BACK IN THE USSR: KEPPLERITES

This glorious chocolate block contains the creamy grey ammonite Kepplerites gowerianus (Sowerby 1827) with a few invertebrate friends, including two brachiopods: Ivanoviella sp., Zeilleria sp. and the deep brown gastropod Bathrotomaria sp. 

There is also a wee bit of petrified wood on the backside.

These beauties hail from Jurassic, Lower Callovian outcrops in the Quarry of Kursk Magnetic Anomaly (51.25361,37.66944), Kursk region, Russia. Diameter ammonite 70мм. 

In the mid-1980s, during the expansion and development of one of the quarries, an unusual geological formation was found. This area had been part of the seafloor around an ancient island surrounded by Jurassic Seas. 

The outcrops of this geological formation turned out to be very rich in marine fossil fauna. This ammonite block was found there years ago by the deeply awesome Emil Black. 

In more recent years, the site has been closed to fossil collecting and is in use solely for the processing and extraction of iron ore deposits. Kursk Oblast is one of Russia's major producers of iron ore. The area of the Kursk Magnetic Anomaly has one of the richest iron-ore deposits in the world. Rare Earth minerals and base metals also occur in commercial quantities in several locations. Refractory loam, mineral sands, and chalk are quarried and processed in the region. 

The Kursk Magnetic Anomaly Quarry is not far from the Sekmenevsk Formation or Sekmenevska Svita in Russian, a Cretaceous (Albian to Cenomanian) terrestrial geologic formation where Pterosaur fossils have been found in the sandstones. 

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!

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.

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.

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

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/

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

MAMMOTH AT THE MUSEUM

Mammoths are a personal favourite of mine and there is a particularly fetching specimen in the Natural History Museum, London. 

Amongst its Ice Age treasures stands the mighty woolly mammoth, Mammuthus primigenius — a shaggy titan of the Pleistocene whose kind roamed the frozen steppes of Europe, Asia, and North America until just 4,000 years ago.

The museum’s mammoth skeleton, with its great spiralled tusks curving forward like ivory crescents, is both imposing and oddly elegant. 

These animals were close cousins of modern elephants, adapted for cold with thick insulating fur, a layer of fat beneath the skin, and small ears to conserve heat. 

Their molars — massive, ridged grinding plates — were built for chewing tough Ice Age grasses across windswept tundra.

Britain itself once hosted mammoths during colder phases of the last Ice Age. As glaciers advanced and retreated, herds wandered across what is now the North Sea basin — then dry land known as Doggerland — and into southern England. 

Fossils dredged from gravel pits and offshore sediments remind us that mammoths were not exotic strangers but part of Britain’s own prehistoric fauna.

Standing beneath those sweeping tusks in the museum, you can almost feel the cold breath of the Ice Age. It is a wonderful place to spend the afternoon. If you go, wear comfortable shoes!

CREAMY APORRHAIS FOSSIL GASTROPOD

This creamy, beige specimen of Aporrhais sp., is a fossil marine gastropod from the Goodland Formation of Fort Worth, Texas, a limestone unit laid down during the Lower Cretaceous (Albian), roughly 113–100 million years ago. 

At that time, north-central Texas lay beneath a warm, shallow epicontinental sea connected to the broader Western Interior Seaway, an environment ideal for shelled invertebrates to flourish.

Aporrhais is a thick-shelled sea snail, part of a lineage well adapted to life on carbonate seafloors. Its inflated, smoothly rounded whorls and robust form suggest a slow-moving grazer or detritivore, creeping across soft sediments in calm, sunlit waters. 

The pale colouration you see today reflects mineral replacement during burial, with the original aragonitic shell long since altered to limestone.

The Goodland Formation is famous for its diverse fossil assemblage. Alongside gastropods, collectors and researchers regularly find ammonites (including forms such as Douvilleiceras), bivalves like oysters and rudists, echinoids (sea urchins), corals, and occasional crustaceans. Together, these fossils paint a vivid picture of a thriving Cretaceous reef-adjacent ecosystem.

Exposures of the Goodland around Fort Worth have been known and collected since the late 19th and early 20th centuries, often through quarrying and construction cuts. Early geological and paleontological work in the region was carried out by figures such as Robert T. Hill, W. S. Adkins, and T. W. Stanton, whose studies helped establish the stratigraphy and fossil content of the Texas Cretaceous. 

Since then, generations of professional paleontologists and dedicated local collectors have continued to document and refine our understanding of this richly fossiliferous formation.

This specimen was collected by Jack Whittles in the 1990s, shared with the Pacific Museum of the Earth (the precursor museum to the one now at UBC, and then shared with me...)

FOSSIL DOLPHIN VERTEBRAE FROM THE NORTH SEA

Dolphin Fossil Vertebrae

Pulled from the cold, turbid bottom of the North Sea, a fossil dolphin vertebra is a small but eloquent survivor of a very different ocean. 

Today, the North Sea is shallow, busy, and heavily worked by trawlers, dredges, and offshore infrastructure. Beneath that modern churn lies a remarkable archive of Cenozoic life, quietly releasing its fossils when nets and dredges scrape sediments that have not seen daylight for millions of years.

Fossil cetacean bones—vertebrae, ribs, mandibles, and the occasional ear bone—are among the most evocative finds recovered from the seafloor. 

Dolphin vertebrae are especially common compared to skulls, as their dense, spool-shaped centra survive transport and burial better than more delicate skeletal elements. 

These fossils are typically dark brown to black, stained by long exposure to iron-rich sediments and phosphates, and often bear the polished surfaces and rounded edges that speak to a history of reworking by currents before final burial.

The North Sea is famous for yielding a mixed assemblage of fossils spanning multiple ice ages and interglacial periods, but many marine mammal remains originate from Miocene deposits, roughly 23 to 5 million years old. During the Miocene, this region was not the marginal, shallow sea we know today. It formed part of a broad, warm to temperate epicontinental sea connected to the Atlantic, rich in plankton, fish, sharks, and early whales and dolphins. 

This was a critical chapter in cetacean evolution, when modern groups of toothed whales, including early delphinids and their close relatives, were diversifying and refining the echolocation-based hunting strategies that define dolphins today.

Most North Sea cetacean fossils are found accidentally rather than through targeted excavation. Commercial fishing trawls, aggregate dredging for sand and gravel, and construction linked to wind farms and pipelines routinely disturb Miocene and Pliocene sediments. 

Fossils are hauled up tangled in nets or mixed with shell hash and glacial debris, often far from their original point of burial. As a result, precise stratigraphic context is usually lost, and age estimates rely on sediment still adhering to the bone, associated microfossils, or comparison with well-dated onshore Miocene marine deposits in the Netherlands, Belgium, Germany, and eastern England.

A dolphin vertebra from this setting tells a story of both life and loss. In life, it was part of a flexible, powerful spine built for speed and agility, driving rapid tail beats through warm Miocene waters. 

After death, the carcass likely sank to the seafloor, where scavengers stripped it and currents scattered the bones. Over time, burial in sand and silt allowed mineral-rich waters to replace organic material with stone, locking the bone into the geological record. 

Much later, Ice Age glaciers reshaped the seafloor, reworking older sediments and concentrating fossils into lag deposits that modern dredges now disturb.

Though often found in isolation, these vertebrae are scientifically valuable. They confirm the long presence of dolphins in northern European seas and help refine our understanding of Miocene marine ecosystems, biogeography, and climate.

MIDDLE TRIASSIC MIXOSAURUS: TAIWAN STYLE

Mixosaurus sp. from Middle Triassic Seas

If you ever wanted to meet an ichthyosaur halfway between “sleek dolphin missile” and “awkward crocodile-fish,” Mixosaurus delivers. 

This extinct marine reptile cruised the Middle Triassic seas around 242–235 million years ago, back when the world’s continents were still shuffling seats and experimenting with new ocean ecosystems.

The Taiwan specimen of Mixosaurus sp. on display at the Natural History Branch of the National Taiwan Museum captures that transitional vibe perfectly. It is a very, very purdy specimen!

With an elongated snout, well-developed fins, and a body still figuring out hydrodynamic fashion, Mixosaurus sits smack in the ichthyosaur family tree between early, lizard-shaped forms and the more streamlined torpedo models that would show up in the Jurassic. 

Think of it as the “adolescent ichthyosaur phase,” complete with growth spurts and evolving lifestyles.

Taxonomically, Mixosaurus belongs to the order Ichthyosauria and is commonly grouped within Mixosauridae. Its relatives include the earlier Utatsusaurus and Grippia (more on the reptilian side of things) and later speed demons like Temnodontosaurus and Stenopterygius. 

While all ichthyosaurs shared adaptations for marine life — big eyes, paddle limbs, and that delightful habit of birthing live young — Mixosaurus kept a few primitive traits, making it a favorite for paleontologists trying to reconstruct evolutionary pathways in Triassic oceans.

As for its museum home: the National Taiwan Museum has a long pedigree. Founded in 1908 during the Japanese era, it’s the oldest museum in Taiwan and houses natural history, anthropology, geology, and zoology collections spanning deep time to present day. 

The Natural History Branch, nestled in a dedicated exhibition space, is where geology, paleontology, and biology truly shine — a quiet refuge where extinct reptiles like Mixosaurus can enjoy their retirement in glass cases while humans politely stare, point, and whisper variants of “whoa.”

If you’re lucky enough to visit, you’ll find Mixosaurus presented not as some dusty relic of a bygone sea, but as a charismatic stepping-stone in reptile evolution — a reminder that even in the Triassic, life was busy experimenting. 

And occasionally, those experiments worked so well they became crowd-pleasers 240 million years later.

The National Taiwan Museum is in Taipei, Taiwan, right in the city’s historic downtown. The main building sits along Xiànběi Road (Xiànběi Rd., Zhongzheng District) facing 228 Peace Memorial Park, making it easy to combine extinct reptiles with a lovely urban stroll.

The Natural History Branch — where the Mixosaurus hangs out — is part of the same museum system and also located in central Taipei. It focuses on geology, biology, and deep time, so it’s very fossil-friendly territory.

If you’re ever in Taipei (or plotting a paleontology-tour itinerary — which, honestly, is something you should do), it’s a fun stop: compact, historic, and just nerdy enough to make Triassic ichthyosaurs feel right at home.

TOXODON: SOUTH AMERICA'S MOST MAGNIFICENT ODDBALL

Toxodon was a hulking, hippo-sized grazing mammal that once roamed the ancient grasslands, wetlands, and scrub of South America. 

The creature first entered the scientific spotlight thanks to Charles Darwin, who stumbled upon its bones during the HMS Beagle expedition. 

On November 26, 1834, while travelling in Uruguay, Darwin heard rumours of “giant’s bones” on a nearby farm. 

Curious, he rode over, investigated the cache, and purchased the skull of a strange beast for eighteen pence — a bargain for a fossil that would later puzzle the greatest minds of the 19th century.

In his journals, Darwin mused: “Toxodon is perhaps one of the strangest animals ever discovered.” And frankly, he wasn’t wrong. 

Once the skeleton was fully reconstructed, it appeared to pull anatomical traits from every corner of the mammalian tree. It was as large and barrel-bodied as a rhinoceros, yet equipped with chisel-shaped incisors reminiscent of oversized rodents — hence its name, meaning “arched tooth.” 

Its high-set eyes and nostrils suggested an animal comfortable in water, much like a hippo or manatee. Darwin marvelled at this evolutionary mash-up: “How wonderfully are the different orders… blended together in the structure of the Toxodon!”

For over a century, the lineage of Toxodon remained a scientific enigma. Traditional morphology bounced it somewhere among ungulates, rodents, and even sirenians. Then, in 2015, ancient DNA changed the game. 

A groundbreaking genomic study revealed that Toxodon — along with the equally bizarre Macrauchenia — belonged to a lineage known as the South American native ungulates, or SANUs. 

These animals were the evolutionary result of South America’s long isolation after the breakup of Gondwana. And here’s the kicker: SANUs are now understood to be distantly related to modern perissodactyls, the group that includes horses, tapirs, and rhinoceroses. 

So Darwin’s instincts weren’t far off — the resemblance to rhinos wasn’t just superficial whimsy.

Toxodon and its relatives (family Toxodontidae) appear in the Late Miocene, roughly 9 million years ago, and flourish throughout the Pliocene and Pleistocene of South America. 

Their fossils have been uncovered across Argentina, Bolivia, Brazil, Paraguay, and Uruguay, with especially rich deposits in the Pampean region where Darwin first collected his specimens.

These creatures were part of a wider radiation of endemic South American mammals — a remarkable fauna that included giant ground sloths, glyptodonts, terror birds, and litopterns. For tens of millions of years, South America functioned almost like a massive evolutionary island, producing lineages found nowhere else on Earth.

Toxodon itself survived until the tail end of the last Ice Age, vanishing about 12,000 years ago, around the time humans arrived on the continent and climate systems shifted dramatically. Its demise mirrors the fate of many Pleistocene megafaunal giants.

Toxodon stands as a fascinating case study in convergent evolution and the challenges of reconstructing deep-time relationships. Its stocky limbs, massive grinding teeth, and robust skull mark it as a grazer well-suited to tough vegetation, while its semi-aquatic adaptations hint at a lifestyle spent wallowing in wetlands and rivers. 

It was, in many ways, a South American answer to the hippo — yet biologically and evolutionarily, it belonged to an entirely different branch of the mammalian tree.

Darwin might have described it as a beautiful blend of mismatched traits, but with DNA in hand, we now see Toxodon not as a puzzle piece forced to fit the wrong box — but as the last great representative of an ancient, isolated ungulate lineage that flourished for millions of years in a continent of evolutionary mischief.

AMMONITES IN CONCRETION

At first glance they look like ordinary stones—rounded, weathered, unassuming. 

But then you notice the delicious hints: a spiral ghosting through the surface, a faint rib, a seam where time is ready to split wide open—it's magic!

Ammonites, long extinct cephalopods, so often appear this way because, shortly after death, their shells became chemical centres of attraction on the seafloor. 

As the soft tissues decayed, they altered the surrounding sediment, triggering minerals—often calcium carbonate or iron-rich compounds—to precipitate rapidly around the shell. 

This early cementation formed a concretion, a protective stone cocoon that hardened long before the surrounding mud was compressed into rock. While everything around it flattened, cracked, and distorted under pressure, the ammonite inside remained cradled and whole.

What you see here is a gathering of these time capsules: a cluster of ammonites preserved in their concretions, each one split or weathered just enough to reveal the coiled story within. 

Some are neatly halved, spirals laid bare like fingerprints from ages past; others are only just beginning to show themselves, teasing their presence beneath rough stone skins. 

Together, they tell a familiar fossil-hunter’s tale—of patience, sharp eyes, and the thrill of knowing that this unassuming rock holds an ancient ocean inside.

BRYCE CANYON NATIONAL PARK

Bryce Canyon National Park 

From above, Bryce Canyon National Park looks less like a place on Earth and more like a revealed secret—an ancient city carved by time, its towers glowing ember-orange against the cool blues and violets of shadow. 

The hoodoos rise by the tens of thousands, slender spires and stacked pinnacles arranged in amphitheatres that curve like giant bowls scooped from the Paunsaugunt Plateau. 

Seen from the air, their geometry becomes mesmerizing: rows and clusters, corridors and cul-de-sacs, each column subtly different, each telling its own long, patient story.

These improbable forms are the product of relentless, delicate violence. Bryce’s hoodoos are sculpted from the Claron Formation, a sequence of sedimentary rocks laid down between about 50 and 35 million years ago, when this high plateau was a landscape of lakes, rivers, and floodplains. 

Limestone, mudstone, and siltstone stacked layer upon layer, later lifted skyward as the Colorado Plateau rose. What followed was not a single dramatic event, but millions of freeze–thaw cycles—water seeping into cracks by day, freezing and expanding by night—paired with rain, snowmelt, and gravity’s quiet insistence.

From the aerial view, colour tells the chemistry of the stone. Iron oxides stain the hoodoos in fiery reds and oranges, while manganese adds purples and lavenders that deepen as shadows lengthen. 

Pale caps of harder rock perch atop many spires like improbable hats, protecting the softer stone beneath and allowing the columns to stand long enough to earn their fantastical shapes. Where caps fall, hoodoos soon follow—proof that this is a living, changing landscape, not a static monument.

Light is the final sculptor. At sunrise, the amphitheatres ignite, each spire rimmed with gold. By midday, the forms sharpen and flatten, revealing the intricate fluting etched into their sides. 

As evening approaches, shadows flood the basins, pooling between the towers until the hoodoos seem to float, suspended in a sea of dusk. From above, those shadows trace the park’s hidden architecture, mapping the slow choreography of erosion.

GRACEFUL BEAUTY: ALBERTONIA

This graceful beauty, with its elegant, sail-like fins and armour of shimmering scales, is Albertonia sp.—an Early Triassic ganoid fish whose lineage once glided through the recovering seas of what is now western Canada. 

Belonging to a group of extinct bony fishes remarkable for their enamel-coated, diamond-shaped ganoid scales, Albertonia offers a rare and intimate glimpse into life shortly after the end-Permian mass extinction, when marine ecosystems were slowly rebuilding themselves.

Specimens of Albertonia have been discovered in two significant rock units: the Sulphur Mountain Formation near Wapiti Lake in British Columbia and the Lower Triassic Montney Formation of Alberta. 

These formations preserve an extraordinary record of Early Triassic marine life—ecosystems shaped by fluctuating sea levels, restricted basins, and the evolutionary experimentation that followed Earth’s most profound biological crisis.

The Sulphur Mountain Formation, in particular, is renowned for its exceptional vertebrate fossils, including fishes, marine reptiles, and rare soft-tissue impressions. Within these beds, Albertonia appears as a slender, streamlined fish with surprisingly tall dorsal and anal fins—features that give it that distinctive “sail-like” profile. These fins likely played a role in stabilization and maneuverability, allowing it to dart through the shallow carbonate-siliciclastic seas with speed and precision.

Ganoid fishes like Albertonia are characterized by their thick, lustrous scales, locking together like a natural chainmail. These scales not only protected the fish from predators but also provide paleontologists with exquisite fossil details. In well-preserved specimens, you can sometimes see the subtle ornamentation—ridges, pits, and patterns—etched into the ganoine coating, each reflecting the biology of a world more than 245 million years removed from our own.

Though Albertonia is long extinct, its fossils help illuminate the pivotal evolutionary story that unfolded during the Early Triassic. As life clawed its way back from catastrophe, species like this little ganoid fish were among the pioneers of new ecological niches, their presence a quiet testament to resilience in ancient oceans.

FOSSIL HUNTRESS PALEONTOLOGY PODCAST

Step into deep time with the Fossil Huntress Podcast—your warm and wonder-filled gateway to dinosaurs, trilobites, ammonites, and the astonishing parade of life that has ever walked, swum, or crawled across our planet.

Close your eyes and travel with me through ancient oceans teeming with early life, lush primeval forests echoing with strange calls, and sunbaked badlands where the bones of giants rest beneath your feet. 

Each episode is a journey into Earth’s secret past, where every fossil tells a story and every stone remembers.

Together, we’ll wander across extraordinary fossil beds, sacred landscapes, and timeworn shores that have witnessed the rise and fall of worlds. 

From tiny single-celled pioneers to mighty dinosaurs, from cataclysms to new dawns, this is where science meets storytelling—and where the past comes vividly alive.

So wherever you are—on the trail, by the sea, or cozy at home—bring your curiosity and join me in the great adventure of discovery. Favourite the show and come fossil-hunting through time with me!

Listen now: Fossil Huntress Podcast on Spotify: https://open.spotify.com/show/1hH1wpDFFIlYC9ZW5uTYVL

LIVING FOSSILS: MASTERS OF MASS EXTINCTION EVENTS

Horseshoe crabs are marine and brackish water arthropods of the order Xiphosura — a slowly evolving, conservative taxa.

Much like (slow) Water Striders (Aquarius remigis), (relatively sluggish) Coelacanth (Latimeria chalumnae) and (the current winner on really slow evolution) Elephant Sharks (Callorhinchus milii), these fellows have a long history in the fossil record with very few anatomical changes. 

But slow change provides loads of great information. It makes our new friend, Yunnanolimulus luoingensis, an especially interesting and excellent reference point for how this group evolved. 

We can examine their genome today and make comparisons all the way back to the Middle Triassic (with this new find) and other specimens from further back in the Ordovician — 445 million years ago. 

These living fossils have survived all five mass extinction events. They are generalists who can live in shallow or deep water and will eat pretty much anything they can find on the seafloor.

The oldest horseshoe crab fossil, Lunataspis aurora, is found in outcrops in Manitoba, Canada. Charmingly, the name means crescent moon shield of the dawn. It was palaeontologist Dave Rudkin and team who chose that romantic name. Finding them as fossils is quite remarkable as their shells are made of protein which does not mineralized like typical fossils.

Even so, the evolution of their exoskeleton is well-documented by fossils, but appendage and soft-tissue preservation are extremely rare. 

A new study analyzes details of the appendage and soft-tissue preservation in Yunnanolimulus luoingensis, a Middle Triassic (ca. 244 million years old) horseshoe crab from Yunnan Province, SW China. The remarkable anatomical preservation includes the chelicerae, five pairs of walking appendages, opisthosomal appendages with book gills, muscles, and fine setae permits comparison with extant horseshoe crabs.

The close anatomical similarity between the Middle Triassic horseshoe crabs and their recent analogues documents anatomical conservatism for over 240 million years, suggesting persistence of lifestyle.

The occurrence of Carcinoscorpius-type claspers on the first and second walking legs in male individuals of Y. luoingensis tells us that simple chelate claspers in males are plesiomorphic for horseshoe crabs, and the bulbous claspers in Tachypleus and Limulus are derived.

As an aside, if you hadn't seen an elephant shark before and were shown a photo, you would likely say, "that's no freaking shark." You would be wrong, of course, but it would be a very clever observation.

Callorhinchus milii look nothing like our Great White friends and they are not true sharks at all. Rather, they are ghost sharks that belong to the subclass Holocephali (chimaera), a group lovingly known as ratfish. They diverged from the shark lineage about 400 million years ago.

If you have a moment, do a search for Callorhinchus milii. The odd-looking fellow with the ironic name, kallos, which means beautiful in Greek, sports black blotches on a pale silver elongate body. And their special feature? It is the fishy equivalent of business in the front, party in the back, with a dangling trunk-like projection at the tip of their snout and well-developed rectal glands near the tail.

As another small point of interest with regards to horseshoe crabs, John McAllister collected several of these while working on his MSc to see if they had microstructures similar to trilobites (they do) and whether their cuticles were likewise calcified. He found no real calcification in their cuticles, in fact, he had a rather frustrating time getting anything measurable to dissolve in acid in his hunt for trace elements. 

Likewise, when looking at oxygen isotopes (16/18) to get a handle on water salinity and temperature, his contacts at the University of Waterloo had tons of fun getting anything at all to analyze. It made for some interesting findings. Sadly, for a number of reasons, he abandoned the work, but you can read his very interesting thesis here: https://dr.library.brocku.ca/handle/10464/1959

Ref: Hu, Shixue & Zhang, Qiyue & Feldmann, Rodney & Benton, Michael & Schweitzer, Carrie & Huang, Jinyuan & Wen, Wen & Zhou, Changyong & Xie, Tao & Lü, Tao & Hong, Shuigen. (2017). Exceptional appendage and soft-tissue preservation in a Middle Triassic horseshoe crab from SW China. Scientific Reports. 7. 10.1038/s41598-017-13319-x.

CAMBRIAN FAUNA FROM THE EAST KOOTENAY REGION

Upper Cambrian Trilobite Outcrops

When most people imagine British Columbia, they picture sky-scraping mountains, temperate rainforests dripping with moss, and coastlines sculpted by Pacific storms. 

But beneath these landscapes lies a vastly older, stranger world—one that thrived more than half a billion years before humans set foot on this continent.

This was the Cambrian, the era of Earth’s first great biological flowering. And ruling those early seas were the trilobites.

Trilobites were among the earliest complex animals to populate Earth’s oceans—marine arthropods with armor-like exoskeletons, jointed legs, compound eyes, and astonishing evolutionary variety. 

Over 270 million years, they adapted to almost every marine habitat imaginable and diversified into more than 20,000 species.

Today, their fossilized forms—ribbed, spined, streamlined, or elaborately ornamented—are found on every continent. But few places on Earth preserve their story with the richness and fidelity of southeastern British Columbia.

A Fossil Time Machine in the Rockies

The province’s Cambrian-aged formations offer a rare window into early marine ecosystems. The world-famous Burgess Shale preserves soft-bodied creatures with near-photographic clarity. But nearby, just outside the city of Cranbrook, another treasure trove reveals the rise of the trilobites in even earlier seas.

This is the Eager Formation—a Burgess Shale–type Lagerstätte from Cambrian Series 2, Stage 4, roughly 515 million years old. Long considered a low-diversity deposit, new research has transformed its scientific importance.

New Species from an Ancient Sea

A sweeping study by Mark Webster, Jean-Bernard Caron and colleagues, published in the Journal of Paleontology in March 2025, combined with new trilobite taxonomy uncover a thriving community of early trilobites—including several species new to science or newly named favourites from some earlier known colloquially from Lisa Bohach's unpublished thesis.

Among them:

• Olenellus santuccii Webster n. sp.
• Wanneria cranbrookense Webster n. sp.
• Olenellus? schofieldi
• Mesonacis eagerensis

These four olenelloids dominate the fauna, forming the backbone of a “typical” benthic trilobite community from the middle Dyeran Stage in Laurentia (ancient North America).

Alongside them are rare representatives from the enigmatic dorypygid and “ptychoparioid” lineages—groups whose fragmentary preservation leaves some species unnamed but no less scientifically important.

This diversity places the Cranbrook trilobite assemblage on par with other remarkable Cambrian deposits across Laurentia, filling a major stratigraphic gap between earlier and later Burgess Shale–type localities.

Even more remarkable: sedimentologic and preservational clues indicate these creatures died close to where they lived, their bodies settling gently into Cambrian muds with minimal transport. This is time travel at its most precise.

Lower Cambrian – The Eager Formation

Wanneria cranbrookense Webster n. sp.

The site outcrops at a few locations as you head east out of Cranbrook towards Fort Steele. 

The first trilobites were discovered with the building of the Kootenay Highway connecting Cranbrook to Fort Steele and beyond. 

Several other localities, including the outcrops at the Silhouette Rife Range — which is literally on a Rifle Range where folks go to shoot at things — is a shade older than the Middle Cambrian Burgess Shale but the fauna here is much less varied. 

The site has been known and collected since the 1920s. Back in the day, fossil collecting was a family affair with folks heading out in their lightly coloured finery to picnic and surface collect the eroding exposures. 

Cranbrook local, Clement Hungerford Pollen was an engineer and avocational palaeontologist. He promoted collecting the exposures of the Eager Formation around 1921. As a pedigreed Englishman of considerable means, he had invested in the Kootenay Central Railway, revitalizing the town by opening up railway access within the region. Locals have been actively collecting at this site ever since. 

Recent work by Mark Webster et al. highlighted other Lower Cambrian species from this area, including:

• Fritzaspis – a small, early olenellid.
• Elliptocephala – known for its elongated head shield.
• Repinaella – a primitive form key to understanding trilobite origins.

Together, these fossils help correlate the Eager Formation with Lower Cambrian deposits across western Laurentia, refining the timeline of trilobite evolution.

Upper Cambrian – The McKay Group

A short drive from the Eager outcrops lies the McKay Group, a sequence of shales and limestones preserving spectacular Upper Cambrian trilobites.

Here, paleontologists such as Brian Chatterton have documented a flourishing array of species, including:

• Pterocephalia norfordi
• Elvinia roemeri
• Calyptaulax
• Prosaukia
• Orygmaspis contracta

Recent fieldwork by dedicated scientists and citizen collectors—Chris New, Chris Jenkins, Guy Santucci, Don Askew, and Stacey Gibb—continues to expand this list, even turning up Pseudagnostus securiger, a Jiangshanian-age species not previously known from southeastern BC.

Names That Tell a Story of Some Very Awesome Folk...

Paleontology is not just about fossils—it’s also about the people who dedicate their lives (and weekends) to uncovering them. In British Columbia, several trilobite species honour those contributions:

• Pterocephalia santuccii – named for geologist Guy Santucci, whose mapping and fieldwork brought attention to the Cranbrook area.
• Orygmaspis newi – recognizing Chris New, a tireless and deeply awesome citizen scientist.
• Calyptaulax jenkinsi – honouring Chris Jenkins, whose meticulous collecting enriched scientific collections.

These names are more than labels—they’re tributes to the collaboration between professionals, institutions, and passionate community members.

A Cast of Characters Spanning Millions of Years

Across the Cambrian rocks of BC, several trilobites stand out as icons of their time:

• Olenoides serratus – the Burgess Shale classic, often preserved with legs and antennae intact.
• Wanneria walcottana – an Early Cambrian form.
• Mesonacis eagerensis – the signature trilobite of the Eager Formation.
• Pterocephalia santuccii, Orygmaspis newi, Calyptaulax jenkinsi – Upper Cambrian forms marking the twilight of trilobite diversity in the region.

Together, these species chart an evolutionary journey from the earliest trilobites to the sophisticated, ornamented forms of the late Cambrian.

Collecting fossils is restricted in national parks like Yoho, but other formations around Cranbrook allow regulated scientific access. Here, fossil hunters navigate weathered shale slopes and scree-covered ridges, scanning for the ribbed arcs and crescent-shaped cephalons of long-dead arthropods.

Trilobites are as beautiful as they are informative. Their perfect bilateral symmetry, paired spines, and geometric patterns have inspired artists and scientists alike for centuries.

Tuzoia, Lower Cambrian, Eager Formation

For those eager to explore this deep past without a rock hammer, the Cranbrook History Centre, located on the traditional territory of the Ktunaxa First Nation, offers superb displays of Cambrian trilobites, including Tuzoia and other arthropods—plus a delightful collection of Devonian fish.

Trilobites may have vanished 250 million years ago, but their legacy endures.

They help us understand:

• How ecosystems rebounded after ancient climate disruptions
• How early animals diversified and competed
• How continents moved and reshaped marine habitats
• How life evolved complex sensory systems and behaviours

Every fossil is a data point from a vanished ocean, a chapter in Earth’s deep-time biography.

Next time you find yourself walking the rocky outcrops of southeastern British Columbia, pause for a moment. Beneath your feet lies the fossilized remains of vibrant, bustling seas—worlds where trilobites crawled, hunted, burrowed, and thrived long before mountains rose or forests took root.

These ancient mariners whisper stories from half a billion years ago. And thanks to ongoing research—from Caron’s foundational work to the newest species described by Webster and dedicated field collectors—we are finally learning to hear them.

Mark Webster and Jean-Bernard Caron "Trilobites of the Cranbrook Lagerstätte (Eager Formation, Cambrian Stage 4), British Columbia," Journal of Paleontology 98(4), 460-503, (6 March 2025). https://doi.org/10.1017/jpa.2023.89