may have been very different for P. perotorum compared to these warm-climate ceratopsids, and we have to wonder how suitable the skin impressions of Chasmosaurus et al. are for reconstructions of Pachyrhinosaurus. We wouldn't, after all, expect the integument of a yak to resemble that of a African buffalo, or consider the fur of a lithe gazelle a suitable model for mountain goat fur. With this philosophy in mind, the question of shaggy pachyrhinosaurs shifts focus from arguments about the cladograms and the skin impressions of their relatives, and on to whether or not Late Cretaceous Alaska was cold enough to promote the development of an extreme integument adaptation in a large dinosaur species.

4) Late Cretaceous Alaska: a struggle for any tourist board
Although nowhere near as bleak as our modern Alaska, the dinosaur faunas inhabiting the northern reaches of latest Cretaceous Alaska would have experienced fairly grim weather for much of the time, perhaps akin to that experienced by modern animals living on the northwest coast of Canada or the more depressing parts of Scotland. In a recent review based on palaeobotanical data from the Cretaceous Arctic, Spicer and Herman (2010) suggested that uppermost Cretaceous Alaska experienced mean average temperatures around 6°C, with summer months attaining a comfortable 14.5°C, but winter months dropping to an average of -2°C. The Pachyrhinosaurus perotorum-bearing Prince Creek Formation may have been a little cooler than other parts of the Late Cretaceous arctic circle, with a mean average temperature between 2.5-5°C. Winter lasts a long time at 80-90° latitude, with 5 of darkness bracketed by 2 months of twilight. A permanent cloud cap over the Late Cretaceous Arctic (detected by the oversize nature of the fossil plant leaves from Cretaceous Alaskan localities) acted as a atmospheric blanket for the region, prohibiting temperatures from plummeting below freezing low for long period. The lowest temperatures - perhaps -10°C - may not have lasted more than a few weeks. Evidence for deep freezes is absent however, with neither the sedimentological or palaeobotanical record indicating nothing more severe than week-long frosts and light freezes. Despite this, rain and snow were probably common, with relative humidity averaging about 80% and even the driest months of the year experiencing over 180 mm of rain. The collective three wettest months, by contrast, collected almost 800 mm. (To put this in perspective, rain-soaked England has an average annual rainfall of 854 mm, according to the UK Met Office [via Wikipedia]). Such a climate was capable of supporting a rich array of plantlife, and evergreen taiga-like forests were common, as were swamps, rivers and other bodies of water. Such conditions seem fairly common right the way through Late Cretaceous Alaska, with conditions a full 8° south of the Prince Creek Formation seeming similarly cold and wet. I should add that this consideration of ancient Alaska  isn't particularly controversial, the palaeobotanical data mentioned here matching palaeoclimate models based on isotope records, animal distribution and sedimentology.

So the Prince Creek palaeoenviroment wasn't exactly an ideal holiday spot, but was it 'extreme' enough to promote the evolution of an fuzzy coat in a 1.5-2 tonne dinosaur species? Given the dense furs we see in large mammals found in similar climates, I think it's certainly a possibility. It would certainly be far weirder if polar dinosaurs of the Late Cretaceous didn't respond to their climate somehow, and a thick coat of protofeathers is one possible adaptation to their cool, wet habitat. A layer of insulating fat would be another (cue an image of some tubby pachyrhinosaurs). Of course, the picture may be different if these animals hibernated or migrated in and out of Alaska annually, enjoying the brief mild period before heading south to escape the winter. The latter is perhaps the most widely discussed concept, but direct evidence for such migrations in Alaskan dinosaurs is as sparse as evidence for their fluffy integuments or fat layers. In the concept proposed here, the protofeather coat may have acted as an insulator against the cold, prevented wind, rain and snow from hitting the naked skin of the animal, or both. The latter function would benefit from the coat being thick and fluffy, but this may not have lead to overheating even in a big animal like Pachyrhinosaurus: the ragged, loose coats of hot-climate adapted ratites appear similarly thick and massive without overheating their owners. Perhaps the concept of shaggy coats in these Alaskan dinosaurs doesn't seem so as implausible as it may first appear, then.

To bring this more-mammoth-than-intended essay to a close, then, I again stress that I'm not saying 'this is what Pachyrhinosaurus looked like!', but attempting to present it as a product of both its phylogenetic history, its environment and habits, and not simply reconstructed via a cladogram. I think there's a lot of scope for these sorts of palaeoartistic renditions, even it does mean more reliance on the 'informed speculation' principle of All Yesterdays. Of course, this whole argument flows back to the core idea behind the All Yesterdays movement: the conservative, 'One Skin Fits All' approach to integument reconstruction is just as likely to be wrong as our more speculative concepts, but at least the use of informed speculation lines the reconstruction up with our knowledge of modern animal diversity.

References
  • Hieronymus, T. L., Witmer, L. M., Tanke, D. H. and Currie, P. J. 2009. The facial integument of centrosaurine ceratopsids: morphological and histological correlates of novel skin structures. Anatomical Record, 292, 1370–1396.
  • Mayr, G., Peters, D. S., Plodowski, G. and Vogel, O. 2002. Bristle-like integumentary structures at the tail of the horned dinosaur Psittacosaurus. Naturwissenschaften 89, 361–365.
  • Spicer, R. A. and Herman, A. B. 2010. The Late Cretaceous environment of the Arctic: A quantitative reassessment based on plant fossils. Palaeogeography, Palaeoclimatology, Palaeoecology, 295, 423–442.
  • Sternberg, C. 1925. Integument of Chasmosaurus belli. The Canadian Field-Naturalist, 39, 108-1 10.
  • Zheng, X., You, H., Xu, X. and Dong, Z. 2009. An Early Cretaceous heterodontosaurid dinosaur with filamentous integumentary structures. Nature, 458, 333–336.