Odobenocetops peruvianus was a small toothed whale that lived during the Miocene, about 7-3 million years ago, in shallow coastal waters around what is now Peru. Around 3m long (~10′), it was a highly unusual cetacean with binocular vision, a vestigial melon, muscular lips, and a pair of tusks – features convergent with walruses that suggest it had a similar lifestyle suction-feeding on seafloor molluscs and crustaceans.
In males the right tusk was much more elongated than the left, measuring around 50cm long (~1’8″) in this species and up to 1.35m (4’5″) in the closely related Odobenocetops leptodon. Since these teeth were quite fragile they probably weren’t used for any sort of combat, and they may have instead served more of a visual display function.
Around 3m tall at the shoulder (~10ft), these hairy proboscideans had very long curving tusks that were used for digging out vegetation from under snow and ice, scraping bark from trees, and for fighting.
The tusks showed a lot of variation in their curvature, and were often rather asymmetrical, a condition also seen in the closely related Columbian mammoth. Like modern elephants mammoths may have also favored using one side over the other for certain tasks, which over their lifetimes could result in uneven wear exaggerating the natural asymmetry even more.
Toothed whales – the branch of cetaceans that includes modern dolphins, porpoises, beaked whales, and sperm whales – have surprisingly asymmetrical skulls, with some of the bones skewed to one side and just the left nostril forming their blowhole.
Some of the most obvious external manifestation of this lopsidedness can be seen in sperm whales, which have their blowhole at the front left side of their head, and in male narwhals, which usually have a single left-side tusk.
This sort of asymmetry first appeared in the skulls of early toothed whales around 30 million years ago. And since the highest amounts of wonkiness have gone on to develop in lineages that hunt in dark, cluttered, or murky waters, this suggests that the trait is somehow linked to the evolution of complex echolocation.
Some ancient members of the river dolphin lineage also had some additional unusual asymmetry, sometimes having slightly sideways-bending snouts.
Ensidelphis riveroi was one of the weirdest of these, living around the coasts of what is now Peru during the Miocene, about 19 million years ago. Around 3m long (~10′), it had a very long narrow toothy snout that curved distinctly off to the right along its length.
It’s not clear what the function of this bend was, or even if the only known skull actually represents the normal condition for this species. But Ensidelphis’ bendy snoot might have been used to probe around in muddy seafloor sediment or to extract prey from crevices, possibly like an underwater version of the modern wrybill.
Antaecetus aithai was an early whale that lived during the late Eocene (~40 million years ago) in what is now Morocco, at a time when northern Africa was covered by a warm shallow sea.
It was part of the “basilosaurids“, some of the first fully aquatic cetaceans – traditionally considered to be a single defined group, but more recently found to be more of an “evolutionary grade” of multiple early whale lineages – and much like Basilosaurus it had elongated back vertebrae that would have given it a very long slender body shape.
Antaecetus also had a proportionally smaller head and smaller teeth than other basilosaurids, along with much denser bones and a stiffer spine that would have made it a rather slow swimmer with reduced maneuverability. It was also fairly small overall compared to most of its relatives, probably around 6m long (~20′).
It was probably a slow-moving coastal water animal somewhat like modern sirenians – except unlike manatees and dugongs it was carnivorous. Its relatively delicate teeth suggest it was feeding on soft-bodied prey like cephalodpods, and with its lack of speed it must have been some sort of ambush predator, waiting around for potential prey to come within striking range.
Cetotheres were a group of small baleen whales, one of three major lineages of these cetaceans alongside the rorquals and the right whales. They first appeared in the fossil record in the mid-Miocene, about 14 million years ago (but are estimated to have actually originated 10-15 million years earlier), and disappeared during the Pleistocene about 2 million years ago.
First recognized in the mid-19th century, for a long time the cetotheres were used as a wastebasket for all fossil baleen whales that didn’t clearly fit into any modern whale families. By the start of the 21st century nearly 30 different genera representing numerous different species were all lumped into the group – and the genus Cetotherium was another wastebasket in itself with at least 12 assigned species, many of which were based on fragmentary or dubious remains.
This was finally cleaned up in the 2000s, when a revision of the cetotheres cut the group down to just 6 genera. Since then a handful of additional new genera and species have been named, and while a few polyphyleticCetotherium species may still need tidying up the cetotheres have overall gone from being a total taxonomic mess to actually being one of the best studied groups of fossil baleen whales.
Their exact evolutionary relationships with each other are still in flux, but the most surprising discovery from the improved understanding of these ancient whales is that they might not be extinct after all.
At this point it seems fairly likely that the pygmy right whale really is either the last surviving representative of the cetothere lineage, or at least is a very close evolutionary “cousin” (a “cetotherioid”) closer related to them than to any other modern baleen whales.
Modern beluga whales and narwhals are the only living representatives of the monodontid lineage, found only in cold Arctic and sub-Arctic waters. But this whale family actually first evolved in much warmer climates – and some of them were downright tropical.
It seems to have had a larger number of functional teeth than modern monodontids, and probably didn’t suction feed like its modern close relatives. Instead it may have fed more like most porpoises and dolphins, relying more on speed and snapping jaws to capture prey.
It inhabited the Mediterranean at a time not long after the sea there had mostly dried up and then been rapidly refilled. The presence of warm-water marine species such as bull sharks, tiger sharks, and dugongs in the same fossil beds as Casatia indicates the local climate at the time was hotter than it is today, with tropical temperatures – and suggests that this whale’s ancestors must have originally moved into the replenishing Mediterranean from lower latitudes alongside these other warmth-adapted animals.
This tropical monodontid was also much closer related to modern belugas than modern narwhals are, which raises the possibility that the two living monodontid species actually specialized for colder conditions completely independently of each other rather than descending from a cold-adapted common ancestor. Instead modern belugas and narwhals may have originated from separate warm-water monodontid ancestors who evolved similar cold-tolerant adaptations in parallel as the climate cooled during the onset of the Quaternary ice age, while the rest of their relatives all went extinct.
Known just from fossilized lower jaws and teeth, with some teeth up to nearly 13cm long (~5″), its full life appearance and size are uncertain – but it may have been slightly larger than a modern bottlenose dolphin at around 4.5m long (~14’9″). It’s traditionally been considered to be part of the kogiid family, closely related to modern pygmy and dwarf sperm whales, but some studies disagree with that classification and instead place it in the true sperm whale lineage.
I’ve reconstructed Kogiopsis here as a kogiid-like animal, with a similar sort of shark-like head shape and “false gill” markings. In the background a second individual is depicted displaying “inking” behavior, releasing a defensive cloud of reddish-brown fluid from a specialized sac in its colon.
Living during the mid-Eocene, about 43 million years ago, in a shallow sea-covered region that is now part of Egypt‘s Western Desert, Phiomicetus was an early protocetid – an amphibious foot-powered swimmer, at a transitional point in the evolution of whales from deer-like terrestrial animals to fully aquatic screaming torpedoes.
About 3m long (~10′), it had large jaw muscles and sharp teeth with wear patterns that suggest it was a raptorial hunter grabbing and snapping at prey with powerful bites. It would have probably tackled fairly big prey compared to other protocetids, hunting things like large fish, turtles, and even smaller whales in an ecological role similar to that of modern orcas.
Along with the distantly-related long-snouted Rayanistes it’s one of the earliest known whales from Africa, giving us further glimpses at a time period when early cetaceans were first dispersing out from the South Asian subcontinent via the ancient Tethys Sea.
Unlike modern baleen whales it was small, about the size of a modern porpoise at around 2m long (6’6″), and the wear on its multi-cusped teeth suggest it was a predator taking slicing bites of fish – possibly using suction-assisted feeding like its close relatives the aetiocetids.
Its fossilized remains are also a rare example of an ancient whale fall, with characteristic bore holes in its bones from Osedax worms.