The Crystal Palace Prehistoric Park is one of the most spectacular and historically significant pieces of palaeoart in the world. Unveiled in 1854, it features more than 30 models of over 20 extinct species captured in concrete, brick and steel. Each model was crafted by a team of sculptors lead by the zoological artist Benjamin Waterhouse Hawkins under the guidance of Britain's preeminent Victorian naturalist, Sir Richard Owen. The Crystal Palace depictions are often overlooked or dismissed in coverage of early palaeontological history, which is entirely unfair. The scale, ambition and success of the project made it a milestone in not only palaeontological outreach but scientific communication in general, and they had a clear impact on future depictions of fossil animals, both scientifically and educationally (Rudwick 1992; McCarthy and Gilbert 1994; Secord 2004). Most of the models still survive today thanks to ongoing work by conservators and the Friends of Crystal Palace Dinosaurs charity, and a trip to Crystal Palace Park is thoroughly recommended if you're a fan of palaeoart or the history of science. The models are National Heritage Grade 1 Listed Monuments but, on account of their age, exposure to weather and vandalism, they are in continuous need of repair. Phases of renovation have been carried out since at least the 1950s (McCarthy and Gilbert 1994) and are ongoing today. Such work is expensive (conservation began in 2015 is expected to cost £1.2 million when completed) so please consider supporting the Friends of Crystal Palace Dinosaurs if you can. The FOCPD also appreciate volunteers to maintain the landscape around the models, which is a great way to visit them up close - keep an eye on their website for opportunities.
Part of the enduring appeal of the Crystal Palace sculptures is the mysteries of their construction. While the generalities of the project are well documented (e.g. Rudwick 1992; Doyle and Robinson 1993; McCarthy and Gilbert 1994; Secord 2004, also see this FOCPD summary), few documents are known specifying how the sculptures were built, and the scientific rationale behind them. Some details of their construction can be deduced by examination of the models themselves, and both Hawkins and Owen put their general scientific approach on record (Owen (1854) in particular reads like a modern summary of palaeoart practises), but it remains difficult to ascertain exactly how Hawkins decided on the form of each species. Adding depth to the mystery are suggestions that Owen's contributions may have not have been as substantial as generally assumed, and that his expertise was only sought as the designs approached their final phase and full-size construction was set to begin - too late, perhaps, for major revisions to Hawkins' drafts (Secord 2004). Moreover, while Hawkins' attention to Owen's work is clear, he also evidently relied on other sources of information and his own intuition on many occassions. This may explain why Owen sometimes distanced himself from aspects of the models in a 1854 guidebook to the models, as well as in newspaper interviews (Secord 2004). Nevertheless, documents authored by both Owen and Hawkins suggest mutual respect and admiration for one another (Owen 1854; Hawkins 1854), although it's interesting that each eventually claimed to be the greater intellectual influence on the project (Secord 2004).
for their website. As part of that process, I've been providing notes on how accurate the models are to current science as well as against fossil data available to Hawkins in the early 1850s. This has proven fascinating, confirming Hawkins' talents and insight while also raising several questions about his process and palaeoart philosophy. We may never know Hawkins' thought process in detail, but we might be able to 'reverse engineer' his models back to specimens known pre-1854 and, through clues worked into his models, establish what science, artworks and extant species influenced his designs. Over the next three posts, I thought it would be of interest to share some of these thoughts, as well as my modern takes on the Crystal Palace species. Edited versions of these notes also appear at the Friends of Crystal Palace Website, and more will follow in the near future as we wrap up this project up. I'm going to tackle the sculptures more or less as they appear in the park as you walk from the geologically oldest models (the Dicynodon) to the youngest (Megaloceros).
Dicynodon
The Crystal Palace Dicynodon are famously turtle-like in form, a circumstance reflecting Dicynodon being almost entirely represented by cranial material in the 1850s. These skulls demonstrated the basic shape of the skull and their strange turtle-meets-walrus nature but, as noted by Owen (1854), the rest of the sculptures are purely conjectural. Owen regarded dicynodonts as amphibious (Owen 1845, 1854) and Hawkins seems to have ran with this concept, presumably also inspired by the turtle-like features of the skull. Details of the sculptures' feet show that Hawkins was probably modelling these creatures on more terrestrially-adept turtles, and I wonder if the three ridged, sculpted keels, developed claws and long, scute-lined tails specifically indicate influence from snapping turtles. As we'll see, Hawkins often took inspiration, and entire anatomies, from living species in his work.
“Labyrinthodon”
A trio of "Labyrinthodon", photographed in 2013. There are two species here, the larger being "L. salamandroides", the smaller "L. pachygnathus". Note the palatal teeth in the right animal and the similarity between L. salamandroides and an Owen sketch of Labyrinthodon as the Chirotherium trackmaker. |
Depicted as giant frog-like creatures, Hawkins’ sculptures show close attention to illustrations of “Labyrinthodon” as interpreted by Owen (e.g. Owen 1841a, 1842; also see Benton and Gower 1997) and capture some details of the skull and tooth material then referred to this genus. Particularly notable are the palatal teeth - this excellent attention to anatomical detail, especially given that visitors have to be right next to the sculptures (or looking with binoculars) to see them. Their mix of smooth and warty skin is surely based on living amphibians, and serves to distinguish the models of “L. pachygnathus” (smaller, warty-skinned) from “L. salamandroides” (the larger, smooth-skinned model) (McCarthy and Gilbert 1994). Owen famously linked "Labyrinthodon" with trackways now referred to pseudosuchians, but in doing so rationalised and illustrated the trackmaker as making prints with opposite limb sets, so the left prints were made with the right feet, and vice versa. This detail is absent from Hawkins’ models, despite his general attention to Owenian ideas. Perhaps even he struggled to make this bizarre hypothesis a reality.
Modern takes on “Labyrinthodon” are very different to the creatures displayed at Crystal Palace. What Owen and Hawkins considered “Labyrinthodon” is now rightfully called Mastodonsaurus, the former name being Owen’s attempt to replace Mastodonsaurus with a title he thought better suited the animal (Owen 1841a). Of the depicted species, “L. salamandroides” has been subsumed into M. jageri, and the fossils referred to “L. pachygnathus” are a mix of mastodonsauroids and archosaurian remains (Benton and Gower 1997; Damiani 2001). The latter point vindicates Hawkins' now archaic-looking approach to restoring Mastodonsaurus. The idea of a sheep-sized prehistoric frog seems outlandish in the 21st century, it was an entirely sensible interpretation of Owen's take on the available fossil material, from the proportions of the body to the upright limbs. I find the capturing of the "L. pachygnathus" jawline and dentition especially commendable.
Hawkins older illustrations and draft Labyrinthodon model (which was presumably shown to Owen) also show flatter heads. Do the fleshy-faced, side-eyed Crystal Palace amphibians reflect Hawkins paying more attention to frogs than Mastodonsaurus fossils? It may, as there are several other examples of Hawkins' models overriding fossil data with extant animal form, as we'll see throughout this review. Alternatively, were they errors? A misguided revision suggested by Owen or someone else? Was Hawkins simply following the illustrations of others, such as that presented in Owen's (1854) guide? Whatever the cause, this is a clear example of Hawkins not using fossil data where he could have done, in contrast to his sometimes exacting reproductions of anatomy in other areas.
Ichthyosaurs
In terms of scientific credibility, Hawkins’ three ichthyosaur statues have probably held up best of all his non-mammalian sculptures. This undoubtedly pertains to ichthyosaur skeletons being entirely known from very early in palaeontological history, as well as their familiar whale- or fish-like form. I consider them a good measure of Hawkins’ skill as a palaeoartist because it puts him on a more equal footing with modern practitioners, and suggests that when he had comprehensive datasets and suitable modern analogues he was able to produce very reasonable interpretations of fossil forms. It was largely a lack of information, not poor knowledge of anatomy and zoology, that lead to the inexactitude of the Crystal Palace models. There are three species of ichthyosaur on display, each distinguished by size and proportions, and once all considered different taxa of Ichthyosaurus. In modern parlance, they are Ichthyosaurus communis (the mid-sized ichthyosaur model), Temnodontosaurus platydon (the largest) and Leptonectes tenuirostris (smallest).An unusual property of the Crystal Palace models is the skin on their flippers, which has a very obvious scaly appearance. This reflects the Owenian hypothesis that the bones of the flippers were somehow reflected in the overlying skin scales (Owen 1841b), which Hawkins faithfully reproduced on his models. This seems unlikely given what we now know of fossilised ichthyosaur skin and the relationships between bone texture and skin anatomy. Hawkins was not solely guided by fossils in his restorations however, with details of the ichthyosaur faces reflecting whales and dolphins. This is particularly evidenced by the dolphin-like grooves and lips along their jaws, and seems entirely reasonable given what we know of ichthyosaurian skulls and the relationship between jaw bone surfaces and facial features.
A modern restoration of Temnodontosaurus eurycephalus (the larger, strand-feeding species) and Ichthyosaurus breviceps (the prey animals). In many ways, not so different from Hawkins' take. |
Plesiosaurians
Complete plesiosaurian skeletons allowed Hawkins to reconstruct them in a generally credible light, though the results were not as precedent as his takes on ichthyosaurs. To be fair, plesiosaurians are not as intuitive to reconstruct as ichthyosaurs and many aspects of their anatomy and functionality are debated even today. Making three-dimensional plesiosaurian sculptures just decades after their fossils were found was no mean feat, and Hawkins' models no less credible than other mid-19th century takes on these animals. Three models were created and, though similar, they have varying proportions and sizes on account of representing three species. Today, we classify these as Plesiosaurus dolichodeirus, “Plesiosaurus” macrocephalus, and Thalassiodracon hawkinsi.There are several major differences between Hawkinsian plesiosaurians and our modern takes. The most obvious of these is their thin, highly flexed necks, which recall those of long-necked birds or snakes even down the obvious neck/skull junction. It is highly unlikely that plesiosaurians could bend their necks as depicted at Crystal Palace, nor do their neck vertebrae imply a light covering of musculature (Noè et al. 2017). Today, we assume plesiosaurians were capable of a reasonable degree of neck flexion, but perhaps only to the extent of forming broad arcs, not multiple tight curves. The Crystal Palace plesiosaurians also have slender, flexible bodies, more like those of lizards (to which they were often compared in early palaeontological literature) than their actual stiffened, barrel-shaped torsos. The P. dolichodeirus and Thalassiodracon hawkinsi models are particularly afflicted with this issue, and their long, flexible tails accentuate their lithe forms further. We can perhaps rationalise this by the holotypes of these plesiosaurs having relatively narrow torsos (a taphonomic influence is probable in both cases) as well as the prevalent early-19th century idea that plesiosaurians were more closely related to lizards than other marine reptiles ("Plesiosaurus", roughly translated, means "allied to lizards" - Owen 1854). Unbeknown to Hawkins and Owen, we would eventually find soft-tissue outlines of plesiosaurians showing substantial soft-tissue around their tails, perhaps reflecting hindlimb musculature (assuming they anchored some major leg muscles on their tails, as is the case for most reptiles) as well as body-contouring fatty tissues (Frey et al. 2017). Their flippers were also augmented with soft-tissue expansions, something Owen knew about for ichthyosaurs, but would not be apparent for plesiosaurians until the late 19th century.
George Scharf's illustration of "P. macrocepahlus", featured in Owen (1840b). The skull is obviously very large in this species, but Hawkins did not capture this in his model. |
Plesiosaurus dolichodeirus as we know it today: not a million miles off the Crystal Palace reconstruction, but significantly different in several aspects. |
That's all for now, but we'll soon move on to teleosaurids, pterosaurs and - the star attractions: dinosaurs! Remember to check out the Friends of Crystal Palace Dinosaurs website if you haven't already, and please consider getting involved with supporting these fantastic, significant models if you can.
Enjoy monthly insights into palaeoart, fossil animal biology and occasional reviews of palaeo media? Support this blog for $1 a month and get free stuff!
This blog is sponsored through Patreon, the site where you can help online content creators make a living. If you enjoy my content, please consider donating $1 a month to help fund my work. $1 might seem a meaningless amount, but if every reader pitched that amount I could work on these articles and their artwork full time. In return, you'll get access to my exclusive Patreon content: regular updates on upcoming books, papers, painting and exhibitions. Plus, you get free stuff - prints, high-quality images for printing, books, competitions - as my way of thanking you for your support. As always, huge thanks to everyone who already sponsors my work!References
- Bajdek, P., Qvarnström, M., Owocki, K., Sulej, T., Sennikov, A. G., Golubev, V. K., & Niedźwiedzki, G. (2016). Microbiota and food residues including possible evidence of pre‐mammalian hair in Upper Permian coprolites from Russia. Lethaia, 49(4), 455-477.
- Benton, M. J., & Gower, D. J. (1997). Richard Owen's giant Triassic frogs: archosaurs from the Middle Triassic of England. Journal of Vertebrate Paleontology, 17(1), 74-88.
- Carpenter, K., Sanders, F., Reed, B., Reed, J., & Larson, P. (2010). Plesiosaur swimming as interpreted from skeletal analysis and experimental results. Transactions of the Kansas Academy of Science, 113(1/2), 1-35.
- Damiani, R. J. (2001). A systematic revision and phylogenetic analysis of Triassic mastodonsauroids (Temnospondyli: Stereospondyli). Zoological Journal of the Linnean Society, 133(4), 379-482.
- Doyle, P., & Robinson, E. (1993). The Victorian ‘Geological Illustrations’ of Crystal Palace Park. Proceedings of the Geologists' Association, 104(3), 181-194.
- Frey, E., Mulder, E. W., Stinnesbeck, W., Rivera-Sylva, H. E., Padilla-Gutiérrez, J. M., & González-González, A. H. (2017). A new polycotylid plesiosaur with extensive soft tissue preservation from the early Late Cretaceous of northeast Mexico. Boletín de la Sociedad Geológica Mexicana, 69(1), 87-134.
- Hawkins, B. W. (1854). On Visual Education as Applied to Geology: Illustrated by Diagrams and Models of the Geological Restorations at the Crystal Palace. W. Trounce
- Kammerer, C. F., Angielczyk, K. D., & Fröbisch, J. (2011). A comprehensive taxonomic revision of Dicynodon (Therapsida, Anomodontia) and its implications for dicynodont phylogeny, biogeography, and biostratigraphy. Journal of Vertebrate Paleontology, 31(sup1), 1-158.
- Lindgren, J., Sjövall, P., Thiel, V., Zheng, W., Ito, S., Wakamatsu, K., ... & Eriksson, M. E. (2018). Soft-tissue evidence for homeothermy and crypsis in a Jurassic ichthyosaur. Nature, 564(7736), 359.
- Liu, S., Smith, A. S., Gu, Y., Tan, J., Liu, C. K., & Turk, G. (2015). Computer simulations imply forelimb-dominated underwater flight in plesiosaurs. PLoS computational biology, 11(12), e1004605.
- McCarthy, S., & Gilbert, M. (1994). The Crystal Palace dinosaurs: The story of the world's first prehistoric sculptures. Crystal Palace Foundation.
- Moser, M., & Schoch, R. (2007). Revision of the type material and nomenclature of Mastodonsaurus giganteus (Jaeger) (Temnospondyli) from the Middle Triassic of Germany. Palaeontology, 50(5), 1245-1266.
- Noè, L. F., Taylor, M. A., & Gómez-Pérez, M. (2017). An integrated approach to understanding the role of the long neck in plesiosaurs. Acta Palaeontologica Polonica, 62(1), 137-162.
- O’Keefe, F. R., & Chiappe, L. M. (2011). Viviparity and K-selected life history in a Mesozoic marine plesiosaur (Reptilia, Sauropterygia). Science, 333(6044), 870-873.
- Owen, R. (1840a). XXXVI.—Note on the Dislocation of the Tail at a certain point observable in the Skeleton of many Ichthyosauri. Transactions of the Geological Society of London, 2(3), 511-514.
- Owen, R. (1840b). XXXVII.—A Description of a Specimen of the Plesiosaurus Macrocephalus, Conybeare, in the Collection of Viscount Cole, MP, DCL, FGS, &c. Transactions of the Geological Society of London, 2(3), 515-535.
- Owen, R. (1841a). On the teeth of species of the genus Labyrinthodon (Mastodonsaurus of Jaeger) common to the German Keuper formation and the lower sandstone of Warwick and Leamington. Transactions of the Geological Society of London, 6, 503-513.
- Owen, R. (1841b). XIX.—A Description of some of the Soft Parts, with the Integument, of the Hind-fin of the Ichthyosaurus, indicating the Shape of the Fin when recent. Transactions of the Geological Society of London, 2(1), 199-201.
- Owen, R. (1842). XXXII.—Description of parts of the Skeleton and Teeth of five species of the Genus Labyrinthodon (Lab. leptognathus, Lab. pachygnathus, and Lab. ventricosus, from the Coton-end and Cubbington Quarries of the Lower Warwick Sandstone; Lab. Jægeri, from Guy’s Cliff, Warwick; and Lab. scutulatus, from Leamington); with remarks on the probable identity of the Cheirotherium with this genus of extinct Batrachians. Transactions of the geological Society of London, 2(2), 515-543.
- Owen, R. (1845). III.—Report on the Reptilian Fossils of South Africa: PART I.—Description of certain Fossil Crania, discovered by AG Bain, Esq., in Sandstone Rocks at the South-eastern extremity of Africa, referable to different species of an Extinct genus of Reptilia (Dicynodon), and indicative of a new Tribe or Sub-order of Sauria. Transactions of the Geological Society of London, 2(1), 59-84.
- Owen, R. (1854). Geology and inhabitants of the ancient world. Crystal palace library.
- Plieninger, T. (1844). Beitra¨ge von Theodor Plieninger. In: von Meyer, H., & Plieninger, T. (eds). Beiträge zur Paläontologie Württemberg's: enthaltend die fossilen wirbelthierreste aus den triasgebilden mit besonderer rücksicht auf die Labyrinthodonten des Keupers. E. Schweizerbart. 51–132.
- Rudwick, M. J. (1992). Scenes from deep time: early pictorial representations of the prehistoric world. University of Chicago Press.
- Secord, J. A. (2004). Monsters at the crystal palace. In: de Chadarevian, S, & Hopwood, N. (eds). Models: the third dimension of science, Stanford University Press. 138-69.
- Witzmann, F. (2009). Comparative histology of sculptured dermal bones in basal tetrapods, and the implications for the soft tissue dermis. Palaeodiversity, 2(233), e270.