Baleen whales are considered underencephalized mammals due to their reduced brain size with respect to their body size (encephalization quotient [EQ] << 1). Despite their low EQ, mysticetes exhibit complex behavioral patterns in terms of motor abilities, vocal repertoire, and cultural learning. Very scarce information is available about the morphological evolution of the brain in this group; this makes it difficult to investigate the historical changes in brain shape and size in order to relate the origin of the complex mysticete behavioral repertoire to the evolution of specific neural substrates. Here, the first description of the virtual endocast of a fossil balaenopterid species, <i>Marzanoptera tersillae</i> from the Italian Pliocene, reveals an EQ of around 3, which is exceptional for baleen whales. The endocast showed a morphologically different organization of the brain in this fossil whale as the cerebral hemispheres are anteroposteriorly shortened, the cerebellum lacks the posteromedial expansion of the cerebellar hemispheres, and the cerebellar vermis is unusually reduced. The comparative reductions of the cerebral and cerebellar hemispheres suggest that the motor behavior of <i>M. tersillae</i> probably was less sophisticated than that exhibited by the extant rorqual and humpback species. The presence of an EQ value in this fossil species that is around 10 times higher than that of extant mysticetes opens new questions about brain evolution and provides new, invaluable information about the evolutionary path of morphological and size change in the brain of baleen whales.
We provide a new study of previously published eurhinodelphinid materials from the early Miocene of Piedmont (NW Italy) based on a new preparation of the fossil specimens. We studied specimens previously assigned to Tursiops miocaenus and Dalpiazella sp. and provide new anatomical data on the eurhinodelphinid skull and ear bones. In particular, we suggest that a skull that was previously assigned to Tursiops miocaenus must be reassigned to Ziphiodelphis sigmoideus (Cetacea, Odontoceti, Eurhinodelphinidae) based on new comparisons of the squamosal. This finding enabled us to provide new anatomical information on the ear bone anatomy of Z. sigmoideus that was previously unknown. The material originally assigned to Tursiops miocaenus is currently lost. For this reason and due to the fact that the partial illustration of this species by Portis does not allow us to find diagnostic characters for this species, we decided that Tursiops miocaenus is a nomen dubium. Analysis of additional isolated teeth previously assigned to Tursiops miocaenus led to the conclusion that these specimens represent Odontoceti incertae sedis. We performed a new phylogenetic analysis by adding newly discovered character states to a previous dataset and a paleobiogeographic analysis of Eurhinodelphinidae. We found two monophyletic clades within this family. The paleobiogeographic pattern found by the present work suggests the existence of North Atlantic and Mediterranean clades with some species distributed among both basins. We analyzed the virtual endocast of Ziphiodelphis sigmoideus and found that it resembles that of Schizodelphis in several respects, suggesting that some of the more derived characters of the odontocete brain were still absent in these early Miocene eurhinodelphinids.
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