We also show that morphology can predict suction feeding in toothed whales, which has implications for inferring suction feeding in the fossil record.
Posts by Rebecca J. Strauch
New pub! @peerj.bsky.social
@paleodm.bsky.social
We quantify morphological specialization and show that the parallel evolution of specialized suction feeding in toothed whales did not result in convergence on skull shape.
peerj.com/articles/211...
New paper out in Proceedings of the Royal Society B: we apply linguistic tools to sperm whale vowels.
The result: sperm whale vowels do not just look like human vowels. They also behave like them.
We found several parallels. Like in Latin, whales have short and long vowels.
I have always struggled with the use of call playback in birds. I reviewed the published evidence & wrote "Ethical Use of Call Playback" together with Dave Bakewell & Andrew Whitehouse. Was surprised at what the data shows. malaysianbird.report/wp-content/u...
New lab paper, this time on phocid limb morphometrics! Lead by former EDDyLab postdoc Dr. Leonard Dewaele, with @narimanechatar.bsky.social, Prof. Mark Uhen, master student Jacques Klassen, and yours truly
anatomypubs.onlinelibrary.wiley.com/doi/10.1002/...
🐬🦷 A new study by Mathes et al on the harbor porpoise reveals that, even with their simple, uniform teeth, toothed whales follow the same developmental stages as other mammals, from early epithelial thickening to full tooth formation.
Read more: anatomypubs.onlinelibrary.wiley.com/doi/10.1002/...
Partial cranium of the balaenid Balaenella brachyrhynus Bisconti, 2005 A. RBINS M.2344 (Kattendijk Formation, Lower Pliocene; Vrasenedok, Belgium), right lateral view: photograph (A1), explanatory line drawing (A2), dorsal view: photograph (A3), explanatory line drawing (A4), posterodorsal (A5) and anterior (A6) views. B. NMB 42001 holotype (Kattendijk Formation, Lower Pliocene, Waaslandkanaal, Belgium), 3D model in right lateral (B1) and dorsal (B2) views provided for comparison. Grey shading indicates main parts covered with sediment; hatching, main break surfaces; red lines, shark bites marks; small blue spot, shark tooth tip interpreted as belonging to the bluntnose sixgill shark Hexanchus griseus (Bonnaterre, 1788); red rectangles in A, the location of detailed photos shown in Figure 3; red rectangles in B, the corresponding preserved part in RBINS M.2344. Bite mark types (TI–V) follow Collareta et al. (2017a). Scale bars 100 mm.
Fig. 4. A, C, D. Monodontid Casatia sp. (RBINS M.1922) from Kattendijk Formation, Lower Pliocene, Vrasenedok, Belgium. A. Partial cranium in dorsal view (A1), detail of the rostrum base in dorsal view: photograph (A2), explanatory line drawing (A3). C. Fragment of the occipital shield in posterior view: photograph (C1), explanatory drawing (C2). D. Proximal part of a single-headed rib in lateral view: photograph (D1), explanatory drawing (D2). B. 3D model of the cranium of the Recent beluga Delphinapterus leucas Pallas, 1776 (USNM 305071) in dorsal (B1) and posterior (B2) views; to indicate the position of the preserved parts (model downloaded from Phenome10k). Red lines, shark bites marks; small blue spot, shark tooth tip interpreted as belonging to the extinct lamnid shark Carcharodon plicatilis (Agassiz, 1843). Bite mark types (TI–V) follow Collareta et al. (2017a). Scale bars A1, B, 100 mm; A2, A3, C, D, 50 mm.
Reconstructed bite sequence corresponding to the set of parallel bite marks observed on the occipital shield of the balaenid Balaenella brachyrhynus Bisconti, 2005 (RBINS M.2344). The shark tooth best matching the bite marks is the large (first) lower tooth of the bluntnose sixgill shark Hexanchus griseus (Bonnaterre, 1788) (RBINS P.968, the Neogene of Antwerp). The proposed sequence includes: (I) contact of the principal cusp and at least five distal cusplets with the supraoccipital bone, followed by a movement of the shark’s jaws towards the right side of the whale cranium and at an angle with the tooth’s mesiodistal axis, (II) break of the tip of the principal cusp, with the tip remaining stuck in compact bone and related local broadening of the main bite mark, and (III) only the truncated principal cusp retains a contact with the bone, together with the more mesial part of the tooth crown, creating an additional mark posterior to the mark made by the principal cusp. The cranium of the holotype of B. brachyrhynus (NMB 42001) is shown in the same orientation to illustrate the position of the bite marks (red rectangle) and the direction of the bite. Large arrows, the proposed direction for the movement of the shark tooth; small arrows, the orientation of the whale cranium; red lines, shark bite marks; blue spot, broken shark tooth tip embedded in whale bone. Scale bar for the cranium 100 mm; interpretive drawings not to scale.
🧵OK it's time for some catch up on recent papers in marine mammal paleontology. First up, out yesterday - bite marks on dwarf baleen whale and a beluga from the early Pliocene (3-4 myo) of Belgium, Lambert et al. 1/ www.app.pan.pl/article/item...
Thank you!
We describe a bit of lower jaw and associated teeth from southern California. This occurrence fills a gap in the geographic range of toothed baleen whales in the North Pacific.
New pub! @royalsocietypublishing.org
New evidence of a toothed mysticete from the Vaqueros Formation of California fills a gap in the palaeobiogeographic range of Aetiocetidae url: royalsocietypublishing.org/rsos/article...
This is amazing.
When the government kills a crucial report, independent scientists decide to write it anyway and release it outside of government channels.
That’s science serving society, even when our political leaders don’t.
Spring is arriving, but there's still snow in the forecast! How do late #winter storms affect our migratory #birds? Out now in @natecoevo.nature.com, we ask that Q with 25+yrs of #CitizenScience data and ~400 museum specimens collected after the 2021 Great TX Freeze: rdcu.be/e7aUy
#EcoEvo #evolution
🧵Happy New Year! 2025 ended up being a decent year for marine mammal paleontology - loads of new fossil whales and dolphins, a couple of sea cow studies, but a bit light on pinnipeds and archaeocetes. Read my new blog here, and this thread for some of this year's highlights! 🧪🐬🦖
Really great to see people quantifying morphological variation across the range of an extant taxon. I saw another paper recently about variation in extant iguanas. It gives us a baseline for what to expect in fossil species academic.oup.com/zoolinnean/a...
My new Gould paper is out today in Paleobiology (OA)! It is, in effect, a synthesis of some of my historical work on Stephen Jay Gould’s early career, which explores the curious position of punctuated equilibria in his early vision for evolutionary paleontology
www.extinctblog.org/palaeonews/2...
New research out! 🐬
We tested 16 NZ toothed whale species to see if habitat predicts PFAS levels.
Results:
• Habitat = weak predictor
• Sex & age = stronger predictors
• Even remote oceans aren’t safe from PFAS
doi.org/10.1016/j.sc...
#PFAS #MarineScience #Cetaceans #MAVELab #CERG
Paleo folks: Please recommend researchers (incl yourselves) interested in phylogenetic reconstruction in deep time, molecular clocks (discord w/ fossil clocks), foundational/methodological issues in phylo/paleo-reconstruction & who'd be interested in hanging w/ historians & philosophers of science ⚒️
This feels mandatory
@rjstrauch.bsky.social investigate the mandibular symphysis in whales. Toothed whales exhibited unfused, partially fused, or fully fused symphyses, while baleen whales evolved a decoupled, highly mobile symphysis that represents a novel condition unobserved in other mammalian clades.
I had a wonderful time at #2025SVP in Birmingham, UK! Gave a talk about suction feeding in fossil odontocetes (“toothed whales”). I thoroughly enjoyed the numerous insightful, engaging conversations I had with colleagues throughout the meeting. Looking forward to Cleveland next year!
This is figure 5, which shows CIRBP overexpression extends lifespan and enhances DNA damage resistance in Drosophila.
The remarkably long lifespan of bowhead whales could be due to an increased ability to repair DNA mutations, according to research in Nature. go.nature.com/4hzvDN7 🌏 🧪
An orca pod has been spotted for the first time repeatedly targeting and flipping young great white sharks onto their backs to paralyze and dismember them
My newest publication is out in @peerj.bsky.social! In this collaboration with Ana Valenzuela, Nick Pyenson & Mario Suarez we describe the most complete skeleton of the #AquaticSloth - #Thalassocnus - from #Chile!
Artwork by @alexboersma-art.bsky.social
1/6
#FossilFriday
peerj.com/articles/198...
Ashbaugh, A.J., Jamniczky, H.A. & Theodor, J.M. Tying the knot between morphology and development: using the patterning cascade model between cheek teeth to study the evolution of molarization in hoofed mammals. J Mammal Evol 32, 23 (2025). doi.org/10.1007/s109...
Very happy to announce that the Handbook of the Historiography of Earth and Environmental Sciences I coedited with Elena Aronova and Marco Tamborini is now available, for free (open access) via this link:
link.springer.com/referencewor...
Frontiers | A global review of operational fishery interactions with killer whales (Orcinus orca): dynamics, impacts, and management strategies
A big shout out to my coauthors @jakeberv.bsky.social @paleodm.bsky.social and everyone who made this work possible @miamiuniversity.bsky.social
Whales span a range of symphyseal morphologies, varying in degree of mobility (fusion) and length (elongation). In this paper, we examine the evolution of these traits across whale phylogeny and geologic time.