Two seismic-scale submarine channel–levee systems exposed in the Karoo Basin, South Africa provide insights into slope conduit evolution. Component channel fills in a levee-confined channel system (Unit C) and an entrenched channel system (Unit D) follow common stacking patterns; initial horizontal stacking (lateral migration) is followed by vertical stacking (aggradation). This architecture is a response to an equilibrium profile shift from low accommodation (slope degradation, composite erosion surface formation, external levee development, sediment bypass) through at-grade conditions (horizontal stacking and widening) to high accommodation (slope aggradation, vertical stacking, internal levee development). This architecture is likely common to other channel–levee systems. Supplementary material: A detailed correlation panel (presented schematically in Figure 2 ) is available at www.geolsoc.org.uk/SUP18456 .

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Although combined molecular and morphological analyses point to a late middle Eocene (38-39 million years ago) origin for the clade Neoceti (Odontoceti, echolocating toothed whales plus Mysticeti, baleen whales, and relatives), the oldest known mysticete fossil dates from the latest Eocene (about 34 million years ago) of Antarctica [1, 2]. Considering that the latter is not the most stemward mysticete in recent phylogenies and that Oligocene toothed mysticetes display a broad morphological disparity most likely corresponding to contrasted ecological niches, the origin of mysticetes from a basilosaurid ancestor and its drivers are currently poorly understood [1, 3-8]. Based on an articulated cetacean skeleton from the early late Eocene (Priabonian, around 36.4 million years ago) of the Pisco Basin, Peru, we describe a new archaic tooth-bearing mysticete, Mystacodon selenensis gen. et sp. nov. Being the geologically oldest neocete (crown group cetacean) and the earliest mysticete to branch off described so far, the new taxon is interpreted as morphologically intermediate between basilosaurids and later toothed mysticetes, providing thus crucial information about the anatomy of the skull, forelimb, and innominate at these critical initial stages of mysticete evolution. Major changes in the morphology of the oral apparatus (including tooth wear) and flipper compared to basilosaurids suggest that suction and possibly benthic feeding represented key, early ecological traits accompanying the emergence of modern filter-feeding baleen whales' ancestors.