Living in what is now Morocco during the late Paleocene and early Eocene, around 56 million years ago, it would have been about the size of a cat, roughly 30cm at the shoulder (~1′) and 60cm long (~2′). It had a fairly low flat head with a proportionally short snout, while the back end of its skull behind it eyes was elongated, supporting large powerful jaw muscles.
Wear patterns on its teeth suggest it ate a lot of tough vegetation, and it may have been a semiaquatic animal behaving somewhat like modern tapirs or pygmy hippos – spending a lot of the daytime lounging in water, and emerging onto land to forage during the night.
(Apologies for the abrupt absence – I’m okay, just having everything break down at once. This is fine.)
So— back to the speculative evolution request list!
TheBigDeepCheatsy requested a “cactus-dwelling/germinating evolution of introduced rosy-faced lovebirds”:
While Agapornis cheatsyi is still quite physically similar to its introduced ancestors, this lovebird has developed a close symbiotic relationship with the cactus Carnegiea ornipolis, a descendant of the modern saguaro.
Naturally fasciated, this cactus grows a splaying fan-like crown which the lovebirds excavate their shallow nest burrows into. Feeding on the cactus’ fruit in early summer, the lovebirds then disperse the seeds via their droppings – a process that significantly improves propagation chances, both due to the birds commonly foraging and defecating around suitable nurse plants and the passage through their gut speeding up germination.
Someone calling themself “LB” asked for some “flying afrotherians”:
Elbeitandraka venenifer is a descendant of tree-climbing Malagasytenrecs that developed gliding membranes – and its lineage is now just about achieving true powered flight.
About 25cm long (~10″), its proportionally short broad wings require it to fly very fast to generate enough lift for its weight. It mostly only actively flies when traveling between roosts and feeding sites (or when escaping from threats), alternating between gliding to save energy and flapping to recover altitude.
It’s an opportunistic omnivore, crawling around in the tree canopy foraging for vegetation, fruits, fungi, invertebrates, and the occasional smaller vertebrate, using its flexible sengi-like nose to probe around in crevices.
Much like modern common tenrecs it’s capable of hibernating for months at a time through periods of scarce food availability. It also accumulates alkaloid toxins in its body from its arthropod prey, advertising its unpalatability to predators with bold contrasting warning coloration on its wing membranes.
And here’s a combination of a couple of anonymous requests for both “flying heterodontosaurs” and “dragons with hind leg wings, a la sharovipteryx”:
Inversodraco rapax is a highly specialized Jurassic descendant of heterodontosaurids that took to climbing and gliding, developing delta-wing-like membranes on their hindlimbs convergently similar to those of the earlier sharovipterygids.
Around 75cm long (~2’6″), it has unusually flexible hip joints for a dinosaur, able to splay its legs out to the sides to deploy wings supported by an elongated outer toe on each foot. Its arms form small forewings for stability, and its long tail ends in a vane of stiffened feathers that aid in steering.
Unlike its herbivorous-to-omnivorous ancestors it’s primarily a carnivore, swooping down onto small prey and grabbing it with its talon-like forelimbs.
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.
Since the last coupleof weeks have featured marine mammals, let’s have one more! This time not a cetacean but a member of the other group of fully aquatic mammals still alive today: the sirenians.
Although commonly known as “sea-cows” due to their herbivorous grazing habits, sirenians’ closest living relatives are actually modern elephants. They’re thought to have originated in Africa over 50 million years ago, starting off as pig-like or hippo-like semi-aquatic animals — but they must have been good swimmers capable of crossing oceans very early in their evolutionary history, since some of the earliest known sirenian fossils actually come from the other side of the Atlantic on the Caribbean island of Jamaica.
Sobrarbesiren cardieli here extends some of our knowledge of early four-legged sirenians to Europe, dating to the mid-Eocene about 42 million years ago. Hundreds of bones were found in Northeastern Spain, representing at least six different individuals and giving us a fairly complete idea of this species’ anatomy.
It was smaller than modern sea-cows, reaching about 2m long (6’6″), and seems to represent a transitional point between the semi-aquatic ancestral sirenians and fully aquatic later forms. It had a head very similar to its modern relatives, and probably a tail fin, but also still retained small functional hind limbs.
It was initially thought to still be somewhat semi-aquatic and capable of quadrupedal locomotion on land, but a later analysis of its hind limb bones suggests that it may actually have been much more aquatic than that. Its hind legs had a wide range of motion and were probably used for otter-like swimming, undulating the body while paddling, but might not have been capable of supporting its weight on land. So if Sobrarbesiren did still haul out of the water, it may have had to move more like a seal.
With their odd-looking skulls, long tusks, and their noses and upper lips modified into tentacle-arm-like trunks, modern elephants are the sort of animal that would seem completely unbelievable if we only had fossils of them.
But not nearly as strange as some of their ancient relatives.
Platybelodon is probably the most famously weird member of the proboscideans (the group that contains both modern elephants and their extinct cousins), looking like some sort of deliberately outrageous speculative creature design.
Living during the mid Miocene, around 15-4 million years ago, several different species of Platybelodon ranged across Africa, Europe, Asia, and North America, with Platybelodon grangeri here known from abundant fossils in Asia.
These strange-looking proboscideans stood around 2.2m tall (7’3″) and had fairly standard elephant-like bodies, but also heads with bizarre-looking elongated lower jaws that ended in a wide flat shovel-like shape tipped by two flat tusks, leading to their nickname of “shovel-tuskers”.
It was originally interpreted as a swamp-dwelling animal using its weird jaw to scoop up soft aquatic vegetation, with a fairly short flat trunk. But more recent studies of the wear patterns on its teeth suggest it actually used them more like a scythe than a shovel, cutting through tough grasses and branches – a feeding style that would also require it to have a much more modern-elephant-like trunk, using it to hold on to plants while it was sawing through them.
Isolated on Crete, with no predators and living at a time when the island was much smaller, it quickly dwarfed and became the tiniest known mammoth to ever exist, standing just 1.1m tall at the shoulder (3’7″). Not much is known about its ecology, but its teeth suggest it was a browser feeding on leaves and shrubs, possibly filling a similar niche to the mid-sized deer that came later.
This mini-mammoth seems to have gone extinct by the mid-Pleistocene, about 1 million years ago, around the time when rising sea levels during an interglacial phase may have submerged so much of the smaller proto-Crete that its population could no longer be supported.
Later in the mid-to-late Pleistocene, after the sea level dropped again and tectonic uplift brought Crete close to its modern dimensions, the small mammoths were replaced by both newly-arriving deer and Palaeoloxodon elephants, which evolved into the much more moderately dwarfed forms of Palaeoloxodon creutzburgi and Palaeoloxodon chaniensis.
To the north and east of Crete the Cyclades and Dodecanese islands had endemic dwarf elephants on at least eight islands, with the best known being the species that lived on Tilos.
Palaeoloxodon tiliensis stood about 1.8m tall (5’11”), on the larger side for a dwarf Mediterranean elephant but still one of the smallest palaeoloxodontines in the Aegean region. Several thousand specimens have been found, and radiocarbon dating shows it was a fairly recent evolutionary development, appearing just 45,000 years ago in the late Pleistocene.
This dwarf elephant was also the very latest surviving of its entire kind, living well into the Holocene until at least 4000 BCE. This is several thousand years after humans first arrived on Tilos, suggesting it was a rare case of an island elephant that managed to endure the effects of a human presence for quite some time.
Over on isolated Cyprus further to the east, the only native large mammals were the miniature hippos and an equally miniature elephant.
Palaeoloxodon cypriotes was smaller than the Aegean palaeoloxodontines, about 1.4m tall (4’7″), and much like its cousin on Tilos seems to have evolved very recently towards the end of the Pleistocene, sometime around 20,000 years ago.
It wasn’t the first dwarf elephant on Cyprus — there was a larger, earlier species known as Palaeoloxodon xylophagou at least 200,000 years ago — but it’s not clear whether these two species represent a single evolutionary line or two entirely different colonizations of the island.
Similarly to the hippos it lived alongside, Palaeoloxodon cypriotes disappeared shortly after humans arrived on Cyprus, between 12,000 and 10,000 years ago. Collections of its bones have been found in a rock shelter with evidence of having been burnt, suggesting that it was being actively hunted and cooked.
And that’s all for the Island Weirdness series! Even over two months there are still plenty of species I didn’t have time to feature, so this definitely won’t be the last we see of strange endemic species.
Thank you for following along — with a shoutout to my Patreon supporters! — and regular weekly art posts will resume here next Monday.
Mammuthus lamarmorai lived on the island of Sardinia during the middle and late Pleistocene, between about 450,000 and 40,000 years ago. Standing around 1.4m tall at the shoulder (4’7″), it was a dwarf form roughly one-third the size of its ancestor, the huge Eurasian steppe mammoth.
Its remains are known only from the west and south of the island. Strangely it appears to be have been absent from the nearby island of Corsica, despite the two being joined as a single landmass a few times during lower sea level periods in the Pleistocene.
It’s not clear why this mini-mammoth disappeared. The date of the earliest human settlement of Sardinia is controversial (ranging from 250,000 to 20,000 years ago), so Mammuthus lamarmorai might never have actually encountered them. Instead it may have struggled to cope with climate changes during the last glacial period towards the end of the Pleistocene, which rapidly turned Sardinia colder and drier.
Over on Sicily and Malta (which were also occasionally a single island when sea levels were lower), there were several different species of miniature elephant during the mid-to-late Pleistocene, each with a different body size and occupying its own ecological niche. They were all descendants of the massive straight-tusked elephant (Palaeoloxodon antiquus) but each resulted from independent colonization waves swimming over to the island(s).
Around 200,000 years ago a sea level drop allowed new colonization from the Italian mainland. If Palaeoloxodon falconeri was still around at that time it likely didn’t survive long with new competition from large herbivores like bison and deer, and being preyed on by newly-arriving large carnivores like wolves, lions, and hyenas.
Another small elephant soon evolved to take its place, although due to the presence of predators it was never able to get nearly so tiny.
Palaeoloxodon mnaidriensis was in fact one of the largest dwarf elephants in the Mediterranean, standing about 1.8-2m tall (5’11”-6’6″), but despite its larger size its limbs still show signs of adaptation for more fast and agile movement. Its tusks also show a lot of variation in shape, with some much more curved and twisted than others.
This elephant had disappeared by about 13,000 years ago, probably due to the climate significantly warming towards the end of the last ice age. Much like Sardinia, the earliest arrival of humans on Sicily and Malta is controversial, and it’s unclear whether they ever encountered Palaeoloxodon mnaidriensis — the earliest definite date for Sicily is about 16,000 years ago, so a human-induced extinction can’t be ruled out entirely.
The subfossil remains of the Siculo-Maltese elephants may have also ended up inspiring legends of the cyclops, as their skulls would have resembled large human ones with the nasal cavity forming a single big “eye socket”.
Actual woolly mammoths (Mammuthus primigenius) were also present in Japan, but the two similar-looking elephants inhabited different environments — Palaeoloxodon naumanni preferred the southern forests, while the true mammoths roamed the colder north.
Humans arrived in Japan around 40,000-30,000 years ago, so Palaeoloxodon naumanni actually coexisted with them for quite some time. Although it was hunted, it seems to have mainly been climate change towards the end of the last glacial maximum that led to its extinction.
Over on the other side of the Pacific Ocean, at least 60,000 years ago, some huge Columbian mammoths (Mammuthus columbi) swam the 6.5km (4 miles) distance to the ancient island of Santa Rosae — a landmass that today is mostly submerged, with its remaining peaks forming the modern California Channel Islands.
With a lack of large predators and then steadily rising sea levels reducing the available habitat on their new home, the mammoths shrank into a dwarfed species known as the Channel Islands pygmy mammoth (Mammuthus exilis). Standing around 1.75-2m at the shoulder (5’9″-6’6″), they were less than half the size of their ancestors and had only about 10% of the body mass.
The pygmy mammoths survived until about 13,000 years ago, around the same time that early Paleoindians arrived. While they may also have been hunted by humans, the warming post-glacial climate is currently thought to be the main factor in their extinction, changing the types of vegetation on their still-shrinking islands and reducing fresh water sources.
We left off last time with the dwarf stegodontids of Flores, but other Indonesian islands also had their own populations of unusually small elephant-relatives — so here’s a few more to start off this month!
Sinomastodon bumiajuensis lived on the island of Java during the early Pleistocene, about 2-1.5 million years ago. It stood around 2m tall at the shoulder (6’6″), less than half the size of most other Sinomastodon species from mainland Asia. Although it looked convergently similar to modern elephants it was actually a member of the gomphotheres, much more closely related to the weird “shovel-tuskers” than to any living species.
Stegodon semedoensis, also from the early Pleistocene of Java about 1.5 million years ago, is only known from a few isolated molar teeth — but the size of those teeth suggest it was one of the smallest known pygmy stegodontids. It was probably no more than 1.2m at the shoulder (3’11”), comparable in size to its close relative Stegodon sondaari over on Flores.
Meanwhile on Sulawesi, Elephas celebensis (sometimes called Stegoloxodon celebensis) was an actual true elephant closely related to the modern Asian elephant. Living during the late Pliocene and early Pleistocene, between about 2.5 million and 800,000 years ago, it was only 1.5m tall (5′) and had a second set of tusks in its lower jaw, a “primitive” feature retained from the gomphothere-like ancestors of modern elephants.
At the same time Sulawesi also had yet another small stegodontid, Stegodon sompoensis, also around 1.5m tall.
The cooling climate of the Pleistocene and dropping sea levels eventually connected the islands of western Indonesia to the Sundaland landmass of mainland Asia. Influxes of new predators and competitors — and early humans — probably drove these endemic small elephants to extinction.
In Africa during the Eocene and Oligocene, the main terrestrial herbivores were a different type of mammal entirely: hyraxes, the close relatives of elephants and manatees. Although their only modern representatives are small climbing rodent-like animals, hyraxes were once a much more diverse and widespread group, filling a variety of ecological niches and ranging from the size of rats up to the size of rhinos.
Antilohyrax pectidens was a mid-sized example of these diverse hyraxes, standing about 50cm tall at the shoulder (1′8″) and living around 34-28 million years ago in Egypt. It had a deer-like snout and long slender limbs adapted for running and leaping, with leg bones incredibly similar in size and proportion to modern springbok.
Its incisor teeth were comb-shaped and resembled those of colugos, so it was probably a similar sort of selective browser eating soft leaves and shoots.