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      Gigantic mysticete predators roamed the Eocene Southern Ocean

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          Abstract

          Modern baleen whales (Mysticeti), the largest animals on Earth, arose from small ancestors around 36.4 million years ago (Ma). True gigantism is thought to have arisen late in mysticete history, with species exceeding 10 m unknown prior to 8 Ma. This view is challenged by new fossils from Seymour Island (Isla Marambio), Antarctica, which suggest that enormous whales once roamed the Southern Ocean during the Late Eocene ( c. 34 Ma). The new material hints at an unknown species of the archaic mysticete Llanocetus with a total body length of up to 12 m. The latter is comparable to that of extant Omura's whales ( Balaenoptera omurai Wada et al. 2003), and suggests that gigantism has been a re-occurring feature of mysticetes since their very origin. Functional analysis including sharpness and dental wear implies an at least partly raptorial feeding strategy, starkly contrasting with the filtering habit of living whales. The new material markedly expands the size range of archaic mysticetes, and demonstrates that whales achieved considerable disparity shortly after their origin.

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          Baleen boom and bust: a synthesis of mysticete phylogeny, diversity and disparity

          A new, fully dated total-evidence phylogeny of baleen whales (Mysticeti) shows that evolutionary phases correlate strongly with Caenozoic modernization of the oceans and climates, implying a major role for bottom-up physical drivers. The phylogeny of 90 modern and dated fossil species suggests three major phases in baleen whale history: an early adaptive radiation (36–30 Ma), a shift towards bulk filter-feeding (30–23 Ma) and a climate-driven diversity loss around 3 Ma. Evolutionary rates and disparity were high following the origin of mysticetes around 38 Ma, coincident with global cooling, abrupt Southern Ocean eutrophication and the development of the Antarctic Circumpolar Current (ACC). Subsequently, evolutionary rates and disparity fell, becoming nearly constant after approximately 23 Ma as the ACC reached its full strength. By contrast, species diversity rose until 15 Ma and then remained stable, before dropping sharply with the onset of Northern Hemisphere glaciation. This decline coincided with the final establishment of modern mysticete gigantism and may be linked to glacially driven variability in the distribution of shallow habitats or an increased need for long-distance migration related to iron-mediated changes in glacial marine productivity.
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            Independent evolution of baleen whale gigantism linked to Plio-Pleistocene ocean dynamics

            Vertebrates have evolved to gigantic sizes repeatedly over the past 250 Myr, reaching their extreme in today's baleen whales (Mysticeti). Hypotheses for the evolution of exceptionally large size in mysticetes range from niche partitioning to predator avoidance, but there has been no quantitative examination of body size evolutionary dynamics in this clade and it remains unclear when, why or how gigantism evolved. By fitting phylogenetic macroevolutionary models to a dataset consisting of living and extinct species, we show that mysticetes underwent a clade-wide shift in their mode of body size evolution during the Plio-Pleistocene. This transition, from Brownian motion-like dynamics to a trended random walk towards larger size, is temporally linked to the onset of seasonally intensified upwelling along coastal ecosystems. High prey densities resulting from wind-driven upwelling, rather than abundant resources alone, are the primary determinant of efficient foraging in extant mysticetes and Late Pliocene changes in ocean dynamics may have provided an ecological pathway to gigantism in multiple independent lineages.
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              Reconstructing Body Size in Extinct Crown Cetacea (Neoceti) Using Allometry, Phylogenetic Methods and Tests from the Fossil Record

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                Author and article information

                Journal
                Antarctic Science
                Antarctic Science
                Cambridge University Press (CUP)
                0954-1020
                1365-2079
                April 2019
                April 02 2019
                April 2019
                : 31
                : 2
                : 98-104
                Article
                10.1017/S095410201800055X
                c35d6845-d89e-4909-8f4d-d6e5834134f6
                © 2019

                https://www.cambridge.org/core/terms

                https://www.cambridge.org/core/terms

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