New material of Chirostenotes pergracilis (Theropoda, Oviraptorosauria) from the Campanian Dinosaur Park Formation of Alberta, Canada

The taxonomy of caenagnathids from the Dinosaur Park Formation of Alberta, Canada, has remained problematic because of incomplete, partial skeletons that do not overlap anatomically. This is particularly problematic for referring mandibular remains, which are the most abundant caenagnathid fossils recovered, but cannot be confidently tied to taxa known from postcranial remains. A new, partial skeleton of Chirostenotes pergracilis preserves the mandibles, cervical and caudal vertebrae, and parts of the hindlimb. Importantly, this is the first specimen with associated mandibles and postcrania of a caenagnathid from the Dinosaur Park Formation, allowing for unambiguous referral of mandibles to this taxon. The mandibles are remarkably similar to those previously suggested to pertain to Chirostenotes pergracilis, and support its distinction from Caenagnathus collinsi. An unfused distal tarsal IV distinguishes the skeleton from Leptorhynchos elegans and supports the referral of small, upturned mandibles to this taxon. Osteohistological analysis indicates that the individual was approaching maximum body size, and provides information on the growth patterns and size of Chirostenotes pergracilis. Accordingly, this supports the division of Dinosaur Park Formation caenagnathids into three taxa of varying body sizes

The origin of placental mammal life histories

After the end-Cretaceous extinction, placental mammals quickly diversified1, occupied key ecological niches2,3 and increased in size4,5, but this last was not true of other therians6. The uniquely extended gestation of placental young7 may have factored into their success and size increase8, but reproduction style in early placentals remains unknown. Here we present the earliest record of a placental life history using palaeohistology and geochemistry, in a 62 million-year-old pantodont, the clade including the first mammals to achieve truly large body sizes. We extend the application of dental trace element mapping9,10 by 60 million years, identifying chemical markers of birth and weaning, and calibrate these to a daily record of growth in the dentition. A long gestation (approximately 7 months), rapid dental development and short suckling interval (approximately 30–75 days) show that Pantolambda bathmodon was highly precocial, unlike non-placental mammals and known Mesozoic precursors. These results demonstrate that P. bathmodon reproduced like a placental and lived at a fast pace for its body size. Assuming that P. bathmodon reflects close placental relatives, our findings suggest that the ability to produce well-developed, precocial young was established early in placental evolution, and that larger neonate sizes were a possible mechanism for rapid size increase in early placentals

The first oviraptorosaur (Dinosauria: Theropoda) bonebed: Evidence of gregarious behaviour in a maniraptoran theropod

A monodominant bonebed of Avimimus from the Nemegt Formation of Mongolia is the first oviraptorosaur bonebed described and the only recorded maniraptoran bonebed from the Late Cretaceous. Cranial elements recovered from the bonebed provide insights on the anatomy of the facial region, which was formerly unknown in Avimimus. Both adult and subadult material was recovered from the bonebed, but small juveniles are underrepresented. The taphonomic and sedimentological evidence suggests that the Avimimus bonebed represents a perimortem gregarious assemblage. The near absence of juveniles in the bonebed may be evidence of a transient age-segregated herd or ‘flock’, but the behaviour responsible for this assemblage is unclear. Regardless, the Avimimus bonebed is the first evidence of gregarious behaviour in oviraptorosaurs, and highlights a potential trend of increasing gregariousness in dinosaurs towards the end of the Mesozoic

How to Live with Dinosaurs: Ecosystems Across the Mesozoic

We continue our trip back in time through the Mesozoic, visiting several different ecosystems across the planet. Each of these was strongly influenced by the continental breakup from a single landmass into several tectonic plates and associated landmasses during this period. We will visit localities on several continents, observe how their vertebrate faunas changed over time, and what external factors might have contributed to these differences. During the Cretaceous, we visit the Iberian Peninsula, where hadrosauroids replaced titanosaurs as the most abundant dinosaur taxon. On the other side of the planet, a succession of geologic formations in Australia shows a gradual change from aquatic to terrestrial faunas resulting from sea-level changes of a now non-existent inland ocean. A visit to two polar ecosystems indicates possible mutual exclusion between amphibians (temnospondyls) and reptiles (crocodylomorphs), because they occupied similar ecological niches. Observing the record of Cretaceous landscapes in what is now Mongolia shows how changes in environment and climate correlate with changes in faunal composition. Heading back, we check if there are distinct differences in vertebrate diversity in space and time in the Late Jurassic of North America. Then we move south, to Argentina, and back to the Middle and Early Jurassic. Here, we will try to understand where these Late Jurassic faunas originated and what influence the fragmentation of the supercontinent Pangea had on their evolution and diversity. Finally, we will stop our trip in the Late Triassic of Central Europe, examining a typical vertebrate fauna from the time when dinosaurs began their domination of the planet