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.

MAMMOTHS LAST MEAL

One of the first scientific accounts of a well-preserved woolly mammoth, Mammuthus primigenius, frozen in Siberia described the meat as enticingly red and marbled but smelling so putrid that researchers could only tolerate a minute in its proximity.

Despite this initial review, numerous apocryphal tales exist of dinners made from centuries-old mammoths found frozen whole in clear blocks of ice. 

These accounts have not only enchanted the public but also heavily influenced early scientific thought on Quaternary extinctions and climate; many researchers resorting to catastrophism to explain the instantaneous freezing necessary to preserve palatable meat.

The possibility of cloning is now the major draw of frozen mammoths but the public remains curious about eating prehistoric meat, especially because some modern paleontologists have credibly described tasting mammoth and extinct bison found preserved in permafrost.

Although less publicized today, eating study specimens was once common practice for researchers. Charles Darwin belonged to a club dedicated to tasting exotic meats, and in his first book wrote almost three times as much about dishes like armadillo and tortoise urine than he did on the biogeography of his Galapagos finches.

One of the most famously strange scientific meals occurred on January 13, 1951, at the 47th Explorers Club Annual Dinner (ECAD) when members purportedly dined on frozen woolly mammoth. The prehistoric meat was supposedly found on Akutan Island in Alaska, USA, by the eminent polar explorers Father Bernard Rosecrans Hubbard, “the Glacier Priest,” and Captain George Francis Kosco of the US Navy.

This much-publicized meal captured the public’s imagination and became an enduring legend and source of pride for the Club, popularizing an annual menu of “exotics” that continues today, making the Club as well-known for its notorious hors d’oeuvres like fried tarantulas and goat eyeballs as it is for its notable members such as Teddy Roosevelt and Neil Armstrong.

The Yale Peabody Museum holds a sample of meat preserved from the 1951 meal, interestingly labelled as a South American Giant Ground Sloth, Megatherium, not Mammoth.

Green Sea Turtle, Chelonia mydas

The specimen of meat from that famous meal was originally designated BRCM 16925 before a transfer in 2001 from the Bruce Museum to the Yale Peabody Museum of Natural History (New Haven, CT, USA) where it gained the number YPM MAM 14399.

The specimen is now permanently deposited in the Yale Peabody Museum with the designation YPM HERR 19475 and is accessible to outside researchers. 

The meat was never fixed in formalin and was initially stored in isopropyl alcohol before being transferred to ethanol when it arrived at the Peabody Museum. DNA extraction occurred at Yale University in a clean room with equipment reserved exclusively for DNA analyses.

In 2016, Jessica Glass and her colleagues sequenced a fragment of the mitochondrial cytochrome-b gene and studied archival material to verify its identity, which if genuine, would extend the range of Megatherium over 600% and alter views on ground sloth evolution. Their results showed that the meat was not Mammoth or Megatherium, but a bit of Green Sea Turtle, Chelonia mydas. So much for elaborate legends. 

The prehistoric dinner was likely meant as a publicity stunt. Glass's study emphasizes the value of museums collecting and curating voucher specimens, particularly those used for evidence of extraordinary claims. Not so long before Glass et al. did their experiment, a friend's mother (and my kayaking partners) served up a steak from her freezer to dinner guests in Castlegar that hailed from 1978. Tough? Inedible? I have it on good report that the meat was surprisingly divine.

Reference: Glass, J. R., Davis, M., Walsh, T. J., Sargis, E. J., & Caccone, A. (2016). Was Frozen Mammoth or Giant Ground Sloth Served for Dinner at The Explorers Club?. PloS one, 11(2), e0146825. https://doi.org/10.1371/journal.pone.0146825

The image of the mammoth you see here is by the very talented Daniel Eskridge. To see more of his work, and indeed purchase it, head over to: https://daniel-eskridge.pixels.com/

FOSSIL FAUNA OF HAIDA GWAII

This lovely slate grey and beige ammonite with the fine ribbing is Brewericeras hulenense (Anderson 1938) — a fast-moving, nektonic (no idle floating here!) carnivorous ammonite from the Lower Cretaceous (Albian) of Haida Gwaii, British Columbia, Canada.

This specimen is just over 12cm in length, a little under the average of 13.4cm. There are several localities in the islands of Haida Gwaii where Brewericeras can be found — six that I know of and likely plenty more.

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

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

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 find multiple beautifully preserved specimens of the spiny ammonite, Douvelleiceras spiniferum along with Brewericeras hulenense (shown here), Cleoniceras perezianum and many cycads in concretion.

The Lower Jurassic ammonite faunas found at Haida Gwaii are very similar to those found in the Eastern Pacific around South America and in the Mediterranean. 

The strata exposed at Maple Island, Haida Gwaii are stratigraphically higher than the majority of Albian localities in Skidegate Inlet. The macrofossil fauna belonged to the Upper part of the Sandstone Member of the Haida formation.

The western end of the island contains numerous well-preserved inoceramids such as Birostrina concentrica and a few rare ammonites of Desmoceras bearskinese. 

The eastern shores are home to unusual ammonite fauna in the finer-grained sandstones. Here we find the fossils as extremely hard concretions while others were loose in the shale. Species include Anagaudryceras sacya and Tetragonites subtimotheanus. A large whorl section of the rare Ammonoceratites crenucostatus has also been found here. 

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.

AMMONITES FROM THE GAULT

The chunky ammonite Proeuhoplites subtuberculatus, bed II (iv), Folkstone Gault Clay, county of Kent, southeast England.

This matrix you see here is the Gault Clay, known locally as the Blue Slipper. This fine muddy clay was deposited 105-110 million years ago during the Lower Cretaceous (Upper and Middle Albian) in a calm, fairly deep-water continental shelf that covered what is now southern England and northern France.

Lack of brackish or freshwater fossils indicates that the gault was laid down in open marine environments away from estuaries. The maximum depth of the Gault is estimated 40-60m a figure which has been reached by the presence of Borings made by specialist Algal-grazing gastropods and supported by a study made by Khan in 1950 using Foraminifera. Estimates of the surface water temperatures in the Gault are between 20-22°c and 17-19°c on the seafloor. These estimates have been reached by bulk analysis of sediments which probably register the sea surface temperature for calcareous nanofossils.

It is responsible for many of the major landslides around Ventnor and Blackgang the Gault is famous for its diverse fossils, mainly from mainland sites such as Folkestone in Kent.

Folkestone, Kent is the type locality for the Gault clay yielding an abundance of ammonites, the same cannot be said for the Isle of Wight Gault, however, the south-east coast of the island has proved to be fossiliferous in a variety of ammonites, in particular, the Genus Hoplites, Paranahoplites and Beudanticeras.

While the Gault is less fossiliferous here on the island it can still produce lovely marine fossils, mainly ammonites and fish remains from these muddy mid-Cretaceous seas. The Gault clay marine fossils include the ammonites (such as Hoplites, Hamites, Euhoplites, Anahoplites, and Dimorphoplites), belemnites (such as Neohibolites), bivalves (notably Birostrina and Pectinucula), gastropods (including the lovely Anchura), solitary corals, fish remains (including shark teeth), scattered crinoid remains, and crustaceans (look for the crab Notopocorystes).

Occasional fragments of fossil wood may also be found. The lovely ammonite you see here is from the Gault Clays of Folkstone. Not all who name her would split the genus Euhoplites. There’s a reasonable argument for viewing this beauty as a very thick form of E. loricatus with Proeuhoplites being a synonym of Euhoplites. Collected, photographed and prepped by Thomas Miller. Approx 35mm across.

Jack Wonfor shared a wealth of information on the Gault and has many lovely examples of the ammonites found here in his collections. If you wish to know more about the Gault clay a publication by the Palaeontological Association called 'Fossils of the Gault clay' by Andrew S. Gale is available in Dinosaur Isle's gift shop.

There is a very good website maintained by Fred Clouter you can look at for reference. It also contains many handy links to some of the best fossil books on the Gault Clay and Folkstone Fossil Beds. Check it out here: http://www.gaultammonite.co.uk/

TURTLE SHELLS: HOME SWEET ARMOUR

Turtle shells are different from the body armour or armoured shells we see adorning dinosaurs like the ankylosaurs. 

Ankylosaurs were blessed with huge plates of bone embedded into their skin that acted as a natural shield against predators. Crocodilians have these same bony plates, or osteoderms, embedded in their skin to give them extra protection. 

We find similar body armour on armadillos. Yet, armadillos, crocodiles and ankylosaurs each evolved body armour that differs significantly from that found in turtles. 

Remarkably, the carapace we see in fully grown turtles is formed from different parts of their skeletons. And, once fully formed, turtle shell fully integrates with the backbone and ribs, growing over the animal in a domed carapace — both protection and home sweet home. 

When we look to the oldest known members of the turtle lineage, Proterochersis and Proganochelys, found as fossils in 210 million-year-old outcrops in present-day Germany and Poland. Like the turtles we find today, these stem-turtles already had fully formed shells — special bony or cartilaginous shell that originates in their ribs. It is a useful adaptation to help deter predators as their soft interior makes for a tasty snack. 

Though I have never eaten turtle (and never will), it was a common and sought after meat for turtle soup. Years ago, I read of Charles Darwin craving it after trying it for the first time on his trip in 1831 aboard the HMS Beagle. It seems Charlie like to taste every exotic new species he had the opportunity to try.

Turtle armour is made of dermal bone and endochondral bones from their vertebrae and rib cage. It is fundamentally different from the armour seen on our other vertebrate friends and the design creates some unique features in turtles. 

Because turtle ribs fuse together with some of their vertebrae, they have to pump air in and out of the lungs with their leg muscles. 

Another unusual feature in turtles is their limb girdles, pectoral and pelvic, which have come to lie within their rib cage, a feature that allows some turtles to pull their limbs inside the shell for protection. 

Sea turtles didn't develop this behaviour or ability and do not retract into their shells like other turtles.

Armadillos have armour formed by plates of dermal bone covered in relatively small, overlapping epidermal scales called scutes, composed of bone with a covering of horn. In crocodiles, their exoskeletons form their armour, similar to ankylosaurs. A bit of genius design, really. It is made of protective dermal and epidermal components that begin as rete Malpighii: a single layer of short, cylindrical cells that lose their nuclei over time as they transform into a horny layer.

Depending on the species and age of the turtle, turtles eat all kinds of food including seagrass, seaweed, crabs, jellyfish, and shrimp,. That tasty diet shows up in the composition of their armour as they have oodles of great nutrients to work with. The lovely example you see here is from the Oxford Museum collections.

PHYLLOCERAS VELLEDAE OF MADAGASCAR

This specimen of Phylloceras velledae (Michelin) has a shell with a small umbilicus, arched, acute venter, and at some growth stage, falcoid ribs that spring in pairs from umbilical tubercles, disappearing on the outer whorls.

This specimen has been polished to show the sutures to great effect. These ammonites are common in rock shops and plentiful on the internet.

These ammonites make a lovely addition to any teaching collection as they provide a lot of detail and can be handled quite well by small, less gentle hands. 

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.

ANCIENT OCTOPUS: KEUPPIA

A sweet as you please example of Keuppia levante (Fuchs, Bracchi & Weis, 2009), an extinct genus of octopus that swam our ancient seas back in the Cretaceous. 

This particular lovely adorns a special place in my heart and my office. His forever home will be within the collections of a local museum but we spend time together—me taking in the remarkable detail and preservation of this specimen and him enjoying a pretty good looking view and regular dustings. Win, win.

I say, he, but we cannot know for sure. 

The dark black and brown area you see here is his ink sac which has been preserved for a remarkable 95 million years.

This cutie is in the family Palaeoctopodidae, and one of the earliest representatives of the order Octopoda — and perhaps my favourite fossil. It was this perfect specimen that inspired the logo for the Fossil Huntress brand.  

These ancient marine beauties are in the class Cephalopoda making them relatives of our modern octopus, squid and cuttlefish.

There are two species of Keuppia, Keuppia hyperbolaris and Keuppia levante, both of which we find as fossils. We find their remains, along with those of the genus Styletoctopus, in Cretaceous-age Hâqel and Hjoula localities in Lebanon. 

For many years, Palaeoctopus newboldi (Woodward, 1896) from the Santonian limestones at Sâhel Aalma, Lebanon, was the only known pre‐Cenozoic coleoid cephalopod believed to have an unambiguous stem‐lineage representative of Octobrachia fioroni. 

With the unearthing of some extraordinary specimens with exquisite soft‐part preservation in the Lebanon limestones, our understanding of ancient octopus morphology has blossomed. The specimens are from the sub‐lithographical limestones of Hâqel and Hâdjoula, in northwestern Lebanon. The localities are about 15 km apart, 45 km away from Beirut and 15 km away from the coastal city of Jbail. Fuchs et al. put a nice little map in their 2009 paper that I have included and referenced here.

Palaeoctopus newboldi had a spherical mantle sac, a head‐mantle fusion, eight equal arms armed with suckers, an ink sac, a medially isolated shell vestige, and a pair of (sub‐) terminal fins. The bipartite shell vestige suggests that Palaeoctopus belongs to the octopod stem‐lineage, as the sister taxon of the Octopoda, the Cirroctopoda, is characterized by an unpaired clasp‐like shell vestige (Engeser 1988; Haas 2002; Bizikov 2004).

It is from the comparisons of Canadian fauna combined with those from Lebanon and Japan that things really started to get interesting with Octobrachia. Working with fossil specimens from the Campanian of Canada, Fuchs et al. (2007a ) published on the first record of an unpaired, saddle‐shaped shell vestige that might have belonged to a cirroctopod. 

Again from the Santonian–Campanian of Canada and Japan, Tanabe et al. (2008) reported on at least four different jaw morphotypes. Two of them — Paleocirroteuthis haggarti (Tanabe et al., 2008) and Paleocirroteuthis Pacifica  (Tanabe et al ., 2008) — have been interpreted as being of cirroctopod type, one of octopod type, and one of uncertain octobrachiate type. 

Interestingly Fuchs et al. have gone on to describe the second species of Palaeoctopus, the Turonian Palaeoctopus pelagicus from limestones at Vallecillo, Mexico. While more of this fauna will likely be recovered in time, their work is based solely on a medially isolated shell vestige.

Five new specimens have been found in the well-known Upper Cenomanian limestones at Hâqel and Hâdjoula in Lebanon that can be reliably placed within the Octopoda. Fuchs et al. described these exceptionally well‐preserved specimens and discuss their morphology in the context of phylogeny and evolution in their 2008 paper (2009 publishing) in the Palaeontology Association Journal, Volume 51, Issue 1.

The presence of a gladius vestige in this genus shows a transition from squid to octopus in which the inner shell has divided into two parts in early forms to eventually be reduced to lateralized stylets, as can be seen in Styletoctopus.

The adorable fellow you see here with his remarkable soft-bodied preservation and inks sack and beak clearly visible is Keuppia levante. He hails from Late Cretaceous (Upper Cenomanian) limestone deposits near Hâdjoula, northwestern Lebanon. The vampyropod coleoid, Glyphiteuthis abisaadiorum n. sp. is also found at this locality. This specimen is about 5 cm long.

Fuchs, D.; Bracchi, G.; Weis, R. (2009). "New octopods (Cephalopoda: Coleoidea) from the Late Cretaceous (Upper Cenomanian) of Hâkel and Hâdjoula, Lebanon". Palaeontology. 52: 65–81. doi:10.1111/j.1475-4983.2008.00828.x.

Photo one: Fossil Huntress. Figure Two: Topographic map of north‐western Lebanon with the outcrop area in the upper right-hand corner. Fuchs et al, 2009.  

BIOLUMINESCENCE: CHEMICAL POETRY

Light in the oceans? It is chemistry, my friends. 

In the inky blackness of the deep sea, more than 90% of the animals are luminescent. It is quite a startling number but makes good sense when you think of the edge bioluminescence provides. 

The ability to generate light helps umpteen animals find mates, attract prey and avoid predation. Handy stuff, light. 

What you know about light above the surface does not hold true for the light you see as bioluminescence. Its energy and luminosity come from a chemical reaction. 

In a luminescent reaction, two types of chemicals — luciferin and luciferase — combine together. Together, they produce cold light — light that generates less than 20% thermal radiation or heat. 

The light you see is produced by a compound called Luciferin. It is the shiny, showy bit in this chemical show. Luciferase acts as an enzyme, the substance that acts as a catalyst controlling the rate of chemical reactions, allowing the luciferin to release energy as it is oxidized. The colour of the light depends on the chemical structures of the chemicals. There are more than a dozen known chemical luminescent systems, meaning that bioluminescence evolved independently in different groups of organisms.

Coelenterazine is the type of luciferin we find in shrimp, fish and jellyfish. Dinoflagellates and krill share another class of unique luciferins, while ostracods or firefleas and some fish have a completely different luciferin. 

The luciferase found in dinoflagellates is related to the green chemical chlorophyll found in plants. Bioluminescent dinoflagellates are a type of plankton — teensy marine organisms that make the seaways shimmer like the Milky Way as you swim through them. 

Their twinkling lights are brief, each containing about 100 million photons that shine for a tenth of a second. While each individual flicker is here and gone in the wink of an eye, en masse they are awe-inspiring. I have spent many wondrous evenings scuba diving amongst these glittering denizens off our shores. 

Cotylorhiza Tuberculata Jellyfish

In this close up of a Cotylorhiza Tuberculata Jellyfish, you can see the luminosity of her blue and white tentacles. The occurrence of identical luciferins for different types of organisms may suggest a dietary source for some groups strengthening the adage, you are what you eat, or perhaps you glow how you eat. 

Bacteria and fireflies have unique luminescent chemistries. Fireflies light up when oxygen combines with calcium, adenosine triphosphate (ATP) and luciferin in the presence of luciferase. 

For bacteria, the world stage of luminosity is quite small — and a bit gormless. Just how much light they emit and when is a free-for-all. Not so for the rest of our bioluminescent friends who have very precise control over when they shine and just how bright. 

Bioluminescence comes in a variety of colours, from blue through red. The colour is based on the chemistry, which involves a substrate molecule called luciferin, the source of energy that goes into light, and an enzyme called luciferase or photoprotein. 

Most of this lighting up of our world happens on land or in saltwater. There are almost no bioluminescent organisms native to freshwater.

In terrestrial plants and animals — fireflies, beetles and fungi like this Ghost Fungus, Omphalotus nidiformis, a gilled basidiomycete mushroom — we commonly find green, yellow, and sometimes red. 

In the ocean, bioluminescence is mostly blue-green or green. You would think that blues and green would not show up all that well in our seas but, surprisingly, they do. While sound travels better through saltwater than air, it is the reverse for light. 

Various colours of light do not transmit equally through saltwater. Once we move deeper than the top layer of the ocean warmed by the sun and brimming with nutrients, the epipelagic zone, and move deeper through the mesopelagic, deeper and deeper still to the bathypelagic, frigid abyssalpelagic and finally the deep trenches of the icy pressure and all but inhospitable hadalpelagic, less and less light — until no light — gets through.

It is the twilight of the mesopelagic, 200 - 1000 metres below the surface, that is the sweet spot for most of our bioluminescent friends. Here, only very faint sunlight gets through. The water pressure is higher than at the surface but still lacks the crushing intensity of the lower zones. It is here that bioluminescence becomes a real advantage — good real estate and the showmanship of light pays gold.

We know that the deeper you go in our oceans, less and less sunlight gets through, so if the purpose of bioluminescence is to provide a signal that is noticed by prey, potential mates and predators alike, it is important that the light moves through the seawater, and not be absorbed or scattered — and this plays out in the colours evolved to be seen here. 

If you have spent any time underwater, you will know that blue-green light transmits best through seawater. The deeper you go, the colours fade. Gone are the reds and yellows until everything looks brown or blue-green. Because of this, it is no surprise that blue-green is the most common colouring of bioluminescence in our oceans. 

There are some exceptions to the blue-green/green colour rule — minuscule planktonic polychaete worms, Tomopteris helgolandica, emit yellow light, and deep-sea fish Malacosteus niger in the family Stomiidae, the barbeled dragonfishes, produce both red and blue. 

Malacosteus niger's unique adaptation of producing red bioluminescence is only found in two other deep-sea dwelling creatures, Aristostomias and Pachystomias. 

This rare form of bioluminescence can reach up to 700 nm in the deep-sea and cannot be perceived by green and blue bioluminescent organisms — granting M. niger a considerable advantage while hunting at depth.

The red light may function as an invisible searchlight of sorts because most animals in the ocean cannot see red light, while the eyes of M. niger are red-sensitive. It is much easier to find and eat something that cannot see you, particularly if it is lit up like a tasty red holiday snack.

Reference: https://latzlab.ucsd.edu/bioluminescence/

DOUVILLEICERAS MAMMILLATUM

Some lovely examples of Douvilleiceras mammillatum (Schlotheim, 1813), ammonites from the Lower Cretaceous (Middle-Lower Albian) Douvilliceras inequinodum zone of Ambarimaninga, Mahajanga Province, Madagascar.

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. The beauties you see here measure 6cm to 10cm.

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.

CANADA'S GREAT BEARS

Look at how this protective mamma bear holds her cub in her arms to give him a bit of a wash. 

Her gentle maternal care is truly touching. This mamma has spent late Autumn to Spring in a cave, having birthed them while still hibernation and staying in the den to feed them on her milk.

Black bear cubs stay with their mamma for the first one to three years of their lives while she protects them and teaches them how to thrive in the wild using their keen sense of smell, hearing, vision and strength. Once they are old enough, they will head off into the forest to live solo until they are ready to mate and start a family of their own. 

Mating is a summer affair with bears socializing shoulder to shoulder with potential mates. Once they have mated, black bears head off on their own again to forage and put on weight for their winter hibernation. If the black bear lives in the northern extent of their range, hibernation lasts longer — they will stay in their dens for seven to eight months longer than their southern counterparts. For those that enjoy the warmer climes in the south, hibernation is shorter. If food is available year-round, the bears do not hibernate at all.

The American black bear, Ursus americanus, is native to North America and found in Canada and the United States. 

They are the most common and widely distributed of the three bear species found in Canada. 

There are roughly 650,000 roaming our forests, swamps and streams — meaning there is a good chance of running into them if you spend any amount of time in the wild. 

Full-grown, these fuzzy monkeys will be able to run 48 kilometres (30 miles)  an hour and smell food up to 32 kilometres (20 miles) away.

With their excellent hearing, black bears usually know you are near well before you realize the same and generally take care to avoid you. Those that come in contact with humans often tend to want to check our garbage and hiking supplies for tasty snacks — hey, a free meal is a free meal.    

In British Columbia, we share our province with nearly half of all black bears and grizzly bears that reside in Canada. The 120,000 - 150,000 black bears who live in the province keep our Conservation Officers busy. They account for 14,000 - 25,000 of the calls the service receives each year. Most of those calls centre around their curiosity for the tasty smells emanating from our garbage. They are omnivores with vegetation making up 80-85% of their diet, but they are flexible around that — berries and seeds, salmon or Doritos — bears eat it all. 

And, as with all wild animals, diet is regional. In Labrador, the local black bear population lives mostly on caribou, rodents and voles. In the Pacific Northwest, salmon and other fish form a large part of the protein in their diet versus the bees, yellow jackets and honey others prefer. The braver of their number have been known to hunt elk, deer and moose calves — and a few showy bears have taken on adults of these large mammals. 

Bears hold a special place within our culture and in First Nation mythology in particular — celebrated in art, dance and song. In the Kwak'wala language of the Kwakiutl First Nations of the Pacific Northwest, the word for black bear is t̕ła'yi — mother is a̱bas and łaxwa̱lap̓a means to love each other. 

Kermode or Spirit Bear, Ursus americanus kermodei

From the photos here you can see that black bears are not always black —  ranging in colour from cinnamon to brown, tan, blonde, red — and even white. 

The Kermode or Spirit Bear, Ursus americanus kermodei, a subspecies of black bear found only in British Columbia — and our official provincial mammal — is a distinctive creamy white. 

They are not albinos, their colouring stems from a recessive mutant gene — meaning that if they receive two copies it triggers a single, nonsynonymous nucleotide substitution that halts all melanin production. Well, not all. They have pigmented eyes and skin but no colour in their fur. The white colour is an advantage when you are hunting salmon by day. Salmon will shy away from their black cousins knowing their intention is to enjoy them as a tasty snack. 

Spirit Bears live in the Great Bear Rainforest on British Columbia's north and central coast alongside the Kitasoo/Xai’xais First Nation who call the Kermode moskgm’ol or white bear.

The Kitasoo/Xai’xais have a legend that tells of Goo-wee, Raven making one in every ten black bears white to remind us of the time glaciers blanketed the land then slowly retreated — their thaw giving rise to the bounty we harvest today.  

Black bears of any colour are a wee bit smaller than their brown bear or grizzly bear cousins, with males weighing in at 45 to 400 kilograms (100 to 900 pounds) and females ranging from 38 to 225 kilograms (85 to 500 pounds). 

Small by relative standards but still very large animals. And they are long-lived or at least can be. Bears in captivity can live up to 30 years but those who dwell in our forests tend to live half as long or less from a mixture of local hazards and humans. 

Reference: Wild Safe BC: https://wildsafebc.com/species/black-bear/

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

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.

STUPENDEMYS GEOGRAPHICUS: A COLOSSAL TURTLE

Freshwater turtles come in all shapes and sizes but one of the most interesting and massive of these is the now-extinct freshwater turtle Stupendemys geographicus.

These aquatic beasties had shells almost three metres long (up to 9.5 feet) making it about a 100 times larger and sharing mixed traits with some of it's nearest living relatives — the giant South American River Turtle, Podocnemis expansa and Yellow-Spotted Amazon River Turtle, Podocnemis unifilis, the Amazon river turtle, Peltocephalus dumerilianus, and twice that of the largest marine turtle, the leatherback, Dermochelys coriacea.

It was also larger than those huge Archelon turtles that lumbered along during the Late Cretaceous at a whopping 15 feet, just over 4.5 metres. Stupendemys geographicus lived during the Miocene in Venezuela and Columbia. South America is a treasure trove of unique fossil fauna.

Throughout its history, the region has been home to giant rodents and an amazing assortment of crocodylians. It was also home to one of the largest turtles that ever lived. But for many years, the biology and systematics of Stupendemys geographicus remained largely unknown. When we found them in the fossil record it is usually as bits and pieces of shell and bone; exciting finds but not enough for us to see the big picture.

Palaeontologist Rodolfo Sánchez with Stupendemys geographicus

Back in 1994, several new shells and the first lower jaws of Stupendemys were found in the Urumaco region near Falcón State, Venezuela. The area is known to palaeontologists as a hotbed rich in well-preserved fossils. Fossil specimens of Stupendemys geographicus were first found here back in the 1970s by Harvard University researchers.

But for almost four decades, very few complete carapaces or other telltale fossils of Stupendemys were found in the region.

This excited Edwin Cadena, Paleontologist at the Universidad del Rosario in Colombia and researchers of the University of Zurich (UZH) and fellow researchers from Colombia, Venezuela, and Brazil. They had very good reason to believe that it was just a matter of time before more complete specimens were to be found. The area is a wonderful place to do fieldwork. It's an arid, desert locality without plant or forest coverage we see at other sites. Fossils weather out but do not wash away like they do at other sites.

Their efforts paid off and the fossils are marvellous. Shown here is Venezuelan Palaeontologist Rodolfo Sánchez with a male carapace (showing the horns) of Stupendemys geographical. This is one of the 8 million-year-old specimens from Venezuela.

Rodolfo Sánchez with Stupendemys geographicus

The team collected the most recent finds from Urumaco and added them fossil specimens from La Tatacoa Desert in Colombia.

Together, they paint a much clearer picture of a large terrestrial turtle that varied its diet and had distinct differences between the males and females in their morphology. Cadena published in February of this year with his colleagues in the journal Science Advances.

The researchers grouped together from multiple sites to help create a better understanding of the biology, lifestyle and phylogenetic position of these gigantic neotropical turtles.

Their paper includes the reporting of the largest carapace ever recovered and argues for a sole giant erymnochelyin taxon, S. geographicus, with extensive geographical distribution in what was the Pebas and Acre systems — pan-Amazonia during the middle Miocene to late Miocene in northern South America).

This turtle was quite the beast with two lance-like horns and battle scars to show it could hold its own with the apex predators of the day.

They also hypothesize that S. geographicus exhibited sexual dimorphism in shell morphology, with horns in males and hornless females. From the carapace length of 2.40 metres, they estimate to total mass of these turtles to be up to 1.145 kg, almost 100 times the size of its closest living relative. The newly found fossil specimens greatly expand the size of these fellows and our understanding of their biology and place in the geologic record.

Their conclusions paint a picture of a single giant turtle species across the northern Neotropics, but with two shell morphotypes, further evidence of sexual dimorphism. These were tuff turtles to prey upon. Bite marks and punctured bones tell us that they faired well from what must have been frequent predatory interactions with large, 30 foot long (over 9 metres) Caimans — big, burly alligatorid crocodilians — that also inhabited the northern Neotropics and shared their roaming grounds. Even with their large size, they were a very tempting snack for these brutes but unrequited as it appears Stupendemys fought, won and lumbered away.

Image Two: Venezuelan Palaeontologist Rodolfo Sánchez and a male carapace of Stupendemys geographicus, from Venezuela, found in 8 million years old deposits. Photo credit: Jorge Carrillo

Image Three: Venezuelan Palaeontologist Rodolfo Sánchez and a male carapace of Stupendemys geographicus, from Venezuela, found in 8 million years old deposits. Photo credit: Edwin Cadena

Reference: E-A. Cadena, T. M. Scheyer, J. D. Carrillo-Briceño, R. Sánchez, O. A Aguilera-Socorro, A. Vanegas, M. Pardo, D. M. Hansen, M. R. Sánchez-Villagra. The anatomy, paleobiology and evolutionary relationships of the largest side-necked extinct turtle. Science Advances. 12 February 2020. DOI: 10.1126/sciadv.aay4593

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

MEET FERGUSONITES HENDERSONAE: HETTANGIAN AMMONITE

Fergusonites hendersonae (Longridge, 2008)

Meet Fergusonites hendersonae, a Late Hettangian (Early Jurassic) ammonite from the Taseko Lakes area of British Columbia, Canadian Rockies.

I had the very great honour of having this fellow, a new species of nektonic carnivorous ammonite, named after me by paleontologist 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.

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. 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 and stunningly beautiful country. We were also blessed with excellent access as the area is closed to collecting except with a permit.

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

Full reference: 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)