FOSSIL CROCODILE

Fossil Crocodile, Lisbon Natural History Museum. Photo: Luis Lima

This well-preserved fossil crocodile is around 12 million years old and hails from Chelas, a locality near the airport in Lisbon. This fellow was quite the beast. The complete crocodile would have been 8-9 meters in length.

This specimen is housed in the Geological Museum of Lisbon. The museum was built in 1857 and is home to beautiful paleontology, archaeology and mineral specimens.

DEVONIAN FISH

CHAMPAGNE-ARDENNE HOPLITES

An excellent example of the ammonite, Hoplites bennettiana (Sowby, 1826) with a pathology. This beauty is from Albian deposits near Carrière de Courcelles, Villemoyenne, laid down in the Cretaceous near la région de Troyes (Aube) Champagne in northeastern France.

L'Albien or Albian is both an age of the geologic timescale and a stage in the stratigraphic column. It was named after Alba, the Latin name for the River Aube, a tributary of the Seine that flows through the Champagne-Ardenne region of northwestern France.

The Albian is the youngest or uppermost subdivision of the Lower Cretaceous, approximately 113.0 ± 1.0 Ma to 100.5 ± 0.9 Ma (million years ago).

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. Interesting times.

Hoplites maritimus / Hoplites rudis

Hoplites are amongst my favourite ammonites. I still have a difficult time telling them apart. To the right, you can see a slightly greyish, Hoplites maritimus, from Sussex England. Below him is a brownish Hoplites rudis from outcrops between Courcelles and Troyes, France. There are many Hoplites species. Each has a nicely raised tire-track ribbing. My preference is for Hoplities bennetianus (or bennettiana). I'm still sorting out the naming of that species. The difference between Hoplites bennettiana and Hoplites dentatus is seen on the venter.

Hoplites shells have compressed, rectangular and trapezoidal whorl sections. They have pronounced umbilical bullae from which their prominent ribs branch out. The ends of the ribs can be both alternate or opposite. Some species have zigzagging ribs and these usually end thickened or raised into ventrolateral tubercules.

Ammonites were predatory, squid-like creatures that lived inside coil-shaped shells. Like other cephalopods, ammonites had sharp, beaklike jaws inside a ring of tentacles that extended from their shells to snare prey such as small fish and crustaceans. Some ammonites grew more than three feet (one meter) across — possible snack food for the giant mosasaur Tylosaurus.

Ammonites constantly built new shell as they grew, but only lived in the outer chamber. They scooted through the warm, shallow seas by squirting jets of water from their bodies. A thin, tubelike structure called a siphuncle reached into the interior chambers to pump and siphon air and helped them move through the water.

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. They were prolific breeders, lived in schools, and are among the most abundant fossils found today. They went extinct with the dinosaurs 65 million years ago. Scientists use the various shapes and sizes of ammonite shells that appeared and disappeared through the ages to date other fossils.

Hoplites sp. from the Early Cretaceous of Dorset, UK

During their evolution, three catastrophic events occurred. The first during the Permian period (250million years ago), only 10% survived.  They went on to flourish throughout the Triassic period, but at the end of this period (206 million years ago), all but one species died. Then they began to thrive from the Jurassic period until the end of the Cretaceous period when all species of ammonites became extinct.

Ammonites began life very tiny, less than 1mm in diameter, and were vulnerable to attack from predators. They fed on plankton and quickly assumed a strong protective outer shell. They also grew quickly with the females growing up to 400% larger than the males; because they needed the larger shell for egg production. Most ammonites only lived for two years.  Some lived longer becoming very large. The largest ever found was in Germany (6.5 feet in diameter).

Ammonites lived in shallow waters of 100 meters or less. They moved through the water by jet propulsion expelling water through a funnel-like opening to propel themselves in the opposite direction. They were predators (cephalopods) feeding on most living marine life including mollusks, fish even other cephalopods. Ammonites would silently stalk their prey then quickly extend their tentacles to grab it.  When caught the prey would be devoured by the Ammonites' jaws located at the base of the tentacles between the eyes.

Hoplites dentalus, from Albian deposits near Troyes, France

Most ammonites have coiled shells. The chambered part of the shell is called a phragmocone.  It contains a series of progressively layered chambers called camerae, which were divided by thin walls called septae. The last chamber is the body chamber.

As the ammonite grew, it added new and larger chambers to the opened end of the shell. A thin living tube called a siphuncle passed through the septa, extending from the body to the empty shell chambers.

This allowed the ammonite to empty water out of the shell chambers by hyperosmotic active transport process. This process controlled the buoyancy of the ammonite's shell.

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

Second Photo: Top: Hoplites maritimus from Sussex, UK. Bottom: Hoplites rudis from near Troyes, France. Collection of Mark O'Dell

Third Photo: Hoplites sp. from the Early Cretaceous of Dorset, UK. Natural Selection Fossils

Fourth Photo: Hoplites dentalus from Albian deposits near Troyes, France. Collection of Stéphane Rolland.

Wright, C. W. (1996). Treatise on Invertebrate Paleontology, Part L, Mollusca 4: Cretaceous Ammonoidea (with contributions by JH Calloman (sic) and MK Howarth). Geological Survey of America and University of Kansas, Boulder, Colorado, and Lawrence, Kansas, 362.

Amédro, F., Matrion, B., Magniez-Jannin, F., & Touch, R. (2014). La limite Albien inférieur-Albien moyen dans l’Albien type de l’Aube (France): ammonites, foraminifères, séquences. Revue de Paléobiologie, 33(1), 159-279.

OSTEOLOGIE DU MEGATHERIUM

This lovely illustration of Megatherium, a fossil sloth discovered in South America was published in 1825 by Georges Cuvier as part of his work comparing specimens from South America to those from the Paris Basin.

Jean Louis Denis was the engraver who created this lovely plate. We have Leonard C. Bruno to thank for access to this image. He took black and white photos of the plate and published them in 1987 to the Library of Congress with full open access. Illus. in: Recherches sur les ossemens fossiles / Georges Cuvier. Third ed. Paris: G. Dufour et E. d'Ocagne, 1825, pl. 16. Published in: The tradition of science / Leonard C. Bruno. Washington, D.C. : Library of Congress, 1987, p. 215.

SLOTHS AND AVOCADOS

In 1788, this magnificent specimen of a Megatherium sloth was sent to the Royal Cabinet of Natural History from the Viceroyalty of Rio de la Plata.

The megaterios were large terrestrial sloths belonging to the group, Xenarthra. These herbivores inhabited large areas of land on the American continent. Their powerful skeleton enabled them to stand on their hind legs to reach leaves high in the trees, a huge advantage given the calories needed to be consumed each day to maintain their large size.

Avocados were one of the food preferences of our dear Giant ground sloths. They ate then pooped them out, spreading the pits far and wide. The next time you enjoy avocado toast, thank this large beastie. One of his ancestors may have had a hand (or butt) in your meal.

In 1788, Bru assembled the skeleton as you see it here. It is exhibited at the Museo Nacional De Ciencias Naturales in Madrid, Spain, in its original configuration for historic value. If you look closely, you'll see it is not anatomically correct. But all good paleontology is teamwork. Based upon the drawings of Juan Bautista Bru, George Cuvier used this specimen to describe the species for the very first time.

GASTROPODA

ZENAPIS PODOLICA

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

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

The lovely 420 million-year-old plate you see here is from Podolia or Podilia, a historic region in Eastern Europe, located in the west-central and south-western parts of Ukraine, in northeastern Moldova. Podolia is the only region in Ukraine where Lower Devonian remains of ichthyofauna can be found near the surface.

For the past 150 years, vertebrate fossils have been found in more than 90 localities situated in outcrops along banks of the Dniester River and its northern tributaries, and in sandstone quarries. At present faunal list of Early Devonian agnathans and fishes from Podolia number 72 species, including 8 Thelodonti, 39 Heterostraci, 19 Osteostraci, 4 Placodermi, 1 Acanthodii, and 1 Holocephali (Voichyshyn 2001a, modified).

In Podolia, Lower Devonian redbeds strata (the Old Red Formation or Dniester Series) can be found up to 1800 m thick and range from Lochkovian to Eifelian in age (Narbutas 1984; Drygant 2000, 2003). In the lower part (Ustechko and Khmeleva members of the Dniester Series) they consist of multicoloured, mainly red, fine-grained cross-bedded massive quartz sandstones and siltstones with seams of argillites (Drygant 2000).

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

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

THE LAST ICE AGE

The massive ice sheets of the Pleistocene covered much of the planet. They contained so much of the Earth's water that sea levels dropped to 100 metres lower than they are today.

FIRST ITALIAN FOSSILS OF AGRIOTHERIUM

Agriotherium / Short-Faced Bear

Fossil remains of Agriotherium, the short-faced giant bear, have been found in Collepardo, Italy. A fragment of a mandible was unearthed back in 2015 in the province of Frosinone. Thanks to several years of research and a recent CT scan, the team from Sapienza University of Rome were finally ready to publish.

Agriotherium is one of the largest of the mighty carnivores that lived in Europe back in the Pleistocene. They weighed as much as 900 kilos (almost 2,000 lbs) and grew up to 2.5 meters tall. These ancient bears roamed prehistoric Italy amid a humid and temperate climate, competing for food resources with some of our ancestors as they only becoming extinct 2.6 million years ago.

CAMBRIAN SEA ANEMONE

A stunning Cambrian soft-bodied Sea Anemone from outcrops near Malong, China. Collection of Marc R. Hänsel

PREHISTORIC BUGS: WANNERIA DUNNAE

Wanneria dunnae, an impressive trilobite from British Columbia's Eager Formation near Cranbrook. Trilobites were among the earliest fossils with hard skeletons. They were the dominant form of life at the beginning of the Cambrian Period. This specimen of Wanneria dunnae from the East Kootenay of British Columbia is typical of the group. Trilobite eyes were compound like those of modern crustaceans and insects. The eyes of these earliest trilobites are not well-known as the visual surface dropped away and was lost during molting long before they ever became fossils.

ZITRONENFALTER: GONEPTERYX RHAMNI

NATURE AS ART: IRIDESCENT EUHOPLITES

This beautiful Euhoplites, measuring just 37 millimetres across, comes from the celebrated fossil beds of Folkestone in southeastern England.

Preserved within the rocks of the Lower Cretaceous, it offers us a glimpse into oceans that existed some 100 million years ago, during the middle to upper Albian Stage. Euhoplites belonged to the ammonoids, an extinct group of cephalopods related, albeit distantly, to the living nautilus and more closely allied to squid and octopus. Its shell was both elegant and elaborate.

Strong ribs sweep across the whorls, sometimes running in graceful curves from the inner margin before folding over the outer edge of the shell. In other species, the ribs form subtle zigzags between small nodules and ventrolateral clavi, giving the shell a richly ornamented appearance.

A narrow groove often traces a path along the centre of the outer rim, accentuating the remarkable symmetry of the spiral. And then there are those curious lumps and bumps — the tubercles that adorn the shell so beautifully. Their precise function remains one of palaeontology's enduring mysteries. They may have served as protection against predators, strengthened the shell against pressure, or perhaps influenced how the animal moved through the water.

Intriguingly, such ornamentation may have increased hydrodynamic drag, suggesting that Euhoplites was not built for speed.

Rather than pursuing prey in rapid bursts, it may have adopted a more measured existence within the warm Cretaceous seas. Though modest in size, with shells typically only reaching a few inches across, Euhoplites was part of a thriving marine community. In the Albian seas of France, it lived alongside ammonites such as Hoplites, Anahoplites, Pleurohoplites, Puzosia, and Desmoceras.

In Brazil, it shared the waters with Anahoplites and the extraordinary corkscrew-shaped Turrilites. Fossils attributed to this genus have even been recorded from rocks of Texas, attesting to the wide distribution of these ancient mariners. Yet nowhere is Euhoplites more closely associated than with the Folkestone Beds of Kent. Here, within the weathered cliffs and clay-rich sediments of England's southeast coast, they are among the most frequently encountered ammonites.

Each specimen recovered from these deposits tells a story of a vanished world — a subtropical sea alive with cephalopods, fishes, marine reptiles, and countless other organisms whose lives have been distilled into stone. This particular specimen, from the collections of José Juárez Ruiz, is a small masterpiece of natural architecture. Its intricate ribs and sculptured ornamentation have survived across immense spans of geological time, inviting us to pause and wonder. For in these delicate spirals lies one of nature's most profound gifts: the ability to connect us, however briefly, with the deep and ancient history of life on Earth.

FIRE-KISSED ARTHROPOD

This fellow is Chengjiangocaris kunmingensis, a rather glorious fuxinhuiid arthropod. While he looks like he could be from the inside of the Lascaux Caves and their fire-kissed Palaeolithic paintings, albeit by a very ancient Picasso, he was found at a Cambian fossil site in southern China.

As his name indicates, he is from a fossil site in the Yunnan region near Kunming. He is unusual in many ways, both because of the remarkable level of preservation and the position in which he was found. This fellow was a bit of a tippy arthropod. His carapace had flipped over before fossilisation, allowing researchers to to examine this fuxianhuiid's head and legs in great detail without a carapace in the way.

The roughly 518-million-year-old site contains a dizzying abundance of beautifully preserved weird and wonderful life-forms, from jellyfish and comb jellies to arthropods and algae and is about 10 million years older than the Burgess Shale. Photo credit: Yie Jang (Yunnan University)

ANCIENT ONES

WASH ON, WASH OFF

If you were a fish living in the warm turquoise waters off the coast of Bonaire, you may not hear those words, but you'd see the shrimp sign language equivalent. It seems Periclimenes yucatanicus or Spotted Cleaner Shrimp is doing a booming business in the local reefs by setting up a fish washing service.

That's right, a Fish Wash. You'd be hard pressed to find a terrestrial Molly Maid with two opposable thumbs as studious and hardworking as this wee marine beauty.

This quiet marine mogul is turning out to be one of the ocean's top entrepreneurs. Keeping its host and diet clean and green, the spotted shrimp hooks up with the locals, in this case, local sea anemones and sets up a fish wash. Picture a car wash but without the noise and teenage boys. The signage posted is the shrimps' natural coloring which attracts fish from around the reefs.

Wash on, wash off.

Once within reach, the shrimp cleans the surface of the fish, giving the fish a buff and the shrimp its daily feed.

FRATERCULA ARCTICA

This lovely fellow is a Puffin or "Sea Parrot" from Skomer Island near Pembrokshire in Wales. 

They live about 20 years making a living in our cold seas dining on herring, hake and sand eels.

They are good little swimmers as you might expect but surprisingly they are great flyers, too! Once they get some speed on board, they can fly up to 88 km an hour. 

The sexy orange beak (dead sexy, right?) shifts from a dull grey to bright orange when it is time to attract a mate. 

While not strictly monogamous, most Puffins will choose the same mate year upon year producing adorable chicks or pufflings (awe) from their mating efforts.

ICHTHYOSAURIA

Ichthyosaurus was an extinct marine reptile first described from fossil fragments found in 1699 in Wales. Shortly thereafter, fossil vertebrae were published in 1708 from the Lower Jurassic.

HOLCOPHYLLOCERAS MEDITERRANEUM

This lovely ammonite is Holcophylloceras mediterraneum (Neumayr 1871) from Late Jurassic (Oxfordian) deposits near Sokoja, Madagasgar.

Amazing suturing on this lovely ammonite and great detail, allowing us to see how he grew, adding to his size, chamber by chamber, building out his spiral shape.

Ammonite shells had many chambers divided by walls called septa. Nautiloids had simple septa with a single arc whereas ammonites developed septa with intricate folds, lobes and saddles. They also developed delicate feather-like or fern-like lacey patterns, called sutures, on the outer shell. You sometimes see them on polished or water worn specimens and in the photos of this fellow below.

The chambers were connected by a tube called a siphuncle which allowed for the control of buoyancy with the hollow inner chambers of the shell acting as air tanks to help them float. A bit like internal water wings you might use to learn how to swim as a kid.

We can see the edges of this specimen's shell where it would have continued out to the last chamber, the body-chamber, where the ammonite lived. Picture a squid or octopus, now add a shell. That's him!

MEGALODON TOOTH

Carcharocles chubutensis, which roughly translates to the "glorious shark of Chubut," from the ancient Greek is an extinct species of prehistoric mega-toothed sharks in the genus Carcharocles.

These big beasties lived during Oligocene to Miocene. This fellow is considered to be a close relative of the famous prehistoric mega-toothed shark, C. megalodon, although the classification of this species is still disputed.

Swiss naturalist Louis Agassiz first identified this shark as a species of Carcharodon in 1843. In 1906, Ameghino renamed this shark as C. chubutensis. In 1964, shark researcher, L. S. Glikman recognized the transition of Otodus obliquus to C. auriculatus. In 1987, shark researcher, H. Cappetta reorganized the C. auriculatus - C. megalodon lineage and placed all related mega-toothed sharks along with this species in the genus Carcharocles.

At long last, the complete Otodus obliquus to C. megalodon progression began to look clear. Since then, C. chubutensis has been re-named into Otodus chubutensis, also the other chronospecies of the Otodus obliquus - O. megalodon lineage. Chubutensis appears at the frontier Upper Oligocene to Lowest Miocene (evolving from O. angustidens which has stronger side cusps) and turns into O. megalodon in the Lower to Middle Miocene, where the side cusps are already absent. Despite previous publications, there is no chubutensis in the Pliocene.

Victor Perez and his team published on the transition between Carcharocles chubutensis and Carcharocles megalodon (Otodontidae, Chondrichthyes): lateral cusplet loss through time in March of 2018. In their work, they look at the separation between all the teeth of Carcharocles chubutensis and Carcharocles megalodon and published that it is next to impossible to divide them up as a complex mosaic evolutionary continuum characterizes this transformation, particularly in the loss of lateral cusplets.

The cuspleted and uncuspleted teeth of Carcharocles spp. are designated as chronomorphs because there is wide overlap between them both morphologically and chronologically. In the lower Miocene Beds (Shattuck Zones) 2–9 of the Calvert Formation (representing approximately 3.2 million years, 20.2–17 Ma, Burdigalian) both cuspleted and uncuspleted teeth are present, but cuspleted teeth predominate, constituting approximately 87% of the Carcharocles spp. teeth represented in their samples.

In the middle Miocene Beds 10–16A of the Calvert Formation (representing approximately 2.4 million years, 16.4–14 Ma, Langhian), there is a steady increase in the proportion of uncuspleted Carcharocles teeth.

In the upper Miocene Beds 21–24 of the St. Marys Formation (representing approximately 2.8 million years, 10.4–7.6 Ma, Tortonian), lateral cusplets are nearly absent in Carcharocles teeth from our study area, with only a single specimen bearing lateral cusplets. The dental transition between Carcharocles chubutensis and Carcharocles megalodon occurs within the Miocene Chesapeake Group. Although their study helps to elucidate the timing of lateral cusplet loss in Carcharocles locally, the rationale for this prolonged evolutionary transition remains unclear.

The specimen you see here is in the Geological Museum in Lisbon. The photo credit goes to the deeply awesome Luis Lima who shared some wonderful photos of his recent visit to their collections.

If you'd like to read the paper from Perez, you can find it here:
https://www.tandfonline.com/doi/full/10.1080/02724634.2018.1546732

ICELAND: TORFAJOKULL

The Northern Lights over a sea of wildflowers in the marsh near Landmannalaugar, part of the Fjallabak Nature Reserve in the Highlands of Iceland.

Landmannalaugar is at the northern tip of the Laugavegur hiking trail that leads through natural geothermal hot springs and an austere yet poetically beautiful landscape. 

Here, you can see the Northern Lights play through the darkness of a night sky without light pollution and bask in the raw geology of this rugged land.

The Fjallabak region takes its name from the numerous wild and rugged mountains with deeply incised valleys, which are found there. The topography of the Torfajokull, a central volcano found within the Fjallabak Nature Reserve, is a direct result of the region being the largest rhyolite area in Iceland and the largest geothermal area (after Grimsvotn in Vatnajokull).

The Torfajokull central volcano is an active volcanic system but is now in a declining fumarolic stage as exemplified by numerous fumaroles and hot springs. The hot pools at Landmannalaugar are but one of many manifestations of geothermal activity in the area, which also tends to alter the minerals in the rocks, causing the beautiful colour variations from red and yellow to blue and green, a good example being Brennisteinsalda. Geologists believe that the Torfajokull central volcano is a caldera, the rim being Haalda, Suðurnamur, Norður-Barmur, Torfajokull, Kaldaklofsfjoll and Ljosartungur.

The bedrock of the Fjallabak Nature Reserve dates back 8-10 million years. At that time the area was on the Reykjanes – Langjokull ridge rift zone. The volcano has been most productive during the last 2 million years, that is during the last Ice Age Interglacial rhyolite lava (Brandsgil) and sub-glacial rhyolite (erupted under ice/water, examples being Blahnukur and Brennisteinsalda are characteristic formations in the area. To the north of the Torfajokull region sub-glacial volcanic activity produced the hyaloclastites (moberg) mountains, such as Lodmundur and Mogilshofdar.

Volcanic activity in recent times (last 10.000 years) has been restricted to a few northeast – southwest fissures, the most recent one, the Veidivotn fissure from 1480, formed Laugahraun (by the hut at Landmannalaugar), Namshraun, Nordurnamshraun, Ljotipollur and other craters which extend 30 km, further to the north Eruptions in the area tend to be explosive and occur every 500 – 800 years, previous known eruptions being around A. D 150 and 900.

MEGALOSAURUS BUCKLANDII

Oxford University Museum of Natural History was established in 1860 to draw together scientific studies from across the University of Oxford. Today, the award-winning Museum continues to be a place of scientific research, collecting and fieldwork and plays host to a number of programmes and exhibitions.

Notable collections include the world's first described dinosaur, Megalosaurus bucklandii, and the world-famous Oxford Dodo, the only soft tissue remains of the extinct dodo. Although fossils from other areas have been assigned to the genus, the only certain remains of Megalosaurus come from Oxfordshire and date to the late Middle Jurassic. In 1824, Megalosaurus was the first genus of non-avian dinosaur to be validly named. The type species is Megalosaurus bucklandii, named in 1827.

In 1842, Megalosaurus was one of three genera on which Richard Owen based his Dinosauria. On Owen's direction, a model was made as one of the Crystal Palace Dinosaurs, which greatly increased the public interest for prehistoric reptiles. Subsequently, over fifty other species would be classified under the genus, originally because dinosaurs were not well known, but even during the 20th century after many dinosaurs had been discovered. Today it is understood these additional species were not directly related to M. bucklandii, which is the only true Megalosaurus species. Because a complete skeleton of it has never been found, much is still unclear about its build.

The Museum is as spectacular today as when it opened in 1860. As a striking example of Victorian neo-Gothic architecture, the building's style was strongly influenced by the ideas of 19th-century art critic John Ruskin. Ruskin believed that architecture should be shaped by the energies of the natural world, and thanks to his connections with a number of eminent Pre-Raphaelite artists, the Museum's design and decoration now stand as a prime example of the Pre-Raphaelite vision of science and art.

On 30 June 1860, the Museum hosted a clash of ideologies that has become known as the Great Debate. Even before the collections were fully installed, or the architectural decorations completed, the British Association for the Advancement of Science held its 30th annual meeting to mark the opening of the building, then known as the University Museum. It was at this event that Samuel Wilberforce, Bishop of Oxford, and Thomas Huxley, a biologist from London, went head-to-head in a debate about one of the most controversial ideas of the 19th century – Charles Darwin's theory of evolution by natural selection.

ALSACE AMMONITE

A lovely example of the nautilus, Cératite Nodosus, from Shell Lime Superior deposits near Alsace in northeastern France on the Rhine River plain. Ammonite and nautilus shells are made up predominantly of calcium carbonate in the form of aragonite and proteinaceous organic matrix or conchiolin arranged in layers: a thin outer prismatic layer, a nacreous layer and an inner lining of prismatic habitat. While their outer shells are generally aragonite, aptychus are distinct as they are composed of calcite.

The aptychus we see here, hard anatomical structures or curved shelly plates now understood to be part of the body of an ammonite or nautilus, are often referred to as beaks. If you look closely at this specimen, you can see the beak of the nautilus, that wee pointed piece, near the centre. Collection of Ange Mirabet, Strasbourg, France.


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GODT NYTT ÅR

JELLYFISH: GAGISAMA

These festive lovelies are jellyfish. Jellyfish are found all over the world, from surface waters to our deepest seas — and they are old. They are some of the oldest animals in the fossil record.

Sea jellies and jellyfish are the common names for the medusa-phase or adult phase of certain gelatinous members of the subphylum Medusozoa, a major part of the phylum Cnidaria — more closely related to anemones and corals.

Jellyfish are not fish at all. Jellyfish evolved millions of years before true fish. 

The oldest conulariid scyphozoans — picture an ice-cream cone with fourfold symmetry — appeared between 635 and 577 million years ago in the Neoproterozoic of the Lantian Formation a 150-meter-thick sequence of rocks deposited in southern China. 

Others are found in the youngest Ediacaran rocks of the Tamengo Formation of Brazil, c. 505 mya, through to the Triassic. Cubozoans and hydrozoans appeared in the Cambrian of the Marjum Formation in Utah, USA, c. 540 mya. Like other soft-bodied organisms, ctenophores (comb jellies), sea jellies and jellyfish only produce fossils only under exceptional taphonomic conditions — think rare.

I have seen all sorts of their brethren growing up on the west coast of Canada. I have seen them in tide pools, washed up on the beach and swam amongst thousands of Moon Jellyfish while scuba diving in the Salish Sea. Their movement in the water is marvellous.  

In the Kwak̓wala language of the Kwakiutl or Kwakwaka'wakw, speakers of Kwak'wala, of the Pacific Northwest, jellyfish are known as ǥaǥisama.

The watercolour ǥaǥisama you see here is a bit of fancy. While I chose blue, purple and pink for these lovelies, they also come in bright yellow, orange and relatively clear — and are often luminescent.

Jellyfish such as comb jellies produce bright flashes to startle a predator, others such as siphonophores can produce a chain of light or release thousands of glowing particles into the water as a mimic of small plankton to confuse the predator.

For most jellyfish bioluminescence is used for defence against predators — and about half of all jellyfish are bioluminescent. Some produce a glowing sticky slime that clings to predators making them vulnerable to other predators. Some jellyfish can release their tentacles as glowing decoys. So you see that there are many strategies for using bioluminescence by jellyfish.

All bioluminescence comes from energy released from a chemical reaction. This is very different from other sources of light, such as from the sun or a light bulb, where the energy comes from heat. In a luminescent reaction, two types of chemicals, called luciferin and luciferase, combine together. The luciferase acts as an enzyme, 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, indicating that bioluminescence evolved independently in different groups of organisms. One type of luciferin is called coelenterazine, found in jellyfish, shrimp, and fish. Dinoflagellates and krill share another class of unique luciferins, while ostracods (firefleas) and some fish have a completely different luciferin. The occurrence of identical luciferins for different types of organisms suggests a dietary source for some groups. Organisms such as bacteria and fireflies have unique luminescent chemistries. In many other groups, the chemistry is still unknown

Some of the most amazing deep-sea jellyfish are the comb jellies, which can get as large as a basketball, and are in some cases so fragile that they are almost impossible to collect intact.

Also spectacular are the siphonophores, some of which can reach several meters in length. Siphonophores deploy many tentacles like a gill net casting for small fish.

ORYGMASPIS OF THE TANGLEFOOT

This calcified beauty is Orygmaspis (Parabolinoides) spinula (Westrop, 1986) an Upper Cambrian trilobite from the McKay Group near Tanglefoot Mountain in the Kootenay Rockies. 

Orygmaspis is a genus of asaphid trilobite with an inverted egg-shaped outline, a wide headshield, small eyes, long genal spines, 12 spined thorax segments and a small, short tail shield, with four pairs of spines. 

Asaphida is comprised of six superfamilies found as marine fossils that date from the Middle Cambrian through to the Ordovician — Anomocaroidea, Asaphoidea, Cyclopygoidea, Dikelocephaloidea, Remopleuridoidea and Trinucleioidea. It was here, in the Ordovician, that five of the six lineages met their end along with 60% of all marine life at the time. They did leave us with some wonderful examples of their form and adaptations. The stubby eyed Asaphids evolved to give us Asaphus kowalewskii with delightfully long eyestalks. These specialized protrusions would have given that lovely species a much better field of view in which to hunt Ordovician seas — and avoid becoming the hunted.

Only the hardy Superfamily Trinucleiodea pushed through. They were to meet their end in the final days of the Silurian where yet another cataclysmic event wiped out much of the life on Earth, including the last remains of Asaphida (Fortey & Chatterton, 1988).

The outline of the exoskeleton Orygmaspis is inverted egg-shaped, with a parabolic headshield — or cephalon less than twice as wide as long. Picture a 2-D egg where the head is wider than the tail.

The glabella, the well-defined central raised area excluding the backward occipital ring, is ¾× as wide as long, moderately convex, truncate-tapering, with 3 pairs of shallow to obsolete lateral furrows. 

The occipital ring is well defined. The distance between the glabella and the border (or preglabellar field) is ±¼× as long as the glabella. This fellow had small to medium-sized eyes, 12-20% of the length of the cephalon. These were positioned between the front and the middle of the glabella and about ⅓ as far out as the glabella is wide. 

The remaining parts of the cephalon, the fixed and free cheeks — or fixigenae and librigenae — are relatively flat. The fracture lines or sutures — that separate the librigenae from the fixigenae in moulting — are divergent just in front of the eyes. These become parallel near the border furrow and strongly convergent at the margin. 

From the back of the eyes, the sutures bend out, then in, diverging outward and backward at approximately 45°, cutting the posterior margin well within the inner bend of the spine — or opisthoparian sutures. 

The thorax or articulating middle part of the body has 12 segments. The anteriormost segment gradually narrows into a sideward directed point, while further to the back the spines are directed outward and the spine is of increasing length up until the ninth spine, while the spine on the tenth segment is abruptly smaller, and 11 and 12 even more so. 

This fellow has a wee pygidium or tail shield that is only about ⅓× as wide as the cephalon. It is narrowly transverse about 2× wider than long. Its axis is slightly wider than the pleural fields to each side, and has up to 4 axial rings and a terminal and almost reaches the margin. Up to 4 pleural segments with obsolete interpleural grooves and shallow pleural furrows. The posterior margin has 3 or 4 pairs of spines, getting smaller further to the back. 

References:

Chatterton, Brian D. E.; Gibb, Stacey (2016). Furongian (Upper Cambrian) Trilobites from the McKay Group, Bull River Valley, Near Cranbrook, Southeastern British Columbia, Canada; Issue 35 of Palaeontographica Canadiana; ISBN: 978-1-897095-79-9

Moore, R.C. (1959). Arthropoda I - Arthropoda General Features, Proarthropoda, Euarthropoda General Features, Trilobitomorpha. Treatise on Invertebrate Paleontology. Part O. Boulder, Colorado/Lawrence, Kansas: Geological Society of America/University of Kansas Press. pp. O272–O273. ISBN 0-8137-3015-5.

KOURISODON PUNTLEDGENSIS

Kourisodon puntledgensis

Mosasaurs were large, globally distributed marine predators who dominated our Late Cretaceous oceans. Since the unearthing of the first mosasaur in 1766 (Mulder, 2003) we've discovered their fossil remains most everywhere around the globe — New Zealand, Antarctica, Africa, North and South America, Europe and Japan.

We've now found the fossil remains of an elasmosaur and two mosasaurs along the banks of the Puntledge River, says Dan Bowen, Chair of the Vancouver Island Palaeontological Society.

The first set of about 10 mosasaurs vertebrae (Platecarpus) was found by Tim O’Bear and unearthed by a team of VIPS and Museum enthusiasts led by Dr. Rolf Ludvigsen. Dan Bowen and Joe Morin of the VIPS prepped these specimens for the Museum.

In 1993, a new species of mosasaur, Kourisodon puntledgensis, a razor-toothed mosasaur, was found upstream from the elasmosaur site by Joe Zembiliwich on a fossil field trip led by Mike Trask. 

A replica of this specimen now calls The Canadian Fossil Discovery Centre in Morden home. What is significant about this specimen is that it is a new genus and species. At 4.5 meters, it is a bit smaller than most mosasaurs and similar to Clidastes, but just as mighty. It shared its environment with a variety of Elasmosaurids, turtles, and other mosasaurs, although it seems that no polycotylids were present in its Pacific environment.

Interestingly, this species has been found in this one locality in Canada and across the Pacific in the basal part of the Upper Cretaceous — middle Campanian to Maastrichtian — of the Izumi Group, Izumi Mountains and Awaji Island of southwestern Japan. We see an interesting correlation with the ammonite fauna from these two regions as well. What we do not see is a correlation between our Pacific fauna and those from our neighbouring province to the east. Betsy Nicholls and Dirk Meckert published on the marine reptiles from the Nanaimo Group (Upper Cretaceous) of Vancouver Island in the Canadian Journal of Earth Sciences in 2002. What we see in our faunal mix reinforces the provinciality of the Pacific faunas and their isolation from contemporaneous faunas in the Western Interior Seaway.

TOTEMS, SETTLER'S & HISTORY: STANLEY PARK

Totem, Welcome & Mortuary Poles at Stanley Park

If you visit Brockton Point in Stanley Park, there are many carved red cedar First Nation poles for you to admire.  

What you are viewing are replicas of First Nation welcome and totem poles that once stood in the park but have been returned to their homes within the province's diverse First Nation communities — or held within museum collections. 

Some of the original totems came from Alert Bay on Cormorant Island, near the Port McNeill on the north coast of Vancouver Island. Others came from communities in Haida Gwaii — and still more from the Wuikinuxv First Nations at Rivers Inlet on British Columbia's central west coast — home of the Great Bear Rainforest with her Spirit Bears.

The exception is the most recent addition carved by Robert Yelton in 2009. Robert is a First Nation carver from the Squamish Nation and his original welcome pole graces Brockton Point, the original settlement site of a group of Squamish-Portuguese settlers.  

If you look at the photo above, the lovely chocolate, red and turquoise pole on the right is a replica of the mortuary pole raised to honour the Raven Chief of Skedans or Gida'nsta, the Haida phrase for from his daughter, the title of respect used when addressing a person of high rank. Early fur traders often took the name of the local Chief and used it synonymously as the place names for the sites they visited — hence Skedans from Gida'nsta.

Chief Skedans Mortuary Pole

Chief Skedans, or Qa'gials qe'gawa-i, to his children, lived in Ḵ’uuna Llnagaay, or village at the edge, in Xaayda Kil — a village on the exposed coast of Louise Island — now a Haida Heritage Site.  

There are some paintings you may have seen by Emily Carr of her visits to the site in 1912, She used the phonetic Q'una from Q:o'na to describe both the place name and title of her work. 

Carr's paintings of the totems have always looked to me to be a mash-up — imagine if painter Tamara de Lempicka and photographer Edward Curtis had a baby — not pretty, but interesting.

Some called this area, Huadju-lanas or Xu'adji la'nas, which means Grizzly-Bear-Town, in reference to resident grizzly bear population and their adornment of many totems and artwork by the local artists.

Upon Chief Skedan's death, the mortuary pole was carved both to honour him and provide his final resting place. Dates are a bit fuzzy, but local accounts have this as sometime between 1870-1878 — and at a cost of 290 blankets or roughly $600 in today's currency. 

The great artistry of the pole was much admired by those in the community and those organizing the celebrations for the 1936 Vancouver Golden Jubilee — witnessed by  350,000 newly arrived residents.

Negotiations were pursued and the pole made its way down from Haida Gwaii to Stanley Park in time for the celebrations. The original totem graced Stanley Park for a little over twenty years before eventually making its way back to Haida Gwaii. It was returned to the community with bits of plaster and shoddy paint marring the original. These bits were scraped off and the pole welcomed back with due ceremony. 

In 1964, respected and renowned Northwest Coast master carver, Bill Reid, from the Kaadaas gaah Kiiguwaay, Raven/Wolf Clan of T'anuu, Haida Gwaii and Scottish-German descent, was asked to carve this colourful replica. 

Mountain Goat Detail, Skedans Mortuary Pole

Reid carved the totem onsite in Stanley Park with the help of German carver Werner True. Interestingly, though I looked at length for information on Werner True, all I can find is that he aided Bill Reid on the carving for a payment of $1000.

Don Yeomans, Haida master carver, meticulously recarved the moon crest in 1998. If you have admired the totem pole in the Vancouver Airport, you will have seen some of Yeoman's incredible work. 

The crest is Moon with the face, wings, legs and claws of a mighty and proud Thunderbird with a fairly smallish hooked beak in a split design. We have Moon to thank for the tides and illuminating our darkest nights. As a crest, Moon is associated with transformation and acting as both guardian and protector.

The original pole had a mortuary box that held the Chief's remains. The crest sits atop a very charming mountain goat. I have included a nice close-up here of the replica for you to enjoy. 

Mountain Goats live in the high peaks of British Columbia and being so close to the sky, they have the supernatural ability to cross over to the sky world. They are also credited as being spirit guardians and guides to First Nation shamans.

I love his horns and tucked in cloven hooves. There is another pole being carved on Vancouver Island that I hope to see during its creation that also depicts a Mountain Goat. With permission and in time, I hope to share some of those photos with you. 

Mountain Goat is sitting atop Grizzly Bear or Huaji or Xhuwaji’ with little human figures placed in his ears to represent the Chief's daughter and son-in-law, who raised the pole and held a potlatch in his honour. 

Beneath the great bear is Seal or Killer Whale in his grasp. The inscription in the park says it is a Killer Whale but I am not sure about that interpretation — both the look and lore make Seal more likely. Perhaps if Killer Whale were within Thunderbird's grasp — maybe. 

Though it is always a pleasure to see Killer Whale carved in red cedar, as the first whales came into being when they were carved in wood by a human — or by Raven — then magically infused with the gift of life.

Siwash Rock on the northern end of Third Beach, Stanley Park

The ground these totems sit upon is composed of plutonic, volcanic and sedimentary layers of rock and exhibits the profound influences of glaciation and glacial retreat from the last ice age. 

Glacial deposits sit atop as a mix of clay, sand, cobbles and larger boulders of glacial till. 

There are a few areas of exposed volcanics within the park that speak to the scraping of the glaciers as they retreated about 12,500 years ago. 

The iconic moss and lichen coated Siwash Rock on the northern end of Third Beach is one of the more picturesque of these. It is a basaltic and andesitic volcanic rock — a blend of black phenocrysts of augite cemented together with plagioclase, hornblende and volcanic glass.

Images not shown: 

Do check out the work of Emily Carr and her paintings of Q:o'na from the 1940s. I'll share a link here but do not have permission to post her works. http://www.emilycarr.org/totems/exhibit/haida/ssintro.htm

PHOTONS: ELECTROMAGNETIC RADIATION

Light is a form of electromagnetic radiation, like radio or microwaves. Some aspects of light, such as its frequency (colour), are based on its wave properties. 

Light can also be considered a stream of particles called photons, each of which contains energy. This concept is called the quantum theory. 

So there are two ways to express how much light there is. One is based on energy (in units of watts, joules, or calories, and the other is based on the number of photons. 

For example, the wavelength of green light is less than 1 millionth of an inch, and the energy of one photon of green light is equivalent to 1 million billionths of a calorie! Even though photons are particles, they are particles of energy and are different from particles in a cell such as molecules.

DANCERS OF THE DEEP: JELLYFISH

This lovely ocean dancer with her long delicate tentacles or lappets and thicker rouched oral arms is a jellyfish. 

Her brethren are playing in the waters of the deep all over the world, from surface waters to our deepest seas — and they are old. They are some of the oldest animals in the fossil record.

Jellyfish and sea jellies are the informal common names given to the medusa-phase or adult phase of certain gelatinous members of the subphylum Medusozoa, a major part of the phylum Cnidaria — more closely related to anemones and corals.

Jellyfish are not fish at all. They evolved millions of years before true fish. The oldest conulariid scyphozoans appeared between 635 and 577 million years ago in the Neoproterozoic of the Lantian Formation, a 150-meter-thick sequence of rocks deposited in southern China. 

Others are found in the youngest Ediacaran rocks of the Tamengo Formation of Brazil, c. 505 mya, through to the Triassic. Cubozoans and hydrozoans appeared in the Cambrian of the Marjum Formation in Utah, USA, c. 540 million years ago.

I have seen all sorts of their brethren growing up on the west coast of Canada. I have seen them in tide pools, washed up on the beach and swam amongst thousands of Moon Jellyfish while scuba diving in the Salish Sea. Their movement in the water is marvellous.  

In the Kwak̓wala language of the Kwakiutl or Kwakwaka'wakw, speakers of Kwak'wala, of the Pacific Northwest, jellyfish are known as ǥaǥisama.

The watercolour ǥaǥisama you see here in dreamy pink and white is but one colour variation. They come in blue, purple, orange, yellow and clear — and are often luminescent. They produce light by the oxidation of a substrate molecule, luciferin, in a reaction catalyzed by a protein, luciferase.