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      Diminutive fleet-footed tyrannosauroid narrows the 70-million-year gap in the North American fossil record

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          Abstract

          To date, eco-evolutionary dynamics in the ascent of tyrannosauroids to top predator roles have been obscured by a 70-million-year gap in the North American (NA) record. Here we report discovery of the oldest Cretaceous NA tyrannosauroid, extending the lineage by ~15 million years. The new taxon— Moros intrepidus gen. et sp. nov.—is represented by a hind limb from an individual nearing skeletal maturity at 6–7 years. With a ~1.2-m limb length and 78-kg mass, M. intrepidus ranks among the smallest Cretaceous tyrannosauroids, restricting the window for rapid mass increases preceding the appearance of colossal eutyrannosaurs. Phylogenetic affinity with Asian taxa supports transcontinental interchange as the means by which iconic biotas of the terminal Cretaceous were established in NA. The unexpectedly diminutive and highly cursorial bauplan of NA’s earliest Cretaceous tyrannosauroids reveals an evolutionary strategy reliant on speed and small size during their prolonged stint as marginal predators.

          Abstract

          Lindsay Zanno et al. report the discovery of a new tyrannosaur that helps to fill in a 70 million year gap in the fossil record. This new species reveals that the earliest North American tyrannosaurs relied on speed and small body size to survive and that apex predator status and large body sizes were not reached until much later in their evolutionary history.

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          Predator interactions, mesopredator release and biodiversity conservation.

          There is growing recognition of the important roles played by predators in regulating ecosystems and sustaining biodiversity. Much attention has focused on the consequences of predator-regulation of herbivore populations, and associated trophic cascades. However apex predators may also control smaller 'mesopredators' through intraguild interactions. Removal of apex predators can result in changes to intraguild interactions and outbreaks of mesopredators ('mesopredator release'), leading in turn to increased predation on smaller prey. Here we provide a review and synthesis of studies of predator interactions, mesopredator release and their impacts on biodiversity. Mesopredator suppression by apex predators is widespread geographically and taxonomically. Apex predators suppress mesopredators both by killing them, or instilling fear, which motivates changes in behaviour and habitat use that limit mesopredator distribution and abundance. Changes in the abundance of apex predators may have disproportionate (up to fourfold) effects on mesopredator abundance. Outcomes of interactions between predators may however vary with resource availability, habitat complexity and the complexity of predator communities. There is potential for the restoration of apex predators to have benefits for biodiversity conservation through moderation of the impacts of mesopredators on their prey, but this requires a whole-ecosystem view to avoid unforeseen negative effects. 'Nothing has changed since I began. My eye has permitted no change. I am going to keep things like this.' From 'Hawk Roosting', by Ted Hughes.
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            Gigantism and comparative life-history parameters of tyrannosaurid dinosaurs.

            How evolutionary changes in body size are brought about by variance in developmental timing and/or growth rates (also known as heterochrony) is a topic of considerable interest in evolutionary biology. In particular, extreme size change leading to gigantism occurred within the dinosaurs on multiple occasions. Whether this change was brought about by accelerated growth, delayed maturity or a combination of both processes is unknown. A better understanding of relationships between non-avian dinosaur groups and the newfound capacity to reconstruct their growth curves make it possible to address these questions quantitatively. Here we study growth patterns within the Tyrannosauridae, the best known group of large carnivorous dinosaurs, and determine the developmental means by which Tyrannosaurus rex, weighing 5,000 kg and more, grew to be one of the most enormous terrestrial carnivorous animals ever. T. rex had a maximal growth rate of 2.1 kg d(-1), reached skeletal maturity in two decades and lived for up to 28 years. T. rex's great stature was primarily attained by accelerating growth rates beyond that of its closest relatives.
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              Bone typology and growth rate: testing and quantifying 'Amprino's rule' in the mallard (Anas platyrhynchos).

              Periosteal bone histology expresses its rate of deposition. This fundamental relationship between bone structure and growth dynamics, first assumed by Amprino many decades ago, was quantified in preliminary studies, but never statistically tested. Moreover, the precise typological characters of bone tissue linked to growth rate remained poorly known. Here, we present the first statistical analysis of 'Amprino's rule', measured on comprehensive growth series of the mallard, Anas platyrhynchos. Growth rates were assessed by fluorescent labelling. Bone typology was described according to Ricqlès' typological classification. Results show that the presence and proportion of primary osteons, two consequences of bone initial porosity at the time of its deposit, are strongly related to bone growth rate. However, no significant relationship between primary osteons orientation and bone growth rate could be detected, at least for osteonal orientations (longitudinal, laminar and reticular) and growth rates values observed in mallard long bones. These results suggest that Amprino's rule holds for some major typological characters of primary compact bone tissues (i.e. primary osteons presence and proportion). However, it is irrelevant to some other characters (i.e. osteonal orientation), the meaning of which remains to be discovered.
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                Author and article information

                Contributors
                lindsay.zanno@naturalsciences.org
                Journal
                Commun Biol
                Commun Biol
                Communications Biology
                Nature Publishing Group UK (London )
                2399-3642
                21 February 2019
                21 February 2019
                2019
                : 2
                : 64
                Affiliations
                [1 ]ISNI 0000 0001 2226 059X, GRID grid.421582.8, Paleontology, , North Carolina Museum of Natural Sciences, ; 11W. Jones, St. Raleigh, NC 27601 USA
                [2 ]ISNI 0000 0001 2173 6074, GRID grid.40803.3f, Department of Biological Sciences, , North Carolina State University, ; 100 Brooks Ave., Raleigh, NC 27607 USA
                [3 ]ISNI 0000 0001 0476 8496, GRID grid.299784.9, Section of Earth Sciences, , Field Museum of Natural History, ; 1400S. Lake Shore Dr., Chicago, IL 60605 USA
                [4 ]ISNI 0000 0001 2214 904X, GRID grid.11956.3a, Department of Earth Sciences, , Stellenbosch University, ; Private Bag X1 Matieland, Stellenbosch, 7602 South Africa
                Author information
                http://orcid.org/0000-0002-1654-1990
                http://orcid.org/0000-0002-4232-1879
                http://orcid.org/0000-0001-9307-9982
                Article
                308
                10.1038/s42003-019-0308-7
                6385174
                30820466
                1cdabc4f-852a-42c6-bb2b-d0ea88613234
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 10 October 2018
                : 8 January 2019
                Funding
                Funded by: Canyonlands Natural History Association
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                © The Author(s) 2018

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