Hesperornithoides miessleriis and the evolution of flight.

Primary blocks of Hesperornithoides specimen WYDICE-DML-001. Images taken by Levi Shinkle. From Hartman et al., 2019.

Birds originated from a theropod lineage more than 150 million years ago. Their evolutionary history is one of the most enduring and fascinating debates in paleontology. In recent years, several discovered fossils as well as innovative studies of living bird behavior, have enriched our understanding of early paravian evolution and flight origins. The discovered fossils demonstrate that distinctive bird characteristics such as feathers, flight, endothermic physiology, unique strategies for reproduction and growth, and a novel pulmonary system have a sequential and stepwise transformational pattern, with many arising early in dinosaur evolution, like the unusually crouched hindlimb for bipedal locomotion,the furcula and the “semilunate” carpal that appeared early in the theropod lineage.

The new paravian theropod, Hesperornithoides miessleriis, from the Late Jurassic Morrison Formation of east–central Wyoming, provides new clues about paravian relationships, as well as the acquisition of flight-related characters in stem avians. Nicknamed “Lori”, and with an estimated length of 89 cm, the new specimen is significantly smaller than other relatively complete theropods from the Morrison Formation. Hesperornithoides lived in a wetland environments with herbaceous plants, but no trees. The habitat, combined with limb proportions indicate that the new specimen was clearly terrestrial.

Association of skeletal elements of Hesperornithoides miessleriis assembled from 3D scans of specimen blocks. Scale bar = 6 cm. From Hartman et al., 2019

Hesperornithoides exhibits the following combination of characters: pneumatic jugal; short posterior lacrimal process; quadrate forms part of lateral margin of paraquadrate foramen; small external mandibular fenestra, humeral entepicondyle >15% of distal humeral width; manual ungual III subequal in size to ungual II; mediodistal corner of tibia exposed anteriorly. The holotype (WYDICE-DML-001) is a partially articulated skeleton consisting of an almost articulated skull, five cervical vertebrae, isolated anterior dorsal rib, portions of 12 caudal vertebrae, five chevrons, partial left scapula and coracoid, portions of the proximal left humerus and distal right humerus, left ulna and radius, radiale, semilunate carpal, left metacarpals I–III, manual phalanges III-2 and 3, manual unguals I, II, and III, ilial fragment, most of an incomplete femur, right and left tibiae and fibulae, left astragalus and calcaneum, portions of right and left metatarsal packets, left pedal phalanges III-1, III-2, III-3, IV-1, IV-2, IV-3, IV-4, and pedal unguals II and III and the proximal portion of IV. The cranial elements are preserved in a separate “skull block”, whereas the axial skeleton is distributed across three blocks.

The acquisition of powered flight in birds was preceded in the course of paravian evolution by a complex sequence of anatomical and functional innovations, and many characters associated with avian flight evolved in a terrestrial context. For this reason, a refined and robust phylogeny of paravians is imperative in order to elucidate the sequence of evolutionary stages that resulted in the acquisition of major avian traits.



Hartman S, Mortimer M, Wahl WR, Lomax DR, Lippincott J, Lovelace DM. 2019A new paravian dinosaur from the Late Jurassic of North America supports a late acquisition of avian flightPeerJ 7:e7247 https://doi.org/10.7717/peerj.7247

Agnolin FL, Motta MJ, Egli FB, Lo Coco G, Novas FE. 2019. Paravian phylogeny and the dinosaur-bird transition: an overview. Frontiers in Earth Science 6:252 https://www.frontiersin.org/articles/10.3389/feart.2018.00252/full

The real Jurassic World.

Global paleogeographic reconstruction of the Earth in the late Jurassic period 150 Ma. From Wikimedia Commons

Global paleogeographic reconstruction of the Earth in the late Jurassic period 150 Ma. Credit: Dr Ron Blakey

The transition from Triassic to Early Jurassic is marked by a major biotic crisis in the marine and terrestrial realms. In the oceans, this event eliminated conodonts and nearly annihilated corals, ammonites, brachiopods and bivalves. In land, most mammal-like reptiles and large amphibians disappeared, as well as early dinosaur groups. During the Jurassic (201-145 mya) the breakup of the supercontinent Pangaea continued and accelerated with the opening of the North Atlantic by the rifting of Africa and North America, giving rise to the supercontinents of Laurasia and Gondwana. The sea level rise flooded continental areas around Pangaea, forming huge epicontinental seas, especially in northern Africa and eastern Laurasia (modern China). The world was predominantly warm with at least four times the present level of atmospheric CO2. The period is also characterized by the explosive adaptive radiation of dinosaurs and the diversification of the cycads.

The Early Jurassic climate was characterized by a global warming, with average summer temperatures that exceeded  35°C in low-latitude regions of western Pangaea where eolian sandstones testify to the presence of vast deserts (Holz, 2015). The early Toarcian Oceanic Anoxic Event  (T-OAE; ∼183 mya) is considered as one of the most severe of the Mesozoic era. It’s associated with a major negative carbon isotope excursion, mass extinction, marine transgression and global warming (Huang, 2014, Ullmann et al., 2014). The T-OAE has been extensively studied in the past three decades although there is no consensus about the causes or triggering mechanisms behind this event.

Painting of a late Jurassic Scene on one of the large island in the Lower Saxony basin in northern Germany (From Wikimedia Commons)

Painting of a late Jurassic Scene on one of the large island in the Lower Saxony basin in northern Germany (From Wikimedia Commons)

After the extinction of many carnivorous crurotarsan lineages (phytosaurs, ornithosuchids, rauisuchians) at the Triassic–Jurassic boundary, theropod dinosaurs increased their diversity and exhibit a greater range of morphological disparity. Sauropodomorphs also achieved a worldwide distribution and become more graviportal and increased their body size. The presence of early armored dinosaurs (thyreophorans) in North America, Asia, and Europe, but their absent from the southern African record, suggests some degree of provinciality in early ornithischian faunas (Brusatte et al., 2010).

By the Mid-Jurassic, Gondwana started to break up in different blocks: Antarctica, Madagascar, India, and Australia in the east, and Africa and South America in the west, with relatively warm sea-surface conditions (26–30◦C) from Mid-Jurassic (∼160Ma) to the Early Cretaceous (∼115Ma) in the Southern Ocean.  There was a drastic climatic decline during the Late Callovian. This decline in temperature lasted about 2.6My and is know as the “Callovian Ice Age”. It has been interpreted in terms of an inverse greenhouse effect, triggered by drawdown of CO2 consequent upon excess carbón burial (Dromart et al, 2003).  The Puchezh-Katunki impact crater in Russia is prior to the Callovian extinction event and is not considered as a factor for this biotic extinction event.

During the Late Jurassic, North America completed its separation from Gondwana, and Gondwana was split into a northern and southern continent by the rift system opening the proto-Indian Ocean. The geological and geochemical record suggest that low-latitude environments were arid and tropical ever-wet conditions were absent. Maximum plant diversity was concentrated at midlatitudes, whith forests dominated by a mixture of conifers, cycadophytes, pteridosperms, ferns, and sphenophytes.


Brusatte, S. L., Nesbitt, S. J., Irmis, R. B., Butler, R. J., Benton, M. J., and Norell, M. A. 2010. The origin and early radiation of dinosaurs. Earth-Science Reviews, 101, 68-100

Holz, M., Mesozoic paleogeography and paleoclimates – a discussion of the diverse greenhouse and hothouse conditions of an alien world, Journal of South American Earth Sciences (2015), doi: 10.1016/j.jsames.2015.01.001

Jenkyns, H. C. (2010), Geochemistry of oceanic anoxic events, Geochem. Geophys. Geosyst., 11, Q03004, doi: 10.1029/2009GC002788.

Sellwood, B.W. & Valdes, P.J. 2006. Mesozoic climates: General circulation models and the rock Record. Sedimentary Geology 190:269–287.

Corwin Sullivan et al. 2014. The vertebrates of the Jurassic Daohugou Biota of northeastern China. Journal of Vertebrate Paleontology, vol. 34, no. 2; doi: 10.1080/02724634.2013.787316