arthropod – Page 5 – Nix Illustration

Kalligrammatids

Did you know butterflies weren’t the first insects to look like butterflies?

Lepidopterans (the group of insects containing moths and butterflies) have been around since the Late Triassic – but it wasn’t until the diversification of flowering plants during the Cretaceous that recognizable moths would have evolved, and true butterflies didn’t actually appear until the early Cenozoic.

Before then, back in the mid-Jurassic about 165 million years ago, a completely different group of insects convergently evolved remarkably butterfly-like features such as large colorful scaled wings and long sucking proboscises.

Known as the kalligrammatids, these insects were giant members of the lacewing group, related to modern forms like antlions and owlflies. But unlike their predatory relatives the kalligrammatids were specialized pollinators, possibly having a mutualistic relationship with the flower-like cones of bennettitales or the pollination drops of some types of conifers. They seem to have originated in China and were found across Asia and Europe by the Late Jurassic, but a few fossils from South America suggest they were even more widespread and may just have a poor fossil record.

They reached wingspans of up to 16cm (~6″), comparable to some of the largest modern butterflies, and often sported conspicuous anti-predator markings on their wings such as stripes and eyespots – so it’s not surprising that they’re often nicknamed the “butterflies of the Jurassic”.

Rather ironically, the extinction of the kalligrammatids was probably linked to the rise of the flowering plants that the true butterflies would later be so dependent on. As flowers diversified and plants like the bennettitales declined, the kalligrammatids dwindled and disappeared, with the last known fossil record coming from the mid-Cretaceous of Brazil about 113 million years ago.

But while they were around, I do wonder if they also exhibited some similar behaviors – such as mud-puddling for extra nutrients, and specifically the habit of drinking the tears of larger animals that we see in some species. Perhaps some non-avian dinosaurs like this Dilong occasionally put up with kalligrammatids sitting on their faces!

Eons Roundup 3

Some more recent work I’ve done for PBS Eons!

The eurypterids Hibbertopterus and Brachyopterus, from “When Giant Scorpions Swarmed the Seas”
https://www.youtube.com/watch?v=1sQXTXbuLYo

The short-faced bears Plionarctos and Arctotherium, from “The Mystery Behind the Biggest Bears of All Time”
https://www.youtube.com/watch?v=KtsOhmBb92E

The big cats Panthera blytheae and Panthera atrox, from “The Ghostly Origins of the Big Cats”
https://www.youtube.com/watch?v=oPJnqWke5n8

Clausocaris

While this might look like a sci-fi alien design, it was actually a very real Earth animal!

This strange-looking creature was Clausocaris lithographica, a member of a group of unique marine arthropods known as thylacocephalans. Only about 3.5cm long (1.4″), it lived in a shallow tropical lagoon environment during the Late Jurassic of Germany, about 150-145 million years ago.

Like most other thylacocephalans it had a narrow flattened shield-like carapace, three pairs of large grasping limbs, and a battery of swimming appendages further back – along with absolutely enormous bulbous eyes. Based on this anatomy it would have been a highly visual hunter, using its huge eyes to locate prey items and then snagging them with its long spiny limbs.

And we’re not even entirely sure what type of arthropods thylacocephalans actually were. They’re generally thought to be some sort of crustacean, but their highly modified anatomy makes linking up their exact evolutionary affinities very difficult. Whatever they were, they must have been incredibly successful as a group because they first appeared in the early Cambrian (~518 mya) and survived all the way into the Late Cretaceous (~94 mya).

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.

Vaderlimulus

Vaderlimulus tricki, a horseshoe crab from the Early Triassic of Idaho, USA (~251-247 mya). Named for its resemblance to the shape of Darth Vader’s helmet, it’s the earliest known Mesozoic horseshoe crab from North America and was closely related to another oddly-shaped form from Australia.

It was much smaller than its modern relatives, only about 10cm long (4″), and probably lived in a brackish estuary environment where seawater and freshwater met.

Almost-Living Fossils Month #08 – A Lot Of Lobsters

Hoploparia was a type of clawed lobster that first appeared in the fossil record in the Early Cretaceous about 140 million years ago. Many many different species within this genus have been found all over the world – over 100 of them have been described! – with quite a lot of anatomical diversity between them, showing that these lobsters were very good at adapting to a wide range of habitats and climates.

Although the vast majority of Hoploparia species lived just in the Cretaceous period, a small number of them did survive the end-Cretaceous mass extinction 66 million years ago. Hoploparia stokesi here was one of them, known from both the Late Cretaceous and Early Paleocene of Antarctica (~70-61 mya) – and was actually one of the first fossils ever described from the continent.

Specimens of this species are usually about 13cm long (5″), and show an evolutionary shift over time, developing much stronger claws and jaws, suggesting they were adapting their diet towards hard-shelled prey.

Various species of Hoploparia persisted on in North America, Europe, and Antarctica for the first half of the Cenozoic, but they never recovered to anywhere close to their Cretaceous levels of diversity. By the Early Miocene (~23-16 mya) there was just one known species left hanging on in Antarctica, and then they were gone.

(However, some modern lobster genera may in fact have originated from somewhere within the huge Hoploparia lineage back in the Cretaceous, so they might at least still have some close living relatives!)

Linguamyrmex

Linguamyrmex vladi, an ant from the Late Cretaceous of Myanmar (~99 mya). Part of an extinct group known as the Haidomyrmecini, or “hell ants”, it measured about 5mm long (0.2″) and is known from several individuals in amber.

It had huge scythe-shaped mandibles and a horn-like appendage on its head which together formed a powerful trap-jaw mechanism, snapping vertically shut when a pair of long sensitive trigger hairs touched against a target. One specimen was preserved close to a large soft-bodied beetle larva, which may have been an intended prey item.

When closed, the mandibles formed a tube-like channel to Linguamyrmex’s mouth, allowing it to suck out the “blood” from its impaled victims – and inspiring its species name, referencing Vlad Dracula.

The horn was also reinforced with metal particles in the chitinous exoskeleton, strengthening it against the impact of its closing jaws.

Synophalos

Synophalos xynos, a shrimp-like arthropod from the Early Cambrian of China (~515 mya). Thought to be closely related to stem-crustaceans like Waptia, it was about 2cm long (0.75″) and had a bivalved carapace with a segmented body ending in a forked tail.

Unlike any other known arthropods, however, it formed long “conga line” chains of up to twenty individuals, with the tail of each animal locking securely into the shell of the next. The function of the these chains is unknown, although suggestions include some sort of mating behavior, migration, or defense against predators.

Only one specimen was found completely on its own, and its slightly longer carapace suggests it may represent a different solitary life stage of these strange little creatures.

Unsolved Paleo Mysteries Month #06 – Tricky Trilobites

Trilobites are common and recognizable fossils, found around the world from the Early Cambrian to the Late Permian (521-250 mya), and ranging in size from 1mm to 72cm (0.03″ – 2′4″). They were some of the first organisms on Earth with complex eyes, and some groups also developed ornamentation like spines, horns, and tridents. The image above depicts a particularly elaborate genus known as Dicranurus.

Occasionally fossils have been found showing fine details of trilobite anatomy like antennae, legs, gills, and digestive organs, and we’ve even recently discovered their eggs.

And yet we don’t really know where they came from. Much like the pterosaurs we started the month off with, trilobites appear suddenly in the fossil record with no intermediate or ancestral forms to definitively link them to other groups. We know they were definitely arthropods, but which arthropods they were most closely related to is still uncertain.

They might be related to the chelicerates (arachnids, horseshoe crabs, and eurypterids), or they might be part of the mandibulates (crustaceans, insects, and myriapods). But the exact relationships of these major arthropod groups are still in dispute, too, and phylogenetic results can vary wildly depending on whether trilobites are included in the analysis or not.

It’s probably going to be some time before any sort of consensus is reached.