Birds are one of the most recognizable and diverse groups of modern vertebrates. Over the past two decades, a wealth of new fossil discoveries and phylogenetic and macroevolutionary studies has transformed our understanding of how birds originated and became so successful. Birds evolved from theropod dinosaurs during the Jurassic (around 165-150 million years ago) and their classic small, lightweight, feathered, and winged body plan was pieced together gradually over tens of millions of years of evolution rather than in one burst of innovation. Early birds diversified throughout the Jurassic and Cretaceous, becoming capable fliers with supercharged growth rates, but were decimated at the end-Cretaceous extinction alongside their close dinosaurian relatives. After the mass extinction, modern birds (members of the avian crown group) explosively diversified, culminating in more than 10,000 species distributed worldwide today.
We report on a new enantiornithine Eopengornis martini gen. et sp. nov. from the lowest horizon of the Jehol Biota in Hebei, China; dated at 130.7 Mya, this is the second oldest avian bearing fossil deposit in the world, recording the First Appearance Datum of Enantiornithes. The new specimen, only the second enantiornithine and third bird reported from this horizon, preserves numerous synapomorphies with the largest Lower Cretaceous enantiornithine Pengornis houi from the Jiufotang Formation dated at 120 Mya. Together, they form a new avian lineage that lasted over 10 Myr, which is longer than any known clade of Lower Cretaceous enantiornithine. Eopengornis reveals new information about basal enantiornithine morphology such as the presence of a metatarsal V, helping to clarify the early evolution of these dominant Cretaceous avians. Furthermore, Eopengornis preserves a previously unrecognized tail morphology: a pair of elongate fully pennaceous rachis dominated feathers. This discovery confirms hypotheses proposing that the rachis dominated racket-plumes in basal birds represent modified pennaceous feathers. We suggest that the ornamental racket-plumes in enantiornithines and Confuciusornis evolved independently from the basal pygostylian condition, which we infer was a tail formed of normal flight feathers.
Enantiornithines are the most speciose avian clade in the Mesozoic, with a fossil record that nearly spans the Cretaceous; however, with less than half of known taxa preserving skull material, our understanding of their cranial morphology remains incomplete. Here we present a comprehensive overview of the current knowledge of enantiornithine skull anatomy and discuss the range of morphologies known for each of the main cranial elements. The typical enantiornithine skull retains numerous ancestral features such as the absence of fusion among bones, the presence of a postorbital bone, a primitive quadrate with a single headed otic process, an unforked dentary, and teeth. The postorbital in at least one taxon is unreduced, suggesting the existence of a complete infratemporal fenestra and thus an unmodified diapsid skull as in confuciusornithids. The rostrum is well known and shows considerable variation, typical of theropods; however, in terms of rostral proportions, enantiornithines are extremely limited within the modern avian spectrum. Although Late Cretaceous skull material is extremely fragmentary, when compared to Early Cretaceous material it reveals a trend towards more specialized morphologies in younger taxa. The foramen magnum in all taxa points caudally, indicating that the 'flexed' type skull morphology may not have evolved in this group. Enantiornithine teeth show considerable diversity in numbers, size, morphology and placement, ranging from taxa with large teeth found throughout the jaws to taxa with small, rostrally restricted teeth, to the fully edentulous. Despite limited preservation of skull material, a number of trophic specializations can be deduced from the range of preserved morphologies, further hinting at the morphological and ecological diversity of the Cretaceous Enantiornithes.
Many palaeobiological analyses have concluded that modern birds (Neornithes) radiated no earlier than the Maastrichtian, whereas molecular clock studies have argued for a much earlier origination. Here, we assess the quality of the fossil record of Mesozoic avian species, using a recently proposed character completeness metric which calculates the percentage of phylogenetic characters that can be scored for each taxon. Estimates of fossil record quality are plotted against geological time and compared to estimates of species level diversity, sea level, and depositional environment. Geographical controls on the avian fossil record are investigated by comparing the completeness scores of species in different continental regions and latitudinal bins. Avian fossil record quality varies greatly with peaks during the Tithonian-early Berriasian, Aptian, and Coniacian–Santonian, and troughs during the Albian-Turonian and the Maastrichtian. The completeness metric correlates more strongly with a ‘sampling corrected’ residual diversity curve of avian species than with the raw taxic diversity curve, suggesting that the abundance and diversity of birds might influence the probability of high quality specimens being preserved. There is no correlation between avian completeness and sea level, the number of fluviolacustrine localities or a recently constructed character completeness metric of sauropodomorph dinosaurs. Comparisons between the completeness of Mesozoic birds and sauropodomorphs suggest that small delicate vertebrate skeletons are more easily destroyed by taphonomic processes, but more easily preserved whole. Lagerstätten deposits might therefore have a stronger impact on reconstructions of diversity of smaller organisms relative to more robust forms. The relatively poor quality of the avian fossil record in the Late Cretaceous combined with very patchy regional sampling means that it is possible neornithine lineages were present throughout this interval but have not yet been sampled or are difficult to identify because of the fragmentary nature of the specimens.
Three-dimensional specimens of the volant fossil bird Gansus yumenensis from the Early Cretaceous Xiagou Formation of northwestern China demonstrate that this taxon possesses advanced anatomical features previously known only in Late Cretaceous and Cenozoic ornithuran birds. Phylogenetic analysis recovers Gansus within the Ornithurae, making it the oldest known member of the clade. The Xiagou Formation preserves the oldest known ornithuromorph-dominated avian assemblage. The anatomy of Gansus, like that of other non-neornithean (nonmodern) ornithuran birds, indicates specialization for an amphibious life-style, supporting the hypothesis that modern birds originated in aquatic or littoral niches.
The wings of birds and their closest theropod relatives share a uniform fundamental architecture, with pinnate flight feathers as the key component. Here we report a new scansoriopterygid theropod, Yi qi gen. et sp. nov., based on a new specimen from the Middle-Upper Jurassic period Tiaojishan Formation of Hebei Province, China. Yi is nested phylogenetically among winged theropods but has large stiff filamentous feathers of an unusual type on both the forelimb and hindlimb. However, the filamentous feathers of Yi resemble pinnate feathers in bearing morphologically diverse melanosomes. Most surprisingly, Yi has a long rod-like bone extending from each wrist, and patches of membranous tissue preserved between the rod-like bones and the manual digits. Analogous features are unknown in any dinosaur but occur in various flying and gliding tetrapods, suggesting the intriguing possibility that Yi had membranous aerodynamic surfaces totally different from the archetypal feathered wings of birds and their closest relatives. Documentation of the unique forelimbs of Yi greatly increases the morphological disparity known to exist among dinosaurs, and highlights the extraordinary breadth and richness of the evolutionary experimentation that took place close to the origin of birds.
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