13Adaptive radiations are long believed to be responsible for the origin of phenotypic diversity and 14 new body plans among higher clades in the fossil record. However, few studies have assessed 15 rates of phenotypic evolution and disparity across broad scales of time to understand the 16 evolutionary dynamics behind the origin of major clades, or how they relate to rates of molecular 17 evolution. Here, we provide a total evidence approach to this problem using the largest available 18 data set on diapsid reptiles. We find a strong decoupling between phenotypic and molecular rates 19 of evolution, with many periods of accelerated phenotypic evolution or expansion of phenotypic 20 disparity at the origin of major reptile clades and body plans that do not correspond to periods of 21 adaptive radiation. We find heterogeneous rates of evolution during the acquisition of similarly 22 23 evolutionary rates. 24 25 26The classical theory of adaptive radiation predicts that such events are characterized by 27 high rates of phenotypic evolution, in combination with an expansion in phenotypic disparity and 28 taxonomic diversity, as new species rapidly transforming to occupy available adaptive zones 29 during times of ecological opportunity 1,2 . Across geological timescales, lineages undergoing 30 exceptionally fast evolutionary rates would give rise to many new lineages, with some of these 31 fast-evolving lineages potentially going extinct. Once niches are occupied, phenotypic disparity 32 stabilizes and species diversification and evolutionary rates decrease and stabilize at lower 33 levels 1 . It has long been assumed that the aftermath of mass extinctions would provide the ideal 34 ecological opportunities for adaptive radiations 1,3 , such as the diversification of placental 35 mammals after the Cretaceous-Palaeogene mass extinction (KPME), or the appearance of several 36 reptile lineages in the fossil record following the Permian-Triassic mass extinction (PTME) 2,3 .
37Therefore, adaptive radiations have long been hypothesized to be responsible for the origin of 38 most of biological diversity (in both taxonomic and phenotypic terms), especially regarding the 39 origin of higher clades (e.g. families or orders) and new body plans, or what Simpson had 40 originally referred to as "mega-evolutionary" processes 4 .
41Although the concept of adaptive radiations is fundamental to our understanding of 42 evolutionary theory, only recently have quantitative tools been developed to rigorously test its 43 predictions at broad taxonomic and deep time scales in the evolutionary paleobiology. For 44 instance, using both relaxed clocks and phylogenetic comparative methods various studies have 45 3 found high rates of evolution at the origin of major clades, including the early evolution of birds, 46 arthropods, and crown placental mammals 5-7 . Fast evolutionary rates during putative periods of 47 adaptive radiations following mass extinctions have also been recovered, such as the radiation of 48 birds 8 and placental mammals...