2015
DOI: 10.1007/s00114-015-1319-y
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Piscivory in a Miocene Cetotheriidae of Peru: first record of fossilized stomach content for an extinct baleen-bearing whale

Abstract: Instead of teeth, modern mysticetes bear hairfringed keratinous baleen plates that permit various bulkfiltering predation techniques (from subsurface skimming to lateral benthic suction and engulfment) devoted to various target prey (from small invertebrates to schooling fish). Current knowledge about the feeding ecology of extant cetaceans is revealed by stomach content analyses and observations of behavior. Unfortunately, no fossil stomach contents of ancient mysticetes have been described so far; the invest… Show more

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Cited by 51 publications
(56 citation statements)
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References 63 publications
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“…The potential decoupling of enamel loss and tooth loss as separate genetic events provides a blueprint by which this hypothesis, involving tooth loss and baleen development as separate events, may be tested. While suction feeding without the aid of a feeding apparatus would seem unlikely for a zooplankton-based diet, it is consistent with the known record of piscivory, which has been documented in Eocene basilosaurids (Uhen, 2004), Miocene mysticetes (Collareta et al, 2015), and extant mysticetes, all of which likely employ some degree of suction during the gape cycle (Werth, 2000). Thus, suction feeding as a basal feeding mode for stem mysticetes best incorporates histological and molecular datasets by proposing a fundamental decoupling between the loss of teeth and the emergence of baleen.…”
Section: Discussionsupporting
confidence: 85%
“…The potential decoupling of enamel loss and tooth loss as separate genetic events provides a blueprint by which this hypothesis, involving tooth loss and baleen development as separate events, may be tested. While suction feeding without the aid of a feeding apparatus would seem unlikely for a zooplankton-based diet, it is consistent with the known record of piscivory, which has been documented in Eocene basilosaurids (Uhen, 2004), Miocene mysticetes (Collareta et al, 2015), and extant mysticetes, all of which likely employ some degree of suction during the gape cycle (Werth, 2000). Thus, suction feeding as a basal feeding mode for stem mysticetes best incorporates histological and molecular datasets by proposing a fundamental decoupling between the loss of teeth and the emergence of baleen.…”
Section: Discussionsupporting
confidence: 85%
“…Brand, Esperante, Chadwick, Poma Porras, & Alomía, 2004;Ehret et al, 2012;Esperante, Brand, Chadwick, & Poma, 2015;Esperante, Brand, Nick, Poma, & Urbina, 2008;Gariboldi et al, 2015;Lambert, Bianucci, & de Muizon, 2008;Lambert, Bianucci, & Post, 2009Lambert, Bianucci, Post, de Muizon, et al, 2010;Lambert, Bianucci, & Beatty, 2014;Lambert, de Muizon, & Bianucci, 2014;Lambert et al, 2015;Collareta et al, 2015). However, despite the growing significance of the vertebrate fauna of the Pisco Formation, a comprehensive stratigraphic framework for individual fossil-bearing localities and their position relative to one another has yet to be established (Brand, Urbina, Chadwick, DeVries, & Esperante, 2011;Di Celma et al, in press).…”
Section: Introductionmentioning
confidence: 99%
“…Acrophyseter sp. ), Ziphiidae (M. gregarius, Chimuziphius coloradensis), Inioidea (Brachydelphis mazeasi and an undescribed taxon), two undescribed kentriodontid-like Delphinida, Balaenopteroidea, and Cetotheriidae (Bianucci et al, 2010(Bianucci et al, , 2016bCollareta et al, 2015;Gioncada et al, 2016;Lambert et al, 2010a). The geological age of the lower allomember is estimated as 9.9-8.9 Ma (Tortonian, Late Miocene) based on the presence of the diatom species Lithodesmium reynoldsii and radiometric dating of a local ash layer .…”
Section: Horizon and Localitymentioning
confidence: 99%