OPHTHALMOPLAX BRASILIANA

Ophthalmoplax brasiliana  / Photo: José F. Ventura‎

Ventral view of the carnivorous portunoid crab Ophthalmoplax brasiliana (Maury, 1930) from the latest Maastrichtian (~66.2 Ma.) deposits near Coahuila, northern Mexico.

This marine species was originally thought to have been found only in the upper Member (Owl Creek Formation) Late/Upper Maastrichtian deposits of Tippah County in Mississippi, USA. 

Sohl and Koch published on the Mississippian finds in the USGS in 1983. Fedorov and Nyborg published on this same species again in 2017. Paleocoordinates: (34.8° N, 88.9° W: 38.3° N, 66.2° W)

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.

AMMONITE OF THE RHÔNE

An exquisite specimen of the delicately ridged ammonite, Porpoceras verticosum, from Middle Toarcian outcrops adjacent the Rhône in southeastern France.

Porpoceras (Buchman, 1911) is a genus of ammonite that lived during the early and middle Toarcian stage of the Early Jurassic. We see members of this genus from the uppermost part of Serpentinum Zone to Variabilis Subzone. These beauties are found in Europe, Asia, North America and South America.

Ammonites belonging to this genus have evolute shells, with compressed to depressed whorl section. Flanks were slightly convex and venter has been low. The whorl section is sub-rectangular. 

The rib is pronounced and somewhat fibulate on the inner whorls — just wee nodes here — and tuberculate to spined on the ventrolateral shoulder. It differs from Peronoceras by not having a compressed whorl section and regular nodes or fibulation. Catacoeloceras is also similar, but it has regular ventrolateral tubercules and is missing the classic nodes or fibulation of his cousins.

This specimen hails from southern France near the Rhône, one of the major rivers of Europe. It has twice the average water level of the Loire and is fed by the Rhône Glacier in the Swiss Alps at the far eastern end of the Swiss canton of Valais then passes through Lake Geneva before running through southeastern France. This 10 cm specimen was prepared by the supremely talented José Juárez Ruiz

H. SAVENYEI: RENE'S BEE

This is a tale of friendship, tragic loss and fossil bees and an introduction to one of the most delightful paleo enthusiasts I have ever had the pleasure to know and collect with — Rene Savenye. He and I enjoyed many years of waxing poetic about our shared love of palaeontology and natural history. 

Rene was a mountain goat in the field, stalking the hills in his signature red t-shirt. He was tremendously knowledgeable about the natural world and delighted in it. For many years, he was Chair of the White Rock and Surrey Naturalists, while I was Chair of the Vancouver Paleontological Society. Together, we would plan and often co-lead field trips to many of the wonderful fossil outcrops in British Columbia and Washington state. 

In 2002, we were planning a very exciting round of field trips. I was offered a fully paid trip to India with Karen Lund to hike to the headwaters of the Ganges, a trip which I was to forgo in favour of a hike up to the outcrops of the Cathedral Escarpment and Burgess Shale and then to yummy Lower Jurassic and Lower Cretaceous, Albian, outcrops accessed only by boat in Haida Gwaii. 

Rene and I had talked about "walking in the shoes" of Joseph Whiteaves, the GSC's chief palaeontologist in Ottawa. He published a paper in 1876 describing the Jurassic and Cretaceous faunas of Skidegate Inlet and spent a significant portion of his career working out the fossil fauna of the Burgess Shale. Combining these two sites within the same field season was a fitting homage. 

John Fam, Vancouver Paleontological Society (VanPS) and Dan Bowen, Vancouver Island Palaeontological Society (VIPS), did much of the planning for that Haida Gwaii trip, they too being inspired by Whiteaves papers and the work of James Richardson and George Dawson — as a whole, we were giddy with the prospect of the year ahead.

Rene and I had planned to do both, but in the end, I had to give up the hike to Burgess that year and Rene never made it back to join me in Haida Gwaii. 

Rene Savenye

In the days before the official trip to Burgess, Rene did some solo hiking in the mountains and hills near Field, British Columbia. He was excited to test his stamina against the steep passes that protect the majestic ridges of Wapta Mountain, Mount Field and Mount Stephen — ever mindful of collecting only with his camera. 

He walked through the hallowed footsteps of Joseph Whiteaves and Charles Doolittle Walcott over ground that should have been named La Entrada de Dios, The Gateway of God, for each footfall brought him closer to meeting the big man. While a naturalist, Rene held to the belief that once his days were done on this Earth, he would be breaking bread in heaven above. 

Rene started with clear skies and a pack full of geology hammers, maps and chisels — the hillside a sea of white and pink flecked wildflowers in the sunlight. As the day went on, the skies filled with rolling clouds, then thunder. Grey sheets of rain covered the landscape. Seeing the danger of being solo in darkening weather, he started down the slope back to his car — his shadow long and thin striking out before him in the fading light — but he never made it. On the afternoon of July 28th, he was struck and killed by lightning — a tragic loss. 

I take heart that he lived and died doing what he loved most. I got the news a few days later and cried for the loss of a great friend. I am sharing my memory of him with you so that you can remember him, too, and share in the delight and loss of one of the loveliest men to ever walk our planet. His years of teaching, mentoring, encouragement and generosity have helped shape natural science and those who have gone on to make it their passion or career — or happily, both.   

Rene's name will not be forgotten to science. His namesake, H. Savenyei, is a lovely fossil halictine bee from Early Eocene deposits near Quilchena, British Columbia — and the first bee body-fossil known from the Okanagan Highlands — and indeed from Canada. 

As a school teacher, Rene once taught the, then student, now SFU biology instructor, Rolf Mathewes. Rene passed his scientifically valuable specimen to Mathews, knowing it was important to science. Mathewes brought it to the attention of Bruce Archibald and Michael Engel, who described Rene's bee in the Canadian Journal of Zoology. Their work is a lovely legacy to a wonderful man and a specimen from one of his favourite collecting sites — Quilchena — a small road-cut exposure of the Coldwater beds of the Princeton Group, one of several depositional basins in the Merritt region of south-central British Columbia.

Rene is also remembered in spirit by the British Columbia Paleontological Alliance (BCPA) Rene Savenye Award. It was established in 2003 to honour those who have demonstrated outstanding service to the science of palaeontology or to palaeontological education in British Columbia. 

Notable past recipients are a veritable who's who from the Pacific Northwest — Graham Beard of Qualicum in 2005, Charles Helm of Tumbler Ridge in 2011, Pat Trask of Courtenay in 2014, Rod Bartlett in 2016, and Joseph "Joe" Haegert in 2018. I'll share a link to the award below so you can read more at your leisure about Rene and those who bear the award with his name.

About H. Savenyei, (Engel & Archibald, 2003): The type specimen is a fairly well preserved complete adult female preserved with portions of the fore-wings and hind-wings. The specimen is 7.04 millimetres (0.277 in) long with the possibility of alteration in length during fossilization. The sections of the forewing which are preserved are approximately 4.8 millimetres (0.19 in) long and show dark brown to black colouration. The presence of a pygidial plate bordered by setae on the fifth metasomal tergum supports the placement into the Halictidae subfamily Halictinae. Placement into the tribe Halictini is based on the lack of a medial cleft in the fifth tergum.

References:

Archibald, B. & R. W. Mathewes. 2000. “Early Eocene Insects from Quilchena, BC, and their Paleoclimatic Implications.” Canadian Journal of Zoology, Volume 78, Number 6: pp 1441-1462.

Grimaldi, D. 1999. “The Co-radiations of Pollinating Insects and Angiosperms in the Cretaceous.” Annals of the Missouri Botanical Garden. 86: 373-406.

Photo: Halictidae sp.; Archibald and Mathewes 2000: 1453.

Rene Savenye Award: https://bcfossils.ca/rene-savenye-award

FOSSILS AND FAUNA OF MADAGASGAR

Aioloceras besairiei (Collingnon, 1949)

A stunning example of the internal suturing with calcite infill in this sliced Aioloceras besairiei (Collingnon, 1949) ammonite from the Upper Cretaceous (Lower Albian) Boeny region of Madagascar. 

This island country is 400 kilometres off the coast of East Africa in the Indian Ocean and a wonderful place to explore off the beaten track.

Madagascar has some of the most spectacular of all the fossil specimens I have ever seen. This beauty is no exception. The shell has a generally small umbilicus, arched to acute venter, and typically at some growth stage, falcoid ribs that spring in pairs from umbilical tubercles, usually disappearing on the outer whorls. I had originally had this specimen marked as a Cleoniceras besairiei, except Cleoniceras and Grycia are not present in Madagascar. 

This lovely, seen in cross-section, is now far from home and in the collection of a wonderful friend. It is an especially lovely example of the ammonite, Aioloceras besairiei, making it a beudanticeratinae. Cleoniceras and Grycia are the boreal genera. If you'd like to see (or argue) the rationale on the name, consider reading Riccardi and Medina's riveting work from back in 2002, or Collingnon from 1949.

The beauty you see here measures in at a whopping 22 cm, so quite a handful. This specimen is from the youngest or uppermost subdivision of the Lower Cretaceous. I'd originally thought this locality was older, but dating reveals it to be from the Lower Albian, so approximately 113.0 ± 1.0 Ma to 100.5 ± 0.9 Ma.

Aioloceras are found in the Cretaceous of Madagascar at geo coordinates 16.5° S, 45.9° E: paleo-coordinates 40.5° S, 29.3° E.; and in four localities in South Africa: at locality 36, near the Mzinene River at 28.0° S, 32.3° E: paleo-coordinates 48.6° S, 7.6° E. 

We find them near the Mziene River, at a second locality north of Hluhluwe where the Mzinene Formation overlies the Aptian-Albian Makatini Formation at 28.0° S, 32.3° E: paleo-coordinates 48.6° S, 7.6° E; and at Haughton Z18, on the Pongola River in the Albian III, Tegoceras mosense beds at 27.3° S, 32.2° E: paleo-coordinates 48.0° S, 7.8° E.

If you happen to be trekking to Madagascar, know that it's big. It’s 592,800 square kilometres (or  226,917 square miles), making it the fourth-largest island on the planet — bigger than Spain, Thailand, Sweden and Germany. The island has an interesting geologic history.

Although there has been a geological survey, which was active extending back well into French colonial times, in the non-French-speaking world our geological understanding of the island is still a bit of a mystery. 

Plate tectonic theory had its beginnings in 1915 when Alfred Wegener proposed his theory of "continental drift." 

Wegener proposed that the continents ploughed through the crust of ocean basins, which would explain why the outlines of many coastlines (like South America and Africa) look like they fit together like a puzzle. Half a century after Wegener there is still no agreement as to whether in continental reconstructions Madagascar should be placed adjacent to the Tanzanian coast to the north (e.g., McElhinny and Embleton,1976), against the Mozambique-Natal coast (Flores 1970), or basically left where it is (Kent 1974, Nairn 1978).

There have been few attempts apart from McKinley’s (1960) comparison of the Karoo succession of southwestern Tanzania with that of Madagascar to follow the famous geological precept of “going to sea.” One critical reason is that although there may be a bibliography of several thousand items dealing with Madagascan geology as Besairie (1971) claims, they are items not generally available to the general public. The vital information gained of the geology of the offshore area by post-World War II petroleum exploration has remained largely proprietary. 

Without this data to draw upon, our understanding remains incomplete. I don't actually mind a bit of a mystery here. It is interesting to speculate on how these geologic puzzle pieces fit together and wait for the big reveal. Still, we have good old Besairie from his 1971, Geologie de Madagascar, and a later précis (Besairie, 1973).

We do know that Madagascar was carved off from the African-South American landmass early on. The prehistoric breakup of the supercontinent Gondwana separated the Madagascar–Antarctica–India landmass from the Africa–South America landmass around 135 million years ago. Madagascar later split from India about 88 million years ago, during the Late Cretaceous, so the native plants and animals on the island evolved in relative isolation. 

It is a green and lush island country with more than its fair share of excellent fossil exposures. Along the length of the eastern coast runs a narrow and steep escarpment containing much of the island's remaining tropical lowland forest. If you could look beneath this lush canopy, you'd see rocks of the Precambrian age stretching from the east coast all the way to the centre of the island. The western edge is made up of sedimentary rock from the Carboniferous to the Quaternary.

Red-Tailed Lemurs, Waiwai & Hedgehog

Madagascar is a biodiversity hotspot. Just as Darwin's finches on the Galápagos were isolated, evolving into distinct species (hello, adaptive radiation), over 90% of the wildlife from Madagascar is found nowhere else. 

The island's diverse ecosystems, like so many on this planet, are threatened by Earth's most deadly species, homo sapien sapiens. 

We arrived back in 490 CE and have been chopping down trees and eating our way through the island's tastier populations ever since. Still, they have cuties like this Red-Tailed Lemur. Awe, right?

Today, beautiful outcrops of wonderfully preserved fossil marine fauna hold appeal for me. The material you see from Madagascar is distinctive — and prolific.

Culturally, you'll see a French influence permeating the language, architecture and legal process. There is a part of me that pictures these lovely Lemurs chatting away in French. "Ah, la vache! Regarde le beau fossile, Hérissonne!"

We see the French influence because good 'ol France invaded sleepy Madagascar back in 1883, during the first Franco-Hova War. Malagasy (the local Madagascarian residents) were enlisted as troops, fighting for France in World War I.  During the Second World War, the island was the site of the Battle of Madagascar between the Vichy government and the British. By then, the Malagasy had had quite enough of colonization and after many hiccuping attempts, reached full independence in 1960. Colonization had ended but the tourist barrage had just begun. You can't stop progress.

If you're interested in learning more about this species, check out the Treatise on Invertebrate Paleontology, Part L (Ammonoidea). R.C. Moore (ed). Geological Soc of America and Univ. Kansas Press (1957), p L394. Or head over to look at the 2002 paper from Riccardi and Medina. 2002. Riccardi, A., C. & Medina, F., A. The Beudanticeratinae and Cleoniceratinae (Ammonitina) from the Lower Albian of Patagonia in Revue de Paléobiologie - 21(1) - Muséum d’Histoire Naturelle de la ville de Genève, p 313-314 (=Aioloceras besairiei (COLLIGNON, 1949). You have Bertrand Matrion to thank for the naming correction. Good to have friends in geeky places!

Collignon, M., 1933, Fossiles cenomaniens d’Antmahavelona (Province d’ Analalave, Madagascar), Ann. Geol. Serv. Min. Madagascar, III, 1934 Les Cephalopods du Trias inferieur de Madagascar, Ann. Paleont. XXII 3 and 4, XXII 1.

Besairie, H., 1971, Geologie de Madagascar, 1. Les terrains sedimentaires, Ann. Geol. Madagascar, 35, p. 463.

J. Boast A. and E. M. Nairn collaborated on a chapter in An Outline of the Geology of Madagascar, that is very readable and cites most of the available geologic research papers. It is an excellent place to begin a paleo exploration of the island.

If you happen to parle français, check out: Madagascar ammonites: http://www.ammonites.fr/Geo/Madagascar.htm

THE SLOW RACE OF TIME: LIVING FOSSILS

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

OIL IN WATER BEAUTY: FOSSILS OF FOLKSTONE

Sheer beauty — a beautiful Euhoplites ammonite from Folkstone, UK. I've been really enjoying looking at all oil-in-water colouring and chunkiness of these ammonites.

Euhoplites is an extinct ammonoid cephalopod from the Lower Cretaceous, characterized by strongly ribbed, more or less evolute, compressed to inflated shells with flat or concave ribs, typically with a deep narrow groove running down the middle.

In some, ribs seem to zigzag between umbilical tubercles and parallel ventrolateral clavi. In others, the ribs are flexious and curve forward from the umbilical shoulder and lap onto either side of the venter.

Its shell is covered in the lovely lumps and bumps we associate with the genus. The function of these adornments are unknown. I wonder if they gave them greater strength to go deeper into the ocean to hunt for food. 

They look to have been a source of hydrodynamic drag, likely preventing Euhoplites from swimming at speed. Studying them may give some insight into the lifestyle of this ancient marine predator. Euhoplites had shells ranging in size up to a 5-6cm. 

We find them in Lower Cretaceous, middle to upper Albian age strata. Euhoplites has been found in Middle and Upper Albian beds in France where it is associated respectively with Hoplites and Anahoplites, and Pleurohoplites, Puzosia, and Desmoceras; in the Middle Albian of Brazil with Anahoplites and Turrilites; and in the Cenomanian of Texas.

This species is the most common ammonite from the Folkstone Fossil Beds in southeastern England where a variety of species are found, including this 37mm beauty from the collections of José Juárez Ruiz.

FIRST DINOSAUR FROM VANCOUVER ISLAND

This dapper fellow is a pine needle and horsetail connoisseur. He's a hadrosaurus — a duck-billed dinosaur. They were a very successful group of plant-eaters that thrived throughout western Canada during the late Cretaceous, some 70 to 84 million years ago.

Hadrosaurs lived as part of a herd, dining on pine needles, horsetails, twigs and flowering plants.

Hadrosaurs are ornithischians — an extinct clade of mainly herbivorous dinosaurs characterized by a pelvic structure superficially similar to that of birds. They are close relatives and possibly descendants of the earlier iguanodontid dinosaurs. 

They had slightly webbed, camel-like feet with pads on the bottom for cushioning and perhaps a bit of extra propulsion in water. They were primarily terrestrial but did enjoy feeding on plants near and in shallow water. There had a sturdy build with a stiff tail and robust bone structure. 

At their emergence in the fossil record, they were quite small, roughly three meters long. That's slightly smaller than an American bison. They evolved during the Cretaceous with some of their lineage reaching up to 20 meters or 65 feet.

Hadrosaurs are very rare in British Columbia but a common fossil in our provincial neighbour, Alberta, to the east. Here, along with the rest of the world, they were more abundant than sauropods and a relatively common fossil find. They were common in the Upper Cretaceous of Europe, Asia, and North America.

There are two main groups of Hadrosaurs, crested and non-crested. The bony crest on the top of the head of the hadrosaurs was hollow and attached to the nasal passages. It is thought that the hollow crest was used to make different sounds. These sounds may have signalled distress or been the hadrosaur equivalent of a wolf whistle used to attract mates. Given their size it would have made for quite the trumpeting sound.

This beautiful specimen graces the back galleries of the Courtenay and District Museum on Vancouver Island, British Columbia, Canada. I was very fortunate to have a tour this past summer with the deeply awesome Mike Trask joined by the lovely Lori Vesper. The museum houses an extensive collection of palaeontological and archaeological material found on Vancouver Island, many of which have been donated by the Vancouver Island Palaeontological Society.

Dan Bowen, Chair of the Vancouver Island Palaeontological Society, shared the photo you see here of the first partly articulated dinosaur from Vancouver Island ever found. The vertebrate photo and illustration are from a presentation by Dr. David Evans at the 2018 Paleontological Symposium in Courtenay.  The research efforts of the VIPS run deep in British Columbia and this new very significant find is no exception. A Hadrosauroid dinosaur is a rare occurrence and further evidence of the terrestrial influence in the Upper Cretaceous, Nanaimo Group, Vancouver Island — outcrops that we traditionally thought of as marine from years of collecting well-preserved marine fossil fauna.

CDM 002 / Hadrosauroid Caudal Vertebrae

The fossil bone material was found years ago by Mike Trask of the Vancouver Island Palaeontological Society. You may recall that he was the same fellow who found the Courtenay Elasmosaur on the Puntledge River.

Mike was leading a fossil expedition on the Trent River. While searching through the Upper Cretaceous shales, the group found an articulated mass of bones that looked quite promising.

Given the history of the finds in the area, the bones were thought to be from a marine reptile.

Since that time, we've found a wonderful terrestrial helochelydrid turtle, Naomichelys speciosa, but up to this point, the Trent had been known for its fossil marine fauna, not terrestrial. Efforts were made to excavate more of the specimen, and in all more than 25 associated vertebrae were collected with the help of some 40+ volunteers. Identifying fossil bone is a tricky business. Encased in rock, the caudal vertebrae were thought to be marine reptile in origin. Some of these were put on display in the Courtenay Museum and mislabeled for years as an unidentified plesiosaur.

In 2016, after years of collecting dust and praise in equal measure, the bones were reexamined. They didn't quite match what we'd expect from a marine reptile. Shino Sugimoto, Fossil Preparator, Vertebrate Palaeontology Technician at the Royal Ontario Museum was called in to work her magic — painstakingly prepping out each caudal vertebrae from the block.

Once fully prepped, seemingly unlikely, they turned out to be from a terrestrial hadrosauroid. This is the second confirmed dinosaur from the Upper Cretaceous Nanaimo Group. The first being a theropod from Sucia Island consisting of a partial left thigh bone — the first dinosaur fossil ever found in Washington state.

Dr. David Evans, Temerty Chair in Vertebrate Palaeontology, Department of Natural History, Palaeobiology from the Royal Ontario Museum, confirmed the ID and began working on the partial duck-billed dinosaur skeleton to publish on the find.

Drawing of Trent River Hadrosauroid Caudal Vertebrae

Now fully prepped, the details of this articulated Hadrosauriod caudal vertebrae come to light. We can see the prominent chevron facets indicative of caudal vertebrae with a nice hexagonal centrum shape on its anterior view.

There are well-defined long, raked neural spines that expand distally — up and away from the acoelous centrum. 

Between the successive vertebrae, there would likely have been a fibrocartilaginous intervertebral body with a gel-like core —  the nucleus pulposus — which is derived from the embryonic notochord. This is a handy feature in a vertebrate built as sturdily as a hadrosaur. Acoelous vertebrae have evolved to be especially well-suited to receive and distribute compressive forces within the vertebral column.

This fellow has kissing cousins over in the state of New Jersey where this species is the official state fossil. The first of his kind was found by John Estaugh Hopkins in New Jersey back in 1838. Since that time, we've found many hadrosaurs in Alberta, particularly the Edmontosuaurs, another member of the subfamily Hadrosaurine.

In 1978, Princeton University found fifteen juvenile hadrosaurs, Maiasaura ("good mother lizard") on a paleontological expedition to the Upper Cretaceous, Two Medicine Formation of Teton County in western Montana. 

Their initial finds of several small skeletons had them on the hunt for potential nests — and they found them complete with wee baby hatchlings!

Photo One: Fossil Huntress / Heidi Henderson, VIPS

Photo Two / Sketch Three: Danielle Dufault, Palaeo-Scientific Ilustrator, Research Assistant at the Royal Ontario Museum, Host of Animalogic. 

The vertebrate photo and illustration were included in a presentation by Dr. David Evans at the 2018 BCPA Paleontological Symposium in Courtenay, British Columbia, Canada.

Photo Four: Illustration by the talented Greer Stothers, Illustrator & Natural Science-Enthusiast.

ATURIA: MIOCENE NAUTILOID

Aturia angustata, Lower Miocene, WA

This lovely Lower Miocene nautiloid is Aturia angustata collected on the foreshore near Clallam Bay, Olympic Peninsula, northwestern Washington. 

Aturia is an extinct genus of Paleocene to Miocene nautiloid within Aturiidae, a monotypic family, established by Campman in 1857 for Aturia (Bronn, 1838), and is included in the superfamily Nautilaceae (Kümmel,  1964).

There are seven living nautiloid species in two genera: Nautilus pompilius, N. macromphalus, N. stenomphalus, N. belauensis, and the three new species being described from Samoa, Fiji, and Vanuatu (Ward et al.). We have specimens of fossil nautiloids dating to the Turonian of California, and possibly the Cenomanian of Australia. There has also been a discovery of what might be the only known fossil of Allonautilus (Ward and Saunders, 1997), from the Nanaimo Group of British Columbia, Canada.

Aturia in the Collection of Rick Ross, VIPS

The exquisite shell preservation of many Nanaimo nautilids has opened up a lens into paleotemperatures and accurate Nitrogen isotope analyses. 

Nautilus and all other known Cretaceous through Paleogene nautiloids were shallow water carnivores. We may see their shells as beautiful bits of art and science today, but they were seen in our ancient oceans as small yet mighty predators. Preferring to dine on shrimp, crab, fish and on occasion, a friendly cousin nautiloid to two.

Aturia lived in cooler water in the Cenozoic, preferring it over the warmer waters chosen by their cousins. Aturia, are commonly found as fossils from Eocene and Miocene outcrops. That record ends with their extinction in the late Miocene. This was a fierce little beast with jaws packed with piranha-like teeth. They grew at least twice that of the largest known Nautilus living today. 

Aturia is characterized by a smooth, highly involute, discoidal shell with a complex suture and subdorsal siphuncle. The shell of Aturia is rounded ventrally and flattened laterally; the dorsum is deeply impressed. The suture is one of the most complex within the subclass Nautiloidea. Of all the nautiloids, he may have been able to go deeper than his brethren.

Nautiloids are known for their simple suturing in comparison to their ammonite cousins. This simplicity of design limited their abilities in terms of withstanding the water pressure experienced when several atmospheres below the sea. Nautiloids were not able to compete with their ammonite cousins in this regard. 

Instead of elaborate and complex sutures capable of withstanding the pressures of the deep, nautiloids have simpler sutures that would have them enfold on themselves and crush at depth.  

Aturia angustata; Rick Ross Collection

It has a broad flattened ventral saddle, narrow pointed lateral lobes, broad rounded lateral saddles, broad lobes on the dorso-umbilical slopes, and a broad dorsal saddle divided by a deep, narrow median lobe. 

The siphuncle is moderate in size and located subdorsally in the adapical dorsal flexure of the septum. Based on the feeding and hunting behaviours of living nautiluses, Aturia most likely preyed upon small fish and crustaceans. 

I've found a few of these specimens along the beaches of Clallam Bay and nearby in a local clay quarry. I've also seen calcified and chalcedony — microcrystalline quartz — agatized beauties of this species collected from river sites within the Olympic Peninsula range. In the bottom photos, you can see Aturia from Washington state and one (on the stand on the left) from Oregon, USA. These beauties are in the collections of the deeply awesome Rick Ross, Vancouver Island Palaeontological Society.

References: Ward, P; Haggart, J; Ross, R; Trask, P; Beard, G; Nautilus and Allonautilus in the Nanaimo Group, and in the modern oceans; 12th British Columbia Paleontological Symposium, 2018, Courtenay, abstracts; 2018 p. 10-11

COAHUILACERATOPS MAGNACUERNA

Coahuilaceratops or "Coahuila Horn Face," is a relatively new genus of Ornithischia Ceratopsidae, a  herbivorous ceratopsian dinosaur who lived during the Upper Cretaceous (late Campanian) near the town of Porvenir de Jalpa (about 64 km / 40 miles west of Saltillo) in what is now southern Coahuila (formerly Coahuila de Zaragoza), northern Mexico.

The Sierra Madre Oriental mountain range runs northwest to southwest forming a spine through the centre of the State. East of the range, the arid landscape slopes gently through the desert terrain down to the Rio Grande. It is home to wonderful common, rare and endangered cacti, beautiful (and one of my favourite) raptors, Aquila chrysaetos and the evolutionarily unlikely pronghorn, Antilocapra americana (if a monkey/owl/ antelope had a baby...)

The world was a much wetter warmer place when these big beauties roamed. Picture them ambling through lush vegetation and rearing young next to freshwater rivers, brackish swamps and salty ancient seas. Many of the dinosaur remains from the area bear the marks or remains of fossilized snails and clams. Perhaps predation vs a symbiotic relationship as proximity isn't always intimacy. Coahuilaceratops magnacuerna is known from holotype CPC 276, a partial skeleton of an adult along with bits and pieces of skull, a section of horn, pretty complete lower jaw, a smidge of the upper jaw and part of the frill.

Another specimen, CPS 277, has been touted as a possible juvenile Coahuilaceratops. All the specimens from Coahuilaceratops come from a single Upper Cretaceous (Campanian) locality of the Cerro del Pueblo Formation, northern Mexico.

This particular species of Coahuilaceratops was formally named C. magnacuerna by Mark A. Loewen, Scott D. Sampson, Eric K. Lund, Andrew A. Farke, Martha C. Aguillón-Martínez, C.A. de Leon, R.A. Rodríguez-de la Rosa, Michael A. Getty and David A. Eberth in 2010. Though the name was in circulation informally by those working in the study of ceratopsian dinosaurs as early as 2008.

Though challenged by examining and interpreting mere bits and pieces, the team posed estimates on the overall size of this new rather largish, 6.7 m / 22 ft, chasmosaurine. Coahuilaceratops' horns are also impressively large, estimated at 1.2 m / 4 feet. Rather long for a ceratopsian (consider that a Triceratops distinctive horn generally comes in under 115 cm / 45 inches and interesting in terms of evolutionary design. The holotypes are available for viewing at the Museo del Desierto in Saltillo, Coahuila. Photo credit: José F. Ventura

NEVADA FOSSILS: CARNIAN-NORIAN BOUNDARY

Time Slows at Berlin-Ichthyosaur State Park

High on the hillside up a long entry road sits the entrance to Berlin-Ichthyosaur State Park in central Nevada.

A worn American flag and sun bleached outbuildings greet you on your way to the outcrops. Away from the hustle and bustle that define the rest of Nevada this place feels remarkably serene. Your eyes squint against the sun as you search for ammonoids and other marine fossil fauna while your nose tends to the assault from the bracing smell of sage brush.

This site holds many stories. The interpretive centre displays wonderful marine reptiles, ichthyosaurs in situ, as you might expect from the name of the park — but it also showcases years of history lovingly tended. This stretch of dry golden low hills dappled with the yellow of creosote and desert grasses is an important locality for our understanding of the Carnian-Norian boundary (CNB) in North America.

The area is known worldwide as one of the most important ichthyosaur Fossil-Lagerstätte because of the sheer volume of remarkably well-preserved, fully articulated (all the sweet bones laid out all in a row...) specimens of Shonisaurus popularis.

Rich ammonoid faunas outcrop in the barren hills of the Upper Triassic (Early Norian, Kerri zone), Luning Formation, West Union Canyon, Nevada. They were studied by N. J. Silberling (1959) and provide support for the definition of the Schucherti and Macrolobatus zones of the latest Carnian — which are here overlain by well-preserved faunas of the earliest Norian Kerri Zone. 

The genus Gonionotites, very common in the Tethys and British Columbia, is for the moment, unknown in Nevada. The Upper Carnian faunas are dominated by Tropitidae, while Juvavitidae are conspicuously lacking. 

Middle Triassic Ammonoids

Despite its importance, no further investigations had been done at this site for a good 50 years. That changed in 2010 when Jim Haggart, Mike Orchard and Paul Smith — all local Vancouverites — collaborated on a project that took them down to Nevada to look at the conodonts and ammonoids. They did a bed-by-bed sampling of ammonoids and conodonts in West Union Canyon during October of that year.

October is an ideal time to do fieldwork in this area. There are a few good weeks between screaming hot and frigid cold. It is also tarantula breeding season so keep your eyes peeled. Those sweet little burrows you see are not from rodents but rather largish arachnids. 

The eastern side of the canyon provides the best record of the Macrolobatus Zone, which is represented by several beds yielding ammonoids of the Tropites group, together with Anatropites div. sp. 

Conodont faunas from both these and higher beds are dominated by ornate metapolygnthids that would formerly have been collectively referred to Metapolygnathus primitius, a species long known to straddle the CNB. Within this lower part of the section, they resemble forms that have been separated as Metapolygnathus mersinensis. Slightly higher, forms close to Epigondolella' orchardi and a single Orchardella n. sp. occur. This association can be correlated with the latest Carnian in British Columbia.

Higher in the section, the ammonoid fauna shows a sudden change and is dominated by Tropithisbites. Few tens of metres above, but slightly below the first occurrence of Norian ammonoids Guembelites jandianus and Stikinoceras, two new species of conodonts (Gen et sp. nov. A and B) appear that also occur close to the favoured Carnian/Norian boundary at Black Bear Ridge, British Columbia. Stratigraphically higher collections continue to be dominated by forms close to M. mersinensis and E. orchardi after BC's own Mike Orchard.

The best exposure of the Kerri Zone is on the western side of the West Union Canyon. Ammonoids, dominated by Guembelites and Stikinoceras div. sp., have been collected from several fossil-bearing levels. Conodont faunas replicate those of the east section. The collected ammonoids fit perfectly well with the faunas described by Silberling in 1959, but they differ somewhat from coeval faunas of the Tethys and Canada. 

The ammonoid fauna paints a compelling picture of Tethyan influence with a series of smoking guns. We see an abundance of Tropitidae in the Carnian, a lack of Pterosirenites in the Norian, copious Guembelites, the Tethyan species G. philostrati, the stratigraphic position of G. clavatus and the rare occurrence of Gonionotites. Their hallelujah moment was likely finding an undescribed species of the thin-shelled bivalve Halobia similar to Halobia beyrichi — the clincher that perhaps seals this deal on Tethyan influence. 

I'll take a boo to see what Christopher McRoberts published on the find. A jolly good idea to have him on this expedition as it would have been easy to overlook if the focus remained solely on the conodonts and ammonoids. McRoberts has published on the much-studied Pardonet Formation up in the Willison Lake Area of Northeastern, British Columbia. He knows a thing or two about Upper Triassic Bivalvia and the correlation to coeval faunas elsewhere in the North American Cordillera, and to the Boreal, Panthalassan and Tethyan faunal realms. 

If you fancy a read, they published a paper: "Towards the definition of the Carnian/Norian Boundary: New data on Ammonoids and Conodonts from central Nevada," which you can find in the proceedings of the 21st Canadian Paleontology Conference; by Haggart, J W (ed.); Smith, P L (ed.); Canadian Paleontology Conference Proceedings no. 9, 2011 p. 9-10.

Fig. 1. Location map of Berlin-Ichthyosaur State Park

Marco Balini, James Jenks, Riccardo Martin, Christopher McRoberts, along with Mike Orchard and Norman Siberling, did a bed by bed sampling in 2013 and published on The Carnian/Norian boundary succession at Berlin-Ichthyosaur State Park (Upper Triassic, central Nevada, USA) and published in January 2014 in Paläontologische Zeitschrift 89:399–433. That work is available for download from ResearchGate. The original is in German, but there is a translation available.

After years of reading about the correlation between British Columbia and Nevada, I had the very great pleasure of walking through these same sections in October 2019 with members of the Vancouver Paleontological Society and Vancouver Island Palaeontological Society. It was with that same crew that I'd originally explored fossil sites in the Canadian Rockies in the early 2000s. Those early trips led to paper after paper and the exciting revelations that inspired our Nevada adventure.

If you plan your own adventure, you'll want to keep an eye out for some of the other modern fauna — mountain lions, snakes, lizards, scorpions, wolves, coyotes, foxes, ground squirrels, rabbits, falcons, hawks, eagles, bobcats, sheep, deer and pronghorns.

Figure One: Location map of Berlin-Ichthyosaur State Park. A detailed road log with access information for this locality is provided in Lucas et al. (2007).

SAKARA MADAGASGAR: OXFORDIAN OUTCROPS

This big beastie is a superb specimen of the ammonite Lobolytoceras costellatum showing the intricate fractal pattern of its septa. This lovely measures to a whopping 230 mm and hails from Oxfordian outcrops near Sakara, Madagascar. Lovingly prepped by the supremely talented José Juárez Ruiz.

Ammonites were predatory, squidlike 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. Ammonites did the equivalent, catching prey in their tentacles. They 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) then they are to shelled nautiloids such as the living Nautilus species.

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.

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.

AMMONITE TIME KEEPERS

Argonauticeras besairei, José Juárez Ruiz

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

Ammonites were predatory, squidlike 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 am 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) Christophe Marot

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 it is found.

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 of rock to match up to specific geologic time periods, rather like 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

Photos: Argonauticeras besairei from the awesome José Juárez Ruiz.

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

SEXUAL DIMORPHISM: PLIENSBACHIAN APODEROCERAS

Apodoceras / Stonebarrow Fossils

Apoderoceras is a wonderful example of sexual dimorphism within ammonites as the macroconch (female) shell grew to diameters in excess of 40 cm – many times larger than the diameters of the microconch (male) shell.

Apoderoceras has been found in the Lower Jurassic of Argentina, Hungary, Italy, Portugal, and most of North-West and central Europe, including as this one is, the United Kingdom. This specimen was found on the beaches of Charmouth in West Dorset.

Neither Apoderoceras nor Bifericeras donovani are strictly index fossils for the Taylori subzone, the index being Phricodoceras taylori. Note that Bifericeras is typical of the earlier Oxynotum Zone, and ‘Bifericeras’ donovani is doubtfully attributable to the genus. The International Commission on Stratigraphy (ICS) has assigned the First Appearance Datum of genus Apoderoceras and of Bifericeras donovani the defining biological marker for the start of the Pliensbachian Stage of the Jurassic, 190.8 ± 1.0 million years ago.

Apoderoceras, Family Coeloceratidae, appears out of nowhere in the basal Pliensbachian and dominates the ammonite faunas of NW Europe. It is superficially similar to the earlier Eteoderoceras, Family Eoderoceratidae, of the Raricostatum Zone, but on close inspection can be seen to be quite different. It is therefore an ‘invader’ and its ancestry is cryptic.

The Pacific ammonite Andicoeloceras, known from Chile, appears quite closely related and may be ancestral, but the time correlation of Pacific and NW European ammonite faunas is challenging. 

Even if Andicoeloceras is ancestral to Apoderoceras, no other preceding ammonites attributable to Coeloceratidae are known. We may yet find clues in the Lias of Canada. Apoderoceras remains present in NW Europe throughout the Taylori Subzone, showing endemic evolution. It becomes progressively more inflated during this interval of time, the adult ribs more distant, and there is evidence that the diameter of the macroconch evolved to become larger. 

At the end of the Taylori Subzone, Apoderoceras disappeared as suddenly as it appeared in the region, and ammonite faunas of the remaining Jamesoni Zone are dominated by the Platypleuroceras–Uptonia lineage, generally assigned (though erroneously) to the Family Polymorphitidae.

In the NW European Taylori Subzone, Apoderoceras is accompanied (as well as by the Eoderoceratid, B. donovani, which is only documented from the Yorkshire coast, although there are known examples from Northern Ireland) by the oxycones Radstockiceras (quite common) and Oxynoticeras (very rare), the late Schlotheimid, Phricoderoceras (uncommon) 

Note: P. taylori is a microconch, and P. lamellosum, the macroconch), and the Eoderoceratid, Tetraspidoceras (very rare). The lovely large specimen (macroconch) of Apoderoceras pictured here is likely a female. Her larger body perfected for egg production.

SPIRALLING BEAUTY: TURRITELLA

Gastropods, or univalves, are the largest and most successful class of molluscs. They started as exclusively marine but have adapted well and now their rank spends more time in freshwater than in salty marine environments.

Many are marine, but two-thirds of all living species live in freshwater or on land. Their entry into the fossil record goes all the way back to the Cambrian.

Slugs and snails, abalones, limpets, cowries, conches, top shells, whelks, and sea slugs are all gastropods. They are the second-largest class of animals with over 60,000–75,000 known living species. The two beauties you see here are Turritella, a genus of medium-sized sea snails with an operculum, marine gastropod mollusks in the family Turritellidae. They hail from the Paris Basin and have tightly coiled shells, whose overall shape is basically that of an elongated cone. The name Turritella comes from the Latin word turritus meaning "turreted" or "towered" and the diminutive suffix -ella.

Many years ago, I had the pleasure of collecting in the Paris Basin with a fellow named Michael. I had stalked the poor man from Sunday market to Sunday market, eventually meeting up with him in the town of Gordes. He graciously shared his knowledge of the local fossil localities from the hills south of Calais to Poitiers and from Caen to the Rhine Valley, east of Saarbrücken. I deeply regret losing my notebook from that trip but cherish the fossils and memories.

The Paris Basin has many fine specimens of gastropods. These molluscs were originally sea-floor predators, though they have evolved to live happily in many other habitats. Many lines living today evolved in the Mesozoic. The first gastropods were exclusively marine and appeared in the Upper Cambrian (Chippewaella, Strepsodiscus). By the Ordovician, gastropods were a varied group present in a variety of aquatic habitats. Commonly, fossil gastropods from the rocks of the early Palaeozoic era are too poorly preserved for accurate identification. Still, the Silurian genus Poleumita contains fifteen identified species.

Most of the gastropods of the Palaeozoic belong to primitive groups, a few of which still survive today. By the Carboniferous, many of the shapes we see in living gastropods can be matched in the fossil record, but despite these similarities in appearance the majority of these older forms are not directly related to living forms. It was during the Mesozoic era that the ancestors of many of the living gastropods evolved.

In rocks of the Mesozoic era, gastropods are more common as fossils and their shells often very well preserved. While not all gastropods have shells, the ones that do fossilize more easily and consequently, we know a lot more about them. We find them in fossil beds from both freshwater and marine environments, in ancient building materials and as modern guests of our gardens.

FOSSILS OF THE NORTH SEA

A lovely 12 cm creamy orange Bottlenose Dolphin, Tursiops sp. lumbar vertebrae found in the Brown Bank area of the North Sea, one of the busiest seaways in the world.

Bottlenose dolphins first appeared during the Miocene and swam the shallow seas of this region. We still find them today in warm and temperate seas worldwide though unlike narwhal, beluga and bowhead whales, Bottlenose dolphins avoid the Arctic and Antarctic Circle regions. 

Their name derives from the Latin tursio (dolphin) and truncatus for their characteristic truncated teeth

We find their remains in the sediments of the North Sea. There are two known fossil species from Italy that include Tursiops osennae (late Miocene to early Pliocene) from the Piacenzian coastal mudstone, and Tursiops miocaenus (Miocene) from the Burdigalian marine sandstone.

Many waterworn vertebrae from the Harbour Porpoise Phocoena sp., (Cuvier, 1816), Bottlenose dolphin Tursiops sp. (Gervais, 1855), and Beluga Whale, Delphinapterus sp. (Lacépède‎, 1804‎) are found by fishermen as they dredge the bottom of the Brown Bank, one of the deepest sections of the North Sea.  

The North Sea is a sea of the Atlantic Ocean located between the United Kingdom, Denmark, Norway, Germany, the Netherlands, Belgium and France. An epeiric sea on the European continental shelf, it connects to the ocean through the English Channel in the south and the Norwegian Sea in the north.

The fishermen use small mesh trawl nets that tend to scoop up harder bits from the bottom. This technique is one of the only ways this Pleistocene and other more recent material is recovered from the seabed, making them relatively uncommon. The most profitable region for fossil mammal material is in the Brown Bank area of the North Sea. I've circled this area on the map below to give you an idea of the region.

Brown Bank, North Sea, Pleistocene Dredging Area

In May 2019, an 11-day expedition by European scientists from Belgium and the United Kingdom was undertaken to explore three sites of potential geologic and archaeologic interest in the southern North Sea. 

It has long been suspected that the southern North Sea plain may have been home to thousands of people, and chance finds by fishermen over many decades support this theory. 

A concentration of archaeological material, including worked bone, stone and human remains, has been found within the area around the Brown Bank, roughly 100 km due east from Great Yarmouth and 80 km west of the Dutch coast. The quantities of material strongly suggest the presence of a prehistoric settlement. As such the Brown Bank provides archaeologists with a unique opportunity to locate a prehistoric settlement in the deeper and more remote areas of the North Sea, known today as Doggerland.

Until sea levels rose at the end of the last Ice Age, between 8-10,000 years ago, an area of land connected Great Britain to Scandinavia and the continent.  It has long been suspected that the southern North Sea plain was home to thousands of people, and chance finds by fishermen over many decades support this theory. 

Over the past decades a concentration of archaeological material, including worked bone, stone and human remains, has been found within the area around the Brown Bank, roughly 100 km due east from Great Yarmouth and 80 km west of the Dutch coast. 

The quantities of material strongly suggest the presence of a prehistoric settlement. 

As such the Brown Bank provides archaeologists with a unique opportunity to locate a prehistoric settlement in the deeper and more remote areas of the North Sea, known today as Doggerland.

Prospecting for such a settlement within the North Sea is a challenging activity.  Multiple utilities cross the area, bad weather is frequent, and visibility underwater is often limited.  Given these challenging conditions, researchers on the Belgian vessel, RV Belgica, used acoustic techniques and physical sampling of the seabed to unravel the topography and history of the areas chosen for the survey.  

During the survey, the team used a novel parametric echosounder from the Flanders Marine Institute (VLIZ). This uses sonar technology to obtain images of the sub-bottom with the highest possible resolution and was combined with the more traditional “sparker” seismic source to explore deeper sediments.  On the Brown Bank, the Belgica also deployed a grab and a Gilson dredge for sampling near-surface stratigraphy. Video footage was collated using VLIZ’s dedicated video frame and a simpler GoPro mounted on the Gilson dredge. A video showing the equipment in operation on the expedition can be seen at https://youtu.be/sGKfyrDCtmw

Additional reading: http://www.vliz.be/en/press-release/update-research-prehistoric-settlements-North-Sea