Introducing Mirarce eatoni, the wonderful winged messenger.

Skeletal reconstruction of Mirarce eatoni showing preserved skeletal elements (white). Illustration: Scott Hartman.

Birds originated from a theropod lineage more than 150 million years ago. By the Early Cretaceous, they diversified, evolving into a number of groups of varying anatomy and ecology. In recent years, several discovered fossils of theropods and early birds have filled the morphological, functional, and temporal gaps along the line to modern birds. Most of these fossils are from the Jehol Biota of northeastern China, dated between approximately 130.7 and 120 million years ago. Among them was the long bony-tailed Jeholornis, only slightly more derived than Archaeopteryx, that lived with Sapeornis, Confuciusornis, and the earliest members of Enantiornithes.

Enantiornithes are the most diverse group of Mesozoic birds. Their remains have been collected on every continent except Antarctica, although their fossil record is particularly poor in North America and limited to the Late Cretaceous. The first probable enantiornithines from North America were collected in the 19th Century, and may be referable to Avisaurus archibaldi. Originally, A. archibaldi was described as a member of a new clade of non-avian theropod dinosaurs, the Avisauridae, the first recognized clade of enantiornithines, defined as “the common ancestor of Neuquenornis volans and Avisaurus archibaldi plus all its descendants”.

Best-preserved cervical and thoracic vertebrae, including the axis of Mirarce (From Atterholt et al., 2018)

The most complete known North American enantiornithine, the so-called “Kaiparowits avisaurid”, was collected in 1992. The specimen was recognized as a new taxon, Mirarce eatoni. Named for its spectacular preservation and level of morphological detail, the holotype (UCMP 139500) of this large, turkey-sized avisaurid enantiornithine is a three-dimensional partial skeleton consisting of several cervical and thoracic vertebrae (including the axis), the pygostyle, almost all phalanges from the left pes and several from the right, a complete humerus, femur, and tarsometatarsus, a partial scapula, coracoid, furcula, and tibiotarsus, as well as fragments of the sternum, radius, ulna, carpometacarpus, and manual phalanges.

The preserved sternal fragment of Mirarce indicates the presence of a well-developed ventral keel, very similar to that observed in Neuquenornis. In modern birds, the narrow furcula and the remige papillae, transfer aerodynamic forces from the feathers to the wing skeleton. These features were also present in Mirarce, and support the hypothesis that at least some lineages of enantiornithines convergently achieved more advanced aerial capabilities by the Late Cretaceous.

Reconstruction of living Mirarce eatoni. Illustration: Brian Engh.

The Enantiornithes have a long evolutionary history, and surviving up to the K–Pg boundary. Several trends have been suggested for the group, including: a general increase in range of body sizes; a greater degree of fusion of compound elements, and the appearance of advanced flight-related features evolved in parallel to the neornithine lineage (like manual reduction, loss of teeth, increase in size of sternal keel). It has been proposed that they were primarily forest dwellers, so they disappeared after the Chicxulub impact triggered widespread destruction of forests.



Atterholt J, Hutchison JH, O’Connor JK. (2018) The most complete enantiornithine from North America and a phylogenetic analysis of the Avisauridae. PeerJ 6:e5910

Daniel J. Field et al. Early Evolution of Modern Birds Structured by Global Forest Collapse at the End-Cretaceous Mass Extinction. Current Biology, published online May 24, 2018; doi: 10.1016/j.cub.2018.04.062


One thought on “Introducing Mirarce eatoni, the wonderful winged messenger.

  1. Pingback: Fossil Friday Roundup: November 16, 2018 | PLOS Paleo Community

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