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 ...

The origin and evolution of clitellate annelids--earthworms, leeches and their relatives--is poorly understood, partly because body fossils of these delicate organisms are exceedingly rare. The distinctive egg cases (cocoons) of Clitellata, however, are relatively common in the fossil record, although their potential for phylogenetic studies has remained largely unexplored. Here, we report the ...

The phylogenetic placement of siricid hymenopterans and especially the relationships among Siricidae are not resolved, and are in need of further investigation. The fossil record helps to illuminate the evolutionary history of this group. In this paper, Xoanon? eocenicus sp. nov. is newly described from the Eocene Fossillagerstätte Grube Messel (Germany). Although several characters of the wing...

14 The fossil record is a rich source of information about biological diversity in the past. However, the fossil 15 record is not only incomplete but has inherent biases due to geological, physical, chemical and biological 16 factors. Our knowledge of past life is also biased because of differences in academic and amateur interests 17 and sampling efforts. As a result, not all individuals or sp...

Approaches quantifying the relative congruence, or incongruence, of molecular divergence estimates and the fossil record have been limited. Previously proposed methods are largely node specific, assessing incongruence at particular nodes for which both fossil data and molecular divergence estimates are available. These existing metrics, and other methods that quantify incongruence across topolo...

The fossil record is a rich source of information about biological diversity in the past. However, the fossil record is not only incomplete but has also inherent biases due to geological, physical, chemical and biological factors. Our knowledge of past life is also biased because of differences in academic and amateur interests and sampling efforts. As a result, not all individuals or species t...

Taxa that fail to become incorporated into the fossil record can reveal much about the biases of this record and provide the information needed to correct such biases in empirical analyses of the history of life. Yet little is known about the characteristics of taxa missing from the fossil record. For the marine Bivalvia, which have become a model system for macroevolutionary and macroecologica...

Two theoretical models have been proposed to describe long-term dynamics of diversification: the equilibrium model considers the Earth as a closed system with a fixed maximum biological carrying capacity, whereas the expansion model hypothesizes a continuously increasing diversification of life. Based on the analysis of the fossil record of all organisms, Benton suggested contrasting models of ...

The timing of the origin and diversification of rodents remains controversial, due to conflicting results from molecular clocks and paleontological data. The fossil record tends to support an early Cenozoic origin of crown-group rodents. In contrast, most molecular studies place the origin and initial diversification of crown-Rodentia deep in the Cretaceous, although some molecular analyses hav...

Characterization of morphological variation in the shells of extant Eastern Box Turtles, Terrapene carolina, provides a baseline for comparison to fossil populations. It also provides an example of the difficulties inherent to recognizing intraspecific diversity in the fossil record. The degree to which variation in fossils of T. carolina can be accommodated by extant variation in the species h...