Phylogenomics and Morphology of Extinct Paleognaths Reveal the Origin and Evolution of the Ratites
نویسندگان
چکیده
The Palaeognathae comprise the flightless ratites and the volant tinamous, and together with the Neognathae constitute the extant members of class Aves. It is commonly believed that Palaeognathae originated in Gondwana since most of the living species are found in the Southern Hemisphere [1-3]. However, this hypothesis has been questioned because the fossil paleognaths are mostly from the Northern Hemisphere in their earliest time (Paleocene) and possessed many putative ancestral characters [4]. Uncertainties regarding the origin and evolution of Palaeognathae stem from the difficulty in estimating their divergence times [1, 2] and their remarkable morphological convergence. Here, we recovered nuclear genome fragments from extinct elephant birds, which enabled us to reconstruct a reliable phylogenomic time tree for the Palaeognathae. Based on the tree, we identified homoplasies in morphological traits of paleognaths and reconstructed their morphology-based phylogeny including fossil species without molecular data. In contrast to the prevailing theories, the fossil paleognaths from the Northern Hemisphere were placed as the basal lineages. Combined with our stable divergence time estimates that enabled a valid argument regarding the correlation with geological events, we propose a new evolutionary scenario that contradicts the traditional view. The ancestral Palaeognathae were volant, as estimated from their molecular evolutionary rates, and originated during the Late Cretaceous in the Northern Hemisphere. They migrated to the Southern Hemisphere and speciated explosively around the Cretaceous-Paleogene boundary. They then extended their distribution to the Gondwana-derived landmasses, such as New Zealand and Madagascar, by overseas dispersal. Gigantism subsequently occurred independently on each landmass.
منابع مشابه
Examining Basal avian divergences with mitochondrial sequences: model complexity, taxon sampling, and sequence length.
Traditional avian classications have generally indicated that the paleognathous birds (ratites and tinamous) represent the earliest divergence within the extant birds and the perching birds (Passeriformes) represent one of the most recently derived lineages (reviewed by Sibley and Ahlquist, 1990; Feduccia, 1995; see Fig. 1A). However, the conclusions of several recent studies using complete mi...
متن کاملScientists reveal new picture in the evolution of flightless birds.
Because of their far-flung geography and colorful examples including the African ostrich, Australian emu, New Zealand kiwi, and long-lost giants such as Madagascar elephant birds and 12-foot-tall New Zealand moa, Baker et al. (2014) have examined a fascinating part in the story of the avian tree of life: Flightless birds, or ratites. Straddling the middle ground and of great debate is the South...
متن کاملPhylogeny and biogeography of ratite birds inferred from DNA sequences of the mitochondrial ribosomal genes.
The origin of the flightless ratite birds of the southern continents has been debated for over a century. Whether dispersal or vicariance (continental breakup) best explains their origin depends largely on their phylogenetic relationships. No consensus has been reached on this issue despite many morphological and molecular studies. To address this question further we sequenced a 2.8-kb region o...
متن کاملA genomic schism in birds revealed by phylogenetic analysis of DNA strings.
The molecular systematics of vertebrates has been based entirely on alignments of primary structures of macromolecules; however, higher order features of DNA sequences not used in traditional studies also contain valuable phylogenetic information. Recent molecular data sets conflict over the phylogenetic placement of flightless birds (ratites - paleognaths), but placement of this clade critical...
متن کاملStructure, ontogeny and evolution of the patellar tendon in emus (Dromaius novaehollandiae) and other palaeognath birds
The patella (kneecap) exhibits multiple evolutionary origins in birds, mammals, and lizards, and is thought to increase the mechanical advantage of the knee extensor muscles. Despite appreciable interest in the specialized anatomy and locomotion of palaeognathous birds (ratites and relatives), the structure, ontogeny and evolution of the patella in these species remains poorly characterized. Wi...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Current Biology
دوره 27 شماره
صفحات -
تاریخ انتشار 2017