In this post, we continue with out exploration of the
Mid-Triassic, 240 MYA. In this post, we look at the Moenkopi and Lykins Formations of
North America, and see what they can tell us about this ancient time. We also delve a bit into the evolution of fin-backs and sails as display structures, like you can see in the picture below.
In the Moenkopi Formation of North America, we can gain a more complete understanding of the terrestrial fauna of this time period. We already discussed the
rauisuchian Ticinosuchus and the
protorosaur Macrocnemus from
Monte San Giorgio, as well as the large temnospondyl
amphibian Eocyclotosaurus from Grès à Voltzia, but there were lots of other very exciting animals alive back then as well.
Arizonasaurus, a
poposaurid archosaur, was likely one of the top predators, and had a back adorned by a
Spinosaurus-like sail, similar to the sail seen in the more primitive
German archosaur
Ctenosauriscus.
We talked about the poposaurs in a recent post which you can read by clicking
HERE. The poposaurs, as well as the rauisuchians, were both members of a large group that many scientists refer to as "
pseudosuchians." These animals were
crocodilian in nature, and fairly closely related to them. But some pseudosuchians, including some rauisuchians and poposaurs, actually evolved a body design similar to some types of
dinosaurs, where they could walk on either two or four feet.
Let's jump back to the sails on the back of
Arizonasaurus,
Ctenosauriscus, and
Spinosaurus. The first two are fairly closely related to each other, but
Spinosaurus is not closely related at all, separated by around 150 MY of geologic time. The question is, why would these animals have
convergently evolved these sails on their backs? The orthodox answer is that the sails help the animal thermoregulate, that by turning the sail towards or away from the sun, it would help the animal warm up or cool off. Similar ideas have been proposed for other animals that feature similar anatomical structures, such as
Stegosaurus with its double row of
plates down its back, or the primitive
synapsids Dimetrodon and
Edaphosaurus.
This idea has some major flaws, however, as argued by
paleontologist Dr. Robert Bakker in his excellent and influential book "
The Dinosaur Heresies." In the book, Bakker points out that very close relatives of these sail-animals don't have these strange fins on their back. If the thermoregulation theory is accepted, then that would suggest that these very closely related animals had very different thermoregulatory needs. For example, Bakker points out that the primitive synapsids
Dimetrodon and
Sphenacodon are very closely related to each other, and most of their anatomy is very similar, other than the fact that
Dimetrodon has that enormous sail on its back, and
Sphenacodon has only a very slight elongation of its vertebrae. If we accept the thermoregulatory hypothesis at face value, it would imply that, despite being very similar in anatomy and lifestyle, for whatever reason
Dimetrodon and
Sphenacodon had drastically different thermoregulatory needs. Below, we have a chart showing a sail-back on the left with a closely related animal on the right, this one lacking a sail.
So what do we propose instead? Most likely a means of attracting a mate. In animals today, it is display structures and behavior pertaining to courtship that changes the most. An excellent example of this is the
birds of paradise from
New Guinea, which we discussed in greater depth in a post with a similar focus, in regards to the plates of
Stegosaurus, which you can read
HERE.
Sharks, such as the very strange-looking
Hybodus, have also been discovered in the Moenkopi Formation.
Where I live in
Colorado, the Lykins Formation is approximately contemporaneous with the Moenkopi Formation. The Lykins Formation isn't the most exciting of Colorado's geologic formations (at least not for people interested in fossils or excitement), but stromatolites can be found in some areas of the formation. Stromatolites are layers of wavy and convoluted cyanobacteria that sometimes form in areas of shallow water. Cyanobacteria by themselves aren't very big, as they are simply single-celled photosynthetic
bacteria. However, together, the gelatinous secretions they produce is enough to trap the sediment that settles out of the water, forming visible laminations that sometimes fossilize.
Stromatolites were much more common prior to the Cambrian Explosion approximately 500 MYA, as back then there wasn't really anything that could eat it. Believe it or not, layers of cyanobacteria are notoriously bad at running away from herbivores, even something as slow as a
snail or a slug. Today, stromatolites are relatively rare, especially considering their past abundance, but you can still find them in isolated areas like Shark Bay,
Australia, and Lake Salda in Turkey. Most stromatolites form in areas that discourage herbivore grazing. Shark Bay and Lake Salda are both hypersaline areas, places where most herbivores simply don't want to go (especially slugs and snails). More recently, stromatolite-like growths were found living in an abandoned asbestos mine in Yukon,
Canada. This indicates to us that the parts of the Lykins Formation in which the stromatolites are found were likely not conducive to supporting herbivores, perhaps also due to hypersaline conditions.
Join us soon for our next post, in which we look at ancestors of both dinosaurs and mammals that were alive during this time! We will also do a little investigating into different types of dentition, so stay tuned!
Works Cited: