AMMONITES FROM THE GAULT

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

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

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

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

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

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

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

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

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

FRACTAL BUILDING: AMMONITES

Argonauticeras besairei, Collection of  José Juárez Ruiz.

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

Ammonites were predatory, 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. But the Ammonites were skilled and successful hunters. They caught their prey while swimming and floating in the water column. Within their shells, they had a number of chambers, called septa, filled with gas or fluid that were interconnected by a wee air tube. By pushing air in or out, they were able to control their buoyancy in the water column.

They lived in the last chamber of their shells, continuously building new shell material as they grew. As each new chamber was added, the squid-like body of the ammonite would move down to occupy the final outside chamber.

They were a group of extinct marine mollusc animals in the subclass Ammonoidea of the class Cephalopoda. These molluscs, commonly referred to as ammonites, are more closely related to living coleoids — octopuses, squid, and cuttlefish) than they are to shelled nautiloids such as the living Nautilus species.

The Ammonoidea can be divided into six orders:

• Agoniatitida, Lower Devonian - Middle Devonian
• Clymeniida, Upper Devonian
• Goniatitida, Middle Devonian - Upper Permian
• Prolecanitida, Upper Devonian - Upper Triassic
• Ceratitida, Upper Permian - Upper Triassic
• Ammonitida, Lower Jurassic - Upper Cretaceous

Ammonites have intricate and complex patterns on their shells called sutures. The suture patterns differ across species and tell us what time period the ammonite is from. If they are geometric with numerous undivided lobes and saddles and eight lobes around the conch, we refer to their pattern as goniatitic, a characteristic of Paleozoic ammonites.

If they are ceratitic with lobes that have subdivided tips; giving them a saw-toothed appearance and rounded undivided saddles, they are likely Triassic. For some lovely Triassic ammonites, take a look at the specimens that come out of Hallstatt, Austria and from the outcrops in the Humboldt Mountains of Nevada.

Hoplites bennettiana (Sowby, 1826).

If they have lobes and saddles that are fluted, with rounded subdivisions instead of saw-toothed, they are likely Jurassic or Cretaceous. If you'd like to see a particularly beautiful Lower Jurassic ammonite, take a peek at Apodoceras. Wonderful ridging in that species.

One of my favourite Cretaceous ammonites is the ammonite, Hoplites bennettiana (Sowby, 1826). This beauty is from Albian deposits near Carrière de Courcelles, Villemoyenne, near la région de Troyes (Aube) Champagne in northeastern France.

At the time that this fellow was swimming in our oceans, ankylosaurs were strolling about Mongolia and stomping through the foliage in Utah, Kansas and Texas. Bony fish were swimming over what would become the strata making up Canada, the Czech Republic and Australia. Cartilaginous fish were prowling the western interior seaway of North America and a strange extinct herbivorous mammal, Eobaatar, was snuffling through Mongolia, Spain and England.

In some classifications, these are left as suborders, included in only three orders: Goniatitida, Ceratitida, and Ammonitida. Once you get to know them, ammonites in their various shapes and suturing patterns make it much easier to date an ammonite and the rock formation where is was found at a glance.

Ammonites first appeared about 240 million years ago, though they descended from straight-shelled cephalopods called bacrites that date back to the Devonian, about 415 million years ago, and the last species vanished in the Cretaceous–Paleogene extinction event.

They were prolific breeders that evolved rapidly. If you could cast a fishing line into our ancient seas, it is likely that you would hook an ammonite, not a fish. They were prolific back in the day, living (and sometimes dying) in schools in oceans around the globe. We find ammonite fossils (and plenty of them) in sedimentary rock from all over the world.

In some cases, we find rock beds where we can see evidence of a new species that evolved, lived and died out in such a short time span that we can walk through time, following the course of evolution using ammonites as a window into the past.

For this reason, they make excellent index fossils. An index fossil is a species that allows us to link a particular rock formation, layered in time with a particular species or genus found there. Generally, deeper is older, so we use the sedimentary layers rock to match up to specific geologic time periods, rather the way we use tree-rings to date trees. A handy way to compare fossils and date strata across the globe.

References: Inoue, S., Kondo, S. Suture pattern formation in ammonites and the unknown rear mantle structure. Sci Rep 6, 33689 (2016). https://doi.org/10.1038/srep33689
https://www.nature.com/articles/srep33689?fbclid=IwAR1BhBrDqhv8LDjqF60EXdfLR7wPE4zDivwGORTUEgCd2GghD5W7KOfg6Co#citeas

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

ACANTHOHOPLITES BIGOURETI

A very pleasing example of the Ammonite Acanthohoplites bigoureti (Seunes, 1887). Lower Cretaceous, Upper Aptian, from a riverbed concretion, Kurdzhips River, North Caucasus Mountains, Republic of Adygea, Russia. 

Geologically, the Caucasus Mountains belong to a system that extends from southeastern Europe into Asia and is considered a border between them. The Greater Caucasus Mountains are mainly composed of Cretaceous and Jurassic rocks with the Paleozoic and Precambrian rocks in the higher regions. 

Some volcanic formations are found throughout the range. On the other hand, the Lesser Caucasus Mountains are formed predominantly of the Paleogene rocks with a much smaller portion of the Jurassic and Cretaceous rocks. 

The evolution of the Caucasus began from the Late Triassic to the Late Jurassic during the Cimmerian orogeny at the active margin of the Tethys Ocean while the uplift of the Greater Caucasus is dated to the Miocene during the Alpine orogeny.

The Caucasus Mountains formed largely as the result of a tectonic plate collision between the Arabian plate moving northwards with respect to the Eurasian plate. As the Tethys Sea was closed and the Arabian Plate collided with the Iranian Plate and was pushed against it and with the clockwise movement of the Eurasian Plate towards the Iranian Plate and their final collision, the Iranian Plate was pressed against the Eurasian Plate. 

As this happened, the rocks that had been deposited in this basin from the Jurassic to the Miocene were folded to form the Greater Caucasus Mountains. This collision also caused the uplift and the Cenozoic volcanic activity in the Lesser Caucasus Mountains.

The preservation of this Russian specimen is outstanding. Acanthohoplites bigoureti are also found in Madagascar, Mozambique, in the Rhone-Alps of France and the Western High Atlas Mountains and near Marrakech in Morocco. This specimen measures 55mm and is in the collection of the deeply awesome Emil Black.

ANAHOPLITES PLANUS OF FRANCE

A beautiful specimen of the ammonite, Anahoplites planus (Mantell, 1822) from Albian deposits in Villemoyenne Quarry, Courcelles, Aube, north-central France. Anahoplites (Hyatt, 1900) is a genus of compressed hoplitid ammonites with flat sides, narrow, flat or grooved venters, and flexious ribs or striae arising from weak umbilical tubercles that end in fine dense ventrolateral nodes.

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

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

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

A. planus from the French Coast

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

This involute (113 mm) specimen shows evidence of cohabitation by some of his marine peers. We see two different bryozoa, an oyster and some serpulids making a living and leaving trace fossils on her flat sides. The top specimen was prepared with potase by José Juárez Ruiz of Spain. 

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

CEPHALOPODS OF HALLSTATT

This beautiful slab of well-preserved Triassic, Carnian, upper Tuvalian ammonoids hails limestone outcrops near the salt-mining town of Hallstatt, Salzburgerland, Austria.

This area of the world boasts one of the richest deposits of Triassic ammonite units — more than five hundred magnificent ammonite species are found here along with a diversified selection of cephalopod fauna  — orthoceratids, nautiloids, ammonoids — we also see gastropods, bivalves (including lovely halobiids), brachiopods, crinoids and a few corals. For microfauna, we see conodonts, foraminifera, sponge spicules, radiolaria, floating crinoids and holothurian sclerites —  polyp-like, soft-bodied "wormy" invertebrate echinozoans. On the left, you can see two specimens of Jovites bosniensis MOJS. The ammonoid in the middle of the plate is Juvavites sp. The right side of the block shows two Hypocladiscites subtornatus MOJS.

The larger specimen (15cm) is a phragmocone. Within its badly crushed body chamber (removed during prep) there are two washed in specimens of Disotropites plinii (MOJS.) You can see them visible in the side view on the top right. The Disotropites plinii subzone is the lower ammonoid subzone of the Tuvalian III.

The second picture here shows Hypocladiscites subtornatus from when it was first described as Arcestes subtornatus, in Mojs, 1873.

In the North American literature (after Tim Tozer) the Tuvalian is split into three Zones; starting with the Dilleri Zone, then the Welleri Zone and finally the Macrolobatus Zone on the very top.

The Dilleri zone is characterized by the rise of the genus Tropites sp. together with later members of the genus Neoprotrachyceras sp.

In the Welleri zone, Neoprotrachyceras sp. disappears and Tropites becomes a very common faunal element. The Macrolobatus zone is named after Klamathites macrolobatus, an endemic ammonite of the North American strata. Other genera of this zone are comparable to the time frame of the latest Tuvalian and the earliest Norian of the Alps. In the Hallstatt (Tethys) realm the following Division is made:

Dilleri Zone= Tuvalian I (literature gives little evidence for this zone). Subbullatus Zone = Tuvalian II — corresponding in most parts to the North American Welleri Zone. These are followed by the Anatropites Zone or Tuvalian III — corresponding in part to the North American Macrolobatus Zone.

In the Alps, the strata are divided between Tuvalian II and Tuvalian III. It is up for debate if all three North American zones can be included in these two alpine zones. It has been postulated by Spatzenegger that there is little evidence for a time gap in the lower Tuvalian of the Alpine strata.

Discotropites sandlingense is in the North America zone — a clear Dilleri faunal element. In the Alps, it is ranged into Tuvalian II (Welleri Zone). The same is true for the genus Traskites sp. — corresponding to alpine Sandlingites sp. Some ammonites of the upper part of the Macrolobatus zone are also placed within the alpine Norian stage. The correlation between the North American and Alpine zones is problematic and matching up the Tuvalian fauna is a tricky business.

Sirenites sp., Upper Triassic, Lower Carnian Julian Zone

Tuvalian 1 is recognizable in the Alps by the composition of the faunal spectrum — the quantity of some special genera. We see more of some, less of others, and this gives us a general sense of time.

In some strata, Trachysagenites sp. Sagenites inermis, Sandlingites sp. occur frequently together, with scarce Tropites sp. and Sirenites sp. and (very rarely) Neoprotrachyceras cf. thyrae.

The transition from Tuvalian to the Norian is confirmed only in one location in the Hallstatt limestone. Clustered onto blocks, the ammonoids show us the faunal mix and allow us to place them in time. The bedded profile of Tuvalian fauna (which is overlain by a Norian fauna) hails from the Feuerkogel near Hallstatt. Here we also find the lower transition of Julian to Tuvalian. Not far from this site are limestone outcrops that show the transition between the Carnian and Norian. Here the latest Tuvalian and lowermost Norian are confirmed only by the microfossil fauna.

The Hallstatt Limestone is the world's richest Triassic ammonite unit, yielding specimens of more than 500 ammonite species. Along with diversified cephalopod fauna — orthoceratids, nautiloids, ammonoids — we also see gastropods, bivalves (esp. halobiids), brachiopods, crinoids and a few corals.

Along with an amazing assortment of macrofossils, we see microfauna that are incredibly helpful in teasing out the geologic history of the area. Fossil conodonts, foraminifera, sponge spicules, radiolaria, floating crinoids and the bizarre holothurian sclerites — polyp-like, soft-bodied invertebrate echinozoans often referred to as sea cucumbers because of their similarities in size, elongate shape, and tough skin over a soft interior — can be found here.

Eduard Suess, Gondwana / Tethys Sea

Franz Ritter von Hauer’s exhaustive 1846 tome describing Hallstatt ammonites inspired renowned Austrian geologist Eduard Suess’s detailed study of the area’s Mesozoic history.

That work was instrumental in Suess being the first person to recognize the supercontinent of Gondwana (proposed in 1861) and the existence of the Tethys Sea, which he named in 1893 after the sister of Oceanus, the Greek god of the ocean.

Suess Land in Greenland, as well as the lunar crater Suess and Suess crater on Mars, are named after him.

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

This area has a rich and interesting geological and human history. I'm sure more studies will be done on the fossil marine fauna to untangle and standardize the Carnian subdivisions. For now, we'll muddle along with regional stratigraphies employing a two-substage subdivision, the Julian and Tuvalian. Others will continue to employ a three-substage organization of the stage: Cordevolian, Julian and Tuvalian. 

As I've pieced together this interesting Tuvalian tale, I have to thank Andreas Spatzenegger from Salzburg, Austria for his insights, work and amazing photos of the area. Kudos to you, my friends. I'd be mesmerized but still well confused about the Carnian subdivisions if not for you!

The genus Hypocladiscites ranges from the base Carnian to the lower Norian stage of the Upper Triassic. Photos and collection of the deeply awesome Andreas Spatzenegger of Salzburg, Austria.

Superfamilia: Arcestaceae MOJSISOVICS, 1875; Familia: Cladiscitidae ZITTEL, 1884; Subfamilia: Cladiscites GAMSJÄGER, 1982; Genus: Hypocladiscites MOJSISOVICS, 1896

Photo: A spectacular example of Sirenites sp., Upper Triassic, Lower Carnian, Julian Zone of Trachyceras aonoides. From Hallstatt Limestone of Austria. This specimen is about 5cm. Photo and collection of the deeply awesome Andreas Spatzenegger.

Photo: Eduard Suess (1831–1914), lithograph by Josef Kriehuber (1800–1876) c. 1869 by Josef Kriehuber - File:Eduard Sueß.jpg (cropped), Public Domain https://commons.wikimedia.org/w/index.php?curid=31526345

DORSOPLANITES: FROM RUSSIA WITH LOVE

Golden light shines on the ammonite, Dorsoplanites dorsoplanus (Vischniakoff, 1882), Upper Jurassic, Volgian Stage, Panderi Zone. If you wanted to visit this beauty today, she is in the collections of the deeply awesome Emil Black. 

If you wanted to travel to the outcrop where she was found, you would want to head to eastern Europe then search through the rock dumps along the new subway in the city of Moscow along the Moskva River in Central Russia.

Eight biohorizons, four of which were previously distinguished in Central Poland and four new ones have been identified as — contradictionis, pommerania, kuteki, and pilicensis, — were identified in the Dorsoplanites panderi zone of the Upper Jurassic Middle Volgian Substage of the European part of Russia on the basis of the succession of ammonites of the Zaraiskites genus. If that sounds like Greek to you, no worries. Just know that they are actively being studied and those geeking out on the finds are happy as clams.

The peculiarities of variations of the ammonite complexes in space and time testify to the stepwise warming during the Panderi Chron and the occurrence of the significant latitudinal temperature gradient in the Middle Russian Sea. Collection & photo of the awesome Emil Black. 

EURYPTERUS SEA SCORPIONS

The impressive homeotype specimen of Eurypterus lacustris from Late Silurian deposits in New York. UCMP Berkeley's palaeontological collections.

Eurypterus is by far the most well-studied and well-known eurypterid and its fossil specimens probably represent more than 90% of all known eurypterid specimens.

About two dozen families of eurypterids “sea scorpions” are known from the fossil record. Although these ancient predators have a superficial similarity, including a defensive needle-like spike or telson at their tail end, they are not true scorpions. They are an extinct group of arthropods related to spiders, ticks, mites and other extant creepy crawlies.

The first fossil of Eurypterus was found in 1818 by S. L. Mitchill, a fossil collector. It was recovered from the Bertie Formation of New York, near Westmoreland, Oneida County. Mitchill interpreted the appendages on the carapace as barbels arising from the mouth. He consequently identified the fossil as a catfish of the genus Silurus. In 1825, American zoologist James Ellsworth De Kay identified the fossil correctly as an arthropod. He named it Eurypterus remipes and established the genus Eurypterus in the process. The name means "wide wing" or "broad paddle", referring to the swimming legs, from Greek εὐρύς (eurús, wide) and πτερόν (pteron, wing).

However, De Kay thought Eurypterus belonged to branchiopods, a group of crustaceans that includes water fleas. Soon after, Eurypterus lacustris was also discovered in New York in 1835 by the palaeontologist Richard Harlan. Another species was discovered in Estonia in 1858 by Jan Nieszkowski. He considered it to be of the same species as the first discovery (E. remipes); though it has since been renamed Eurypterus tetragonophthalmus.

Jan Nieszkowski's 1858 dissertation

These specimens from Estonia are often of extraordinary quality, retaining the actual cuticle of their exoskeletons. In 1898, the Swedish palaeontologist Gerhard Holm separated these fossils from the bedrock with acids. Holm was then able to examine the almost perfectly preserved fragments under a microscope. His remarkable study led to the modern breakthrough in eurypterid morphology.

More fossils were recovered in great abundance in New York in the 19th century, and elsewhere in eastern Eurasia and North America. Today, Eurypterus remains one of the most commonly found and best-known eurypterid genera, comprising more than 95% of all known eurypterid fossils.

Eurypterids hunted fish in the muddy bottoms of warm shallow seas some 460 to 248 million years ago before moving on to hunting grounds in fresh and brackish water during the latter part of their reign. Their numbers diminished greatly during the Permian-Triassic extinction, becoming extinct by 248 million years ago.

Image: Dorsal and ventral aspects of Eurypterus tetragonophthalmus, from Jan Nieszkowski's 1858 dissertation; By Jan Nieszkowski (1833-1866) - Nieszkowski J. De euryptero remipede: dissertatio inauguralis. Dorpat: H. Laakmann, 1858, Public Domain, https://commons.wikimedia.org/w/index.php?curid=11225856

TRACKING THROUGH THE TRIASSIC

Grambergia sp. Middle Triassic Ammonoid of  BC, Canada

In the early 1980s, Tim Tozer, Geological Survey of Canada was looking at the spread of marine invertebrate fauna in the Triassic of North America. 

In the western terranes of the Cordillera, marine faunas from southern Alaska and Yukon to Mexico are known from the parts that are obviously allochthonous with regard to the North American plates.

Lower and upper Triassic faunas of these areas, as well as some that are today up to 63 ° North, have the characteristics of the lower palaeo latitudes. In the western Cordillera, these faunas of the lower paleo latitudes can be found up to 3,000 km north of their counterparts on the American plate. This indicates a tectonic shift of significant magnitude. There are marine triads on the North American plate over 46 latitudes from California to Ellesmere Island. 

For some periods, two to three different faunal provinces can be distinguished. The differences in faunal species are linked, not surprisingly, to their palaeolatitude. They are called LPL, MPL, HPL (lower, middle, higher palaeolatitude).

Nevada provides the diagnostic features of the lower (LPL); northeastern British Columbia that of the middle (MPL) and Sverdrup Basin, the large igneous province on Axel Heiberg Island and Ellesmere Island, Nunavut, Canada near the rifted margin of the Arctic Ocean, that of the higher palaeolatitude (HPL).

A distinction between the provinces of the middle and the higher palaeo-situations can not be made for the lower Triassic and lower Middle Triassic (anise). However, all three provinces can be seen in the deposits of Ladin, Kam and Nor.

In the early 2000s, as part of a series of joint UBC, VIPS and VanPS fossil field trips (and then Chair of the VanPS), I explored much of the lower faunal outcrops of northeastern British Columbia. It was my first time seeing many of British Columbia's Triassic outcrops. Years later, and fueled by seeing paper after paper correlating the faunal assemblages of BC to those of Nevada, I had the very great pleasure of walking through the Nevada strata with John Fam (VanPS, Vice-Chair), Dan Bowen (VIPS, Chair) and Betty Franklin (VIPS, Goddess of Everything and BCPA, Treasurer) — and witnessing first-hand the correlation between the Nevada fauna and those from the Triassic of British Columbia, Canada.

Triassic ammonoids, West Humboldt Mountains, Nevada, USA

The Nevada faunal assemblages are a lovely match. The quality of preservation at localities like Fossil Hill in the Humboldt Mountains of Nevada, perhaps the most famous and important locality for the Middle Triassic (Anisian/Ladinian) of North America, is truly outstanding.

Aside from sheer beauty and spectacular preservation, the ammonoids and belemnites were tucked in cozily with very well preserved ichthyosaur remains.

Tozer's interest in our marine invert friends was their distribution. How and when did certain species migrate, cluster, evolve — and for those that were prolific, how could their occurrence — and therefore significance — aide in an assessment of plate and terrane movements that would help us to determine paleolatitudinal significance. I share a similar interest but not exclusive to our cephalopod fauna. The faunal collection of all of the invertebrates holds appeal.

Middle Triassic (Anisian/Ladinian) Fauna

This broader group held an interest for J.P. Smith who published on the marine fauna in the early 1900s based on his collecting in scree and outcrops of the West Humboldt Mountains, Nevada. He published his first monograph on North American Middle Triassic marine invertebrate fauna in 1914.

N. J. Siberling from the US Geological Survey published on these same Nevada outcrops in 1962. His work included nearly a dozen successive ammonite faunas, many of which were variants on previously described species. Both their works would inform what would become a lifelong piecing together of the Triassic puzzle for Tozer.

If one looks at the fauna and the type of sediment, the paleogeography of the Triassic can be interpreted as follows: a tectonically calm west coast of the North American plate that bordered on an open sea; in the area far from the coast, a series of volcanic archipelagos delivered sediment to the adjacent basins. Some were lined or temporarily covered with coral wadding and carbonate banks. Deeper pools were in between. The islands were probably within 30 degrees of the triadic equator. They moved away from the coast up to about 5000 km from the forerunner of the East Pacific Ridge. The geographical situation west of the back was probably similar.

Jurassic and later generations of the crust from near the back have brought some of the islands to the North American plate; some likely to South America; others have drifted west, to Asia. There are indications that New Guinea, New Caledonia and New Zealand were at a northern latitude of 30 ° or more during the Triassic period.

The terranes that now form the western Cordillera were probably welded together and reached the North American plate before the end of the Jurassic period.

Marine Triassic occurs on the North American Plate over a latitudinal spread of 46 degrees, from California to Ellesmere Island. At some intervals of time faunas on the Plate permit the discrimination of two or three provinces with distinctively different coeval faunas. The faunal differences are evidently related to paleolatitude and the provinces are designated LPL, MPL, HPL (low, mid, high paleolatitude). Nevada provides the diagnostic characters of the LPL province; northeastern British Columbia the MPL; the Sverdrup Basin the HPL. In the Lower Triassic and early Middle Triassic (Anisian), the distinction between the MPL and HPL provinces cannot be made. All three provinces are recognized in the Ladinian, Carnian and Norian deposits.

Juvavites sp. Geological Survey of Canada. Photo: John Fam

In the western tracts of the Cordillera, the part formed of suspect terranes, apparently allochthonous with respect to the North American Plate, marine faunas are known all the way from southern Alaska and Yukon to Mexico.

Lower and Upper Triassic faunas from these terranes, including some which today are at 63 degrees north, have the characters of the LPL province.

Middle Triassic faunas from the terranes, as presently known, do not contribute significant data. In the terranes of the Western Cordillera, LPL faunas were now up to 3,000 km north of their counterparts on the American Plate. Through the fossil fauna assemblages, we can see this level of tectonic displacement.

Taking into account the faunas and the nature of the rocks, the Triassic paleogeography is interpreted as a tectonically quiet west shore for the North American Plate, bordered by an open sea or ocean; then, well off-shore, a series of volcanic archipelagos shedding sediment into adjacent basins. Some were fringed or intermittently covered by coralline shoals and carbonate banks. Deeper basins were in between. The islands probably were within 30 degrees of the Triassic equator and extended offshore for about 5000 km, to the spreading ridge directly ancestral to the East Pacific Rise. The geography west of the spreading ridge was probably comparable.

Jurassic and later generation of crust at the ridge had driven some of the islands into the North American Plate; some probably to South America; others have gone west to Asia. Evidence is given that northern New Guinea, New Caledonia and New Zealand may have been at a north latitude of 30 degrees or more in the Triassic. The terranes now forming the Western Cordillera had probably amalgamated, and reached the North American Plate, before the end of the Jurassic.

At the end of the Rhaetian (part of the Triassic period), most of the ammonites had died out. The Hettangian, a rather poorly understood 3 million year time interval followed the Triassic-Jurassic mass extinction event.

During the Hettangian, the new or  Neoammonites developed quite quickly. Within a million years, a fairly large, diverse selection of genera and species had risen to fill the void. The gap created by the Triassic-Jurassic extinction event was re-filled and our ability to "read the rocks' to understand their continued movement through tectonic plate shifting recommenced.

Alsatites proaries, Hettangian Ammonite

It is during the Hettangian that the smooth shelled ammonite genus Psiloceras first appears. They span the time between 201.3 ± 0.2 Ma and 199.3 ± 0.3 Ma (million years ago). For my European friends, the Hettangian is the time span in which the marine limestone, shales and clay Lias of western Europe were deposited.

This Hettangian ammonite, Alsatites proaries, is a lovely example of the cephalopods cruising our ancient oceans at that time. Alsatites is an extinct genus of cephalopod belonging to the Ammonite subclass. They lived during the Early Jurassic, Hettangian till the Sinemurian and are generally extremely evolute, many whorled with a broad keel. Or, as described by one of my very young friends, he looks like a coiled snake you make in pottery class.

The Hettangian is an interesting little period of our history. It spans the time between 201.3 ± 0.2 Ma and 199.3 ± 0.3 Ma (million years ago). For my European friends, the Hettangian is the time in which the marine limestone, shales and clay Lias of western Europe were deposited. In British Columbia, Canada, we see the most diverse middle and late Hettangian (Early Jurassic) ammonite assemblages in the Queen Charlotte Islands (Haida Gwaii), an archipelago about 50 km off British Columbia's northern Pacific coast. In total, 53 ammonite taxa are described of which Paradasyceras carteri, Franziceras kennecottense, Pleuroacanthites charlottensis, Ectocentrites pacificus and Curviceras haidae are new.

In general, North American Early Jurassic ammonites are of Tethyan affinity or endemic to the eastern Pacific. For this reason, a separate zonation for the Hettangian and Sinemurian of the Western Cordillera of North America was established. Taylor et al. (2001), wrote up and published on much of this early research though, at the time, very little Canadian information was included.

Longridge, L. M., et al. “Three New Species of the Hettangian (Early Jurassic) Ammonite Sunrisites from British Columbia, Canada.” Journal of Paleontology, vol. 82, no. 1, 2008, pp. 128–139. JSTOR, www.jstor.org/stable/20144175. Accessed 27 Jan. 2020.

Tozer, ET (Tim): Marine Triassic faunas of North America: Their significance for assessing plate and terrane movements. Geol Rundsch 71, 1077-1104 (1982). https://doi.org/10.1007/BF01821119

Danner, W. (Ted): Limestone resources of southwestern British Columbia. Montana Bur. Mines & Geol., Special publ. 74: 171-185, 1976.

Davis, G., Monger, JWH & Burchfiel, BC: Mesozoic construction of the Cordilleran “collage”, central British Columbia to central California. Pacific Coast Paleography symposium 2, Soc. Economic Paleontologists and Mineralogists, Los Angeles: 1-32, 1978.

Gibson, DW: Triassic rocks of the Rocky Mountain foothills and front ranges of northeastern British Columbia and west-central Alberta. Geol. Surv. Canada Bull. 247, 1975.

Photo of the large belemnite (Atractites sp?) and ammonites (Sunrisites & Badouxia) from the Lower Jurassic (Late Hettangian), Last Creek Formation (Castle Pass member), Taseko Lakes area, British Columbia, Canada in the collection of the deeply awesome John Fam.

Photo: A drawer of Juvavites sp. in the collections of the Geological Survey of Canada. These rarely seen Upper Triassic (Carnian to Norian) ammonoids were collected over many decades by geologists of the Geological Survey of Canada from Northeastern British Columbia. Photo care of the deeply awesome John Fam.

Photo: Grambergia sp. from the Early Anisian (Middle Triassic) ammonoid biostratigraphy of northeastern British Columbia, Canada. Collection of Fossil Huntress.

Photo: Alsatites proaries, Coll. Reiter, Neoammoniten, 30 July 2011, 19:26:10

LOWER PLIENSBACHIAN: ANDROGYNOCERAS

This gorgeous Lower Pliensbachian macroconch of the ammonite Androgynoceras lataecosta was found as a nodule from the Green Ammonite beds, Lower Pliensbachian, Stonebarrow Marl Member, Charmouth Mudstone Formation (190 MYA) at Charmouth Beach, Dorset Coast in the summer of 2020. 

This specimen was found, prepped and photographed by the lovely and talented folk at Stonebarrow Fossils. 

And what a delightful surprise! The large macroconch specimen here is 12 cm but is cuddled in with her is a lovely grouping of  the diminutive male microconchs of Androgynoceras (Hyatt, 1867) if you are lucky — sometimes a Tragophylloceras loscombi (Sowerby, 1814) — or nothing at all if you are not. 

We see a great variation in this species and the ammonite species that make up this population. Murray Edmunds from Chipping Norton, UK shared some of his insights on why we see such variation and how a phylogenetic species concept may be masking a continuum that tells a very different story.  

We are starting to recognise that these could all be variants of one interbreeding population — with a highly variable duration of a juvenile Capricorn stage. Palaeontologists use a phylogenetic species concept as you cannot test reproductive isolation in any but the most recent of fossils.

By definition, individuals within an interbreeding population cannot belong to different species, let alone different genera. In palaeontology, we can only interpret what we see with reference to what we understand of biology. 

In the Davoei Zone Liparoceratidae, we have a single lineage that evolves into Oistoceras. The microconchs (putative males) are small Capricorns, and the macroconchs (putative females) are very variable: they have a Capricorn juvenile stage that can be expressed for only a few mm (or not at all), or for many cm. But eventually, the adult macroconch body chamber acquires liparoceratid ornament — inflated and bipinnate with numerous secondary ribs. 

Unfortunately, the green ammonite beds at Charmouth preserve only juvenile macroconchs so we do not get to appreciate the similarity and differences of the mature adult shell form. These beauties can look very different from one another but are all the same species. 

Historically, this difference in appearance led to all the individuals — both micro and macroconchs — with prolonged Capricorn morphology being assigned to Androgynoceras and those macroconchs lacking the juvenile Capricorn stage (as is typical in their Ibex zone ancestors) to be Liparoceras. 

Different species were named for different variants. But this is a purely morphological approach to nomenclature and does not reflect the taxonomy used for extant organisms where we try to reflect phylogeny.

But as more and more examples are collected, we start to see that these specimens form a continuum. And as we follow them up through time, we see that all of them (microconchs and macroconchs, regardless of the extent of the Capricorn stage — although that tends to become more prolonged through time — simultaneously evolve progressively forwardly projected ribs across the venter, culminating in Oistoceras. 

This simultaneous evolutionary change across the entire Liparoceratid population more or less proves that we have a single interbreeding clade. And that it is separate from Becheiceras – through that’s another story! And they all go extinct simultaneously too, whereas Becheiceras carries on into the Margaritatus Zone. If you're a grad student looking to do your thesis, there is a very interesting story you could tell.

If you fancy a web stroll through some beautifully prepped specimens from Jurassic Coast, UK, or if you'd like to get some prepped, you can check out Stonebarrow Fossils here: https://www.stonebarrowfossils.co.uk/  / Photos: Stonebarrow Fossils

If you like podcasts, check out the Fossil Huntress — Palaeo Sommelier Podcast at https://anchor.fm/fossil-huntress / Spotify / Google Play / Apple Podcasts

HIKING TO THE FERNIE AMMONITE

The Fernie ammonite, Titanites occidentalis, from outcrops on Coal Mountain near Fernie, British Columbia, Canada. 

This beauty is the remains of a carnivorous cephalopod within the family Dorsoplanitidae that lived and died in a shallow sea some 150 million years ago.

If you would like to get off the beaten track and hike up to see this ancient beauty, you will want to head to the town of Fernie in British Columbia close to the Alberta border. 

Driving to the trail base is along an easy access road just east of town along Fernie Coal Road. There are some nice exposures of Cretaceous plant material on the north side (left-hand side) of the road as you head from Fernie towards Coal Creek. I recently drove up to Fernie to look at Cretaceous plant material and locate the access point to the now infamous Late Jurassic (Tithonian) Titanites (S.S. Buckman, 1921) site. While the drive out of town is on an easy, well-maintained road, the slog up to the ammonite site is a steep 3-hour push.

The first Titanites occidentalis was about one-third the size and was incorrectly identified as Lytoceras, a fast-moving nektonic carnivore. The specimen you see here is significantly larger at 1.4 metres (about four and a half feet) and rare in North America. 

Titanites occidentalis, the Western Giant, is the second known specimen of this extinct fossil species. The first was discovered in 1947 in nearby Coal Creek by a British Columbia Geophysical Society mapping team. When they first discovered this marine fossil high up on the hillside, they could not believe their eyes — both because it is clearly marine at the top of a mountain and the sheer size of this ancient beauty.

In the summer of 1947, a field crew was mapping coal outcrops for the BC Geological Survey east of Fernie. One of the students reported finding “a fossil truck tire.” Fair enough. The similarity of size and optics are pretty close to your average Goodridge. 

A few years later, GSC Paleontologist Hans Frebold described and named the fossil Titanites occidentalis after the large Jurassic ammonites from Dorset, England. The name comes from Greek mythology. Tithonus, as you may recall, was the Prince of Troy. He fell in love with Eos, the Greek Goddess of the Dawn. Eos begged Zeus to make her mortal lover immortal. Zeus granted her wish but did not grant Tithonus eternal youth. He did indeed live forever — ageing hideously. Ah, Zeus, you old trickster. It is a clever play on time placement. Dawn is the beginning of the day and the Tithonian being the latest age of the Late Jurassic. Clever Hans!

Hiking to the Fernie Ammonite

From the town of Fernie, British Columbia, head east along Coal Creek Road towards Coal Creek. The site is 3.81 km from the base of Coal Creek Road to the trailhead as the crow flies. I have mapped it here for you in yellow and added the wee purple GPS marker for the ammonite site proper. There is a nice, dark grey to black roadcut exposure of Cretaceous plants on the north side of the dirt road that is your cue to pull over and park.  

You access the trailhead on the south side of the road. You'll need to cross the creek to begin your ascent. There is no easy way across the creek and you'll want to tackle this one with a friend when the water level is low. 

The beginning of the trail is not clear but a bit of searching will reveal the trailhead with its telltale signs of previous hikers. This is a 2-3 hour moderate 6.3-kilometre hike up & back bush-whacking through scrub and fallen trees. Heading up, you'll make about a 246-metre elevation gain. You won't have a cellular signal up here but if you download the Google Map to your mobile, you'll have GPS to guide you. 

If you're coming in from out of town, the closest airport is Cranbrook. Then it is about an hour and change to Fernie and another 15-minutes or so to the site.

You will want to leave your hammers with your vehicle (no need to carry the weight) as this site is best enjoyed with a camera. This is a site you will want to wear hiking boots to access. Know that these will get wet as you cross the creek. If you'd like to see the ammonite but are not keen on the hike, a cast has been made by fossil preparator Rod Bartlett and is on display at the Courtenay Museum in Courtenay, Vancouver Island, Canada. Fernie Ammonite Palaeo Coordinates: 49°29'04"N 115°00'49"W

MADAGASCAR GIANT: LOBOLYTOCERAS

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.

DELICATELY RIDGED PORPOCERAS

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 the 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. The flanks are slightly convex and the 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 tubercles 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

PLAZA DE ESPANA, SEVILLE

The Plaza de España is a plaza in the Parque de María Luisa, in Seville, Spain. It was built in 1928 for the Ibero-American Exposition of 1929. 

It is a landmark example of Regionalism Architecture, mixing elements of the Baroque Revival, Renaissance Revival and Moorish Revival styles of Spanish architecture. You can stroll through the grounds and explore each of the buildings. There is amazing tile work.

The Plaza de España, designed by Aníbal González, was a principal building built on the Maria Luisa Park's edge to showcase Spain's industry and technology exhibits. González combined a mix of 1920s Art Deco and Spanish Renaissance Revival, Spanish Baroque Revival and Neo-Mudéjar styles. The Plaza de España complex is a huge half-circle; the buildings are accessible by four bridges over the moat, which represent the ancient kingdoms of Spain. In the centre is the Vicente Traver fountain.

Many tiled alcoves were built around the plaza, each representing a different province of Spain. Each alcove is flanked by a pair of covered bookshelves, now used by visitors in the manner of a "Little Free Library". Each bookshelf often contains works with information about each province. Visitors have also donated favourite novels and other books for others to read.

Today the buildings of the Plaza de España have been renovated and adapted for use as offices for government agencies. The central government departments, with a sensitive adaptive redesign, are located within it. Toward the end of the park, the grandest mansions from the fair have been adapted as museums. The most distant museum contains the city's archaeology collections. The main exhibits are Roman mosaics and artefacts from nearby Italica.

The Plaza de España has been used as a filming location, including scenes for Lawrence of Arabia (1962). The building was used as a location in the Star Wars movie series Star Wars: Episode II – Attack of the Clones (2002) — in which it featured in shots of the City of Theed on the Planet Naboo. It also featured in the 2012 film The Dictator.

METASEQUOIA GLYPTOSTROBOIDES

Metasequoia, Dawn Redwood, is a fast-growing, deciduous tree native to Lichuan county in Hubei province in central China. It is the sole living species of Metasequoia glyptostroboides and one of three species of conifers known as redwoods.

Metasequoia has experienced morphological stasis for the past 65 million years, meaning they have not changed much. The modern Metasequoia glyptostroboides looks identical to its late Cretaceous ancestors.

They are remarkably similar to and sometimes mistaken for Sequoia at first glance but are easily distinguishable if you look to their needles. Metasequoia has paired needles that attach opposite to each other on the compound stem. Sequoia needles are offset and attach alternately. Think of the pattern or jumping versus walking. Metasequoia needles are paired as if you were jumping forward, one print beside the other, while Sequoia needles have the one-in-front-of-the-other pattern of walking.

Although the least tall of the redwoods, it grows to at least Sixty meters (200 feet) in height. Local villagers refer to the original tree from which most others derive as Shui-sa, or "water fir", which is part of a local shrine. Since its rediscovery in 1944, the dawn redwood has become a popular ornamental tree in the Pacific Northwest.

Metasequoia fossils are known from many areas in the Northern Hemisphere. And folk love naming them. More than twenty fossil species have been named over time —  some even identified as the genus Sequoia in error — but for all their collective efforts to beef up this genus there are just three species: Metasequoia foxii, Metasequoia milleri, and Metasequoia occidentalis.

Alder & Metasequoia Fossils from McAbee

During the Paleocene and Eocene, extensive forests of Metasequoia thrived as far north as Strathcona Fiord on Ellesmere Island and sites on Axel Heiberg Island (northern Canada) at around 80° N latitude.

We find lovely examples of Metasequoia occidentalis in the Eocene outcrops at McAbee near Cache Creek, British Columbia, Canada. The McAbee Fossil Beds are known for their incredible abundance, diversity and quality of fossils including lovely plant, insect and fish species that lived in an old lake bed setting 52-53 million years ago.

The McAbee fossil beds are 30 metres of fossiliferous shale in the Eocene Kamloops Group. The fossils are preserved here as impressions and carbonaceous films.

We see gymnosperm (16 species); a variety of conifers (14 species to my knowledge); two species of ginkgo, a large variety of angiosperm (67 species); a variety of insects and fish remains, the rare feather and a boatload of mashed deciduous material. Nuts and cupules are also found from the dicotyledonous Fagus and Ulmus and members of the Betulaceae, including Betula and Alnus.

We see many species that look very similar to those growing in the Pacific Northwest today. Specifically, cypress, dawn redwood, fir, spruce, pine, larch, hemlock, alder, birch, dogwood, beech, sassafras, cottonwood, maple, elm and grape. By far, we see the lovely Metasequoia the most.

Metasequoia was first described as a fossil from the Mesozoic Era by Shigeru Miki in 1941. Later in 1944, a small stand of an unidentified tree species was discovered in China in Modaoxi (磨刀溪; presently, Moudao (谋道), in Lichuan County, Hubei province by Zhan Wang.

Hubei province, central China.

While the find was exciting, it was overshadowed by China's ongoing conflict. In 1937, a clash between Chinese and Japanese troops at the Marco Polo Bridge, just outside Beijing, led to an all-out war.

A year later, by mid-1938, the Chinese military situation was dire. Most of eastern China lay in Japanese hands: Shanghai, Nanjing, Wuhan. Many outside observers assumed that China could not hold out, and the most likely scenario was a Japanese victory over China.

Yet the Chinese hung on, and after Pearl Harbor, the war became genuinely global. The western Allies and China were now united in their war against Japan, a conflict that would finally end on September 2, 1945.

With World War II behind them, the Chinese researchers were able to re-focus their energies on the sciences. In 1946, Wan Chun Cheng and Hu Hsen Hsu went back to examine the trees from Lichuan County. Two years later, they published a paper describing a new living species of Metasequoia. That same year, Arnold Arboretum of Harvard University sent an expedition to collect seeds and, soon after, seedling trees were distributed to various universities and arboreta worldwide for growth trials.

BACK IN THE USSR: KEPPLERITES

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

There is also a wee bit of petrified wood on the backside. These beauties hail from Jurassic, Lower Callovian outcrops in the Quarry of Kursk Magnetic Anomaly (51.25361,37.66944), Kursk region, Russia. Diameter ammonite 70мм. Back in the USSR — in the mid-1980s — during the expansion and development of one of the quarries, an unusual geological formation was found. This area had been part of the seafloor around an ancient island surrounded by Jurassic Seas. 

The outcrops of this geological formation turned out to be very rich in marine fossils. This ammonite block was found there years ago by the deeply awesome Emil Black. It has been many years since he has been able to collect there as the site is now closed to fossil collecting and employed solely for the processing and extraction of iron ore deposits.

BACK IN THE USSR: BEADANTICERAS

This lovely oil in water coloured ammonite is the beauty Beudanticeras sp. from the Lower Cretaceous (Upper Aptian), Krasnodar region, Northern Caucasus, southern Russia. 

This area of the world has beautiful fossil specimens with their distinct colouring. The geology and paleontological history of the region are fascinating as is its more recent history. 

The territory of present Krasnodar Krai was inhabited as early as the Paleolithic, about 2 million years ago. It was inhabited by various tribes and peoples since ancient times. There were several Greek colonies on the Black Sea coast, which later became part of the Kingdom of the Bosporus. In 631, the Great Bulgaria state was founded in the Kuban. In the 8th-10th centuries, the territory was part of Khazaria.

In 965, the Kievan Prince Svyatoslav defeated the Khazar Khanate and this region came under the power of Kievan Rus, Tmutarakan principality was formed. At the end of the 11th century, in connection with the strengthening of the Polovtsy and claims of Byzantium, Tmutarakan principality came under the authority of the Byzantine emperors (until 1204).

In 1243-1438, this land was part of the Golden Horde. After its collapse, Kuban was divided between the Crimean Khanate, Circassia, and the Ottoman Empire, which dominated in the region. Russia began to challenge the protectorate over the territory during the Russian-Turkish wars.

In 1783, by decree of Catherine II, the right-bank Kuban and Taman Peninsula became part of the Russian Empire after the liquidation of the Crimean Khanate. In 1792-1793, Zaporozhye (Black Sea) Cossacks resettled here to protect new borders of the country along the Kuban River. 

During the military campaign to establish control over the North Caucasus (Caucasian War of 1763-1864), in the 1830s, the Ottoman Empire for forced out of the region and Russia gained access to the Black Sea coast.

Prior to the revolutionary events of 1917, most of the territory of present Krasnodar Krai was occupied by the Kuban region, founded in 1860. In 1900, the population of the region was about 2 million people. In 1913, it ranked 2nd by the gross harvest of grain, 1st place for the production of bread in the Russian Empire.

The Kuban was one of the centres of resistance after the Bolshevik revolution of 1917. In 1918-1920, there was a non-Bolshevik Kuban People’s Republic. In 1924, North-Caucasian krai was founded with the centre in Rostov-on-Don. In 1934, it was divided into Azov-Black Sea krai (Rostov-on-Don) and North Caucasus krai (Stavropol).

September 13, 1937, the Azov-Black Sea region was divided into the Rostov region and Krasnodar Krai that included Adygei autonomous oblast. During the Second World War, the region was captured by the Germans. After the battle for the Caucasus, it was liberated. There are about 1,500 monuments and memorials commemorating heroes of the war on the territory of Krasnodar Krai.

The lovely block you see here is in the collections of the awesome John Fam, Vice-Chair of the Vancouver Paleontological Society in British Columbia, Canada.

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

AMMONITES IN PYRITE

We sometimes find fossils preserved by pyrite. They are prized as much for their pleasing gold colouring as they are for their scientific value as windows into the past. 

Sometimes folk add a coating of brass to increase the aesthetic appeal — a practice is frowned upon in paleontological communities.

Pyrite, sometimes called Fool's Gold, is a brass-yellow mineral with a bright metallic lustre. I popped a photo of some pyrite below so you can see the characteristic shape of its cubic crystal system.

Fool's Gold has a chemical composition of iron sulfide (FeS2) and is the most common sulfide mineral. It forms at high and low temperatures usually in small quantities, in igneous, metamorphic, and sedimentary rocks. If these sulfide minerals are close at hand when a fossil is forming, they can infuse specimens, replacing their mineral content to beautiful effect.

When we find a fossil preserved with pyrite, it tells us a lot about the conditions on the seabed where the organism died. Pyrite forms when there is a lot of organic carbon and not much oxygen in the vicinity. 

The reason for this is that bacteria in sediment usually respire aerobically (using oxygen), however, when there is no oxygen, they respire without oxygen (anaerobic) typically using sulphate. 

Sulphate is a polyatomic anion with the empirical formula SO2−4. It is generally highly soluble in water. Sulfate-reducing bacteria, some anaerobic microorganisms, such as those living in sediment or near deep-sea thermal vents, use the reduction of sulfates coupled with the oxidation of organic compounds or hydrogen as an energy source for chemosynthesis.

The sulfide mineral Pyrite, FeS2

High quantities of organic carbon in the sediment form a barrier to oxygen in the water. This also works to encourage anaerobic respiration. Anaerobic respiration using sulphate releases hydrogen sulphide, which is one of the major components in pyrite. 

So, when we find a fossil preserved in pyrite, we know that it died and was buried in sediment with low quantities of oxygen and high quantities of organic carbon. 

If you have pyrite specimens and want to stop them from decaying, you can give them a 'quick' soak in water (hour max) then wash them off, dry thoroughly in a warm oven. 

Cool, then soak in pure acetone for a couple of days. Then soak in paraloid, a thermoplastic resin surface coating or acetone for a couple of days. Keep in a sealed container with a desiccant pack afterwards to keep them dry — or leave them out on display to enjoy knowing that the decay will come in time. We do this with cut flowers so why not fossils sometimes.

I have a friend who gives her pyrite fossils on display a quick thumb wipe with vasoline or petroleum jelly. I'm not sure if the hydrocarbons there will play nice over time but it will act as a protective barrier.