QUENSTEDTOCERAS WITH PATHOLOGY

What you are seeing here is a protuberance extruding from the venter of Quenstedtoceras cf. leachi (Sowerby). It is a pathology in the shell from hosting immature bivalves that shared the seas with these Middle Jurassic, Upper Callovian, Lamberti zone fauna from the Volga River basin. 

The collecting site is the now inactive Dubki commercial clay quarry and brickyard near Saratov, Russia. 

The site has produced thousands of ammonite specimens. A good 1,100 of those ended up at the Black Hills Institute of Geological Research in Hill City, South Dakota. 

Roughly 1,000 of those are Quenstedtoceras (Lamberticeras) lamberti and the other 100 are a mix of other species found in the same zone. These included Eboraciceras, Peltoceras, Kosmoceras, Grossouvria, Proriceras, Cadoceras and Rursiceras. 

What is especially interesting is the volume of specimens — 167 Quenstedtoceras (Lamberticeras) lamberti and 89 other species in the Black Hills collection — with healed predation injuries. It seems Quenstedtoceras (Lamberticeras) lamberti are the most common specimens found here and so not surprisingly the most common species found injured. 

Of the 1,000, 655 of the Quenstedtoceras (Lamberticeras) lamberti displayed some sort of deformation or growth on the shell or had grown in a tilted manner. 

Again, some of the Q. lamberti had small depressions in the centre likely due to a healed bite and hosting infestations of the immature bivalve Placunopsis and some Ostrea. 

The bivalves thrived on their accommodating hosts and the ammonites carried on, growing their shells right up and over their bivalve guests. 

This relationship led to some weird and deformities of their shells. They grow in, around, up and over nearly every surface of the shell and seem to have lived out their lives there. It must have gotten a bit unworkable for the ammonites, their shells becoming warped and unevenly weighted. 

Over time, both the flourishing bivalves and the ammonite shells growing up and over them produced some of the most interesting pathology specimens I have ever seen.    

In the photo here from Emil Black, you can see some of the distorted shapes of Quenstedtoceras sp. 

Look closely and you see a trochospiral or flattened appearance on one side while they are rounded on the other. 

All of these beauties hail from the Dubki Quarry near Saratov, Russia. The ammonites were collected in marl or clay used in brick making. The clay particles suggest a calm, deep marine environment. 

One of the lovely features of the preservation here is the amount of pyrite filling and replacement. It looks like these ammonites were buried in an oxygen-deficient environment. 

The ammonites were likely living higher in the water column, well above the oxygen-poor bottom. An isotopic study would be interesting to prove this hypothesis. 

There's certainly enough of these ammonites that have been recovered to make that possible. It's estimated that over a thousand specimens have been recovered from the site but that number is likely much higher. But these are not complete specimens. We mostly find the phragmocones and partial body chambers. Given the numbers, this may be a site documenting a mass spawning death over several years or generations.

If you fancy a read on all things cephie, consider picking up a copy of Cephalopods Present and Past: New Insights and Fresh Perspectives edited by Neil Landman and Richard Davis. Figure 16.2 is from page 348 of that publication and shows the hosting predation quite well. 

Photos: Courtesy of the deeply awesome Emil Black. These are in his personal collection that I hope to see in person one day. 

It was his sharing of the top photo and the strange anomaly that had me explore more about the fossils from Dubki and the weird and wonderful hosting relationship between ammonites and bivalves. Thank you, my friend!

ZENASPIS: DEVONIAN FISH MORTALITY PLATE

A Devonian fish mortality plate showing all lower shields of Zenaspis podolica (Lankester, 1869) and Stensiopelta pustulata (or Victoraspis longicornualis) from Lower Devonian deposits of Podolia, Ukraine.

Zenaspis is an extinct genus of jawless fish which existed during the early Devonian period. Due to it being jawless, Zenaspis was probably a bottom feeder.

The lovely 420 million-year-old plate you see here is from Podolia or Podilia, a historic region in Eastern Europe, located in the west-central and south-western parts of Ukraine, in northeastern Moldova. 

Podolia is the only region in Ukraine where Lower Devonian remains of ichthyofauna can be found near the surface.

For the past 150 years, vertebrate fossils have been found in more than 90 localities situated in outcrops along banks of the Dniester River and its northern tributaries, and in sandstone quarries. 

At present faunal list of Early Devonian agnathans and fishes from Podolia number 72 species, including 8 Thelodonti, 39 Heterostraci, 19 Osteostraci, 4 Placodermi, 1 Acanthodii, and 1 Holocephali (Voichyshyn 2001a, modified).

In Podolia, Lower Devonian redbeds strata (the Old Red Formation or Dniester Series) can be found up to 1800 m thick and range from Lochkovian to Eifelian in age (Narbutas 1984; Drygant 2000, 2003). 

In the lower part (Ustechko and Khmeleva members of the Dniester Series) they consist of multicoloured, mainly red, fine-grained cross-bedded massive quartz sandstones and siltstones with seams of argillites (Drygant 2000).

We see fossils beds of Zenaspis in the early Devonian of Western Europe. Both Zenaspis pagei and Zenaspis poweri can be found up to 25 centimetres long in Devonian outcrops of Scotland.

Reference: Voichyshyn, V. 2006. New osteostracans from the Lower Devonian terrigenous deposits of Podolia, Ukraine. Acta Palaeontologica Polonica 51 (1): 131–142. Photo care of Fossilero Fisherman.

BACK IN THE USSR: BEADANTICERAS OF THE NORTHERN CAUCASUS

This lovely oil in water coloured ammonite is the beauty Beudanticeras sp. from the Lower Cretaceous (Upper Aptian), Krasnodar region, Northern Caucasus, southern Russia. 

This area of the world has beautiful fossil specimens with their distinct colouring. The geology and paleontological history of the region are fascinating as is its more recent history. 

The territory of present Krasnodar Krai was inhabited as early as the Paleolithic, about 2 million years ago. It was inhabited by various tribes and peoples since ancient times. 

There were several Greek colonies on the Black Sea coast, which later became part of the Kingdom of the Bosporus. In 631, the Great Bulgaria state was founded in the Kuban. In the 8th-10th centuries, the territory was part of Khazaria.

In 965, the Kievan Prince Svyatoslav defeated the Khazar Khanate and this region came under the power of Kievan Rus, Tmutarakan principality was formed. At the end of the 11th century, in connection with the strengthening of the Polovtsy and claims of Byzantium, Tmutarakan principality came under the authority of the Byzantine emperors (until 1204).

In 1243-1438, this land was part of the Golden Horde. After its collapse, Kuban was divided between the Crimean Khanate, Circassia, and the Ottoman Empire, which dominated in the region. Russia began to challenge the protectorate over the territory during the Russian-Turkish wars.

In 1783, by decree of Catherine II, the right-bank Kuban and Taman Peninsula became part of the Russian Empire after the liquidation of the Crimean Khanate. 

In 1792-1793, Zaporozhye (Black Sea) Cossacks resettled here to protect new borders of the country along the Kuban River. 

During the military campaign to establish control over the North Caucasus (Caucasian War of 1763-1864), in the 1830s, the Ottoman Empire for forced out of the region and Russia gained access to the Black Sea coast.

Prior to the revolutionary events of 1917, most of the territory of present Krasnodar Krai was occupied by the Kuban region, founded in 1860. In 1900, the population of the region was about 2 million people. In 1913, it ranked 2nd by the gross harvest of grain, 1st place for the production of bread in the Russian Empire.

The Kuban was one of the centres of resistance after the Bolshevik revolution of 1917. In 1918-1920, there was a non-Bolshevik Kuban People’s Republic. In 1924, North-Caucasian krai was founded with the centre in Rostov-on-Don. In 1934, it was divided into Azov-Black Sea krai (Rostov-on-Don) and North Caucasus krai (Stavropol).

September 13, 1937, the Azov-Black Sea region was divided into the Rostov region and Krasnodar Krai that included Adygei autonomous oblast. During the Second World War, the region was captured by the Germans. After the battle for the Caucasus, it was liberated. There are about 1,500 monuments and memorials commemorating heroes of the war on the territory of Krasnodar Krai.

The lovely block you see here is in the collections of the awesome John Fam, Vice-Chair of the Vancouver Paleontological Society in British Columbia, Canada.

AVES: LIVING DINOSAURS

Cassowary, Casuariiformes

Wherever you are in the world, it is likely that you know your local birds. True, you may call them des Oiseaux, pássaros or uccelli — but you'll know their common names by heart.

You will also likely know their sounds. The tweets, chirps, hoots and caws of the species living in your backyard.

Birds come in all shapes and sizes and their brethren blanket the globe. It is amazing to think that they all sprang from the same lineage given the sheer variety. 

If you picture them, we have such a variety on the planet — parrots, finches, wee hummingbirds, long-legged waterbirds, waddling penguins and showy toucans. 

But whether they are a gull, hawk, cuckoo, hornbill, potoo or albatross, they are all cousins in the warm-blooded vertebrate class Aves. 

The defining features of the Aves are feathers, toothless beaked jaws, the laying of hard-shelled eggs, a high metabolic rate, a four-chambered heart, and a strong yet lightweight skeleton. The best features, their ability to dance, bounce and sing, are not listed, but it is how I see them in the world.

These modern dinosaurs live worldwide and range in size from the 5 cm (2 in) bee hummingbird to the 2.75 m (9 ft) ostrich. 

There are about ten thousand living species, more than half of which are passerine, or "perching" birds. Birds have wings whose development varies according to species; the only known groups without wings are the extinct moa and elephant birds.

Wings evolved from forelimbs giving birds the ability to fly

Wings, which evolved from forelimbs, gave birds the ability to fly, although further evolution has led to the loss of flight in some birds, including ratites, penguins, and diverse endemic island species. 

The digestive and respiratory systems of birds are also uniquely adapted for flight. Some bird species of aquatic environments, particularly seabirds and some waterbirds, have further evolved for swimming.

Wee Feathered Theropod Dinosaurs

We now know from fossil and biological evidence that birds are a specialized subgroup of theropod dinosaurs, and more specifically, they are members of Maniraptora, a group of theropods that includes dromaeosaurs and oviraptorids, amongst others. As palaeontologists discover more theropods closely related to birds, the previously clear distinction between non-birds and birds has become a bit muddy.

Recent discoveries in the Liaoning Province of northeast China, which include many small theropod feathered dinosaurs — and some excellent arty reproductions — contribute to this ambiguity. 

Still, other fossil specimens found here shed a light on the evolution of Aves. Confuciusornis sanctus, an Early Cretaceous bird from the Yixian and Jiufotang Formations of China is the oldest known bird to have a beak.

Like modern birds, Confuciusornis had a toothless beak, but close relatives of modern birds such as Hesperornis and Ichthyornis were toothed, telling us that the loss of teeth occurred convergently in Confuciusornis and living birds.

The consensus view in contemporary palaeontology is that the flying theropods, or avialans, are the closest relatives of the deinonychosaurs, which include dromaeosaurids and troodontids.

Together, these form a group called Paraves. Some basal members of this group, such as Microraptor, have features that may have enabled them to glide or fly. 

The most basal deinonychosaurs were wee little things. This raises the possibility that the ancestor of all paravians may have been arboreal, have been able to glide, or both. Unlike Archaeopteryx and the non-avialan feathered dinosaurs, who primarily ate meat, tummy contents from recent avialan studies suggest that the first avialans were omnivores. Even more intriguing...

Avialae, which translates to bird wings, are a clade of flying dinosaurs containing the only living dinosaurs, the birds. It is usually defined as all theropod dinosaurs more closely related to modern birds — Aves — than to deinonychosaurs, though alternative definitions are occasionally bantered back and forth.

The Earliest Avialan: Archaeopteryx lithographica

Archaeopteryx, bird-like dinosaur from the Late Jurassic

Archaeopteryx lithographica, from the late Jurassic Period Solnhofen Formation of Germany, is the earliest known avialan that may have had the capability of powered flight. 

However, several older avialans are known from the Late Jurassic Tiaojishan Formation of China, dating to about 160 million years ago.

The Late Jurassic Archaeopteryx is well-known as one of the first transitional fossils to be found, and it provided support for the theory of evolution in the late 19th century. 

Archaeopteryx was the first fossil to clearly display both traditional reptilian characteristics — teeth, clawed fingers, and a long, lizard-like tail—as well as wings with flight feathers similar to those of modern birds. It is not considered a direct ancestor of birds, though it is possibly closely related to the true ancestor.

Unlikely yet true, the closest living relatives of birds are the crocodilians. Birds are descendants of the primitive avialans — whose members include Archaeopteryx — which first appeared about 160 million years ago in China.

DNA evidence tells us that modern birds — Neornithes — evolved in the Middle to Late Cretaceous, and diversified dramatically around the time of the Cretaceous–Paleogene extinction event 66 mya, which killed off the pterosaurs and all non-avian dinosaurs.

In birds, the brain, especially the telencephalon, is remarkably developed, both in relative volume and complexity. Unlike most early‐branching sauropsids, the adults of birds and other archosaurs have a well‐ossified neurocranium. In contrast to most of their reptilian relatives, but similar to what we see in mammals, bird brains fit closely to the endocranial cavity so that major external features are reflected in the endocasts. What you see on the inside is what you see on the outside.

This makes birds an excellent group for palaeoneurological investigations. The first observation of the brain in a long‐extinct bird was made in the first quarter of the 19th century. However, it was not until the 2000s and the application of modern imaging technologies that avian palaeoneurology really took off.

Understanding how the mode of life is reflected in the external morphology of the brains of birds is but one of several future directions in which avian palaeoneurological research may extend.

Although the number of fossil specimens suitable for palaeoneurological explorations is considerably smaller in birds than in mammals and will very likely remain so, the coming years will certainly witness a momentous strengthening of this rapidly growing field of research at the overlap between ornithology, palaeontology, evolutionary biology and the neurosciences.

Reference: Cau, Andrea; Brougham, Tom; Naish, Darren (2015). "The phylogenetic affinities of the bizarre Late Cretaceous Romanian theropod Balaur bondoc (Dinosauria, Maniraptora): Dromaeosaurid or flightless bird?". PeerJ. 3: e1032. doi:10.7717/peerj.1032. PMC 4476167. PMID 26157616.

Reference: Ivanov, M., Hrdlickova, S. & Gregorova, R. (2001) The Complete Encyclopedia of Fossils. Rebo Publishers, Netherlands. p. 312

WHEN GORGON REIGNED SUPREME

Step back into the deep Paleozoic—an era that began some 540 million years ago with oceans bustling with trilobites, early fish, and soft-bodied wonders, while the continents themselves hosted little more than humble mats of mosses and fungi. Life’s great drama was still mostly underwater.

Fast-forward 240 million years, and the evolutionary landscape had transformed dramatically. 

Vertebrates had conquered the land, ecosystems had diversified, and Earth’s surface teemed with reptilian innovators, amphibians the size of crocodiles, and the early ancestors of mammals. Among these emerging terrestrial titans strode the Gorgonopsians, or “Gorgons”—ferocious sabre-toothed therapsids that dominated the Middle to Late Permian, from about 265 to 252 million years ago.

These were no sluggish proto-reptiles. Gorgons were highly specialized predators, boasting elongated canine teeth worthy of any future saber-toothed cat, powerful jaws, and sleek, muscular bodies built for pursuit. Their anatomy blended the primitive and the prophetic: reptile-like postures paired with early mammalian traits such as differentiated teeth and strong jaw musculature. 

Their clawed limbs, keen forward-facing eyes, and cutting-edge predatory adaptations placed them firmly at the top of the Permian food chain. In a world long before dinosaurs, they were the undisputed apex hunters.

My own fascination with these remarkable creatures was ignited by Gorgons, Peter Ward’s wonderfully wry and insightful dive into the ancient landscapes of South Africa. Ward’s vivid tales of fieldwork in the blistering, bone-dry vastness of the Karoo Basin—ancestral home of the Gorgons—captured both the hardships and the sheer exhilaration of unearthing deep time. 

His descriptions of sunburn and scientific revelations in that arid world made me laugh more than once. It is a highly enjoyable read.

The Great Karoo itself is a geological and paleontological marvel. This enormous, semi-arid expanse formed within a vast inland basin roughly 320 million years ago, at a time when the part of Gondwana destined to become Africa lay draped across the South Pole. 

Layer upon layer of sedimentary rock accumulated as glaciers advanced and retreated, rivers meandered, lakes dried, and ecosystems rose and fell. Today, those layers read like a grand evolutionary chronicle, preserving a world populated by beaked herbivores, hulking amphibians, and the charismatic, toothy Gorgonopsians.

This was a pivotal chapter in Earth’s history—just before the catastrophic Permian-Triassic extinction swept away nearly 90% of life. Yet in the twilight of the Permian, before that great dying, the Karoo thrived with innovation and ecological complexity. It was a world where the early steps toward warm-bloodedness were being taken, where synapsids (our own deep ancestors) were experimenting with new forms, and where the Gorgons reigned supreme.

FOSSIL BEES, FIRST NATION HISTORY

Welcome to the world of bees. This fuzzy yellow and black striped fellow is a bumblebee in the genus Bombus sp., family Apidae. 

We know him from our gardens where we see them busily lapping up nectar and pollen from flowers with their long hairy tongues.

My Norwegian cousins on my mother's side call them humle. Norway is a wonderful place to be something wild as the wild places have not been disturbed by our hands. Head out for a walk in the wild flowers and the sounds you will hear are the wind and the bees en masse amongst the flowers.   

There are an impressive thirty-five species of bumblebee species that call Norway hjem (home), and one, Bombus consobrinus, boasts the longest tongue that they use to feast solely on Monkshood, genus Aconitum, you may know by the name Wolf's-bane.

In the Kwak̓wala language of the Kwakwaka'wakw, speakers of Kwak'wala, and my family on my father's side in the Pacific Northwest, bumblebees are known as ha̱mdzalat̕si — though I wonder if this is actually the word for a honey bee, Apis mellifera, as ha̱mdzat̕si is the word for a beehive.

I have a special fondness for all bees and look for them both in the garden and in First Nation art.

Bumblebees' habit of rolling around in flowers gives us a sense that these industrious insects are also playful. In First Nation art they provide levity — comic relief along with their cousins the mosquitoes and wasps — as First Nation dancers wear masks made to mimic their round faces, big round eyes and pointy stingers. 

A bit of artistic license is taken with their forms as each mask may have up to six stingers. The dancers weave amongst the watchful audience and swoop down to playfully give many of the guests a good, albeit gentle, poke. 

Honey bees actually do a little dance when they get back to the nest with news of an exciting new place to forage — truly they do. Bumblebees do not do a wee bee dance when they come home pleased with themselves from a successful foraging mission, but they do rush around excitedly, running to and fro to share their excitement. They are social learners, so this behaviour can signal those heading out to join them as they return to the perfect patch of wildflowers. 

Bumblebees are quite passive and usually sting in defense of their nest or if they feel threatened. Female bumblebees can sting several times and live on afterwards — unlike honeybees who hold back on their single sting as its barbs hook in once used and their exit shears it off, marking their demise.

They are important buzz pollinators both for our food crops and our wildflowers. Their wings beat at 130 times or more per second, literally shaking the pollen off the flowers with their vibration. 

And they truly are busy bees, spending their days fully focused on their work. Bumblebees collect and carry pollen and nectar back to the nest which may be as much as 25% to 75% of their body weight. 

And they are courteous — as they harvest each flower, they mark them with a particular scent to help others in their group know that the nectar is gone. 

The food they bring back to the nest is eaten to keep the hive healthy but is not used to make honey as each new season's queen bees hibernate over the winter and emerge reinvigorated to seek a new hive each Spring. She will choose a new site, primarily underground depending on the bumblebee species, and then set to work building wax cells for each of her fertilized eggs. 

Bumblebees are quite hardy. The plentiful hairs on their bodies are coated in oils that provide them with natural waterproofing. They can also generate more heat than their smaller, slender honey bee cousins, so they remain productive workers in cooler weather.    

We see the first bumblebees arise in the fossil record 100 million years ago and diversify alongside the earliest flowering plants. Their evolution is an entangled dance with the pollen and varied array of flowers that colour our world. 

We have found many wonderful examples within the fossil record, including a rather famous Eocene fossil bee found by a dear friend and naturalist who has left this Earth, Rene Savenye.

His namesake, H. Savenyei, is a lovely fossil halictine bee from Early Eocene deposits near Quilchena, British Columbia — and the first bee body-fossil known from the Okanagan Highlands — and indeed from Canada. 

It is a fitting homage, as bees symbolize honesty, playfulness and willingness to serve the community in our local First Nation lore and around the world — something Rene did his whole life.

FOSSIL FISHAPODS FROM THE CANADIAN ARCTIC

Qikiqtania wakei, a fishapod & relative to tetrapods

You will likely recall the amazing tetrapodomorpha fossil found on Ellesmere Island in the Canadian Arctic in 2004, Tiktaalik roseae. 

These were advanced forms transitional between fish and the early labyrinthodonts playfully referred to as fishapods — half-fish, half-tetrapod in appearance and limb morphology. 

Up to that point, the relationship of limbed vertebrates (tetrapods) to lobe-finned fish (sarcopterygians) was well known, but the origin of significant tetrapod features remained obscure for the lack of fossils that document the sequence of evolutionary changes — until Tiktaalik. 

While Tiktaalik is technically a fish, this fellow is as far from fish-like as you can be and still be a card-carrying member of the group. 

Interestingly, while Neil Shubin and crew were combing the icy tundra for Tiktaalik, another group was trying their luck just a few kilometres away. 

A week before the eureka moment of Tiktaalik's discovery, Tom Stewart and Justin Lemberg unearthed material that we now know to be a relative of Tiktaalik's. 

Meet Qikiqtania wakei, a fishapod and close relative to our dear tetrapods — and cousin to Tiktaalik — who shares features in the flattened triangular skull, shoulders and elbows in the fin. 

Qikiqtania (pronounced kick-kick-TAN-ee-ya)

But, and here’s the amazing part, its upper arm bone (humerus) is specialised for open water swimming, not walking. 

The story gets wilder when we look at Qikiqtania’s position on the evolutionary tree— all the features for this type of swimming are newly evolved, not primitive. 

This means that Qikiqtania secondarily reentered open water habitats from ancestors that had already had some aspect of walking behaviour. 

And, this whole story was playing out 365 million years ago — the transition from water to land was going both ways in the Devonian.

Why is this exciting? You and I descend from those early tetrapods. We share the legacy of their water-to-land transition and the wee bony bits in their wrists and paddles that evolved to become our hands. I know, mindblowing!

Thomas Stewart and Justin Lemberg put in thousands of hours bringing Qikiqtania to life. 

The analysis consisted of a long path of wild events— from a haphazard moment when it was first spotted, a random collection of a block that ended up containing an articulated fin, to a serendipitous discovery three days before Covid lockdowns in March 2020.

Both teams acknowledge the profound debt owed to the individuals, organizations and indigenous communities where they had the privilege to work — Grise Fiord and Resolute Bay— Ellesmere Island in Nunavut, the largest and northernmost territory of Canada. 

Part of that debt is honoured in the name chosen for this new miraculous species. 

Aerial View of Ellesmere Island

The generic name, Qikiqtania (pronounced kick-kick-TAN-ee-ya), is derived from the Inuktitut words Qikiqtaaluk and Qikiqtani which are the traditional place name of the region where the fossil was discovered. 

The specific name, wakei, is in memory of the evolutionary biologist David Wake — colleague, mentor and friend. 

He was a professor of integrative biology and Director and curator of herpetology at the Museum of Vertebrate Zoology at the University of California, Berkeley who passed away in April 2021. 

Wake is known for his work on the biology and evolution of salamanders and vertebrate evolutionary biology. 

If you look at the photo on the left you can imagine visiting these fossil localities in Canada's far north.

Qikiqtania was found on Inuit land and belongs to the community. Thomas Stewart and his colleagues were able to conduct this research because of the generosity and support of individuals in the hamlets of Resolute Bay and Grise Fiord, the Iviq Hunters and Trappers of Grise Fiord, and the Department of Heritage and Culture, Nunavut.

To them, on behalf of the larger scientific community — Nakurmiik. Thank you! 

Here is the link to Tom Stewart's article in The Conversation & paper in Nature:

• Stewart, Thomas A.; Lemberg, Justin B.; Daly, Ailis; Daeschler, Edward B.; Shubin, Neil H. (2022-07-20). "A new elpistostegalian from the Late Devonian of the Canadian Arctic". Nature. doi:10.1038/s41586-022-04990-w. ISSN 0028-0836.
• Stewart, Thomas. "Meet Qikiqtania, a fossil fish with the good sense to stay in the water while others ventured onto land" The Conversation. Retrieved 2022-07-20.

Image One: An artist’s vision of Qikiqtania enjoying its fully aquatic, free-swimming lifestyle. Alex Boersma, CC BY-ND

Image Two: A new elpistostegalian from the Late Devonian of the Canadian Arctic, T. A. Stewart, J. B. Lemberg, A. Daly, E. B. Daeschler, & N. H. Shubin.

A huge shout out to the deeply awesome Neil Shubin who shared that the paper had been published and offered his insights on what played out behind the scenes!

CLALLAM BAY FOSSIL HEIST

Vertipecten fucanus (Dall, 1900)

Some water-worn samples of the bivalve Verdipectin fucanus, Clallam Formation, Clallam Bay, Washington State. Miocene.

It all began one gloriously sunny summer weekend when the planets aligned, the calendar gods smiled, and my mother and I were simultaneously free. 

Naturally, this meant one thing: we were going fossil hunting. I still get out collecting regularly but back in the day it was every weekend of the year with the bigger trips planned a few years in advance. 

Many of those were "reckie trips" scouting out new localities. The Olympic Peninsula was duly scouted and now it was back to the regular haunts. 

We rattled down through Port Angeles and set up camp at the Lyre River—mosquitoes, campfire smoke, and all the rustic feels. 

I took Mom on a grand tour of my favourite haunts: Majestic Beach (where we found some amazing fossil whale verts), a private-land site with ghost shrimp claws and urchins (with permission), and finally down to Clallam Bay and its dreamy beach exposures.

The Clallam Formation stretches along the north coast of the Olympic Peninsula, tracing the rugged edge of the Strait of Juan de Fuca from Slip Point at the eastern end of Clallam Bay to the headland of Pillar Point. Here, sandstone beds push the coastline outward in a subtle bulge, their weathered flanks dropping abruptly to a broad, wave-washed bedrock platform.

Pillar Point, Clallam Bay

Imagine standing on that foreshore: waves crash rhythmically against the stone, sending up bursts of cool spray. The surf’s deep, steady thunder pulses underfoot, while the sharper cries of gulls wheel above, carried on the wind. 

The air is rich with the briny scent of kelp and cold saltwater, a sharp, clean smell that settles in the back of the throat. Each retreating wave leaves a gleaming sheen on the rock, swirling with foam before sliding back to the sea.

Its cliffs and tidal benches have long drawn geologists—and especially paleontologists—who were captivated by the formation’s abundance of beautifully preserved fossils. 

William Healey Dall, a pioneering American geologist and paleontologist whose career spanned more than six decades. Dall loved to explore this rugged bit of coastline, studying and describing many of the mollusks now known from the Clallam Formation, adding his work to the early scientific tapestry woven from these windswept rocks.

He became one of the most prolific describers of North Pacific mollusks, naming hundreds of new species—from marine snails and clams to chitons—many of which still bear the names he assigned or honour him through genera such as Dallina and Dallididae. His work laid much of the early scientific foundation for the paleontology of the Pacific Coast.

Retracing his footsteps and to catch the tides just right, we collected in the early afternoon, blissfully unaware that we were setting up the perfect comedy plot twist. 

After a full day of hauling home the ocean’s Miocene leftovers, we decided to stash some of our fossil booty under a log—just until morning. A little paleo treasure cache. Perfectly safe. Nothing could possibly go wrong.

The next morning, we strolled back down the beach, coffees in hand, ready to retrieve our hoard like triumphant pirates.

Enter: A very enthusiastic gaggle of high school students.

There they were, marching toward us, each clutching a fossil like they’d just won the geological lottery. “Look what we found!” they cried, beaming, displaying our carefully cached treasures.

Yes. Our stash. Our carefully curated, lovingly positioned, absolutely-not-meant-for-public-consumption stash.

But honestly? They were so thrilled, we couldn’t help but be charmed. Besides, most of what I collect ends up in museums or teaching collections anyway. These young fossil hunters had simply… expedited the process. Efficient, really.

We gathered the Verdipectin together for one glamorous group photo, wished the kids well, and sent them off with pockets full of deep time. 

And our grand prize for the weekend? Some very fetching water-worn whale vertebrae—one of which was briefly enscripted into service as the crown of the King of the Lemon People, while my mother created elaborate beach sculptures to our shared amusement.. All in all, a perfect weekend.

Image: Vertipecten fucanus (Dall, 1900) is the most characteristic mollusk in assemblages from the Clallam Formation.

BEARDED SEALS OF SVALBARD

The Bearded Seal

Bartrobbe — the bearded seal (Erignathus barbatus) — is a familiar and charismatic presence in the high Arctic waters surrounding Svalbard, Norway. 

Large, solitary, and unmistakable with its luxuriant moustache of stiff vibrissae, this species is superbly adapted to life along the drifting margins of sea ice. 

Adults can exceed 400 kilograms in mass, with thick blubber for insulation and broad, flexible foreflippers that allow them to haul out on ice floes or shallow shorelines with surprising ease.

Bearded seals are benthic specialists. Rather than chasing fast-moving prey in the water column, they forage along the seafloor, using their extraordinarily sensitive whiskers to detect vibrations and textures in soft sediments. 

Their diet reflects this lifestyle and includes clams, mussels, polychaete worms, crabs, shrimp, snails, and demersal fishes such as sculpins and flatfish. Powerful suction feeding allows them to extract prey directly from shells or sediment, leaving distinctive feeding pits on the seabed—clear signatures of their presence even when the seals themselves are out of sight.

The Bearded Seal

Unlike many other pinnipeds, bearded seals are not strongly colonial. Outside of the breeding season they are largely solitary, loosely distributed across ice-covered continental shelves. 

Mating occurs in spring, typically from April to May, when males establish underwater display areas rather than surface territories. 

Courtship is acoustic: males produce long, haunting trills and sweeping calls beneath the ice, audible over kilometres, to attract receptive females. 

After mating, implantation of the embryo is delayed, a reproductive strategy shared with many seals, resulting in a total gestation of roughly 11 months. 

Pups are born the following spring on drifting sea ice and are remarkably precocial, entering the water within hours and weaned after only two to three weeks—one of the shortest lactation periods among seals.

In the fossil record, bearded seals belong to the family Phocidae, a lineage that diversified during the Miocene as cold-adapted marine ecosystems expanded in the Northern Hemisphere. 

While Erignathus barbatus itself does not appear as a clearly identifiable species until the late Pleistocene, its ancestry is represented by fossil phocids from Miocene and Pliocene deposits across the North Atlantic and Arctic margins. 

Fragmentary remains—skulls, mandibles, and limb bones—document the emergence of large, bottom-feeding seals adapted to shallow continental shelves, particularly in regions influenced by cooling climates and seasonal ice. 

Pleistocene deposits in northern Europe, Siberia, Alaska, and Arctic Canada contain remains attributable to Erignathus, telling us that bearded seals expanded their range alongside advancing ice sheets during glacial cycles.

Today, Bartrobbe and its kin remain tightly bound to Arctic sea ice, making them sensitive indicators of environmental change. Their long evolutionary history, traced through shifting climates and frozen seas, underscores just how finely tuned they are to the rhythms of ice, sound, and sediment in the polar oceans—a living echo of the Arctic’s deep past.

THE LOST SEA BENEATH THE PYRAMIDS: TETHYS

Tethys Ocean

Long before the first pharaohs ruled the Nile, Egypt lay beneath the warm, shallow waters of the Tethys Ocean—a vanished sea that once divided the ancient supercontinents of Gondwana and Laurasia. 

Stretching from what is now the Mediterranean to the Indian Ocean, the Tethys existed from the late Paleozoic through the early Cenozoic, roughly 250 to 50 million years ago.

The concept of this long-lost ocean was first proposed in 1893 by Austrian geologist Eduard Suess, one of the founders of modern geology. While studying the distribution of marine fossils in rocks found high in mountain ranges such as the Alps and Himalayas, Suess realized that these fossils—corals, ammonites, and foraminifera—must once have lived in a vast tropical sea. 

His revolutionary conclusion: the mountains had been uplifted from the floor of an ancient ocean that no longer existed. He named this vanished sea the Tethys, after the Greek sea goddess and wife of Oceanus.

Evidence for the Tethys Ocean comes from both geology and fossil assemblages. Layers of marine limestone rich in Nummulites, ammonites, and other marine fossils are found across Europe, North Africa, and southern Asia—often thousands of meters above current sea level. 

These rocks record an ocean teeming with life during the Mesozoic and early Cenozoic, later compressed and folded as the African, Indian, and Eurasian plates collided to form the Alps, the Himalayas, and the Zagros Mountains.

Its tropical lagoons once hosted coral reefs, sea urchins, mollusks, and the foraminifera that would later become Nummulites. As these tiny organisms lived, died, and settled onto the seafloor, their calcium carbonate shells accumulated in thick beds of lime mud. Over millions of years, these sediments hardened into the fossil-rich Eocene limestones that now form much of Egypt’s geology—including the very stone quarried for the pyramids of Giza.

Today, the remnants of the Tethys survive as the Mediterranean, Black, Caspian, and Aral Seas, but its story lives on in every fossil-bearing limestone block of the Great Pyramid—a geological time capsule of an ocean that vanished long before humankind emerged.

POETRY IN MOTION: ORCA

There are days here on the coast when the sea turns to slate, and the light slips low behind Vancouver Island, and that is when they come. 

Black fins cutting clean arcs through the water, moving with a calm that feels almost ceremonial. 

The water barely whispers around them. Gulls quiet. Even the currents seem to soften. 

To watch a pod of orca move through the water is magical. I was once lucky enough to be right down at the dock when a lovely Mamma and her new baby swam within 20 feet of me. 

I squealed out loud at that breathtaking sight. So very special. I have been so very lucky to have many of those experiences growing up on the coast, and they never fail to leave me awe-struck. 

Orca, Orcinus orca, are the ocean’s most cosmopolitan dolphins — yes, dolphins — and they have been cruising the seas in recognisable form for millions of years. In the fossil record, their lineage appears clearly by the Pliocene. 

A species called Orcinus citoniensis, described from fossils in Italy and dating back roughly three to five million years, shows us that these powerful hunters were already evolving the robust skulls and teeth suited for taking down large prey. 

Their broader family tree stretches deeper still into the Miocene, when early dolphin ancestors were diversifying in ancient seas that looked nothing like today’s familiar coastlines.

And yet, for all their evolutionary gravitas, there is something profoundly intimate about seeing them here at home. 

The Southern Resident pods, the Bigg’s (transient) orca, the subtle differences in dorsal fins and saddle patches that let devoted watchers recognise individuals as old friends. 

Orca are matriarchal, led by wise elder females who carry cultural knowledge — hunting strategies, travel routes, even dialects — passed down through generations. They are not just apex predators; they are keepers of memory.

Their black-and-white colouring may help camouflage them, breaking up their outline in the shifting light of the sea. 

They have the second-largest brain of any marine mammal, and distinct ecotypes do not interbreed, even when they share the same waters. Some specialise in salmon, others in seals, and their teeth tell the tale — worn differently depending on diet. 

They can live remarkably long lives, especially the females, who may guide their pods well into their 80s or beyond. 

Longevity, it seems, has its advantages when you are teaching your grandchildren how to read a tide rip.

When I watch them glide past at dusk, the Narrows breathing in and out with the tide, I cannot help but think of the fossil ancestors entombed in stone and the unbroken thread that connects them to these living, breathing beings. 

Deep time meets present moment in a single exhale of mist. 

The sea holds their story — and on evenings like this, if you are very still, it feels as though it is willing to share it.

FOSSILS AND FIRST NATIONS HISTORY: NOOTKA

Nootka Fossil Field Trip. Photo: John Fam

The rugged west coast of Vancouver Island offers spectacular views of a wild British Columbia. Here the seas heave along the shores slowly eroding the magnificent deposits that often contain fossils. 

Just off the shores of Vancouver Island, east of Gold River and south of Tahsis is the picturesque and remote Nootka Island.

This is the land of the proud and thriving Nuu-chah-nulth First Nations who have lived here always. 

Always is a long time, but we know from oral history and archaeological evidence that the Mowachaht and Muchalaht peoples lived here, along with many others, for many thousands of years — a time span much like always. 

While we know this area as Nootka Sound and the land we explore for fossils as Nootka Island, these names stem from a wee misunderstanding. 

Just four years after the 1774 visit by Spanish explorer Juan Pérez — and only a year before the Spanish established a military and fur trading post on the site of Yuquot — the Nuu-chah-nulth met the Englishman, James Cook.  

Captain Cook sailed to the village of Yuquot just west of Vancouver Island to a very warm welcome. He and his crew stayed on for a month of storytelling, trading and ship repairs. Friendly, but not familiar with the local language, he misunderstood the name for both the people and land to be Nootka. In actual fact, Nootka means, go around, go around. 

Two hundred years later, in 1978, the Nuu-chah-nulth chose the collective term Nuu-chah-nulth — nuučaan̓uł, meaning all along the mountains and sea or along the outside (of Vancouver Island) — to describe themselves. 

It is a term now used to describe several First Nations people living along western Vancouver Island, British Columbia. 

It is similar in a way to the use of the United Kingdom to refer to the lands of England, Scotland and Wales — though using United Kingdom-ers would be odd. Bless the Nuu-chah-nulth for their grace in choosing this collective name.  

An older term for this group of peoples was Aht, which means people in their language and is a component in all the names of their subgroups, and of some locations — Yuquot, Mowachaht, Kyuquot, Opitsaht. While collectively, they are the Nuu-chah-nulth, be interested in their more regional name should you meet them. 

But why does it matter? If you have ever mistakenly referred to someone from New Zealand as an Aussie or someone from Scotland as English, you have likely been schooled by an immediate — sometimes forceful, sometimes gracious — correction of your ways. The best answer to why it matters is because it matters.

Each of the subgroups of the Nuu-chah-nulth viewed their lands and seasonal migration within them (though not outside of them) from a viewpoint of inside and outside. Kla'a or outside is the term for their coastal environment and hilstis for their inside or inland environment.

It is to their kla'a that I was most keen to explore. Here, the lovely Late Eocene and Early Miocene exposures offer up fossil crab, mostly the species Raninid, along with fossil gastropods, bivalves, pine cones and spectacularly — a singular seed pod. These wonderfully preserved specimens are found in concretion along the foreshore where time and tide erode them out each year.

Five years after Spanish explorer Juan Pérez's first visit, the Spanish built and maintained a military post at Yuquot where they tore down the local houses to build their own structures and set up what would become a significant fur trade port for the Northwest Coast — with the local Chief Maquinna's blessing and his warriors acting as middlemen to other First Nations. 

Following reports of Cook's exploration British traders began to use the harbour of Nootka (Friendly Cove) as a base for a promising trade with China in sea-otter pelts but became embroiled with the Spanish who claimed (albeit erroneously) sovereignty over the Pacific Ocean. 

Dan Bowen searching an outcrop. Photo: John Fam

The ensuing Nootka Incident of 1790 nearly led to war between Britain and Spain (over lands neither could actually claim) but talk of war settled and the dispute was settled diplomatically. 

George Vancouver on his subsequent exploration in 1792 circumnavigated the island and charted much of the coastline. His meeting with the Spanish captain Bodega y Quadra at Nootka was friendly but did not accomplish the expected formal ceding of land by the Spanish to the British. 

It resulted however in his vain naming the island "Vancouver and Quadra." The Spanish captain's name was later dropped and given to the island on the east side of Discovery Strait. Again, another vain and unearned title that persists to this day.

Early settlement of the island was carried out mainly under the sponsorship of the Hudson's Bay Company whose lease from the Crown amounted to 7 shillings per year — that's roughly equal to £100.00 or $174 CDN today. Victoria, the capital of British Columbia, was founded in 1843 as Fort Victoria on the southern end of Vancouver Island by the Hudson's Bay Company's Chief Factor, Sir James Douglas. 

With Douglas's help, the Hudson's Bay Company established Fort Rupert on the north end of Vancouver Island in 1849. Both became centres of fur trade and trade between First Nations and solidified the Hudson's Bay Company's trading monopoly in the Pacific Northwest.

The settlement of Fort Victoria on the southern tip of Vancouver Island — handily south of the 49th parallel — greatly aided British negotiators to retain all of the islands when a line was finally set to mark the northern boundary of the United States with the signing of the Oregon Boundary Treaty of 1846. Vancouver Island became a separate British colony in 1858. British Columbia, exclusive of the island, was made a colony in 1858 and in 1866 the two colonies were joined into one — becoming a province of Canada in 1871 with Victoria as the capital.

Dan Bowen, Chair of the Vancouver Island Palaeontological Society (VIPS) did a truly splendid talk on the Fossils of Nootka Sound. With his permission, I have uploaded the talk to the ARCHEA YouTube Channel for all to enjoy. Do take a boo, he is a great presenter. Dan also graciously provided the photos you see here. The last of the photos you see here is from the August 2021 Nootka Fossil Field Trip. Photo: John Fam, Vice-Chair, Vancouver Paleontological Society (VanPS).

Know Before You Go — Nootka Trail

The Nootka Trail passes through the traditional lands of the Mowachaht/Muchalat First Nations who have lived here since always. They share this area with humpback and Gray whales, orcas, seals, sea lions, black bears, wolves, cougars, eagles, ravens, sea birds, river otters, insects and the many colourful intertidal creatures that you'll want to photograph.

This is a remote West Coast wilderness experience. Getting to Nootka Island requires some planning as you'll need to take a seaplane or water taxi to reach the trailhead. The trail takes 4-8 days to cover the 37 km year-round hike. The peak season is July to September. Permits are not required for the hike. 

Access via: Air Nootka floatplane, water taxi, or MV Uchuck III

• Dan Bowen, VIPS on the Fossils of Nootka: https://youtu.be/rsewBFztxSY
• https://www.thecanadianencyclopedia.ca/en/article/sir-james-douglas
• file:///C:/Users/tosca/Downloads/186162-Article%20Text-199217-1-10-20151106.pdf
• Nootka Trip Planning: https://mbguiding.ca/nootka-trail-nootka-island/#overview

PRETTY IN PINK: FLAMINGOS

At ungodly-o’clock in the morning, while the rest of us are still grumbling into our pillows, European flamingos are out there looking like someone spilled a sunrise into the Mediterranean. 

Pale peach, rose, and full-on “salmon mousse,” these birds glide across mirror-flat lagoons on legs that appear to have been stolen from a straw factory.

Their down-curved bills are evolutionary multi-tools — built not for glamour, but for vacuuming up brine shrimp and algae with the intensity of someone cleaning nacho dust out of a keyboard. It’s not chic, but it works, and in science points, it’s a 10/10.

But here’s the kicker: Phoenicopterus roseus isn’t just a pretty face in a wetland spa. It’s the last surviving branch of a lineage forged way back — we’re talking more than 30 million years, mid-Eocene hangover era, when Europe had giant lakes, strange mammals, and nobody worrying about the price of olive oil.

The flamingo story starts with Palaelodus — the awkward teen phase of flamingo evolution. Imagine a tall bird, very leggy, somewhat unsure of its angles, but tragically lacking the extreme bendy straw beak we now know and love. Fossils in France, Germany, and North America show it poking around ancient alkaline lakes like a bird who had not yet received the memo about being fabulous.

Then came the Miocene (aka the “Let’s Try Flamingos For Real” chapter). Suddenly, ancient Spain, Italy, Hungary, and Greece are full of lakebeds stuffed with flamingo bones and trackways. Flamingo highways! Flamingo stomping grounds! Flamingos everywhere! 

And honestly — they looked more or less like the modern ones, suggesting evolution took one glance and said: “Perfect. Don’t change a thing.”

For years, scientists tried to figure out who flamingos were related to. Were they storks? Herons? Ducks? Feathered mystery cryptids? At one point the evolutionary family tree was basically a messy group chat. 

Then genetics swooped in and declared flamingos and grebes — yes, the chunky diving birds — as siblings in a clade called Mirandornithes. 

One is a pink runway model, the other is a potato with scuba certification, but the ancestry checks out.

Modern flamingos have claimed the best real estate the Mediterranean can offer: the Camargue, Doñana, Sicily, Sardinia, Turkey’s salt pans, and the lagoons of North Africa. Their blushing pink comes from carotenoid pigments in their food, proving once and for all that you literally are what you eat — even if what you eat is tiny shrimp smoothies.

Their mud-tower nests are a direct callback to their Miocene ancestors, preserved not just in rock but in behaviour, which is basically evolution’s way of saying, “If it ain’t broke, don’t reinvent the flamingo.”

So the next time you see a flock drifting across a salt lagoon like pastel confetti on stilts, remember you’re looking at one of evolution’s longest-running success stories. Flamingos nailed their niche early, kept the receipts, and have been slaying the alkaline wetlands scene ever since.

Thirty million years. Zero design revisions. Pink forever. Epic and awesome. Bless them!

STEGOSAURUS: PLATED GIANT OF THE JURASSIC

Few dinosaurs are as instantly recognizable as Stegosaurus, with its double row of towering bony plates and spiked tail. 

This herbivore, whose name means “roofed lizard,” roamed western North America about 155–150 million years ago during the Late Jurassic. 

Fossils of Stegosaurus have been found primarily in the Morrison Formation, a magnificent rock unit famous for preserving one of the most diverse dinosaur ecosystems ever discovered.

Stegosaurus could reach up to 9 meters (30 feet) in length but had a disproportionately small head with a brain roughly the size of a walnut. 

Despite this, it thrived as a low-browser, feeding on ferns, cycads, and other ground-level plants using its beak-like mouth and peg-shaped teeth. Its most iconic features were the dermal plates, some nearly a meter tall, running down its back. 

Their function remains debated—some have proposed they were used for display, species recognition, or thermoregulation.

At the end of its tail, Stegosaurus bore four long spikes, known as the thagomizer. 

Evidence from fossilized injuries on predator bones suggests these were formidable weapons, capable of piercing the flesh of even the largest carnivores.

Stegosaurus did not live in isolation. It shared its world with a cast of iconic dinosaurs and other ancient animals:

• Sauropods such as Apatosaurus, Diplodocus, and Brachiosaurus dominated the floodplains, their long necks sweeping across the tree canopy.
• Predators like Allosaurus and Ceratosaurus stalked the ecosystem, preying on herbivores. The spikes of Stegosaurus would have been a key defense against these hunters.
• Ornithopods, including Camptosaurus and Dryosaurus, grazed alongside Stegosaurus, representing smaller, quicker plant-eaters.
• Early mammals, small and shrew-like, scurried through the underbrush, while flying pterosaurs soared overhead.
• Freshwater systems hosted fish, turtles, and crocodile relatives, rounding out the ecosystem.

Interesting Facts

• The brain-to-body ratio of Stegosaurus is one of the smallest of any dinosaur, fueling the myth that it had a “second brain” in its hips—an idea no longer supported by science.
• Tracks attributed to stegosaurs suggest they may have moved in small groups, possibly for protection.
• Despite its fearsome appearance, Stegosaurus was strictly an herbivore. Its teeth were too weak to chew tough vegetation, meaning it likely swallowed food in large chunks.
• And, being one of my best loved dinosaurs, I chose Stegosaurus as one of my logos for the Fossil Huntress. This gentle giant is one of my all time favourites!

Stegosaurus lived tens of millions of years before the rise of dinosaurs like Tyrannosaurus rex, and remains one of the most beloved prehistoric creatures. 

Its strange mix of delicate feeding adaptations and heavy defensive weaponry highlights the balance of survival in the Jurassic ecosystem.

For those that love paleo art, check out the work of Daniel Eskridge (shared with permission here) to see more of his work and purchase some to bring into your world by visiting:https://daniel-eskridge.pixels.com/

HUNTERS OF PANTHALASSAN SEAS: SHONISAURUS

Shonisaurus sikanni / Sikanni Chief River

More than 200 million years ago, when the supercontinent Pangaea was still knitting the world together, a leviathan moved through the warm Panthalassan seas that covered what is now northeastern British Columbia. 

Shonisaurus sikanniensis was colossal. At an estimated 21 metres (about 70 feet) in length, it rivals or exceeds the largest whales alive today. 

This was no scaly sea dragon but an ichthyosaur: a dolphin-shaped marine reptile with immense paddle-like limbs, a long, tapering snout, and eyes built for the dim light of deep water. 

Its vertebrae alone are the size of dinner plates. When it swam, it would have moved with powerful sweeps of its crescent tail, master of a Late Triassic ocean teeming with ammonites and early marine reptiles.

The type specimen of Shonisaurus sikanniensis was discovered along the banks of the Sikanni Chief River and painstakingly excavated over three ambitious field seasons led by Dr. Betsy Nicholls of the Royal Tyrrell Museum. 

A Rolex Laureate and one of Canada’s most respected vertebrate palaeontologists, Dr. Nicholls undertook what remains one of the most formidable fossil excavations ever attempted in this country. 

The animal lay entombed in limestone, and freeing it required extraordinary logistics, teamwork, and resolve over many field seasons.  

That immense skeleton — the largest marine reptile ever described — reshaped our understanding of just how big ichthyosaurs could become.

Many dedicated researchers have contributed to expanding the story of Shonisaurus and its kin. Scholars such as Dean Lomax and Sven Sachs, among others, continue to refine our understanding of ichthyosaur anatomy, growth patterns, and evolutionary relationships. 

Recent work on giant ichthyosaurs from the Triassic of Europe and North America suggests that extreme body size evolved rapidly after the end-Permian mass extinction. New discoveries of enormous jaw fragments and vertebrae hint that multiple lineages independently pushed the limits of marine reptile gigantism. 

These animals were likely deep-diving specialists, feeding on abundant soft-bodied cephalopods and fish, filling ecological roles that whales would not occupy for another 150 million years.

The Sikanni Chief River flows through the traditional territory of the Kaska Dena, whose stewardship of these lands spans countless generations. Any scientific work in this region exists within that broader and much older human story, and it is important to acknowledge the enduring relationship between the land, the river, and the people who know it best.

Today, the bones of Shonisaurus sikanniensis rest in Alberta, but its story stretches far beyond a museum gallery. It is a tale of deep time, bold fieldwork, collaboration across continents, and the simple human wonder that arises when we uncover something vast and ancient from stone. 

From the warm Triassic seas to the careful hands of modern researchers, the story of Shonisaurus reminds us that our planet has always been capable of producing giants — and that with patience, teamwork, and curiosity, we can bring their stories joyfully back into the light.

FRACTAL BUILDING: AMMONITES

Argonauticeras besairei, Collection of José Juárez Ruiz.

An exceptional example of fractal building of an ammonite septum, in this clytoceratid Argonauticeras besairei from the awesome José Juárez Ruiz.

Ammonites were predatory, squid-like creatures that lived inside coil-shaped shells.

Like other cephalopods, ammonites had sharp, beak-like jaws inside a ring of squid-like tentacles that extended from their shells. They used these tentacles to snare prey, — plankton, vegetation, fish and crustaceans — similar to the way a squid or octopus hunt today.

Catching a fish with your hands is no easy feat, as I'm sure you know. But the Ammonites were skilled and successful hunters. They caught their prey while swimming and floating in the water column. Within their shells, they had a number of chambers, called septa, filled with gas or fluid that were interconnected by a wee air tube. By pushing air in or out, they were able to control their buoyancy in the water column.

They lived in the last chamber of their shells, continuously building new shell material as they grew. As each new chamber was added, the squid-like body of the ammonite would move down to occupy the final outside chamber.

They were a group of extinct marine mollusc animals in the subclass Ammonoidea of the class Cephalopoda. These molluscs, commonly referred to as ammonites, are more closely related to living coleoids — octopuses, squid, and cuttlefish) than they are to shelled nautiloids such as the living Nautilus species.

The Ammonoidea can be divided into six orders:

• Agoniatitida, Lower Devonian - Middle Devonian
• Clymeniida, Upper Devonian
• Goniatitida, Middle Devonian - Upper Permian
• Prolecanitida, Upper Devonian - Upper Triassic
• Ceratitida, Upper Permian - Upper Triassic
• Ammonitida, Lower Jurassic - Upper Cretaceous

Ammonites have intricate and complex patterns on their shells called sutures. The suture patterns differ across species and tell us what time period the ammonite is from. If they are geometric with numerous undivided lobes and saddles and eight lobes around the conch, we refer to their pattern as goniatitic, a characteristic of Paleozoic ammonites.

If they are ceratitic with lobes that have subdivided tips; giving them a saw-toothed appearance and rounded undivided saddles, they are likely Triassic. For some lovely Triassic ammonites, take a look at the specimens that come out of Hallstatt, Austria and from the outcrops in the Humboldt Mountains of Nevada.

Hoplites bennettiana (Sowby, 1826).

If they have lobes and saddles that are fluted, with rounded subdivisions instead of saw-toothed, they are likely Jurassic or Cretaceous. If you'd like to see a particularly beautiful Lower Jurassic ammonite, take a peek at Apodoceras. Wonderful ridging in that species.

One of my favourite Cretaceous ammonites is the ammonite, Hoplites bennettiana (Sowby, 1826). This beauty is from Albian deposits near Carrière de Courcelles, Villemoyenne, near la région de Troyes (Aube) Champagne in northeastern France.

At the time that this fellow was swimming in our oceans, ankylosaurs were strolling about Mongolia and stomping through the foliage in Utah, Kansas and Texas. Bony fish were swimming over what would become the strata making up Canada, the Czech Republic and Australia. Cartilaginous fish were prowling the western interior seaway of North America and a strange extinct herbivorous mammal, Eobaatar, was snuffling through Mongolia, Spain and England.

In some classifications, these are left as suborders, included in only three orders: Goniatitida, Ceratitida, and Ammonitida. Once you get to know them, ammonites in their various shapes and suturing patterns make it much easier to date an ammonite and the rock formation where is was found at a glance.

Ammonites first appeared about 240 million years ago, though they descended from straight-shelled cephalopods called bacrites that date back to the Devonian, about 415 million years ago, and the last species vanished in the Cretaceous–Paleogene extinction event.

They were prolific breeders that evolved rapidly. If you could cast a fishing line into our ancient seas, it is likely that you would hook an ammonite, not a fish. They were prolific back in the day, living (and sometimes dying) in schools in oceans around the globe. We find ammonite fossils (and plenty of them) in sedimentary rock from all over the world.

In some cases, we find rock beds where we can see evidence of a new species that evolved, lived and died out in such a short time span that we can walk through time, following the course of evolution using ammonites as a window into the past.

For this reason, they make excellent index fossils. An index fossil is a species that allows us to link a particular rock formation, layered in time with a particular species or genus found there. Generally, deeper is older, so we use the sedimentary layers rock to match up to specific geologic time periods, rather the way we use tree-rings to date trees. A handy way to compare fossils and date strata across the globe.

References: Inoue, S., Kondo, S. Suture pattern formation in ammonites and the unknown rear mantle structure. Sci Rep 6, 33689 (2016). https://doi.org/10.1038/srep33689
https://www.nature.com/articles/srep33689?fbclid=IwAR1BhBrDqhv8LDjqF60EXdfLR7wPE4zDivwGORTUEgCd2GghD5W7KOfg6Co#citeas

Photo: Hoplites Bennettiana from near Troyes, France. Collection de Christophe Marot