JURASSIC SEA URCHIN: AM'DA'MA

This lovely little biscuit is a Holectypus sea urchin from 120 million-year-old deposits from the Lagniro Formation of Madagascar.

The specimen you see here is in the collections of my beautiful friend Ileana. She and I were blessed to meet in China many years ago and formed an unbreakable bond that happens so few times in one's life. 

Holectypus are a genus of extinct echinoids related to modern sea urchins and sand dollars. They were abundant from the Jurassic to the Cretaceous (between 200 million and 65.5 million years ago).

This specimen is typical of Holectypus with his delicate five-star pattern adorning a slightly rounded test and flattened bottom. The specimen has been polished and was harvested both for its scientific and aesthetic value. 

I have many wonderful memories of collecting their modern cousins that live on the north end of Vancouver Island and along the beaches of Balaklava Island. In the Kwak̓wala language of the Kwakiutl or Kwakwaka'wakw, speakers of Kwak'wala, of the Pacific Northwest, sea urchins are known as a̱m'da̱'ma and it is this name that I hear in my head when I think of them.

In echinoids, the skeleton is almost always made up of tightly interlocking plates that form a rigid structure or test — in contrast with the more flexible skeletal arrangements of starfish, brittle stars, and sea cucumbers. Test shapes range from nearly globular, as in some sea urchins, to highly flattened, as in sand dollars. 

Sea Urchin Detail

Living echinoids are covered with spines, which are movable and anchored in sockets in the test. These spines may be long and prominent, as in typical sea urchins and most have lovely raised patterns on their surface. 

In sand dollars and heart urchins, however, the spines are very short and form an almost felt-like covering. The mouth of most echinoids is provided with five hard teeth arranged in a circle, forming an apparatus known as Aristotle’s lantern.

Echinoids are classified by the symmetry of the test, the number and arrangement of plate rows making up the test, and the number and arrangement of respiratory pore rows called petals. Echinoids are divided into two subgroups: regular echinoids, with nearly perfect pentameral (five-part) symmetry; and irregular echinoids with altered symmetry.

Because most echinoids have rigid tests, their ability to fossilize is greater than that of more delicate echinoderms such as starfish, and they are common fossils in many deposits. The oldest echinoids belong to an extinct regular taxon called the Echinocystitoidea. 

They first appeared in the fossil record in the Late Ordovician. Cidaroids or pencil urchins appear in the Mississippian (Early Carboniferous) and were the only echinoids to survive the mass extinction at the Permo-Triassic boundary. Echinoids did not become particularly diverse until well after the Permo-Triassic mass extinction event, evolving the diverse forms we find them in today. 

True sea urchins first appear in the Late Triassic, cassiduloids in the Jurassic, and spatangoids or heart urchins in the Cretaceous. Sand dollars, a common and diverse group today, do not make an appearance in the fossil record until the Paleocene. They remain one of my favourite echinoderms and stand tall amongst the most pleasing of the invertebrates.

CHUCKANUT DRIVE: EOCENE TROPICAL PARADISE

A trip along Chuckanut Drive, in northwestern Washington is a chance to view incredible diversity from sea to sky.

An amazing array of plants and animals call this coastline home. 

For the fossil enthusiast, it is a chance to slip back in time and have a bird’s eye view of a tropical paradise preserved in the Eocene strata of various fossil sites. 

Snug up against the Pacific Ocean, this 6000m thick exposure yields a vast number of tropical and flowering plants that you might see in Mexico today. Easily accessible by car, this rich natural playground makes for an enjoyable daytrip just one hour south of the US Border.

Over vast expanses of time, powerful tectonic forces have massaged the western edge of the continent, smashing together a seemingly endless number of islands to produce what we now know as North America and the Pacific Northwest. Intuition tells us that the earth’s crust is a permanent, fixed outer shell – terra firma.

Aside from the rare event of an earthquake or the eruption of Mount St. Helen’s, our world seems unchanging, the landscape constant. In fact, it has been on the move for billions of years and continues to shift each day. As the earth’s core began cooling, some 4.5 billion years ago, plates, small bits of continental crust, have become larger and smaller as they are swept up in or swept under their neighboring plates. 

Large chunks of the ocean floor have been uplifted, shifted and now find themselves thousands of miles in the air, part of mountain chains far from the ocean today or carved by glacial ice into valleys and basins.

Two hundred million years ago, Washington was two large islands, bits of continent on the move westward, eventually bumping up against the North American continent and calling it home. Even with their new fixed address, the shifting continues; the more extreme movement has subsided laterally and continues vertically. 

The upthrusting of plates continues to move our mountain ranges skyward – the path of least resistance. This dynamic movement has created the landscape we see today and helped form the fossil record that tells much of Washington’s relatively recent history – the past 50 million years.

Chuckanut Drive is much younger than other parts of Washington. The fossils found there lived and died some 40-55 million years ago, very close to where they are now, but in a much warmer, swampy setting. The exposures of the Chuckanut Formation were once part of a vast river delta; imagine, if you will, the bayou country of the Lower Mississippi. The siltstones, sandstones, mudstones and conglomerates of the Chuckanut Formation were laid down about 40-54 million years ago during the Eocene epoch, a time of luxuriant plant growth in the subtropical flood plain that covered much of the Pacific Northwest.

This ancient wetland provided ideal conditions to preserve the many trees, shrubs & plants that thrived here. Plants are important in the fossil record because they are more abundant and can give us a lot of information about climate, temperature, the water cycle and humidity of the region. 

The Chuckanut flora is made up predominantly of plants whose modern relatives live in tropical areas such as Mexico and Central America. If you are interesting in viewing a tropical paradise in your own backyard, look no further than the Chuckanut. 

Images and tag lines: Glyptostrobus, the Chinese swamp cypress, is perhaps the most common plant found here. Also abundant are fossilized remains of the North American bald cypress, Taxodium; Metasequoia (dawn redwood), Lygodium (climbing fern), large Sabal (palm) and leaves from a variety of broad leaf angiosperm plants such as (witch hazel), Laurus (laurel), Ficus (fig) and Platanus (sycamore), and several other forms.

While less abundant, evidence of the animals that called this ancient swamp home are also found here. Rare bird, reptile, and mammal tracks have been immortalized in the outcrops of the Chuckanut Formation. Tracks of a type of archaic mammal of the Orders Pantodonta or Dinocerata (blunt foot herbivores), footprints from a small shorebird, and tracks from an early equid or webbed bird track give evidence to the vertebrates that inhabited the swamps, lakes and river ways of the Pacific Northwest 50 million years ago.

The movement of these celebrity vertebrates was captured in the soft mud on the banks of a river, one of the only depositional environments favorable for track preservation.

INKY BEAUTY: AMMONITE OF PONGO DE MANSERICHE

This inky beauty is Prolyelliceras ulrichi (Knechtel, 1947) a fast-moving nektonic carnivorous ammonite from Cretaceous lithified, black, carbonaceous limestone outcrops in the Pongo de Manseriche gorge in northwest Peru. 

If you look closely, you can see that this specimen shows a pathology, a slight deviation to the side of the siphonal of the ammonite. We see Prolyelliceras from the Albian to Middle Albian from five localities in Peru.

The canyons of the Amazon River system in the eastern ranges of the Andes of Peru are known by the Indian name pongo. 

The most famous of these is the Pongo de Manseriche, cut by the Marañon River through the eastern range of the Andes, where it emerges from the cordillera into the flat terrane of the Amazon Basin. The fossil exposures here are best explored by boat. The reality of the collecting is similar to the imagined. I was chatting with Betty Franklin, VIPS, about this. They float along and pick up amazing specimen after amazing specimen. When the water rises, the ammonites are aided in their erosion out of the cliffs.  

The Pongo de Manseriche lies nearly 500 miles upstream from Iquitos, and consequently nearly 3,000 miles above the mouth of the Amazon River. It is situated in the heart of the montaña, in a vast region the ownership of which has long been in dispute between Peru and Ecuador, but over which neither country exercises any police or other governmental control. There is an ancient tradition of the indigenous people of the vicinity that one of their gods descended the Marañón and another ascended the Amazon to communicate with him. Together they opened the pass called the Pongo de Manseriche.

Reference: M. M. Knechtel. 1947. Cephalopoda. In: Mesozoic fossils of the Peruvian Andes, Johns Hopkins University Studies in Geology 15:81-139

W. J. Kennedy and H. C. Klinger. 2008. Cretaceous faunas from Zululand and Natal, South Africa. The ammonite subfamily Lyelliceratinae Spath, 1921. African Natural History 4:57-111. The beauty you see here is in the collection of the deeply awesome José Juárez Ruiz.

EXPLORING WRANGELLIA: HAIDA GWAII

Misty shores, moss covered forests, a rich cultural history, dappled light, fossils and the smell of salt air—these are my memories of Haida Gwaii.

The archipelago of Haida Gwaii lays at the western edge of the continental shelf due west of the central coast of British Columbia.

They form part of Wrangellia, an exotic tectonostratigraphic terrane that includes Vancouver Island, parts western British Columbia and Alaska.

The Geological Survey of Canada sponsored many expeditions to these remote islands and has produced numerous reference papers on this magnificent terrain, exploring both the geology and palaeontology of the area.

Joseph Whiteaves, the GSC's chief palaeontologist in Ottawa, published a paper in 1876 describing the Jurassic and Cretaceous faunas of Skidegate Inlet, furthering his reputation globally as both a geologist, palaeontologist as well as a critical thinker in the area of science.

The praise was well-earned and foreshadowed his significant contributions to come. Sixteen years later, he wrote up and published his observations on a strange Mount Stephen fossil that resembled a kind of headless shrimp with poorly preserved appendages. 

Because of the unusual pointed shape of the supposed ventral appendages and the position of the spines near the posterior of the animal, Whiteaves named it Anomalocaris canadensis. The genus name "Anomalocaris" means "unlike other shrimp" and the species name "canadensis" refers to the country of origin.

Whiteaves work on the palaeontology of Haida Gwaii provided excellent reference tools, particularly his work on the Cretaceous exposures and fauna that can be found there.

One of our fossil field trips was to the ruggedly beautiful Cretaceous exposures of Lina Island. We had planned this expedition as part of our “trips of a lifetime.” 

Both John Fam, the Vice Chair of the Vancouver Paleontological Society and Dan Bowen, the Chair of both the British Columbia Paleontological Alliance and Vancouver Island Palaeontological Society, can be congratulated for their efforts in researching the area and ably coordinating a warm welcome by the First Nations community and organizing fossil field trips to some of the most amazing fossil localities in the Pacific Northwest.

With great sandstone beach exposures, the fossil-rich (Albian to Cenomanian) Haida formation provided ample specimens, some directly in the bedding planes and many in concretion. Many of the concretions contained multiple specimens of typical Haida Formation fauna, providing a window into this Cretaceous landscape.

It is always interesting to see who was making a living and co-existing in our ancient oceans at the time these fossils were laid down. We found multiple beautifully preserved specimens of the spiny ammonite, Douvelleiceras spiniferum along with Brewericeras hulenense, Cleoniceras perezianum and many cycads in concretion.

Douvelliceras spiniferum, Cretaceous Haida Formation

Missing from this trip log are tales of Rene Savenye, who passed away in the weeks just prior. While he wasn't there in body, he was with us in spirit. I thought of him often on the mist-shrouded days of collecting. 

Many of the folk on who joined me on those outcrops were friends of Rene's and would go on to receive the Rene Savenye Award for their contributions to palaeontology. There is a certain poetry in that. 

The genus Douvilleiceras range from Middle to Late Cretaceous and can be found in Asia, Africa, Europe and North and South America. 

We have beautiful examples in the early to mid-Albian from the archipelago of Haida Gwaii in British Columbia. Joseph F. Whiteaves was the first to recognize the genus from Haida Gwaii when he was looking over the early collections of James Richardson and George Dawson.

My collections from Haida Gwaii will all be lovingly prepped and donated to the Haida Gwaii Museum in Skidegate, British Columbia.

DINOSAURS OF THAILAND

This beautiful dinosaur track is from Kalasin Dinosaur Park in northeastern Thailand. 

Thailand boasts some of the finest Mesozoic trackways from five endemic dinosaur species.  

Since 1976, the Department of Mineral Resources with Thai-French Paleontological Project had continuously investigated the dinosaurs in the Phu Wiang mountains. The project found so many vertebrae, teeth, and footprints of the dinosaurs mainly from the sandstones of the Early Cretaceous Sao Khua Formation (about 130 million years old). These include sauropods and theropods ranging in size from adorable chickens to beasties up to 15 meters long. 

The Thai dinosaur record from the continental rocks of the Khorat Plateau is the best in Southeast Asia. The oldest footprints are those from small dinosaurs from the Middle to Late Jurassic Phra Wihan Formation. The most varied dinosaur assemblages come from the Late Jurassic Sao Khua Formation. Here we see the sauropods dominate the fossil beds interspersed with a variety of theropods. Large theropod footprints are known from the Early Cretaceous Phu Phan Formation. Theropods and the primitive ceratopsian Psittacosaurus occur in the Aptian-Albian Khok Kruat Formation. We find dinosaur material further north along the Mekong River region of Laos. Thai fossils show a close relationship to those found in China and Mongolia. 

If you'd like to go visit them, there is a rather nice display at the Phu Wiang Dinosaur Museum in the newly established Wiang Kao district about 80 kilometres to the west of the provincial capital of Khon Kaen. They have several species on display, including: Phuwiangosaurus sirindhornae, Siamosaurus suteethorni, Siamotyrannus isanensis, Kinnareemimus khonkaenensis, Compsognathus (awe, a wee vicious chicken...) and, of course, the Phu Wiang dinosaur footprints.

If you'd like to visit Kalasin Dinosaur Park, follow route 227 towards Lam Pao Dam and Dok Ket Beach. Instead of turning left towards the dam, continue up towards Sirindhorn Dinosaur Museum. You'll see it on your left about 5km before the museum. For some GPS help, pop this into Google Maps: Dinosaur Park, Ni Khom, Sahatsakhan District, Kalasin 46140, Thailand.

References: 

• Ingavat, R., Janvier, R., and Taquet, P. (1978) Decouverte en Thailande d'une portion de femur de dinosaure sauropode (Saurischia, Reptilia). C.R. Soc.Geol.France 3: 140-141
• Wickanet Songtham and Benja Sektheera (2006) Phuwiangosaurus sirindhornae Bangkok: Department of Mineral Resources: 100 pages
• Buffetaut, E., Suteethorn, V., and Tong, H. (2009) An earliest 'ostrich dinosaur' (Theropoda: Ornithomosauria) from the Early Cretaceous Sao Khua Formation of NE Thailand, pp. 229-243, in E. Buffetaut, G. Cuny, J. Le Loeuff, and V. Suteethorn (eds.), Late Palaeozoic and Mesozoic Ecosystem in SE Asia. Geological Society, London, Special Publication 315.

ARMOURED ANIMALS: ANCIENT ARMADILLOS

Glyptodonts are the early ancestors of our modern armadillos that roamed North and South America during the Pleistocene. 

Armadillos, both living and extinct, range in size from the size of an armoured car to the size of a small, family dog. As they evolved over time, the smaller they have become. 

Glyptodonts became extinct at the end of the last ice age. They, along with a large number of other megafaunal species, including pampatheres, the giant ground sloths, and the Macrauchenia, left this Earth but their bones tell a story of brief and awesome supremacy.

Today, Glyptodonts live on through their much smaller, more lightly armoured and flexible armadillo relatives. They defended themselves against Sabre Tooth Cats and other predators but could not withstand the arrival of early humans in the Americas. Archaeological evidence suggests that these humans made use of the animal's armoured shells and enjoyed the meat therein. Glyptodonts possessed a tortoise-like body armour, made of bony deposits in their skin called osteoderms or scutes. Beneath that hard outer coating was a food source that our ancestors sought for their survival.

Each species of glyptodont had a unique osteoderm pattern and shell type. With this protection, they were armoured like turtles; glyptodonts could not withdraw their heads, but their armoured skin formed a bony cap on the top of their skull. Glyptodont tails had a ring of bones for protection. Doedicurus possessed a large mace-like spiked tail that it would have used to defend itself against predators and, possibly, other Doedicurus. Glyptodonts had the advantage of large size.

Many, such as the type genus, Glyptodon, were the size of modern automobiles. The presence of such heavy defences suggests they were the prey of a large, effective predator. At the time that glyptodonts evolved, the apex predators in the island continent of South America were phorusrhacids, a family of giant flightless carnivorous birds.

The ancient Armadillo Glyptodon asper

In physical appearance, glyptodonts superficially resembled the much earlier dinosaurian ankylosaurs and, to a lesser degree, the recently extinct giant meiolaniid turtles of Australia.

These are examples of the convergent evolution of unrelated lineages into similar forms. The largest glyptodonts could weigh up to 2,000 kilograms. Like most of the megafauna in the Americas, they all became extinct at the end of the last ice age 10,000 years ago. The deeper you get in time, the larger they were. Twenty thousand years ago, they could have ambled up beside you in what would become Argentina and outweighed a small car.

A few years back, some farmers found some interesting remains in a dried-out riverbed near Buenos Aires. The find generated a ton of palaeontological excitement. Fieldwork revealed this site to contain two adults and two younger specimens of an ancient armadillo. These car-size beasties would have been living and defending themselves against predators like Sabre Tooth Cats and other large predators of the time by employing their spiked club-like tails and thick bony armour.

Glyptodonts were unlikely warriors. They were grazing herbivores. Like many other xenarthrans, they had no incisor or canine teeth but had a number of cheek teeth that would have been able to grind up tough vegetation, such as grasses. They also had distinctively deep jaws, with large downward bony projections that would have anchored their powerful chewing muscle.

Image Two: By Arentderivative work: WolfmanSF (talk) -  http://de.wikipedia.org/wiki/Bild:Glyptodon-1.jpg, CC BY-SA 3.0, https://commons.wikimedia.org/w/index.php?curid=665483

AMYLASE: YOU ARE WHAT YOU EAT

The old adage, you are what you eat, might be best amended to you are what you can digest. 

For all the mammals, you and I included, we need the amylase gene (AMY). It codes for a starch-digesting enzyme needed to break down the vegetation we eat. 

Humans, dogs and mice have record numbers of the amylase gene. The AMY gene copy number increases in mammal populations where starch-based foods are more abundant. Think toast and jam versus raw chicken.

A good example of this is seen when we compare wolves living in the wild to dogs from agricultural societies. Dogs split off the lineage from wolves around 30,000–40,000 years ago. 

Domesticated dogs have extra copies of amylase and other genes involved in starch digestion that contribute to an increased ability to thrive on a starch-rich diet, allowing Fido to make the most of those table scraps. Similar to humans, some dog breeds produce amylase in their saliva, a clear marker of a high starch diet. So do mice, rats, and pigs, as expected as they live in concert with humans. Curiously, so do some New World monkeys, boars, deer mice, woodrats, and giant African pouched rats. 

More like cats and less like other omnivores, dogs can only produce bile acid with taurine and they cannot produce vitamin D, which they obtain from animal flesh. Also, more like cats, dogs require arginine to maintain their nitrogen balance. These nutritional requirements place dogs halfway between carnivores and omnivores.

The amount of AMY and starch in the diet varies among subspecies, and sometimes even amongst geographically distinct populations of the same species. I was at a talk recently given by Alaskan wolf researchers who shared that two individual packs of wolves separated by less than a kilometre ate vastly different diets. This had me thinking about what we eat and it is mostly driven by what is on offer. 

Diet impacts our genetics and this, in turn, allows the fittest to eat, digest and survive. While wolves win the carnivore contest, they will still eat opportunistically and that includes vegetation when other food is scarce. Would they evolve similar levels of AMY as humans, dogs and mice? Maybe if their diets evolved to be similar. Likely. The choice would be that or starvation.

The evolution of amylase in other domesticated or human commensal mammals remains an alluring area of inquiry.

Reference: 

Amylase in Dietary Food Preferences in Mammals: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6516957/

DESMOCERAS OF MAHAJANGA

This lovely dark rust chunky monkey is the ammonite Desmoceras (Pseudouhligella) latidorsatum from the Lower Cretaceous, Lower Albian, Douvilliceras inequinodum Zone, Ambarimaninga, Mahajanga Province, Madagascar.

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. 

They used their tentacles to snare prey, — plankton, vegetation, fish and crustaceans — similar to the way a squid or octopus hunt today.

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

JAPANESE CORKSCREW AMMONITE: HYPHANTOCERAS ORIENTALE

A stunning example of the heteromorph ammonite, Hyphantoceras orientale macroconch. This beauty corresponds to 'Morphotype C' from Aiba (2017). 

The specimen is a handful at 136 mm and was lovingly prepared by the hand holding it, that of the talented José Juárez Ruiz.

This an adult specimen (not the juvenile stage) from Upper Santonian outcrops near Ashibetsu, Hokkaido, Japan.

Aiba published on a possible phylogenetic relationship of two species of Hyphantoceras (Ammonoidea, Nostoceratidae) earlier this year, proposing that a phylogenetic relationship may exist based on newly found specimens with precise stratigraphic occurrences in the Kotanbetsu and Obira areas, northwestern Hokkaido.

Two closely related species, Hyphantoceras transitorium and H. orientale, were recognized in the examined specimens from the Kotanbetsu and Obira areas. Specimens of H. transitorium show wide intraspecific variation in the whorl shape. The stratigraphic occurrences of the two species indicate that they occur successively in the Santonian–lowermost Campanian, without stratigraphic overlapping. 

The similarity of their shell surface ornamentations and the stratigraphic relationships possibly suggest that H.orientale was derived from H. transitorium. The presumed lineage is likely indigenous to the northwestern Pacific realm in the Santonian–earliest Campanian. Hyphantoceras venustum and H. heteromorphum might stand outside a H. transitorium–H. orientale lineage, judging from differences of their shell surface ornamentation.

Aiba, Daisuke. (2019). A Possible Phylogenetic Relationship of Two Species of Hyphantoceras (Ammonoidea, Nostoceratidae) in the Cretaceous Yezo Group, Northern Japan. Paleontological Research. 23. 65-80. 10.2517/2018PR010.

DRIFTWOOD CANYON FOSSIL BEDS / KUNGAX

Puffbird similar to Fossil Birds found at Driftwood Canyon 

Driftwood Canyon Provincial Park 

Driftwood Canyon Provincial Park covers 23 hectares of the Bulkley River Valley, on the east side of Driftwood Creek, a tributary of the Bulkley River, 10 km northeast of the town of Smithers in northern British Columbia. 

Wet'suwet'en First Nation

The parklands are part of the asserted traditional territory of the Wet'suwet'en First Nation which includes lands around the Bulkley River, Burns Lake, Broman Lake, and François Lake in the northwestern Central Interior of British Columbia. 

The Wetʼsuwetʼen are part of the Dakelh or Carrier First Nation, and in combination with the Babine First Nation are referred to as the Western Carrier. They speak Witsuwitʼen, a dialect of the Babine-Witsuwitʼen language which, like its sister language Carrier, is a member of the Athabaskan family.

Their oral history or kungax recounts a time when their ancestral village, Dizkle or Dzilke, once stood upstream from the Bulkley Canyon. This cluster of cedar houses on both sides of the river was said to be abandoned because of an omen of impending disaster. The exact location of the village has been lost but their stories live on. 

The neighbouring Gitxsan, collectively the People of Smooth Waters—the Gilseyhu Big Frog Clan, the Laksilyu Small Frog Clan, the Tsayu Beaver Clan, the Gitdumden Wolf and Bear Clan and the Laksamshu Fireweed and Owl Clan—each phratry or kinship group calling the Lax Yip home—33,000 km2 of land and water in northwestern ​British Columbia along the waters of the Skeena River and its tributaries—have a similar tale—though the village in their versions is referred to as Dimlahamid or Temlahan depending on which house group or wilp is sharing the tale—as well as where they are located as dialects differ. 

Gitksan speak Sim'algax—the real or true language. Within the Gitxsan communities there are two slightly different dialects. The Gyeets (Downriver) dialect spoken in Gijigyukwhla (Gitsegukla), Gitwangax, and Gitanyow—and the Gigeenix (Upriver) dialect is spoken in Ansbayaxw (Kispiox), Sik-E-Dakh and Gitanmaax.

Driftwood Canyon Fossil Beds

Driftwood Canyon's Fossil Beds record life in the earlier portion of the Eocene when British Columbia — and indeed our world — was much warmer than it is today. This site was discovered in the beginning of the 20th century and is now recognized as containing significant fossil material. 

The fossils found here—and their superb preservation—provide a fascinating opportunity to understand the area’s evolutionary processes of both geology and biology over the past fifty million years or so. The fossils themselves are 51.7 million years old and look remarkably like many of the species we recognize today. 

The park that contains these beautiful fossils is fifty-seven years old. It was created in 1967 by the generosity of the late Gordon Harvey (1913–1976). He donated the land to protect fossil resources that he truly loved and wanted to see preserved. The fossil beds are on the east side of Driftwood Creek. 

Metasequoia, the Dawn Redwood

Exploring the region today, we see a landscape dominated by conifers blanketing the area. 

Forests teem with the aromatic Western Red Cedar, Pacific Silver Fir with its many medicinal properties, the tall and lanky Subalpine Fir with its soft, brittle and quickly decaying wood, the slender scaly Lodgepole Pine, the graceful and slightly forlorn looking Western Hemlock. Across the landscape you see several species of Spruce, including the impressive Sitka. 

Some of the tallest on view would have been mere seedlings, colonizing the glacial moraines centuries ago when the glaciers retreated. Collectively, these conifers tell the tale of the region's cool climate today. 

The Gitsan territory boasts seven of the 14 biogeoclimatic zones of the province—the Alpine Tundra, Spruce-Willow-Birch, Boreal White and Black Spruce, Sub-Boreal Pine-Spruce, Sub-Boreal Spruce, Engelmann Spruce-Subalpine Fir and Interior Cedar-Hemlock. 

The fossil material we find here speaks to a warmer climate in this region's past. We find fossil plants, fish—including specimens of salmon, suckerfish and bowfin, a type of air breathing fish—and insect fossil here—wasps and water striders—fossil plants including Metasequoia, the Dawn Redwood, alder—and interesting vertebrate material. Bird feathers are infrequently collected from the shales; however, two bird body fossils have been found here.

In 1968, a bird body fossil was collected in the Eocene shales of the Ootsa Lake Group in Driftwood Canyon Provincial Park by Pat Petley of Kamloops. 

Pat donated the specimen in 2000 to the Thompson Rivers University (TRU) palaeontology collections. This fossil bird specimen is tentatively identified as the puffbird, Piciformes bucconidae, of the genus Primobucco.

Primobucco is an extinct genus of bird placed in its own family, Primobucconidae. The type species, Primobucco mcgrewi, lived during the Lower Eocene of North America. It was initially described by American paleo-ornithologist Pierce Brodkorb in 1970, from a fossil right-wing, and thought to be an early puffbird. However, the discovery of a further 12 fossils in 2010 indicate that it is instead an early type of roller.

Related fossils from the European Messel deposits have been assigned to the two species P. perneri and P. frugilegus. Two specimens of P. frugilegus have been found with seeds in the area of their digestive tract, which suggests that these birds were more omnivorous than the exclusively predaceous modern rollers. The Driftwood specimen has never been thoroughly studied. If there is a grad student out there looking for a worthy thesis, head on down to the Thompson Rivers University where you'll find the specimen on display.

Another fossil bird, complete with feathers, was collected at Driftwood Canyon in 1970, This one was found by Margret and Albrecht Klöckner who were travelling from Germany. Theirs is a well-travelled specimen, having visited many sites in BC as they toured around, then to Germany and finally back to British Columbia when it was repatriated and donated to the Royal British Columbia Museum in Victoria. 

I am not sure if it is still on display or back in collections, but it was lovingly displayed back in 2008. There is a new grad student, Alexis, looking at Eocene bird feathers down at the RBCM, so perhaps it is once again doing the rounds. 

This second bird fossil is of a long-legged water bird and has been tentatively identified by Dr. Gareth Dyke of the University of Southampton as possibly from the order Charadriiformes, a diverse order of small to medium-ish water birds that include 350 species of gulls, plovers, sandpipers, terns, snipes, and waders. Hopefully, we'll hear more on this find in the future.

A Tapir showing off his prehensile nose trunk

Tapirs and Tiny Hedgehogs

The outcrops at Driftwood Canyon are also special because they record a record of some of the first fossil mammals ever to be found in British Columbia at this pivotal point in time. 

Wee proto-hedgehogs smaller than your thumb lived in the undergrowth of that fossil flora. They shared the forest floor with an extinct tapir-like herbivore in the genus Heptodon that looked remarkably similar to his modern, extant cousins (there is a rather cheeky fellow shown here so you get the idea) but lacked their pronounced snout (proboscis). I am guessing that omission made him the more fetching of his lineage.

In both cases, it was a fossilized jaw bone that was recovered from the mud, silt and volcanic ash outcrops in this ancient lakebed site. And these two cuties are significant— they are the very first fossil mammals we've ever found from the early Eocene south of the Arctic.

How can we be sure of the timing? The fossil outcrops here are found within an ancient lakebed. Volcanic eruptions 51 million years ago put loads of fine dust into the air that settled then sank to the bottom of the lake, preserving the specimens that found their way here — leaves, insects, birds, mammals.

 As well as turning the lake into a fossil making machine—water, ash, loads of steady sediment to cover specimens and stave off predation—the volcanic ash contains the very chemically inert—resistant to mechanical weathering—mineral zircon which we can date with uranium/lead (U/Pb). 

The U/Pb isotopic dating technique is wonderfully accurate and mighty helpful in dating geologic events from volcanic eruptions, continental movements to mass extinctions. This means we know exactly when these lovelies were fossilized and, in turn, their significance.

Know Before You Go

If you fancy a visit to Driftwood Canyon Park, the park is accessible from Driftwood Road from Provincial Highway 16. You are welcome to view and photograph the fossils found here but collecting is strictly forbidden. 

Driftwood Canyon is recognized as one of the world’s most significant fossil beds. It provides park users with a fascinating opportunity to understand the area’s evolutionary processes of both geology and biology. The day-use area is open from May 15 to September 2. There is a short, wheelchair-accessible interpretative trail that leads from the parking are to the fossil beds. Pets are welcome on leash. Signs along the trail provide information on fossils and local history. 

Below a cliff face at the end of the trail is a viewing area that has interpretive information and viewing area overlooking Driftwood Creek.

This park proudly operated by Mark and Anais Drydyk

Email: kermodeparks@gmail.com / Tel: 1 250 877-1482 or 1 250 877-1782

Palaeo Coordinates: Latitude: 50° 51' 59" N / Longitude: 116° 27' 37" W

Lat/Long (dec): 50.86665,-116.46042 / GUID: d3a6bd3e-68d6-42cf-9b2c-d20a30576988

Driftwood Canyon Provincial Park Brochure: 

https://bcparks.ca/explore/parkpgs/driftwood_cyn/driftwood-canyon-brochure.pdf?v=1638723136455

LOTUS FLOWER FRUIT

Lotus Flower Fruit, Nelumbo

This beauty is the fruit of the lotus, Nelumbo. This specimen was found by Green River Stone (GRS) in early Eocene outcrops of the Fossil Lake Member of the Green River Formation. 

The awesome possums from GRS are based out of North Logan, Utah, USA and have unearthed some world-class specimens. They've found Nelumbo leaves over the years but this is their first fossil specimen of the fruit.

And what a specimen it is! The spectacularly preserved fruit measures 6-1/2" round. Here you can see both the part and counterpart in fine detail. Doug Miller of Green River Stone sent copies to me this past summer and a copy to the deeply awesome Kirk Johnson, resident palaeontologist over at the Smithsonian Institute, to confirm the identification.

There is another spectacular specimen from Fossil Butte National Monument. They shared photos of a Nelumbo just yesterday. Nelumbo is a genus of aquatic plants in the order Proteales found living in freshwater ponds. You'll recognize them as the emblem of India, Vietnam and many wellness centres.

Nelumbo Fruit, Green River Formation

There is residual disagreement over which family the genus should be placed in. Traditional classification systems recognized Nelumbo as part of the Nymphaeaceae, but traditional taxonomists were likely misled by convergent evolution associated with an evolutionary shift from a terrestrial to an aquatic lifestyle. 

In the older classification systems, it was recognized under the biological order Nymphaeales or Nelumbonales. Nelumbo is currently recognized as the only living genus in Nelumbonaceae, one of several distinctive families in the eudicot order of the Proteales. Its closest living relatives, the (Proteaceae and Platanaceae), are shrubs or trees.

Interestingly, these lovelies can thermoregulate, producing heat. Nelumbo uses the alternative oxidase pathway (AOX) to exchange electrons. Instead of using the typical cytochrome complex pathway most plants use to power mitochondria, they instead use their cyanide-resistant alternative. 

This is perhaps to generate a wee bit more scent in their blooms and attract more pollinators. The use of this thermogenic feature would have also allowed thermo-sensitive pollinators to seek out the plants at night and possibly use the cover of darkness to linger and mate.

So they functioned a bit little like a romantic evening meeting spot for lovers and a wee bit like the scent diffuser in your home. This lovely has an old lineage with fossil species in Eurasia and North America going back to the Cretaceous and represented in the Paleogene and Neogene. Photo Two: Doug Miller of Green River Stone Company

LATE HETTANGIAN FOSSIL FAUNA FROM THE TASEKO LAKES: BRITISH COLUMBIA

The late Hettangian ammonite fauna from Taseko Lakes is diverse and relatively well‐preserved. Over three field seasons, thirty-five taxa from the Mineralense and Rursicostatum zones were studied and three new species discovered and named: Fergusonites hendersonae, Eolytoceras constrictum and Pseudaetomoceras victoriense. 

This material is very important as it greatly expands our understanding of the fauna and ranges of ammonites currently included in the North American regional ammonite zonation. 

I had the very great honour of having the fellow below, Fergusonites hendersonae, a new species of nektonic carnivorous ammonite, named after me by palaeontologist Louse Longridge from the University of British Columbia. 

I'd met Louise as an undergrad and was pleased as punch to hear that she would be continuing the research by Dr. Howard Tipper, the authority on this area of the Chilcotins and Haida Gwaii — which he dearly loved. 

"Tip" was a renowned Jurassic ammonite palaeontologist and an excellent regional mapper who mapped large areas of the Cordillera. He made significant contributions to Jurassic paleobiogeography and taxonomy in collaboration with Dr. Paul Smith, Head of Earth and Ocean Science at the University of British Columbia. 

Tip’s regional mapping within BC has withstood the test of time and for many areas became the regions' base maps for future studies. The scope of Tip’s understanding of Cordilleran geology and Jurassic palaeontology will likely never be matched. He passed away on April 21, 2005. His humour, knowledge and leadership will be sorely missed. 

Fergusonites hendersonae

Before he left us, he shared that knowledge with many of whom who would help to secure his legacy for future generations. We did several trips over the years up to the Taseko Lake area of the Rockies joined by many wonderful researchers from Vancouver Island Palaeontological Society and Vancouver Paleontological Society, as well as the University of British Columbia. 

Both Dan Bowen and John Fam were instrumental in planning those expeditions and each of them benefited greatly from the knowledge of Dr. Howard Tipper. 

If not for Tipper's early work in the region, our shared understanding and much of what was accomplished in his last years and after his passing would not have been possible. 

Over the course of three field seasons, we endured elevation sickness, rain, snow, grizzly bears and very chilly nights  — we were sleeping right next to a glacier at one point — but were rewarded by the enthusiastic crew, helicopter rides — which really cut down the hiking time — excellent specimens including three new species of ammonites, along with a high-spired gastropod and lobster claw that have yet to be written up. This area of the world is wonderful to hike and explore — stunningly beautiful country. We were also blessed with access as the area is closed to all fossil collecting except with a permit.

This fauna understanding helps us to understand the correlations between different areas: (1) the Mineralense and Rursicostatum zones are present in Taseko Lakes and can be readily correlated with contemporaneous strata elsewhere in North America; (2) the Mineralense and Rursicostatum zones of North America are broadly equivalent to the Canadensis Zone and probably the Arcuatum horizon of the South American succession; (3) broad correlations are possible with middle–late Hettangian and earliest Sinemurian taxa in New Zealand; (4) the Mineralense and Rursicostatum zones are broadly equivalent to the circum‐Mediterranean Marmoreum Zone; (5) the Mineralense Zone and the lower to middle portion of the Rursicostatum Zone are probably equivalent to the Complanata Subzone whereas the upper portion of the Rursicostatum Zone may equate to the Depressa Subzone of the north‐west European succession.

Taseko Lake Area, BC

The Taseko Lakes area has yielded the best preserved and most diverse collection of late Hettangian ammonites yet discovered in British Columbia (BC). Early studies of the fauna were undertaken by Frebold (1951, 1967). At that time, eastern Pacific ammonite faunas were poorly understood and species were frequently shoehorned into established north‐west European taxa. 

Since then, knowledge of eastern Pacific Hettangian ammonite faunas has improved considerably. 

Detailed systematic studies have been completed on faunas from localities in other areas of BC, Alberta, Alaska, Oregon, Nevada, Mexico and South America (e.g. Guex 1980, 1995; Imlay 1981; Hillebrandt 1981, 1988, 1990, 1994, 2000a–d; Smith and Tipper 1986; Riccardi et al. 1991; Jakobs and Pálfy 1994; Pálfy et al. 1994, 1999; Taylor 1998; Hall et al. 2000; Taylor and Guex 2002; Hall and Pitaru 2004). 

These studies have demonstrated that Early Jurassic eastern Pacific ammonites had strong Tethyan affinities as well as a high degree of endemism (Guex 1980, 1995; Taylor et al. 1984; Smith et al. 1988; Jakobs et al. 1994; Pálfy et al. 1994). Frebold’s early studies were also hampered because they were based on small collections, which limited understanding of the diversity of the fauna and variation within populations. However, recent mapping has greatly improved our understanding of the geology of Taseko Lakes (Schiarizza et al. 1997; Smith et al. 1998; Umhoefer and Tipper 1998) and encouraged further collecting that has dramatically increased the size of the sample.

A study of the ammonite fauna from Taseko Lakes is of interest for several reasons. The data are important for increasing the precision of the late Hettangian portion of the North American Zonation. 

Owing to the principally Tethyan or endemic nature of Early Jurassic ammonites in the eastern Pacific, a separate zonation for the Hettangian and Sinemurian of the Western Cordillera of North America has been established by Taylor et al. (2001). Except for information available from the early studies by Frebold (1951, 1967), the only Taseko Lakes taxa included in the North American Zonation of Taylor et al. (2001) were species of Angulaticeras studied by Smith and Tipper (2000). 

Since then, Longridge et al. (2006) made significant changes to the zonation of the late Hettangian and early Sinemurian based on a detailed study of the Badouxia fauna from Taseko Lakes (Text‐fig. 2). An additional taxonomic study was recently completed on the late Hettangian ammonite Sunrisites (Longridge et al. 2008) and this information has not yet been included within the zonation. 

Hettangian Zonation

The systematics of the remaining ammonite fauna from Taseko Lakes are presented here. A comprehensive study of this material is important because the exceptional quality and diversity of the fauna provide important data for updating the North American Zonation, making it more comprehensive and more widely applicable, especially in Canada.

The Taseko Lakes fauna can improve Hettangian correlations within North America as well as between North America and the rest of the world. 

North‐west European ammonite successions (e.g. Dean et al. 1961; Mouterde and Corna 1997; Page 2003) are considered the primary standard for Early Jurassic biochronology (Callomon 1984). 

In north‐west Europe, the turnover from schlotheimiid dominated faunas in the late Hettangian to arietitid dominated faunas in the early Sinemurian was sharp (e.g. Dean et al. 1961; Bloos 1994; Bloos and Page 2002). In other areas, by contrast, these faunas were not so mutually exclusive and the transition was much more gradual. 

This makes correlations between north‐west Europe and other areas difficult (e.g. Bloos 1994; Bloos and Page 2000, 2002). Correlations are further impeded by endemism and provincialism. 

The Taseko Lakes fauna addresses these problems because it contains many taxa that are common throughout the eastern Pacific as well as several cosmopolitan taxa that make intercontinental correlation possible. Correlation between North America and other areas is of particular significance in that the interbedded volcanic and fossiliferous marine rocks in North America permit the calibration of geochronological and biochronological time scales (Pálfy et al. 1999, 2000). 

This correlation between the late Hettangian fauna in the Taseko Lakes area and contemporaneous faunas in other areas of North America, South America, New Zealand, western and eastern Tethys, and north‐west Europe is of particular interest to me — especially the correlation of the faunal sequences of Nevada, USA. 

Reference: PaleoDB 157367 M. Clapham GSC C-208992, Section A 09, Castle Pass Angulata - Jurassic 1 - Canada, Longridge et al. (2008)

L. M. Longridge, P. L. Smith, and H. W. Tipper. 2008. Late Hettangian (Early Jurassic) ammonites from Taseko Lakes, British Columbia, Canada. Palaeontology 51:367-404

PaleoDB taxon number: 297415; Cephalopoda - Ammonoidea - Juraphyllitidae; Fergusonites hendersonae Longridge et al. 2008 (ammonite); Average measurements (in mm): shell width 9.88, shell diameter 28.2; Age range: 201.6 to 196.5 Ma. Locality info: British Columbia, Canada (51.1° N, 123.0° W: paleo coordinates 22.1° N, 66.1° W)

Photo One: Hettangian Ammonites and Gastropods, Taseko Lakes. Photo Two: Fergusonites hendersonae, a Late Hettangian (Early Jurassic) ammonite from the Taseko Lakes area of British Columbia, Canadian Rockies, named by Dr. Louise Longridge after Heidi Henderson, Chair, Vancouver Paleontological Society who collected and subsequently donated many Hettangian specimens from Taseko Lakes to the GSC collections. Holotype. GSC 127423 from the Rursicostatum Zone, Castle Pass section A, level 06, Taseko Lakes.

Map: Localities of sections and isolated outcrops bearing late Hettangian ammonites in the Taseko Lakes map area. Figure Two: Zonation for the Hettangian showing correlation of North American zones with South America, north‐west Europe, western Tethys (circum‐Mediterranean), eastern Tethys and New Zealand. Only approximate correlations are implied. 

UPTHRUSTING PLATES: WASHINGTON GEOLOGY

Two hundred million years ago, Washington was two large islands, bits of the continent on the move westward, eventually bumping up against the North American continent and calling it home. The shifting continues, subtly changing the landscape like a breath. We only notice when pockets of resistance manifest as earthquakes, some newsworthy, some all but unnoticed. For now, the more extreme movement has subsided laterally and continues vertically, pushing California towards the North Pole. Hello Baja-BC.

The upthrusting of plates move our mountain ranges skyward – the path of least resistance. And it is this dynamic movement that's created the landscape we see today.

The 3,000 meters of the stratigraphic section of the Chuckanut Formation along Chuckanut Drive span an age range of just a few million years. The lower part is late Paleocene with a radiometric age of around 56 million years. The upper part of the section is early Eocene. The fossils found here lived and died very close to where they are now but in a much warmer, wetter, swampy setting. The exposures of the Chuckanut Formation were once part of a vast river delta; imagine, if you will, the bayou country of the Lower Mississippi. The siltstones, sandstones, mudstones and conglomerates of this formation were laid down during a time of luxuriant plant growth in the subtropical flood plain that covered much of the Pacific Northwest.

This ancient wetland provided ideal conditions to preserve the many trees, shrubs and plants that thrived here giving us a lot of information about climate, temperature, the water cycle and humidity of the region. The Chuckanut flora is made up predominantly of plants whose modern relatives live in tropical areas such as Mexico and Central America. While less abundant, evidence of the animals that called this ancient swamp home are also found here. Rare bird, reptile, and mammal tracks have been immortalized in the outcrops of the Chuckanut Formation.

Sumas Eocene Shorebird Trackway

Tracks of a type of archaic mammal of the Orders Pantodonta or Dinocerata (blunt foot herbivores), footprints from a small shorebird, and tracks from an early equid or webbed bird track give evidence to the vertebrates that inhabited the swamps, lakes and riverways of the Pacific Northwest 50 million years ago.

Fossil mammals and bird trackways from Washington State have caused great excitement over the past few years. Many new trackways have been discovered since the 2009 slides near Sumas. George Mustoe and team collected these important finds, bringing them to the Burke Museum in Washington State to study and make available for display.

The movement of these vertebrates was captured in the soft mud on the banks of an ancient river, one of the only depositional environments favourable for track preservation. The terrestrial paleontological record of Washington State at sites like Chuckanut and Racehorse Creek (U-Pb 53 Ma.) is primarily made up of plant material with some wonderfully enticing mammal, shorebird (seen here) and large Diatryma bird tracks on rare occasions.

JUVENILE HAMITES SUBROTUNDUS

A tremendously delicate juvenile Hamites subrotundus (J. Sowerby 1814) from Upper Albian outcrops in Mallorca, the largest of the three Balearic Islands in the Mediterranean at more than 3,600 square kilometers. 

Mallorca has been home to various inhabitants for thousands of years. Sitting some 200 kilometers off Spain’s southeastern, it is a idyllic setting for exploring the rich human and geologic history of this part of the world.

The island is made up of dolomite and limestone from a huge expanse of time, the Mesozoic and Cenozoic—170 million to 10 million years ago— and bookended by two parallel mountain chains top and bottom on its southern and northern coasts. 

As you walk the mountain passes northwest to northeast, you stroll across Miocene deposits 20 million to 13 million years ago that speak of the time in our Earth's recent past when part of the African continent collided with Europe. 

It is famous for its limestone mountains and Roman and Moorish remains. As you can see here, it is also home to some rather nice fossils including this specimen of Hamites subrotundus.

While H. subrotundus is generally a Middle Albian species, this specimen was found in the lower part of Upper Albian in the Cristatum zone by José Juárez Ruiz. José had to piece this lovely together from seven fragments. His labour of love was worth the effort. The final piece is sheer perfection and a beautiful specimen approximately 2.5 cm long.

Mallorca and the other Balearic Islands are geologically an extension of the Baetic Cordillera mountain chain of western Andalusia that extends to Murcia and Valencia. 

They are made up of sediments deposited in the Tethys Sea during the Mesozoic.

Exploring the islands, you can collect from deposits from the Triassic, Cretaceous, Jurassic, and Neogene periods. 

The limestone outcrops contain lovely examples of foraminifers—mainly the species Globigerina.

We also see lovely examples of Hamites (Hamites) subrotundus in the Euhoplites loricatus zone; Euhoplites meandrinus subzone from the Middle Albian (Lower Gault) of Folkestone, Kent, UK. 

Photo, preparation and in the collection of the deeply awesome José Juárez Ruiz. Wright C. W. 1996. Treatise on Invertebrate Paleontology (Part L Mollusca 4 Revised) Volume 4: Cretaceous Ammonoidea

FOSSILS, LIMESTONE & SALT: HALLSTATT

Hallstatt Salt Mines, Austria / Permian Salt Diapir

The Hallstatt Limestone is the world's richest Triassic ammonite unit, yielding specimens of more than 500 ammonite species.

Along with diversified cephalopod fauna  — orthoceratids, nautiloids, ammonoids — we also see gastropods, bivalves, especially the late Triassic pteriid bivalve Halobia (the halobiids), brachiopods, crinoids and a few corals. We also see a lovely selection of microfauna represented. 

For microfauna, we see conodonts, foraminifera, sponge spicules, radiolaria, floating crinoids and holothurian sclerites —  polyp-like, soft-bodied invertebrate echinozoans often referred to as sea cucumbers because of their similarities in size, elongate shape, and tough skin over a soft interior. 

Franz von Hauer’s exhaustive 1846 tome describing Hallstatt ammonites inspired renowned Austrian geologist Eduard Suess’s detailed study of the area’s Mesozoic history. That work was instrumental in Suess being the first person to recognize the former existence of the Tethys Sea, which he named in 1893 after the sister of Oceanus, the Greek god of the ocean. As part of the Northern Limestone Alps, the Dachstein rock mass, or Hoher Dachstein, is one of the large karstic mountains of Austria and the second-highest mountain in the Northern Limestone Alps. It borders Upper Austria and Styria in central Austria and is the highest point in each of those states.

Parts of the massif also lie in the state of Salzburg, leading to the mountain being referred to as the Drei-Länder-Berg or three-state mountain. Seen from the north, the Dachstein massif is dominated by the glaciers with the rocky summits rising beyond them. By contrast, to the south, the mountain drops almost vertically to the valley floor. The karst limestones and dolomites were deposited in our Mesozoic seas. The geology of the Dachstein massif is dominated by the Dachstein-Kalk Formation — the Dachstein limestone — which dates back to the Triassic.

Hallstatt and the Hallstatt Sea, Austria

There were several phases of mountain building in this part of the world pushing the limestone deposits 3,000 metres above current sea level. The rock strata were originally deposited horizontally, then shifted, broken up and reshaped by the erosive forces of ice ages and erosion.

The Hallstatt mine exploits a Permian salt diapir that makes up some of this area’s oldest rock. 

The salt accumulated by evaporation in the newly opened, and hence shallow, Hallstatt-Meliata Ocean. This was one of several small ocean basins that formed in what is now Europe during the late Paleozoic and early Mesozoic when the world’s landmasses were welded together to form the supercontinent Pangea. 

Pangea was shaped like a crescent moon that cradled the famous Tethys Sea. Subduction of Tethyian oceanic crust caused several slivers of continental crust to separate from Pangea, forming new “back-arc basins” (small oceans formed by rifting that is associated with nearby subduction) between the supercontinent and the newly rifted ribbon continents.

The Hallstatt-Meliata Ocean was one such back-arc basin. As it continued to expand and deepen during the Triassic, evaporation ceased and reefs flourished; thick limestone deposits accumulated atop the salt. When the Hallstatt-Meliata Ocean closed in the Late Jurassic, the compression squeezed the low-density salt into a diapir that rose buoyantly, injecting itself into the Triassic limestones above.

The Hallstatt salt diapir and its overlying limestone cap came to rest in their present position in the northern Austrian Alps when they were shoved northward as nappes (thrust sheets) during two separate collision events, one in the Cretaceous and one in the Eocene, that created the modern Alps. It is from the Hallstatt salt diapir that Hallstatt, like so many cities and towns, gets its name.

Deposits of rock salt or halite, the mineral name of sodium chloride with the chemical formula of NaCl, are found and mined around the globe. These deposits mark the dried remains of ancient oceans and seas. Names of rivers, towns and cities in Europe — Salzburg, Halle, Hallstatt, Hallein, La Salle, Moselle — all pay homage to their connection to halite and salt production. The Greek word for salt is hals and the Latin is sal. The Turkish name for salt is Tuz, which we see in the naming of Tuzla, a salt-producing region of northeastern Bosnia-Herzegovina and in the names of towns that dot the coast of Turkey where it meets the Black Sea. Hallstatt with its salt diapir is no exception.

The salt-named town of Hallstatt sits on the shores of the idyllic Hallstätter Sea at the base of the Dachstein massif. Visiting it today, you experience a quaint traditional fishing village built in the typical upper Austrian style. Tourism drives the economy as much as salt as this area of the world is picture-perfect from every angle.

Space is at a minimum in the town. For centuries, every ten years the local cemetery exhumes the bones of those buried there and moves them to an ossuary to make room for new burials. The Hallstatt Ossuary is called Karner, Charnel House, or simply Beinhaus (Bone House). Karners are places of secondary burials. They were once common in the Eastern Alps, but that custom has largely disappeared.

Hallstatt Beinhaus Ossuary, Hallstatt, Austria

A collection of over 700 elaborately decorated skulls rest inside the ossuary. They are lined up on rows of wooden shelves that grace the walls of the chapel. Another 500 undecorated skulls, bare and without any kind of adornment, are stacked in the corners.

Each is inscribed and attached to a record with the deceased's name, profession and date of death. The Bone House is located in a chapel in the basement of the Church of Saint Michael. The church dates from the 12th century CE. 

Decorating the skulls was traditionally the job of the local gravedigger and an honour granted to very few. At the family's request, garlands of flowers were painted on the skulls of deceased as decorative crowns if they were female. The skulls of men and boys were painted wreaths of oak or ivy.

Every building in Hallstatt looks out over the Hallstätter Sea. This beautiful mountain lake considered one of the finest of Austria's Salzkammergut region. It lies at the northern foot of the Dachstein mountain range, sitting eight-and-a-half kilometres long and two kilometres wide. The shoreline is dotted by the villages of  Obertraun, Steeg, and Hallstatt.

The region is habitat to a variety of diverse flora and fauna, including many rare species such as native orchids, in the wetlands and moors in the south and north.

Linked by road to the cities of Salzburg and Graz, Hallstatt and its lake were declared one of the World Heritage sites in Austria in 1997 and included in the Hallstatt-Dachstein Salzkammergut Alpine UNESCO World Heritage Site. The little market village of Hallstatt takes its name from the local salt mine.

Hallstatt, Salzkammergut region, Austria

The town is a popular tourist destination with its quaint shops and terraced cafes. In the centre of town, the 19th-century Evangelical Church of Hallstatt with its tall, slender spire is a lakeside landmark. You can see it here in the photo on the left.

Above the town are the Hallstatt Salt mines located within the 1,030-meter-tall Salzburg Salt Mountain. They are accessible by cable car or a three-minute journey aboard the funicular railway. There is also a wonderful Subterranean Salt Lake.

In 1734, there was a corpse found here preserved in salt. The fellow became known as the Man in Salt. Though no archaeological analysis was performed at the time — the mummy was respectfully reburied in the Hallstatt cemetery — based on descriptions in the mine records, archaeologists suspect the miner lived during the Iron Age. This Old Father, Senos ph₂tḗr, 'ɸatīr 'father' may have been a local farmer, metal-worker, or both and chatted with his friends and family in Celtic or Proto-Celtic.

Salt mining in the area dates back to the Neolithic period, from the 8th to 5th Centuries BC. This is around the time that Roman legions were withdrawing from Britain and the Goths sacked Rome. In Austria, agricultural settlements were dotting the landscape and the alpine regions were being explored and settled for their easy access to valuable salt, chert and other raw materials.

The salt-rich mountains of Salzkammergut and the upland valley above Hallstatt were attractive for this reason. The area was once home to the Hallstatt culture, an archaeological group linked to Proto-Celtic and early Celtic people of the Early Iron Age in Europe, c.800–450 BC.

Bronze Age vessel with cow and calf

In the 19th century, a burial site was discovered with 2,000 individuals, many of them buried with Bronze Age artefacts of amber and ivory.

It was this find that helped lend the name Hallstatt to this epoch of human history. The Late Iron Age, between around 800 and 400 BC, became known as the Hallstatt Period.

For its rich history, natural beauty and breathtaking mountainous geology, Hallstatt is a truly irresistible corner of the world.

Salzbergstraße 1, 4830 Hallstatt.  https://www.salzwelten.at/en/home/

Photo: Bronze vessel with cow and calf, Hallstatt by Alice Schumacher - Naturhistorisches Museum Wien - A. Kern – K. Kowarik – A. W. Rausch – H. Reschreiter, Salz-Reich. 7000 Jahre Hallstatt, VPA 2 (Wien, 2008) Seite 133 Abbildung 6. Hallstatt Village & Ossuary Photos: P. McClure Photography ca. 2015.

Bernoulli D, Jenkyns HC (1974) Alpine, Mediterranean, and Central Atlantic Mesozoic facies in relation to the early evolution of the Tethys. Soc Econ Paleont Mineral Spec Publ 19:129–160

Bernoulli D, Jenkyns H (2009) Ancient oceans and continental margins of the Alpine-Mediterranean Tethys: deciphering clues from Mesozoic pelagic sediments and ophiolites. Sedimentology 56:149–190

ANAHOPLITES PLANUS OF FRANCE

A beautiful specimen of the ammonite, Anahoplites planus (Mantell, 1822) from Albian deposits in Villemoyenne Quarry, Courcelles, Aube, north-central France.

Anahoplites (Hyatt, 1900) is a genus of compressed hoplitid ammonites with flat sides, narrow, flat or grooved venters, and flexious ribs or striae arising from weak umbilical tubercles that end in fine dense ventrolateral nodes.

This lovely has attracted some roommates — an oyster, some bryozoans and worm tubes are attached to her shell.

Anahoplites is now included in the subfamily Anahoplitinae and separated from the Hoplitinae where it was placed in the older in the 1957 edition of the Treatise on Invertebrate Paleontology, Part L (Ammonoidea). Genera of the Hoplitinae tend to be more robust, with broader whorls and stronger ribs.

Anahoplites is found in Cretaceous (Middle to the Late Albian) deposits from England, through Europe, all the way to the Transcaspian Oblast region in Russia to the east of the Caspian Sea. The Aube department, named after the local river, is the type locality of the Albian stage (d'ORBIGNY, 1842). 

A. planus from the French Coast

Two formations are recognized in the clay facies (the "Gault" auct.) of the stratotype, the Argiles tégulines de Courcelles (82 m), overlain by the Marnes de Brienne (43 m). The boundary between the two formations is well-defined at the top of an indurated bed and readily identifiable in the field.

This involute (113 mm) specimen shows evidence of cohabitation by some of his marine peers. 

We see two different bryozoa, an oyster and some serpulids making a living and leaving trace fossils on her flat sides. The top specimen was prepared with potase by José Juárez Ruiz of Spain. 

The lovely Anahoplites planus you see here to the lower right was found by Bertus op den Dries on the French coast in Albian deposits near Wissant, P5 and measures in at 8 cm. This on edge view gives you a very good sense of the keel.