The stratigraphic position of the lower Miocene Kiel Sand Member of the Berchem Formation in the Antwerp area (northern Belgium) is not well constrained and its depositional environments are poorly known. Due to a spatial limited decalcification front, the Kiel Sand Member is completely decalcified in southern Antwerp and gradually becomes fossiliferous to the north-east of the city. The stratigraphy and palaeontology of the fossiliferous sediments in three temporary exposures are presented. The dinoflagellate cyst analysis of fossiliferous horizons shows the relative progress of a transgression in the southern North Sea Basin during the early–middle Burdigalian, that probably initiated in the late Aquitanian. The Kiel Sand Member contains an important mollusc fauna, with several species reported for the first time from this member. The taphonomy and fauna of the shell beds indicate a shallow marine, high energetic depositional environment, strongly influenced by storms, currents, waves and a rather low sedimentation rate. The climate was warm-temperate to subtropical. In all studied sections, the Kiel Sand Member could be clearly distinguished from the Antwerpen Sand Member: similarities and differences are discussed. Moving to the north of Antwerp, the erosive base of the Antwerpen Sand Member cuts deeper into the Kiel Sand Member. The Early Miocene Unconformity (EMU) is suggested at this contact.

The family Cetotheriidae has played a major role in recent discussions of baleen whale phylogenetics. Within this group, the enigmatic, monotypic Metopocetus durinasus has been interpreted as transitional between herpetocetines and other members of the family, but so far has been restricted to a single, fragmentary cranium of uncertain provenance and age. Here, we expand the genus and shed new light on its phylogenetic affinities and functional morphology by describing Metopocetus hunteri sp. nov. from the Late Miocene of the Netherlands. Unlike the holotype of M. durinasus, the material described here is confidently dated and preserves both the tympanic bulla and additional details of the basicranium. M. hunteri closely resembles M. durinasus, differing primarily in its somewhat less distally expanded compound posterior process of the tympanoperiotic. Both species are characterised by the development of an unusually large fossa on the ventral surface of the paroccipital process, which extends anteriorly on to the compound posterior process and completely floors the facial sulcus. In life, this enlarged fossa may have housed the posterior sinus and/or the articulation of the stylohyal. Like other cetotheriids, Metopocetus also bears a well-developed, posteriorly-pointing dorsal infraorbital foramen near the base of the ascending process of the maxilla, the precise function of which remains unclear.

In 1941, Abel established Balaena belgica based on a series of fused cervical vertebrae and citing other cranial fragments from the late Neogene of the Antwerp harbor (northern Belgium). Later, Plisnier-Ladame & Quinet (1969) added a neurocranium and other skeletal remains from the same area to this species. Recently, the neurocranium was re-assigned to the genus Eubalaena thanks to newer phylogenetic analyses. Here, a new description is provided of materials previously assigned to “Balaena” belgica together with taxonomic revisions. Our work suggests that the cervical complex originally designated as the type of “Balaena” belgica is too poorly preserved to be used as such and is assigned to Balaenidae gen. et sp. indet., thus making “Balaena” belgica a nomen dubium. In addition to the neurocranium, the other remains consist in a fragment of maxilla assigned to Balaenidae gen. et sp. indet. and in a humerus assigned to Eubalaena sp. Discovered in the Kruisschans Sands Member of the Lillo Formation (3.2–2.8 Ma, Piacenzian, Late Pliocene), the neurocranium is designated as the holotype of the new species Eubalaena ianitrix. Our phylogenetic analysis supports a sister-group relationship of Eubalaena ianitrix and Eubalaena glacialis, and helps constraining the ages of origin for balaenid clades. Ecological and phylogenetic data suggest that Eubalaena ianitrix may represent the direct ancestor of Eubalaena glacialis, the latter having evolved through phyletic transformation including body size increase during the temperature decline of the Late Pliocene.

The taxonomic revision of Isocetus depauwi Van Beneden, 1880 was carried out through the description of a number of specimens assigned to this species by Van Beneden and Abel in the last decades of the 19th and the early decades of the 20th centuries. After detailed comparisons with the published record of archaic mysticetes, the genus and species are considered valid despite the incompleteness and poor preservation of the material. Diagnostic features are found in the morphology of the mandibular condyle, the angular process of the dentary and the thoracic vertebrae. The new species Parietobalaena campiniana is established based on a partial skeleton, including most of the skull and ear bones, previously assigned to Isocetus depauwi by Abel. Parietobalaena campiniana is described and compared in detail, and its phylogenetic relationships are assessed by a new large-scale cladistic analysis of 246 morphological characters scored for 46 taxa. The results support a basal position of the genus Parietobalaena in the radiation of Miocene 'cetotheres', the monophyly of Balaenoidea (Neobalaenidae and Balaenidae), Balaenopteroidea (Eschrichtiidae and Balaenopteridae), and Cetotheriidae and the paraphyly of 'cetotheres' s.l. The new superfamily Thalassotherii is established based on high bootstrap support and a number of morphological characters; Thalassotherii includes Balaenopteridae, Eschrichtiidae, Cetotheriidae and the basal 'cetothere' mysticetes with the exclusion of Balaenoidea, Eomysticetoidea and toothed mysticetes.

A new extinct genus, Fragilicetus gen. nov., is described here based on a partial skull of a baleen-bearing whale from the Early Pliocene of the North Sea. Its type species is Fragilicetus velponi sp. nov. This new whale shows a mix of morphological characters that is intermediate between those of Eschrichtiidae and those of Balaenopteridae. A phylogenetic analysis supported this view and provided insights into some of the morphological transformations that occurred in the process leading to the origin of Balaenopteridae. Balaenopterid whales show specialized feeding behaviour that allows them to catch enormous amounts of prey. This behaviour is possible because of the presence of specialized anatomical features in the supraorbital process of the frontal, temporal fossa, glenoid fossa of the squamosal, and dentary. Fragilicetus velponi gen. et sp. nov. shares the shape of the supraorbital process of the frontal and significant details of the temporal fossa with Balaenopteridae but maintains an eschrichtiidand cetotheriid-like squamosal bulge and posteriorly protruded exoccipital. The character combination exhibited by this cetacean provides important information about the assembly of the specialized morphological features responsible for the highly efficient prey capture mechanics of Balaenopteridae.