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Morphological Innovation and the Evolution of Hadrosaurid Dinosaurs

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Morphological Innovation and the Evolution of Hadrosaurid Dinosaurs Paleobiology, 45(2), 2019, pp. 347–362 DOI: 10.1017/pab.2019.9 Morphological innovation and the evolution of hadrosaurid dinosaurs Thomas L. Stubbs , Michael J. Benton, Armin Elsler , and Albert Prieto-Márquez Abstract.—The hadrosaurids were a successful group of herbivorous dinosaurs. During the Late Cret- aceous, 100 to 66 million years ago, hadrosaurids had high diversity, rapid speciation rates, and wide geo- graphic distribution. Most hadrosaurids were large bodied and had similar postcranial skeletons. However, they show important innovations in the skull, including disparate crests that functioned as socio-sexual display structures, and a complex feeding apparatus, with specialized jaws bearing dental batteries. Little is known about the macroevolutionary processes that produced these evolutionary novel- ties. Here we provide novel perspectives using evolutionary rate and disparity analyses. Our results show that hadrosaurid cranial evolution was complex and dynamic, but their postcranial skeleton and body size were conservative. High cranial disparity was achieved through multiple bursts of phenotypic innovation. We highlight contrasting evolutionary trends within hadrosaurids between the disparate facial skeleton and crests, which both showed multiple high-rate shifts, and the feeding apparatus, which had low vari- ance and high rates on a single phylogenetic branch leading to the diverse Saurolophidae. We reveal that rapid evolutionary rates were important for producing the high disparity of exaggerated crests and present novel evidence that the hadrosaurid diversification was linked to both a key adaptive innovation in the feeding apparatus and multiple bursts of innovation in socio-sexual displays. Thomas L. Stubbs, Michael J. Benton, and Armin Elsler. School of Earth Sciences, University of Bristol, 24 Tyndall Avenue, Bristol BS8 1TQ, U.K. E-mail: [email protected], [email protected], armin.elsler@ bristol.ac.uk Albert Prieto-Márquez.* Field Museum of Natural History, 1400 S. Lake Shore Drive, Chicago, Illinois 60605, U.S.A. *Present address: Institut Català de Paleontologia Miquel Crusafont, Universitat Autònoma de Barcelona, Carrer de l’Escola Industrial 23, 08201 Sabadell, Spain. E-mail: [email protected] Accepted: 3 February 2019 Data available from the Dryad Digital Repository: https://doi.org/10.5061/dryad.0dt2h6c Introduction successful groups (e.g., Brusatte et al. 2014; Evolutionary diversifications are commonly Hopkins and Smith 2015; Close et al. 2015; Ben- associated with adaptive radiations, when son et al. 2018). “key innovations” open new adaptive zones Hadrosauroids were a hugely diverse and linked to ecological opportunities (Simpson abundant clade of herbivorous ornithopod 1953; Schluter 2000; Yoder et al. 2010; Simões dinosaurs (Horner et al. 2004; Prieto-Márquez et al. 2016). However, not all evolutionary 2010a). These megaherbivores were important diversifications are directly linked to new eco- components in the Late Cretaceous (100–66 logical adaptations (Rabosky 2017). For million years ago) ecosystems of Eurasia, Ant- example, speciation, high diversity, and mor- arctica, and the Americas (Prieto-Márquez phological variation may be driven by socio- 2010b). Within hadrosauroids, the clade sexual selective factors (Wagner et al. 2012; Hadrosauridae (hadrosaurids) radiated signifi- Rabosky 2017). The fossil record provides cantly during the latest Cretaceous (Santonian– insights into evolutionary diversifications Maastrichtian) (Fig. 1). Quantitative studies across large spatiotemporal scales in geological show that hadrosaurids had high taxic diver- time (Benton 2015). Methodological advance- sity (Lloyd et al. 2008; Butler et al. 2009) and ments and the availability of large phylogenies notably high speciation rates when compared and morphological data sets allow researchers with other contemporaneous dinosaurian to test patterns and processes of morphological clades (Sakamoto et al. 2016). The postcranial evolution quantitatively, including evolution- skeleton of hadrosaurids was apparently mor- ary rate and disparity dynamics in highly phologically conservative, with a consistent © 2019 The Paleontological Society. All rights reserved. This is an Open Access article, distributed under the terms of the DownloadedCreative from https://www.cambridge.org/core Commons Attribution licence. IP address: (http://creativecommons.org/licenses/by/4.0/), 170.106.203.74, on 05 Oct 2021 at 06:59:50, subject to the which Cambridge permits Core unrestrictedterms of use, available re- at https://www.cambridge.org/core/termsuse, distribution, and reproduction. https://doi.org/10.1017/pab.2019.9 in any medium, provided the original work is properly cited. 0094-8373/19 https://www.cambridge.org/core/terms Downloaded from 348 https://www.cambridge.org/core . https://doi.org/10.1017/pab.2019.9 . IPaddress: THOMAS L. STUBBS ET AL. 170.106.203.74 , on 05 Oct2021 at06:59:50 , subjectto theCambridgeCore termsofuse,available at FIGURE 1. Time-scaled phylogeny of hadrosauroids. The cladogram is a strict consensus tree generated using the four most parsimonious trees from Prieto-Márquez et al. (2016). The thicker lines illustrate the upper and lower bounds of stratigraphic ranges. Major clades are highlighted. The figured skulls are from Equijubus normani, Parasaur- olophus walkeri, Lambeosaurus lambei, Gryposaurus notabilis, and Saurolophus angustirostris (from top to bottom). MORPHOLOGICAL INNOVATION IN HADROSAURID DINOSAURS 349 body plan, and most species were large-bodied 2009; Cuthbertson et al. 2012). The success of (7–14 m in length) (Horner et al. 2004). How- hadrosaurids has been attributed to this unique ever, their cranial and mandibular anatomy feeding apparatus, and previous macroevolu- shows unique and specialized innovations, tionary work on ornithopod dental disparity potentially linked to their success. proposed that, once this complex dental battery Hadrosaurids are famed for their elaborate emerged rapidly in hadrosaurids, there was solid (most species of the subclade Saurolophi- limited further innovation (Strickson et al. nae) and hollow (subclade Lambeosaurinae) cra- 2016). Hadrosaurids therefore present an inter- nial crests (Evans 2010; Prieto-Márquez et al. esting test case for comparing agencies of nat- 2015)(Fig. 1). These exaggerated ornamental ural and socio-sexual selection, namely their structures were formed by extensive modifica- conservative, but highly successful, feeding tions to the nasal and frontal bones in saurolo- apparatus, a classic key innovation, and their phines and the premaxilla and nasal bones in highly variable “nonadaptive” cranial crests. lambeosaurines, and they manifested as an In this study, we present a series of evolu- impressive array of shapes, including tubes, tionary rate and disparity analyses that uncover lobes, fans, and rounded plates. Crests could the patterns and processes of morphological also be formed by soft tissues (Bell et al. 2014). evolution during the diversification of hadro- Hadrosauridcrestsfunctionedprimarilyasvis- sauroids. We address several key questions ual displays (Hopson 1975; Bell et al. 2014; based on our current understanding of hadro- Prieto-Márquez et al. 2015), and in lambeosaur- sauroid morphological evolution. First, how ines the hypertrophied nasal passages inside do evolutionary rate and disparity dynamics the crests may have been used for sound produc- vary between their disparate skulls and seem- tion (Weishampel 1997). The visual and potential ingly conservative postcranial skeletons? Was auditory signals of hadrosaurid crests were likely hadrosaurid cranial disparity achieved through important factors in socio-sexual selection, a single evolutionary burst at one position in potentially being used for mate competition the tree, or through multiple bursts of innov- (Evans 2010; Knell and Sampson 2011;Hone ation? Did the two major hadrosaurid evolu- et al. 2011; Bell et al. 2014). Socio-sexual selection tionary novelties, the disparate cranial crests can lead to a great variety of specialized adapta- and the successful feeding apparatus, evolve tions, with important macroevolutionary conse- in the same way—were both associated with a quences, including higher speciation rates single or multiple evolutionary bursts? Finally, (Panhuis et al. 2001;Knelletal.2013). Crests, as body-size disparity was a key aspect of dino- such as those in hadrosaurids, represent an saurian evolution and a potential factor in important innovation and a source of morpho- niche partitioning (Barrett 2014; Benson et al. logical disparity that is disconnected from trad- 2018), we test whether rates of hadrosauroid itional macroevolutionary “adaptive zones” body-size evolution were homogeneous or a (Simpson 1953), as they have no role in the acqui- potentially important morphological variable. sition of food resources or escape from predators. Our results confirm that hadrosauroid skull Important adaptive innovations are seen evolution was dynamic, while their postcranial in the hadrosaurid feeding apparatus. They skeleton was morphologically conservative. evolved histologically and biomechanically Body-size change is ruled out as an important complex grinding structures made from multi- source of innovation. Importantly, we show toothed dental batteries with complex struc- that the unique hadrosaurid jaw apparatus tures (Erickson et al. 2012). This dentition evolved fast and then stabilized at the root of facilitated crushing and
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