Aging, Maturation and Growth of Sauropodomorph Dinosaurs

Griebeler, E. M., Klein, N., and  P. M. Sander. 2013. Aging, Maturation and Growth of Sauropodomorph Dinosaurs as Deduced from Growth Curves Using Long Bone Histological Data: An Assessment of Methodological Constraints and Solutions. PLoS ONE 8(6): e67012. doi:10.1371/journal.pone.0067012

Abstract - Information on aging, maturation, and growth is important for understanding life histories of organisms. In extinct dinosaurs, such information can be derived from the histological growth record preserved in the mid-shaft cortex of long bones. Here, we construct growth models to estimate ages at death, ages at sexual maturity, ages at which individuals were fully-grown, and maximum growth rates from the growth record preserved in long bones of six sauropod dinosaur individuals (one indeterminate mamenchisaurid, two Apatosaurus sp., two indeterminate diplodocids, and one Camarasaurus sp.) and one basal sauropodomorph dinosaur individual (Plateosaurus engelhardti). Using these estimates, we establish allometries between body mass and each of these traits and compare these to extant taxa. Growth models considered for each dinosaur individual were the von Bertalanffy model, the Gompertz model, and the logistic model (LGM), all of which have inherently fixed inflection points, and the Chapman-Richards model in which the point is not fixed. We use the arithmetic mean of the age at the inflection point and of the age at which 90% of asymptotic mass is reached to assess respectively the age at sexual maturity or the age at onset of reproduction, because unambiguous indicators of maturity in Sauropodomorpha are lacking. According to an AIC-based model selection process, the LGM was the best model for our sauropodomorph sample. Allometries established are consistent with literature data on other Sauropodomorpha. All Sauropodomorpha reached full size within a time span similar to scaled-up modern mammalian megaherbivores and had similar maximum growth rates to scaled-up modern megaherbivores and ratites, but growth rates of Sauropodomorpha were lower than of an average mammal. Sauropodomorph ages at death probably were lower than that of average scaled-up ratites and megaherbivores. Sauropodomorpha were older at maturation than scaled-up ratites and average mammals, but younger than scaled-up megaherbivores.

Osteoderm Microstructure of “Rauisuchian” Archosaurs from South America

Cerda, I. A., J. B. Desojo, T. M. Scheyer and C. L. Schultz. In Press. Osteoderm microstructure of “rauisuchian” archosaurs from South America. Geobios (accepted manuscript) doi: http://dx.doi.org/10.1016/j.geobios.2013.01.004

Abstract - In this contribution we analyze and discuss the microanatomy and histology of postcranial osteoderms of a number of “rauisuchians” from different localities of South America (Argentina and Brazil). The studied sample includes osteoderms of Fasolasuchus tenax, Prestosuchus chiniquensis, Saurosuchus galilei and an undetermined rauisuchian from Brazil. The bone microanatomy of the osteoderms is variable: whereas some specimens have a rather compact structure, others show a diploe architecture with a central cancellous core bordered by two compact cortices. Both external and basal cortices are mainly composed of poorly vascularized, fine and coarse parallel fibred bone and networks of interwoven and mineralized fiber bundles. The internal region of the non-remodeled specimens consists of a well-vascularized core in which the intrinsic fibers exhibit important variations (even in the same specimen), ranging from coarse, parallel-fibred to woven-fibred bone tissues. Lines of arrested growth (LAGs) are well recorded in both basal and external cortices. Differences in the bone microstructure (compact vs. diploe) could be related to the age, sex and reproductive status of the sampled individuals. Hence, age estimation based on the count of LAGs in rauisuchian osteoderms appears to be reliable only in the early stages of ontogeny. The bone microstructure suggests that rauisuchian osteoderms were originated through a mechanism that involves both intramembranous and metaplastic ossifications.

Paleohistological Estimation of Bone Growth Rate in Extinct Archosaurs

Cubo, J., LeRoy, N., Martinez-Maza, C., and L. Montes. 2012. Paleohistological estimation of bone growth rate in extinct archosaurs. Paleobiology 38:335-339. doi: http://dx.doi.org/10.1666/08093.1

Abstract - The clade Archosauria contains two very different sister groups in terms of diversity (number of species) and disparity (phenotypic variation): Crurotarsi (taxa more closely related to crocodiles than to birds) and Ornithodira (pterosaurs and dinosaurs including birds). The extant species of Crurotarsi may constitute a biased sample of past biodiversity regarding growth patterns and metabolic rates. Bone histological characters can be conserved over hundreds of millions of years in the fossil record and potentially contain information about individual age at death, age at sexual maturity, bone growth rates, and basal metabolic rates of extinct vertebrates. Using a sample of extant amniotes, we have constructed a paleobiological model to estimate bone growth rate from bone histological traits. Cross-validation tests show that this model is reliable. We then used it to estimate bone growth rates in a sample of extinct archosaurs including Crurotarsi and Ornithodira. After testing for phylogenetic signal, optimization of femoral growth rates through squared change parsimony onto a time-calibrated tree of amniotes shows two divergent evolutionary trends: whereas bone growth rates increase from the last common ancestor of Ornithodira to extant birds, they decrease from the last common ancestor of Crurotarsi to extant crocodiles. However, we conclude, on the basis of recent evidence for unidirectional airflow in the lungs of alligators, that crocodiles may have retained the capacity of growing at high rates.

Guest Post - Roland Sookias Discusses His New Study Examining How Dinosaurs Came to Fill Most Ecological Niches During the Mesozoic

Why were dinosaurs, and other archosauromorphs (the group of animals including crocodiles, dinosaurs, pterosaurs and several other extinct groups), so big? Was natural selection for increasing size responsible for archosauromorphs’ dramatic rise to larger sizes and did selection for decreasing size drive therapsids’ (‘mammal-like reptiles’, which were the dominant land vertebrates before archosauromorphs) reduction in size during the Triassic (see picture)? These are the questions which my, Richard Butler’s and Roger Benson’s recent publication in Proceedings of the Royal Society B – “Rise of dinosaurs reveals major body size transitions are driven by passive processes of trait evolution” – attempts to answer.
Most of the work in the paper was done as part of my MSc thesis project, which Richard, Roger and Andrew Smith supervised. To carry out the project I spent a good deal of last summer collecting femur and skull length measurements (which we used as proxies for body mass) in the Natural History Museum Library, London. Though barely seeing daylight for a month or two, I managed to collect measurements for ~200 species, which, in combination with data from Benson et al. 2011 got us to >400 species in total. To answer the questions above we focused on getting data for archosauromorphs and therapsids from the Late Permian to Middle Jurassic. This allowed comparison between the two groups, and the interval brackets the rise of archosauromorphs to become the dominant terrestrial vertebrates, replacing therapsids. Thus it allowed us to look at body size evolutionary dynamics during a major faunal transition.

Archosauromorphs (dinosaurs, crocodiles, pterosaurs and their relatives) increased greatly in maximum size (black line, black triangles) from the Permian to Jurassic, and therapsids (‘mammal-like reptiles’) decreased. However in both this was due to expansion in the size variance (i.e. both size increase and decrease), but with subsequent extinction of larger therapsid species. Figure from Sookias et al. 2012, Proc Roy Soc B.

Once we’d got the data together we analysed them using maximum likelihood model fitting approaches. We tried both phylogenetic – i.e. incorporating evolutionary relationships – and time series (ignoring within-group evolutionary relationships and simply averaging size within time ‘bins’) models. Time series models confirmed that on average archosauromorphs tended to increase across the time interval, and that therapsids got smaller. However when we included phylogeny (evolutionary relationships) we found that there was no directional trend in either group along individual lineages. Thus the apparent trends through time were in fact due to ‘passive expansion’ in size, but as the original size was nearer the bottom than the top of the eventual size range the average size tended to increase (see picture). We thus can say that the long-repeated idea of “Cope’s rule” – that taxa in a clade tend to get larger over time due to within-lineage natural selection for larger body sizes – is not found in either archosauromorphs or therapsids during this time interval.

Our work excludes larger size in archosauromorphs as an explanation for their success, as if larger size was especially beneficial one would expect a directional evolutionary trend towards larger sizes. Instead, archosauromorphs probably replaced therapsids opportunistically, as many have hypothesized before. However, the exceptionally high growth, and thus reproductive, rates of archosauromorphs may have allowed them to re-fill empty ecological niches especially easily and rapidly after they went empty due to extinction of therapsids. Thus, while size and growth rate probably did not allow archosauromorphs to outcompete therapsids, it did allow them to fill up free niches quickly.

We also found that archosauromorph predators exceeded the size of the largest herbivores – anomodont therapsids – during the Middle-early Late Triassic. This finding – that the largest carnivores are larger than herbivores - is extremely rare in ecosystems throughout time. It demonstrates that extinct archosauromorphs really were exceptionally large, and that they were able to grow to larger sizes than therapsids given the same resources.

Well, there’s not much more to say about that paper except hope you enjoy it! However, we should be publishing some more work based on my MSc thesis in the near future, so stay tuned, and I’ve just started a PhD with Richard Butler on the early archosauromorph radiation, so hopefully I’ll be involved in answering a few more interesting questions in the coming years. Finally, a very big thank you to Bill Parker for giving us a guest slot here on the esteemed Chinleana.

The paper’s full citation is:


Sookias, R. B., Butler, R. J., Benson, R. B. J. (2012). Rise of dinosaurs reveals major body size transitions are driven by passive processes of trait evolution. Proceedings of the Royal Society B.
doi: 10.1098/rspb.2011.2441 



Abstract- A major macroevolutionary question concerns how long-term patterns of body-size evolution are underpinned by smaller scale processes along lineages. One outstanding long-term transition is the replacement of basal therapsids (stem-group mammals) by archosauromorphs, including dinosaurs, as the dominant large-bodied terrestrial fauna during the Triassic (approx. 252–201 million years ago). This landmark event preceded more than 150 million years of archosauromorph dominance. We analyse a new body-size dataset of more than 400 therapsid and archosauromorph species spanning the Late Permian–Middle Jurassic. Maximum-likelihood analyses indicate that Cope’s rule (an active within-lineage trend of body-size increase) is extremely rare, despite conspicuous patterns of body-size turnover, and contrary to proposals that Cope’s rule is central to vertebrate evolution. Instead, passive processes predominate in taxonomically and ecomorphologically more inclusive clades, with stasis common in less inclusive clades. Body-size limits are clade-dependent, suggesting intrinsic, biological factors are more important than the external environment. This clade-dependence is exemplified by maximum size of Middle–early Late Triassic archosauromorph predators exceeding that of contemporary herbivores, breaking a widely accepted ‘rule’ that herbivore maximum size greatly exceeds carnivore maximum size. Archosauromorph and dinosaur dominance occurred via opportunistic replacement of therapsids following extinction, but were facilitated by higher archosauromorph growth rates.



Popular press coverage:

http://news.discovery.com/animals/how-dinosaurs-got-so-big-120131.html

http://news.sciencemag.org/sciencenow/2012/01/the-secret-of-dinos-success.html?ref=hp