Tag: convergent evolution

Island Weirdness #23 – The Bibymalagasy

One of the most mysterious members of Madagascar’s pre-human ecosystem was a creature known as Plesiorycteropus, or the “bibymalagasy”.

It’s known only from fragmentary remains, including a few limb bones, vertebrae, partial skulls, and partial pelvises – with two different species identified, the larger Plesiorycteropus madagascariensis and the smaller Plesiorycteropus germainepetterae. For a long time it was it was unclear what type of mammal it even was and the best guess seemed to be “some sort of small aardvark-relative” based on anatomical similarities, but various studies disagreed and some even considered it to represent a completely unique order of mammals.

In 2013 an analysis of preserved collagen from one bone finally gave a better answer – Plesiorycteropus was most closely related to tenrecs, which arrived in Madagascar via ocean rafting during the mid-Cenozoic, and the skeletal resemblance to aardvarks was due to convergent evolution.

It was built for scratch-digging, using its strong forelimbs and claws to dig while bracing itself with its hindlimbs and long thick tail. Its snout had large nasal cavities, indicating a good sense of smell, and similarities to the skulls of armadillos suggest it had the same sort of diet of insects, grubs, worms, and other soft foods. It may also have fed on ants and termites.

Since it’s only known from fragments its full size is hard to determine, but rough estimates suggest Plesiorycteropus madagascariensis was “small dog-sized” – possibly having a head-and-body length of 60-80cm (2′-2′7), and a total length of over 1m (3′3″).

Unlike some other extinct Malagasy animals there are no historical or folkloric accounts of anything resembling the bibymalagasy. One bone has been carbon dated to just over 2000 years ago, shortly after the arrival of human settlers, and it seems to have gone extinct very soon after that date.

Island Weirdness #20 – Megaladapis

While some of the lemurs of Madagascar were surprisingly sloth-like, another lineage of these primates evolved in a different direction entirely.

Megaladapis was built similarly to a koala, with a rather squat body and hands and feet adapted for clinging onto branches. Three different species have been identified, with the largest measuring around 1.5m long (4′11″).

Its skull resembled that of a cow, with eyes on the sides of its head, a long snout, and powerful chewing jaw muscles for processing its diet of tough leaves. It also had a very unusual nose for a primate, with nasal bones similar to rhinos – suggesting it may have had an enlarged prehensile upper lip used for grasping foliage.

Much like some of the sloth lemurs, carbon dating of subfossil remains indicates that these “koala lemurs” may have survived until surprisingly recently – possibly only going extinct about 500-600 years ago.

Island Weirdness #19 – Archaeoindris fontoynontii

The small and medium-sized sloth lemurs of Madagascar were incredibly convergent with modern tree sloths, and the biggest member of the group likewise seems to have been the closest they came to evolving a ground sloth equivalent.

Archaeoindris was the largest known lemur – and one of the largest primates – similar in size to a modern gorilla at about 1.5m tall (4′11″). It would have been a slow-moving animal which fed mostly on leaves, and while it was still capable of climbing around in larger trees it was probably much too bulky for upside-down suspension like its smaller relatives, and would likely have had to regularly traverse the ground to reach new feeding sites.

It seems to have been a fairly rare member of the ecosystem, living only in the Central Highlands, and the last known remains date to just over 2000 years ago – around the same time that humans first reached that area of the island. Sadly a combination of factors such as the giant lemurs’ slow reproductive rate, habitat loss, and hunting pressure was too much for their population to recover from all at once, and they probably went extinct very soon after that date.

Island Weirdness #18 – Palaeopropithecus

The island of Madagascar has been isolated from other landmasses for almost 90 million years, and as a result there are many lineages present there found nowhere else on Earth.

Lemurs are one of the island’s most famous residents, having arrived from Africa via a rafting event sometime early in the Cenozoic and evolving to fill the ecological niches occupied elsewhere by monkeys and apes. But while there are around 100 lemur species alive today, there used to be more before the arrival of humans – subfossil remains from the last 25,000 years hint at an ecology with even greater diversity, and types of lemurs much larger than any still living today.

The sloth lemurs, as their name suggests, resembled modern sloths in a remarkable case of convergent evolution. With long limbs and long hooked fingers and toes they were adapted for swinging through trees and hanging from branches, feeding on a wide range of plant material such as leaves, fruit, and seeds.

Palaeopropithecus was one of the larger members of this group, and the most specialized for sloth-like upside-down suspension. Three different species have been identified, with the biggest (Palaeopropithecus maximus) possibly measuring around 1m long (3′3″).

It probably spent almost its entire life in the trees, and would have been slow and awkward on the ground. Malagasy folklore about a creature known as the tretretretre or tratratratra, which couldn’t navigate on smooth flat surfaces, may even represent a cultural memory of Palaeopropithecus from before its extinction – which may have happened as recently as within the last 500-1000 years.

Triopticus

What Triassic animal has a name that sounds like a Transformers character?

Triopticus primus!

Living in Texas, USA, during the Late Triassic, about 229-226 million years ago, Triopticus was a type of archosauriform reptile (a “cousin” to crocodiles, pterosaurs, and dinosaurs). Classifying it any more specifically than that is rather difficult since it’s only known from a single partial skull.

It had five large bony bosses on its head that convergently resembled the domes of pachycephalosaurs, suggesting it may have engaged in similar headbutting or flank-butting behavior. At the back of its skull there was also a distinctive deep pit that looked like a “third eye socket”, inspiring it its name – although this feature probably wasn’t actually a parietal eye, instead just being the result of the way several of the bosses came together at that point.

The rest of its appearance is unknown, and this reconstruction is rather speculative as a result. But based on other archosauriformes it was likely to have been a small semi-sprawling quadruped, possibly around 80cm in length (2′7″).

Sanctacaris

Nicknamed “Santa Claws”, Sanctacaris uncata was a marine arthropod from the Middle Cambrian (~505 mya) Burgess Shale deposits of Canada. Its exact evolutionary relationships are unclear, but it’s thought to have been very closely related to or part of an early branch of the chelicerates – the lineage that includes modern arachnids and horseshoe crabs.

Measuring up to about 9cm long (3.5″), it had forward-facing eyes and five pairs of grasping appendages on the underside of its head, adaptations that suggest it was an active predator convergently similar to anomalocaridids. It probably swam around grabbing onto whatever small prey items it could catch, trapping them in its “limb basket” while it ate them.

Peltephilus

Peltephilus ferox, an armadillo from the Early Miocene of Argentina (~17-16 mya) that was similar in size to a large dog, probably around 1.5m long (5′). It had less solid armor than its modern relatives, with its bony osteoderms being arranged more like chain mail, loosely connected to each other and slightly overlapping, creating a much more flexible body covering.

Its most unusual features were the horns on its snout, convergently resembling the later horned gophers of North America. But unlike other mammals Peltephilus‘ horns were actually modified plates of its face armor, enlarged pointed osteoderms that were only connected to its skull by soft tissue membranes – meaning that after death they tended to fall off, and the exact number and position of them is still a little uncertain.

Its unusually broad snout and large teeth were originally interpreted as evidence of it being an active carnivore, but more recent studies of its anatomy have suggested that it was much more likely to have been a herbivorous or omnivorous digger, mainly feeding on underground plant matter like roots and tubers.

Ichthyosaur Blubber

In early 2017 evidence of blubber was found in plesiosaurs, indicating that they were probably much more chubby than they’re usually reconstructed, and now in late 2018 it’s been found in an ichthyosaur, too!

Living during the Early Jurassic (~183-179 mya) in the shallow seas that covered most of Europe at the time, Stenopterygius was an average-sized ichthyosaur growing up to about 4m in length (13′). A fossil found in Germany has some incredibly good soft-tissue preservation, showing smooth flexible scaleless skin, a layer of insulating blubber very convergently similar to that found in cetaceans, and even evidence of countershaded coloration.

While the confirmation of blubber is amazing, and gives further evidence that ichthyosaurs were warm-blooded, the color preservation might actually be even more interesting. The skin pigmentation is preserved in enough fine detail for branched melanophores to be visible under a microscope – a type of cell associated with the ability to change color. So there’s a possibility that ichthyosaurs could actively darken or lighten their color patterns, for purposes such as better camouflage, UV protection, or temperature regulation.

Almost-Living Fossils Month #24 – Sabertoothed Sparassodonts

Along with the marsupials and the polydolopimorphs, the sparassodonts were one of the lineages of metatherian mammals that inhabited South America during its “great isolation” for most of the Cenozoic. And despite having to share the large carnivore niches with both the terror birds and the sebecosuchian crocs, they still managed to become the main mammalian predators of the region.

Their first definite fossils come from the start of the Paleocene (~65 mya), but they probably actually originated sometime in the Late Cretaceous before the mass extinction. A currently-unnamed skull from Mongolia (~70 mya) appears to be either an early sparassodont or a very close relative, and a North American metatherian called Varalphadon (~90 mya) may also be linked to the group. It’s possible that, like the marsupials, they may have first evolved in North America and later spread into South America before it became isolated.

Like their marsupial relatives they would have given birth to tiny undeveloped young, although we don’t know for certain if they actually had pouches or not. Their epipubic bones were highly reduced, so it’s possible they didn’t have pouches – but they also might have had mostly cartilaginous epipubics (like thylacines) that just didn’t fossilize.

Over the course of the Cenozoic the sparassodonts convergently evolved many similar features to placental carnivorans, with carnassial teeth for shearing through flesh and a wide variety of body shapes ranging from small weasel-like forms to long-snouted ambush hunters to large hyaena-like bone-crushers.

But by far the most famous members of the group were the thylacosmilids. First appearing in the Early Miocene, about 20-15 million years ago, these sparassodonts developed huge elongated canine teeth that resembled those of sabertoothed cats. Unlike the felid sabertooths, however, thylacosmilids’ fangs grew continuously and their lower jaws had long bony flanges that supported and protected their teeth when theirs jaws were closed.

Thylacosmilus atrox was the last and most highly specialized of the thylacosmilids, living from the Late Miocene to the Late Pliocene, around 9-3 million years ago. About 1.2-1.5m long (~4-5′) and standing 60cm tall at the shoulder (2′) it was similar in size to a modern jaguar – not huge compared to some placental predators, but still one of the largest of all known carnivorous metatherians.

Despite its huge fangs it actually had a fairly weak bite force, instead relying on its strong forelimbs to immobilize its prey before delivering precise deep stabs into soft body parts using powerful neck muscles. The structure of its limbs also suggests it wasn’t a fast runner, and it probably had to stalk or ambush its targets.

Although the extinction of Thylacosmilus and the other last sparassodonts is often blamed on being out-competed by similar placental carnivores arriving during the Great American Interchange, it seems like that wasn’t actually the case. Many of their northern placental equivalents such as Smilodon didn’t enter South America until the mid-Pleistocene (~1-0.7 mya), over 1.5 million years after the last record of any living sparassodonts. So it’s likely they never actually met each other, and the disappearance of the sparassodonts may be more linked to cooling climates in the Pliocene and early Pleistocene.

Almost-Living Fossils Month #20 – Some Very Spiky Turtles

The meiolaniformes were a group of terrestrial turtles that first appeared in the fossil record in the Early Cretaceous, around 125 million years ago. Although they were originally thought to be cryptodirans, more recent studies suggest they weren’t actually quite true turtles at all, instead being close evolutionary cousins to them in a much older and more “primitive” lineage that may go back as far as the Triassic.

They’re known mainly from South America and Oceania, but they may have had a more global distribution during the Cretaceous, with some fossils from the northern continents sometimes being classified as members of the group. However, only the South American meiolaniformes seem to have actually survived through the end-Cretaceous extinction.

The most distinctive meiolaniformes were the heavily armored meiolaniids, which first appeared in Patagonia during the Early Eocene (~48 mya). With large horns on their heads and thorn-like spikes along their long tails, they seem to have convergently evolved to fill the same sort of large-herbivore-tank niche as ankylosaurs and glyptodonts.

They also had fairly large nasal cavities, which might indicate a well-developed sense of smell – or may have been an adaptation for regulating the heat and moisture content of each breath, similar to the complex noses of ankylosaurs.

The South American meiolaniformes all went extinct around the end of the Eocene (~33 mya), but some meiolaniids had already dispersed across to Australia via Antarctica (before the continents had fully separated, and before Antarctica had frozen over) and they continued to survive there for most of the rest of the Cenozoic. They even went on to spread to various islands around Oceania, suggesting they were able to float and swim like modern giant tortoises.

The largest Australian meiolaniids reached sizes of around 2.5m long (8′2″), making them some of the biggest of all known terrestrial turtles. These giant forms went extinct in the Late Pleistocene, around 50,000 years ago, alongside much of the other Australian megafauna.

A few smaller varieties hung on in smaller islands to the east, with one of the latest-surviving species being Meiolania platyceps on Lord Howe island. It was only about half the size of its biggest Australian relatives – an example of insular dwarfism – and lived into the Late Holocene just 3000-2000 years ago.

Meiolania species on other islands seem to have gone extinct after the arrival of humans. But Lord Howe Island appears to have never been inhabited prior to European settlement in the late 1700s, so it’s unclear why this last of the meiolaniformes disappeared.

[Edit: A 2018 study of Meiolania platyceps’ anatomy suggests it may have been more aquatic than previously thought. It might have been something like a giant herbivorous snapping turtle or an armored reptilian hippo, bottom-walking around in coastal lagoons, with its big nasal cavity housing salt glands.]