MAMMOTH LAST MEAL

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

Despite this initial review, numerous apocryphal tales exist of dinners made from centuries-old mammoths found frozen whole in clear blocks of ice. These accounts have not only enchanted the public but also heavily influenced early scientific thought on Quaternary extinctions and climate; many researchers resorting to catastrophism to explain the instantaneous freezing necessary to preserve palatable meat.

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

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

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

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

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

Green Sea Turtle, Chelonia mydas

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

The specimen is now permanently deposited in the Yale Peabody Museum with the designation YPM HERR 19475 and is accessible to outside researchers. The meat was never fixed in formalin and was initially stored in isopropyl alcohol before being transferred to ethanol when it arrived at the Peabody Museum. DNA extraction occurred at Yale University in a clean room with equipment reserved exclusively for aDNA analyses.

In 2016, Jessica Glass and her colleagues sequenced a fragment of the mitochondrial cytochrome-b gene and studied archival material to verify its identity, which if genuine, would extend the range of Megatherium over 600% and alter views on ground sloth evolution. Their results showed that the meat was not Mammoth or Megatherium, but a bit of Green Sea Turtle, Chelonia mydas. So much for elaborate legends. The prehistoric dinner was likely meant as a publicity stunt. Glass's study emphasizes the value of museums collecting and curating voucher specimens, particularly those used for evidence of extraordinary claims. Not so long before Glass et al. did their experiment, a friend's mother (and my kayaking partners) served up a steak from her freezer to dinner guests in Castlegar that hailed from 1978. Tough? Inedible? I have it on good report that the meat was surprisingly divine.

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

SUNSHINE AND SUPERNOVAE

Sunsets — pure visual poetry: peaceful, meditative, mesmerizing.

What is sunlight, actually? Yes, it's light from the Sun but so much more than that. Sunlight is both light and energy. Once it reaches Earth, we call this energy, "insolation," a fancy term for solar radiation. The amount of energy the Sun gives off changes over time in a never-ending cycle.

Solar flares (hotter) and sunspots (cooler) on the Sun's surface impact the amount of radiation headed to Earth. These periods of extra heat or extra cold (well, cold by Sun standards...) can last for weeks, sometimes months. The beams that reach us and warm our skin are electromagnetic waves that bring with them heat and radiation, by-products of the nuclear fusion happening as hydrogen nuclei fuse and shift violently to form helium, a process that fires every star in the sky.

Our bodies convert the ultraviolet rays to Vitamin D. Plants use the rays for photosynthesis, a process of converting carbon dioxide to sugar and using it to power their growth (and clean our atmosphere!) That process looks something like this: carbon dioxide + water + light energy — and glucose + oxygen = 6 CO2(g) + 6 H2O + photons → C6H12O6(aq) + 6 O2(g).

Photosynthetic organisms convert about 100–115 thousand million metric tonnes of carbon to biomass each year, about six times more power than used us mighty homo sapien sapiens. Our plants, forests and algae soak up this goodness and much later in time, we harvest this energy from fossil fuels.

We've yet to truly get a handle on the duality between light as waves and light as photons. The duality of the two-in-oneness of light; of their waves and alter-ego, particle photons is a physicists delight. Einstein formulated his special theory of relativity in part by thinking about what it would be like to ride around on these waves. What would space look and feel like? How would time occur? It bends the mind to consider. His wave-particle view helped us to understand that these seemingly different forms change when measured. To put this in plain English, they change when viewed, ie. you look them "in the eye" and they behave as you see them.

Light fills not just our wee bit of the Universe but the cosmos as well, bathing it in the form of cosmic background radiation that is the signature of the Big Bang and the many mini-big bangs of supernovae as they go through cycles of reincarnation and cataclysmic death — exploding outward and shining brighter than a billion stars.

In our solar system, once those electromagnetic waves leave the Sun headed for Earth, they reach us in a surprising eight minutes. We experience them as light mixed with the prism of beautiful colours. But what we see is actually a trick of the light. As rays of white sunlight travel through the atmosphere they collide with airborne particles and water droplets causing the rays to scatter.

We see mostly the yellow, orange and red hues (the longer wavelengths) as the blues and greens (the shorter wavelengths) scatter more easily and get bounced out of the game rather early.

HOLDERNESS AMMONITE

An unusual Yorkshire Holderness ammonite about 5cm across found by Harry Tabiner. He’s found a few of these specimens preserved completely with calcite making them hard to prepare. It’s possibly Kosmoceras, a middle Jurassic ammonite.

The Geology of Yorkshire in northern England shows a very close relationship between the major topographical areas and the geological period in which their rocks were formed. The rocks of the Pennine chain of hills in the west are of Carboniferous origin whilst those of the central vale are Permo-Triassic.

The North York Moors in the north-east of the county are Jurassic in age while the Yorkshire Wolds to the southeast are Cretaceous chalk uplands. The plain of Holderness and the Humberhead levels both owe their present form to the Quaternary ice ages. The strata become gradually younger from west to east. Much of Yorkshire presents heavily glaciated scenery as few places escaped the direct or indirect impact of the great ice sheets as they first advanced and then retreated during the last ice age. This beauty is in the collection of the deeply awesome Harry Tabiner.

CORAL: CLIMATE CHANGE INDICATORS

A lovely specimen of fossilized coral. Corals are marine invertebrates within the class Anthozoa of the phylum Cnidaria. They typically live in compact colonies of many identical individual polyps.

Annual growth bands in some corals, such as the deep-sea bamboo coral, Isididae, may be among the first signs of the effects of ocean acidification on marine life. The growth rings allow geologists to construct year-by-year chronologies, a form of incremental dating, which underlies high-resolution records of past climatic and environmental changes using geochemical techniques.

Certain species form communities called microatolls, which are colonies whose top is dead and mostly above the waterline, but whose perimeter is mostly submerged and alive. The average tide level limits their height. By analyzing the various growth morphologies, microatolls offer a low-resolution record of sea-level change. Fossilized microatolls can also be dated using Radiocarbon dating. Such methods can help to reconstruct Holocene sea levels.

Increasing sea temperatures in tropical regions, ~1 degree C, over the last century have caused major coral bleaching, death, and collapsing of coral populations since although they are able to adapt and acclimate. It is uncertain if this evolutionary process will happen quickly enough to prevent a major reduction of their numbers.

Though coral has large sexually-reproducing populations, their evolution can be slowed by abundant asexual reproduction. Gene flow is variable among coral species. According to the biogeography of coral species gene flow cannot be counted on as a dependable source of adaptation as they are very stationary organisms. Also, coral longevity might factor into their adaptivity.

However, adaptation to climate change has been demonstrated in many cases. These are usually due to a shift in coral and zooxanthellae genotypes. These shifts in allele frequency have progressed toward more tolerant types of zooxanthellae. Scientists found that a certain scleractinian zooxanthella is becoming more common where sea temperature is high. Symbionts able to tolerate warmer water seem to photosynthesize more slowly, implying an evolutionary trade-off.

In the Gulf of Mexico, where sea temperatures are rising, cold-sensitive staghorn and elkhorn coral have shifted in location. Not only have the symbionts and specific species been shown to shift, but there seems to be a certain growth rate favorable to selection. Slower-growing but more heat-tolerant corals have become more common. The changes in temperature and acclimation are complex. Some reefs in current shadows represent a refugium location that will help them adjust to the disparity in the environment even if eventually the temperatures may rise more quickly there than in other locations. This separation of populations by climatic barriers causes a realized niche to shrink greatly in comparison to the old fundamental niche.

CORAL COLONIES

Coral colony and Soldier Fish, Great Barrier Reef, Australia

Corals are marine invertebrates within the class Anthozoa of the phylum Cnidaria. They typically live in compact colonies of many identical individual polyps.

Corals are important reef builders that inhabit tropical oceans and secrete calcium carbonate to form a hard skeleton.

A coral "group" is a colony of a myriad of genetically identical polyps. Each polyp is a sac-like animal typically only a few millimetres in diameter and a few centimetres in length. A set of tentacles surround a central mouth opening. Each polyp excretes an exoskeleton near the base. Over many generations, the colony thus creates a skeleton characteristic of the species which can measure up to several meters in size. Individual colonies grow by asexual reproduction of polyps. Corals also breed sexually by spawning: polyps of the same species release gametes simultaneously overnight, often around a full moon. Fertilized eggs form planulae, a mobile early form of the coral polyp which when mature settles to form a new colony.

Although some corals are able to catch plankton and small fish using stinging cells on their tentacles, most corals obtain the majority of their energy and nutrients from photosynthetic unicellular dinoflagellates of the genus Symbiodinium that live within their tissues. These are commonly known as zooxanthellae and gives the coral colour. Such corals require sunlight and grow in clear, shallow water, typically at depths less than 60 metres (200 ft). Corals are major contributors to the physical structure of the coral reefs that develop in tropical and subtropical waters, such as the Great Barrier Reef off the coast of Australia. These corals are increasingly at risk of bleaching events where polyps expel the zooxanthellae in response to stress such as high water temperature or toxins.

Other corals do not rely on zooxanthellae and can live globally in much deeper water, such as the cold-water genus Lophelia which can survive as deep as 3,300 metres (10,800 ft). Some have been found as far north as the Darwin Mounds, northwest of Cape Wrath, Scotland, and others off the coast of Washington State and the Aleutian Islands.

TUZOIA OF THE BALANG FORMATION

A large extinct bivalved arthropod, Tuzoia sinesis (Pan, 1957) from Cambrian deposits of the Balang Formation. The Balang outcrops in beautiful Paiwu, northwestern Hunan Province in southern China. The site is intermediate in age between the Lower Cambrian Chengjiang fauna of Yunnan and the Lower to Middle Cambrian, Kaili Lagerstätten of Guizhou in southwestern China.

This specimen was collected in October 2019. It is one of many new and exciting arthropods to come from the site. Balang has a low diversity of trilobites and many soft-bodied fossils similar in preservation to Canada's Burgess Shale.

Some of the most interesting finds include the first discovery of anomalocaridid appendages (Appendage-F-type) from China along with the early arthropod Leanchoiliids with his atypical frontal appendages (and questionable phylogenetic placement) and the soft-shelled trilobite-like arthropod, Naraoiidae.

Jianheaspis jiaobangensis, is a newly described trilobite also from the Lower Cambrian Balang Formation of Guizhou Province, China. While the site is not as well-studied as the Chengjiang and Kaili Lagerstätten, it looks very promising. The exceptionally well-preserved fauna includes algae, sponges, chancelloriids, cnidarians, worms, molluscs, brachiopods, trilobites and a few non-mineralized arthropods. It is an exciting time for Cambrian paleontology. The Balang provides an intriguing new window into our ancient seas and the profound diversification of life that flourished there.

ZEACINITIES MAGNOLIAEFORMIS

This lovely specimen is Zeacrinites magnoliaeformis, an Upper Mississippian-Chesterian crinoid found by Keith Metts in the Glen Dean Formation, Grayson County, Kentucky, USA.

Crinoids are unusually beautiful and graceful members of the phylum Echinodermata. They resemble an underwater flower swaying in an ocean current. But make no mistake they are marine animals. Picture a flower with a mouth on the top surface that is surrounded by feeding arms. Awkwardly, add an anus right beside that mouth. That's him!

Crinoids with root-like anchors are called Sea Lilies. They have graceful stalks that grip the ocean floor. Those in deeper water have longish stalks up to 3.3 ft or a meter in length.

Then there are other varieties that are free-swimming with only vestigial stalks. They make up the majority of this group and are commonly known as feather stars or comatulids. Unlike the sea lilies, the feather stars can move about on tiny hook-like structures called cirri. It is these same cirri that allows crinoids to latch to surfaces on the seafloor. Like other echinoderms, crinoids have pentaradial symmetry. The aboral surface of the body is studded with plates of calcium carbonate, forming an endoskeleton similar to that in starfish and sea urchins.

These make the calyx somewhat cup-shaped, and there are few, if any, ossicles in the oral (upper) surface called a tegmen. It is divided into five ambulacral areas, including a deep groove from which the tube feet project, and five interambulacral areas between them. The anus, unusually for echinoderms, is found on the same surface as the mouth, at the edge of the tegmen.

Crinoids are alive and well today. They are also some of the oldest fossils on the planet. We have lovely fossil specimens dating back to the Ordovician.

PHYLLOCERAS PONTICULI DE CORDOBA

Phylloceras (Hypophylloceras) ponticuli from the Subbético Externo de Córdoba, a fast-moving carnivorous ammonite. This classical Tethyan Mediterranean specimen is very well preserved, showing much of his delicate suturing in intricate detail. Phylloceras were primitive ammonites with involute, laterally flattened shells.

They were smooth, with very little ornamentation, which led researchers to think of them resembling plant leaves and gave rise to their name, which means leaf-horn. They can be found in three regions that I know of.  In the Jurassic of Italy near western Sicily's Rosso Ammonitico Formation, Lower Kimmeridgian fossiliferous beds of Monte Inici East and Castello Inici (38.0° N, 12.9° E: 26.7° N, 15.4° E) and in the Arimine area, southeastern Toyama Prefecture, northern central Japan, roughly, 36.5° N, 137.5° E: 43.6° N, 140.6° E. And in Madagascar, in the example seen here found near Sokoja, Madagascar, off the southeast coast of Africa at 22.8° S, 44.4° E: 28.5° S, 18.2° E. Photo: Manuel Peña Nieto

PHYLLOCERAS VELLEDAE

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

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

These ammonites make a lovely addition to any teaching collection as they provide a lot of detail and can be handled quite well by small, less gentle hands. Like other cephalopods, ammonites had sharp, beak-like jaws inside a ring of squid-like tentacles that extended from their shells. They used these tentacles to snare prey, — plankton, vegetation, fish and crustaceans — similar to the way a squid or octopus hunt today.

Catching a fish with your hands is no easy feat, as I'm sure you know. But the Ammonites were skilled and successful hunters. They caught their prey while swimming and floating in the water column. Within their shells, they had a number of chambers, called septa, filled with gas or fluid that were interconnected by a wee air tube. By pushing air in or out, they were able to control their buoyancy in the water column.

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

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

LENS ON SEPTARIAN NODULES

Septarian Nodule, Dan Bowen, 2020 Tucson Gem and Mineral Show

An exceptional polished septarian nodule with an ammonite heart. Septarian concretions or septarian nodules are concretions containing angular cavities or cracks, called "septaria." These septaria can be filled 

The word comes from the Latin word septum; "partition", and refers to the cracks/separations in this kind of rock.

The process that created the septaria that characterize septarian concretions remains unclear. A number of mechanisms have been proposed, including the dehydration of clay-rich, gel-rich, or organic-rich cores; shrinkage of the concretion's center; expansion of gases produced by the decay of organic matter; or brittle fracturing or shrinkage of the concretion interior by either earthquakes or compaction.

The cracks or patterns you see here are highly variable in shape and volume, as well as the degree of shrinkage they indicate. Although it has commonly been assumed that concretions grew incrementally from the inside outwards, the fact that radially oriented cracks taper towards the margins of septarian concretions is taken as evidence that in these cases the periphery was stiffer while the inside was softer, presumably due to a gradient in the amount of cement precipitated.

A spectacular example of septarian concretions, which are as much as 3 meters (9.8 feet) in diameter, are the Moeraki Boulders. These concretions are found eroding out of Paleocene mudstone of the Moeraki Formation exposed along the coast near Moeraki, South Island, New Zealand. They are composed of calcite-cemented mud with septarian veins of calcite and rare late-stage quartz and ferrous dolomite.

Beautiful smaller septarian concretions are found in the Kimmeridge Clay exposed in cliffs along the Wessex Coast of England. As as you walk the beach, look for exposures of Speeton Clay beds D6 and D7, the bentonite horizons that weather to yellow colouration. Beneath the Speeton Shell Bed cliff exposures is an exposure of Kimmeridge Clay, UK. This outcrop contains concretions that show the characteristic 'turtle-stone' patterns of these septarian nodules.

Photo top: Dan Bowen, Chair, VIPS, 2020 Tucson Gem and Mineral Show.

References: Humberside Geologist No. 14, Humberside Geologist Online, The geology of East Yorkshire coast.http://www.hullgeolsoc.co.uk/hg146t.htm

Dale, P.; Landis, C. A.; Boles, J. R. (1985-05-01). "The Moeraki Boulders; anatomy of some septarian concretions". Journal of Sedimentary Research. 55 (3): 398–406.

Milliken, Kitty L.; Picard, M. Dane; McBride, Earle F. (2003-05-01). "Calcite-Cemented Concretions in Cretaceous Sandstone, Wyoming and Utah, U.S.A." Journal of Sedimentary Research. 73 (3): 462–483. Bibcode:2003JSedR..73..462M. doi:10.1306/111602730462. ISSN 1527-1404.

AMMONITES: INDEX FOSSILS

Ammonites 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 their fossilized remains (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. Photo: Dan Bowen, 2020 Tucson Gem and Mineral Show.

HOLCOPHYLLOCERAS MEDITERRANEUM

There is tremendously robust suturing on this lovely ammonite, Holcophylloceras mediterraneum, (Neumayr 1871) from Late Jurassic (Oxfordian) deposits near Sokoja, Madagasgar.

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.

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.

The shells had many chambers divided by walls called septa. The chambers were connected by a tube called a siphuncle which allowed for the control of buoyancy with the hollow inner chambers of the shell acting as air tanks to help them float. We can see the edges of this specimen's shell where it would have continued out to the last chamber, the body chamber, where the ammonite lived. Picture a squid or octopus, now add a shell and a ton of water.

ANDROGYNOCERAS OF YORKSHIRE

A stunning example of the ammonite Androgynoceras from the Yorkshire Coast, England.

The Geology of Yorkshire in northern England shows a very close relationship between the major topographical areas and the geological period in which their rocks were formed. The rocks of the Pennine chain of hills in the west are of Carboniferous origin whilst those of the central vale is Permo-Triassic.

The North York Moors in the north-east of the county are Jurassic in age while the Yorkshire Wolds to the southeast are Cretaceous chalk uplands.

The plain of Holderness and the Humberhead levels both owe their present form to the Quaternary ice ages. The strata become gradually younger from west to east. Much of Yorkshire presents heavily glaciated scenery as few places escaped the direct or indirect impact of the great ice sheets as they first advanced and then retreated during the last ice age. This beauty is in the collection of the deeply awesome Harry Tabiner.

MIDDLE TRIASSIC HUMBOLDT RANGE

Looking out over the Middle Triassic exposures of the Humboldt Mountain Range.

These hills were the site of the 1905 Expedition of the University of California’s Department of Geology in Berkeley funded by the beautiful and bold, Annie Alexander, the women to whom the UCMP owes both its collection and existence. Annie brought together a paleontological crew to explore these localities and kept an expedition journal of their trip which is now on display at the University of California Museum of Paleontology at Berkeley.

Annie's interest was the ichthyosaurs and she was well pleased with the results. They dodged rattlesnakes and tarantulas, finding many new specimens as they opened up new quarries in the hills of the Humboldt Range of Nevada.

Ichthyosaurs range from quite small, just a foot or two, to well over twenty-six metres in length and resembled both modern fish and dolphins. The specimens from Nevada are especially large and well-preserved. They hail from a time, some 217 million years ago, when Nevada, and parts of the western USA, was covered by an ancient ocean that would one day become our Pacific Ocean. Many ichthyosaur specimens have come out of Nevada. So many, in fact, that they named it their State Fossil back in 1977.

Fossil fragments and complete specimens of these marine reptiles have been collected in the Blue Lias near Lyme Regis and the Black Ven Marls. More recently, specimens have been collected from the higher succession near Seatown. Paddy Howe, Lyme Regis Museum geologist, found a rather nice Ichthyosaurus breviceps skull a few years back. A landslip in 2008 unveiled some ribs poking out of the Church cliffs and a bit of digging revealed the ninth fossil skull ever found of a breviceps, with teeth and paddles to boot.

Specimens have since been found in Europe in Belgium, England, Germany, Switzerland and in Indonesia. Many tremendously well-preserved specimens come from the limestone quarries in Holzmaden, southern Germany.

AMMONITE: INDEX FOSSILS

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.

UPPER CRETACEOUS NANAIMO GROUP AT HORNBY ISLAND

Hornby is a delightful island off the east coast of Vancouver Island, just east of Denman Island. Texada and Lasqueti lie just to the west of Hornby. It is home to about 1,000 residents made up of artists, retirees and those wanting to enjoy the quiet, rural, community-oriented lifestyle.

Hornby Island is formed from sediments of the upper Nanaimo Group which are also widely exposed on adjacent Denman Island and the southern Gulf Islands. Peter Mustard, a geologist from the Geologic Survey of Canada, did considerable work on the geology of the island. It has a total stratigraphic thickness of 1350 m of upper Nanaimo Group marine sandstone, conglomerate and shale.

These are partially exposed in the Campanian to the lower Maastrichtian outcrops at Collishaw Point on the northwest side of Hornby Island. Four formations underlie the island from oldest to youngest, and from west to east: the Northumberland, Geoffrey, Spray and Gabriola.

During the upper Cretaceous, between ~90 to 65 Ma, sediments derived from the Coast Belt to the east and the Cascades to the southeast poured seaward to the west and northwest into what was the large ancestral Georgia Basin. This major forearc basin was situated between Vancouver Island and the mainland of British Columbia.

The island's soils have developed from marine deposits of variable texture, except for the higher elevations and steeper slopes where weathered clastic sedimentary rock provides the parent material. Most of Hornby's soils are sandy or gravelly, but some deep black loams occur in the northwestern part and many of the sands at the southern end have loam-textured topsoils.

Collishaw Point, known locally as Boulder Point, Hornby Island

Podzols are common and the bleached sand grains associated with their eluvial (A2, Ae or E) horizons lend a salt-and-pepper appearance to many forest trails. In most cases, though, the E is not very thick and may, in fact, be discontinuous. For this reason, the soils were mostly classified as Brown Podzolic in a soil survey published in 1959.

All of the island's soils are strongly acidic in their natural state except for those which have developed on shoreline shell middens.

And it is to the shore that many are drawn — locals, tourists, geologists and paleontologists alike. Hornby is a wonderful place to explore. The island is beautiful in its own right and the fossils from here often keep some of their original shell or nacre which makes them quite fetching.

The Nanaimo Group as a whole represents largely coarse-grained units deposited in deep-sea fan systems. In this environment, deeper channels continuously cut through successive shale and sandstone bodies. The channels funnelled density currents into the basin, while also building levee deposits. Turbidity currents travelled down the channels, and also overtopped the levees spilling across backslope areas. The sequential sediment formations, from significantly coarse-grained sandstones and conglomerates to fine silts and shale units of the Nanaimo Group, are considered to be partly due to eustacy, but more significantly related to relative sea-level changes induced by regional tectonics in an active forearc setting.

The Northumberland Formation consists of a massive, dark-grey mudstone which is locally interlaminated and interbedded with siltstone and fine-grained sandstone.

There are abundant calcium carbonate concretions, parallel and current ripple laminations, clastic dikes and folded layers due to slumping. In the Gulf Islands to the south, this formation has been found to contain abundant and diverse foraminifera indicating marine paleodepths of 150-1200 m.

The more resistive Geoffrey Formation consists of thick-bedded sandstone and conglomerate. It is highly channelized, and some sandstone has exposed parallel and ripple laminations. The Spray Fm exposed on the east end of the island is a massive olive-grey mudstone with interlaminations of sandstone.

Furthest to the east, the youngest exposures on Hornby Island are from the Gabriola Formation, which outcrops on the eastern peninsula. This is again a thick-bedded and channelized sequence of conglomerates and massive sandstone with minor mudstone interbeds. South, in the Gulf Islands, this formation has contained ammonites, gastropods and pelecypods. Paleowater-depth from foraminiferal assemblages has been set at 200 m.

Katnick, D.C. and P.S. Mustard (2001): Geology of Denman and Hornby Islands, British Columbia (NTS 92F/7E, 10); British Columbia Geological Survey Branch, Geoscience Map 2001-3.

England, T.D.J. and R. N. Hiscott (1991): Upper Nanaimo Group and younger strata, outer Gulf Islands, southwestern British Columbia: in Current Research, Part E; Geological Survey of Canada, Paper 91-1E, p. 117-125.

LIVING FOSSIL: HEDGEHOGS

This little cutie is a Western European hedgehog, Erinaceus europaus, in the subfamily Erinaceinae (Fischer, 1814). They are native to western Europe, Asia, Africa and have been introduced (oops!) to New Zealand.

There are seventeen species of hedgehog in five genera. They share distant ancestry with the family Soricidae (shrews) and the gymnures.

Hedgehogs are considered "Living Fossils" as they have changed very little over the past 15 million years. These small mammals are loners with their own kind but live in close proximity to our human population. They dwell in inhabited areas, farmland, deciduous forests and desert. You'll know them by their distinctive spiny look (which may remind you of very tasty chocolates from Purdy's in Canada) and their adorable piglike snorts and grunts as they make their way through the underbrush looking for tasty snacks.

Look for them in the evening in hedgerows and undergrowth as they hunt for frogs, toads, snails, bird eggs, grassroots, berries, insects, worms and snakes. They fatten themselves up in preparation for hibernation. They'll find a nice burrow or built a nest in leaves or compost heaps. In Europe, they generally hibernate by October or November and become active again in March to mid-April once temperatures reach over 15 degrees.

JURASSIC STILL LIFE

This beautiful block, an ancient Still Life of the Jurassic (Callovian) hails from outcrops near Anwil, a municipality in the district of Sissach in the canton of Basel-Country in Switzerland.

It is a tremendous block showing the fauna from that time. Ammonites and Trigonia are clustered together. This specimen was found and prepared by the talented Tim Haye. Tim made the find during his inspection of a 2014 excavation through the Bern and Basel Museums.

PALEONTOLOGIE FRANCAISE

Paléontologie Française: Alcide d'Orbigny

L'un des grands classiques, Paléontologie Française: Zoologique Et Géologique de Tous les Animaux Mollusques Et Rayonnés Fossiles de France, Comprenant Leur Application A la Reconnaissance des Couches; Terrains Crétacés, Supplément. Voici une citation de cette édition:

"Eepl. Des fig. Pl. 4, fig. 4, cône alvéolaire de grandeur naturelle, vu de profil; a la tige: la partie ombrée est ce qu'on connaît en nature, le reste est supposé fig.

Le même, vu en dessus; fig. 3, godet terminal, supposé d'après les lignes d'accroissement; fig. 4, coquille entière, supposée d'après les lignes d'accroissement marquées sur le cône alvéolaire; fig. 5, la figure 2 grossie, la partie non ombrée supposée; fig. 6, la figure grossie; et, partie supposée; b, partie positive; fig. 7, cône alvéolai're vu en dessus, avec son siphon ventre, de ma collection."

PRIMITIVE PTERASPIDOMORPHS

The oldest and most primitive pteraspidomorphs were the Astraspida and the Arandaspida.

They evolved in shallow equatorial seas, as a large diverse and widespread group of armoured, jawless fishes: the Pteraspidomorphi. The first of three groups of ostracoderms.

The Pteraspidomorphi are divided into three major groups: the Astraspida, Arandaspida and the Heterostraci. You'll notice that their taxon names contain 'aspid', which means shield. This is because these early fishes and many of the Pteraspidomorphi possessed large plates of dermal bone at the anterior end of their bodies. This dermal armour was very common in early vertebrates, but it was lost in their descendants.

Arandaspida is represented by two well-known genera: Sacabampaspis, from South America and Arandaspis from Australia. Arandaspis have large, simple, dorsal and ventral head shields. Their bodies were fusiform, which means they were shaped sort of like a spindle, fat in the middle and tapering at both ends. Picture a sausage that is a bit wider near the centre with a crisp outer shell.

Photo by Nobu Tamura (http://spinops.blogspot.com) - Own work, CC BY-SA 3.0, https://commons.wikimedia.org/w/index.php?curid=19460450

JUVENILE HAMITES SUBROTUNDUS

A tremendously delicate juvenile Hamites subrotundus (J. Sowerby 1814) from Upper Albian outcrops in Mallorca, the largest of the Spanish Balearic Island in the Mediterranean. It is famous for its limestone mountains and Roman and Moorish remains. As you can see here, it is also home to some rather nice fossils including this specimen of Hamites subrotundus.

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

Mallorca and the other Balearic Islands are geologically an extension of the Betic Cordillera of Andalusia. They are made up of sediments deposited in the Tethys Sea during the Mesozoic.

Exploring the islands, you can collect from deposits from the Triassic, Cretaceous, Jurassic, and Neogene periods. The limestone outcrops contain many foraminifers of the species Globigerina.

We also see lovely examples of Hamites (Hamites) subrotundus in the Euhoplites loricatus zone; Euhoplites meandrinus subzone from the Middle Albian (Lower Gault) of Folkestone, Kent, UK. Photo, preparation and in the collection of the deeply awesome José Juárez Ruiz. Wright C. W. 1996. Treatise on Invertebrate Paleontology (Part L Mollusca 4 Revised) Volume 4: Cretaceous Ammonoidea

GRAPTOLITES: DARLINGS OF THE DARRIWILIAN

Back in 2009, Jörg Maletz from St. Francis Xavier University, Antigonish, Nova Scotia, did a paper looking at the Les Méchins region in Quebec to compare the Darriwilian graptolite succession found there against other outcrops of eastern North America.

The graptolite faunas of the upper member of the Anse au Crapaud Formation include the Arienigraptus gracilis, Oncograptus upsilon, Undulograptus austrodentatus, and Holmograptus spinosus biozone faunas and, thus, complement the well known Darriwilian faunas of the Cow Head, Table Head, and Goose Tickle groups of western Newfoundland. In particular, the Holmograptus spinosus Biozone interval of calcarenitic limestones bears a rare combination of benthic (shelly) and planktic (graptolitic) faunas with conodonts, brachiopods, ostracods, sponge spicules, and algal remains associated with common graptolites that allow an inter-continental correlation.

The Holmograptus spinosus Biozone is introduced for the interval based on a diverse and characteristic graptolite fauna. The fauna includes among others, Atopograptus woodwardi, recognized for the first time in North America. The Holmograptus spinosus Biozone fauna can be found worldwide and is easily correlated into the conodont biofacies using species of the genus Histiodella. He looked at ties between graptolite and conodont biozonations for the Darriwilian. Some lovely silicified ostracods were illustrated for the first time from the interval and a new species, Hustedograptus quebecensis, was introduced.

The Darriwilian or late Middle Ordovician time interval shows a dramatic re-organization of graptolite faunas, both in their taxonomic composition and in their rhabdosome developmental style.

The Early Ordovician graptolite faunas, composed of multiramous to pauciramous “Dichograptaceans” (Bulman 1970), are slowly replaced by dipleural biserial graptolites of the “Diplograptaceans” (Mitchell et al. 1995, 2007) or Axonophorans (Maletz et al. 2009).

This shift started with the introduction of the reclined isograptids and glossograptids in the Dapingian and culminated with the extinction of multiramous sinograptids and stem reclinatids in the Darriwilian (Da 2 – Da 3), leaving but few survivors to reach the Late Ordovician. The monopleural glossograptids, as a second clade of the Bireclinata, enjoyed moderate success in the mid and Late Ordovician, but never attained the high diversity of the Axonophorans.

The Darling Darriwilian

The Darriwilian is a significant stage in the Middle Ordovician. It is here we see the first land plants and the introduction of the Undulograptus austrodentatus graptolite zone. These graptolite outcrops from around the world help us establish the base of the Darriwilian as an easily correlatable marker in time. Yet, for so many reasons, the charming Darriwilian has not received the attention in graptolite studies it deserves and little is known about many of the graptolites from the interval.

The biostratigraphy within this time interval remains only partially explored due to a scarcity of uninterrupted successions. The Darriwilian in Victoria, Australia (Vandenberg and Cooper 1992) is based on numerous spot collections, but successions spanning more than a single graptolite zone are not available. The base of the Darriwilian is now defined at the first appearance datum (FAD) of Undulograptus austrodentatus in the Huangnitang section (Zhejiang, China), but the graptolitic succession is less detailed and complete in the higher part of the interval (see Chen et al. 2006).

The northern Appalachian successions in Quebec and western Newfoundland provide numerous successions from which detailed biostratigraphical data are available, but most sections are poorly studied. Recent advances show the presence of good Darriwilian graptolite faunas in the Cow Head, Table Head, and Goose Tickle groups of western Newfoundland (Williams and Stevens 1988; Maletz 1992c; Taylor 1997) and China (Chen et al. 2006) that provide a better insight into the biostratigraphy and evolutionary history of graptolites in this interval.

Lithostratigraphic Succession at Les Méchins

The southern shore of the St. Lawrence River along the coast of the Gaspé Peninsula of Quebec exposes Cambrian to Ordovician continental slope sequences, representing the allochthonous thrust slices of the Humber tectonostratigraphic zone of Williams (1979). The successions were thrust westwards across the eastern rim of Laurentia during the Taconic Orogeny in the Middle Ordovician. Because of the complexity of the successions, the stratigraphy is only well defined in part and detailed biostratigraphic work is lacking for most regions.

Bernstein et al. (1992) described the lithostratigraphic succession at Les Méchins and provided detailed information on the location of the sections along the northern side of route 132, directly west of the entrance to Les Méchins.

As graptolites are the most important biostratigraphic indicators, their record can shed light on the structural complexity of the successions and help us to understand the geological evolution of this region. Newly discovered faunal successions at Les Méchins, Quebec have provided important biostratigraphical and biogeographical data and yielded taxa not previously found in North America.

Maletz, Jörg. Holmograptus spinosus and the Middle Ordovician (Darriwilian) graptolite biostratigraphy at Les Méchins (Quebec, Canada) Canadian Journal of Earth Sciences, 2009, 46:739-755, https://doi.org/10.1139/E09-048.

Albanesi, G., Hünicken, M.A., and Barnes, C.R. 1998. Bioestratigrafia de conodontes de las secuencias ordovicicas del Cerro Potrerillo, Precordillera central de San Juan, R. Argentina. Actas XII Academia Nacional de Ciencias., Córdoba, 12, pp. 7–72.

Bulman, O.M.B. 1970. Graptolithina with sections on Enteropneusta and Pterobranchia. In Treatise on invertebrate paleontology, Part V. 2nd ed. Edited by K. Teichert and R.C. Moore. Geological Society of America and University of Kansas Press, Boulder, Colo. and Lawrence, Kans., pp. 1–163.

Chen X, Zhang YD, Bergström SM, Xu H-G. 2006. Darriwilian graptolite and conodont zonation in the global stratotype section of the Darriwilian stage (Ordovician) at Huangnitang, Changshan, Zhejiang, China. Palaeoworld 15(2): 150-170.

ARIENIGRAPTUS OF BOLIVIA

Graptolites (Graptolita) are a group of colonial animals known primarily from Ordovician deposits. The biological affinities of the graptolites have always been debatable.

Originally regarded as being related to the hydrozoans, graptolites are now considered to be related to the pterobranchs, a rare group of modern marine animals.

The graptolites are classed as hemichordates (phylum Hemichordata), a phylum of marine deuterostome animals and come in a variety of weird and wonderful designs. They were a major component of the zooplankton in our early Paleozoic ecosystems, most likely living as suspension feeders, drifting freely on the surface of ancient seas or attached to floating seaweed by means of a slender thread. Some forms of graptolite lived attached to the sea-floor by a root-like base. The deceased planktonic graptolites would sink down to and settle on the seafloor, eventually becoming entombed in the sediment and are thus well-preserved.

Graptolite fossils are often found in shales and slates and can be mistaken for scratches on the rock. The name graptolite comes from the Greek graptos meaning "written", and lithos meaning "rock." It is a very suitable name as many graptolites look very much like hieroglyphs written on rock and not the impressions of animals.

Graptolites are common fossils and have a worldwide distribution. The preservation, quantity and gradual change over a geologic time scale of graptolites allow the fossils to be used to date strata of rocks throughout the world. They are important index fossils for dating Palaeozoic rocks as they evolved rapidly with time and formed many different species.

We find graptolite fossils flattened along the bedding planes of the rocks in which they occur. My first graptolite finds were from roadcuts up near Cranbrook, British Columbia, Canada. I was on a fossil field trip looking for Cambrian trilobites. It was a thrilling experience and completely unexpected when the first graptolite met my eyes.

They vary in shape, but are most commonly dendritic or branching (such as Dictoyonema), saw-blade like, or "tuning fork" shaped, such as Didymograptus murchisoni. The lovely specimen of Arienigraptus sp. you see here is from the Lower Darriwilian of Bolivia and in the collections of the deeply awesome Gilberto Juárez Huarachi‎. The second photo is from the Encyclopaedia Brittanica - From the Encyclopaedia Brittanica, Public Domain, https://commons.wikimedia.org/w/index.php?curid=6886878

PERSISTISTROMBUS LATUS

A beautiful example of two water-worn specimens of the gastropod Persististrombus latus (Gmelin, 1791) captured after a storm captured by the deeply awesome José Juárez Ruiz from Palma De Mallorca, Spain.

In his original description of Strombus latus, Gmelin describes this new species in his paper from 1791, page 3520: "latus. 35. Str. testae labro prominulo inferne bis emarginato, spirae anfractu primo medio laevi utrinque transversim striato, reliquis nodis obtusis coronatis."

Persististrombus latus is the most iconic representative of the Senegalese fauna, a fossil assemblage of tropical water organisms thought to have colonized the Mediterranean Sea during the last interglacial period.

Persististrombus latus has become an important stratigraphic marker of Marine Isotope Stage (MIS) 5.5, which allows for the correlation of raised coastal deposits, useful in studying sea-level variations and tectonic uplift.

Persististrombus latus is found in shallow marine sediments of Tyrrhenian age (∼124 ka) in several localities of the Italian peninsula. Gmelin's early work on the species is from upper Pleistocene deposits of the marine terraces of the Crotone peninsula of southern Italy. If you fancy a visit to this locality, head to: N38°45'00" - N39°04'60", E17°04'60" - E17°19'60".

Commonly known as the Bubonian Conch, this species of sea snail is a marine gastropod mollusk in the family Strombidae, the true conchs. These fellows are herbivorous, dining on wee bits of algae, seagrass and other detritus found along the seafloor. They grow to around 2.76" - 6.5" (7cm - 16.5cm). We find them in the fossil record and also as modern shells in the Atlantic Ocean along West Africa, Senegal, Gabon, Cape Verde, Ascension Island and Angola. They like it warm, preferring seas of 57.2 °F - 68 °F (14°C - 20°C).

Ronald Nalin, Valentina Alice Bracchi, Daniela Basso, Francesco Massari; Persististrombus latus (Gmelin) in the upper Pleistocene deposits of the marine terraces of the Crotone peninsula (southern Italy). Italian Journal of Geosciences ; 131 (1): 95–101. doi: https://doi.org/10.3301/IJG.2011.25

Gmelin J.F. (1791). Vermes. In: Gmelin J.F. (Ed.) Caroli a Linnaei Systema Naturae per Regna Tria Naturae, Ed. 13. Tome 1(6). G.E. Beer, Lipsiae [Leipzig]. pp. 3021-3910.

BAETIC CORDILLERA

This beautiful ammonite is Neocomites (Teschenites) flucticulus (Thieuloy, 1977) sharing a large boulder with a delicate, straight-shelled, heteromorph ammonite Bochianites. These beauties were found on a fossil field trip to Hauterivian, Early Cretaceous deposits in the Baetic Cordillera in the Spring of 2019. The Baetic Cordillera is one of the main systems of mountain ranges in Spain along the southern and eastern Iberian Peninsula. There are several productive outcrops here that yield lovely Cretaceous ammonites and other marine species.

Neocomites are known from about a dozen offshore marine deep subtidal Cretaceous deposits in France, Hungary, Italy, Romania, Slovakia and Ukraine. We also find Neocomites in the Cretaceous of British Columbia, Canada.

This lovely specimen is the first Neocomites I've seen come out of fossil deposits in Spain. It was found and prepped by the talented Manuel Peña Nieto of Córdoba, Spain.

RHACOLEPSIS AND CARDIAC OUTFLOW

This concretion contains a partially exposed Rhacolepis Buccalis, an extinct genus of ray-finned fossil fish in carbonate concretion from the Lower Cretaceous, Santana Formation, Brazil.

These ancient fish swam our Cretaceous seas 122-109 million years ago. Interestingly, we've been able to recover complete fossilized hearts from this species using X-ray synchrotron microtomography.

Lara Maldanis and her team published a paper on this back in 2016. They were looking at the evolution of cardiac outflow tracts in vertebrates and had a breakthrough moment when an x-ray revealed enough detail to show that Rhacolepis hearts contain a conus arteriosus containing at least five-valve rows making them a transitional morphology between the primitive, multivalve, conal condition and the derived, monovalvar, bulbar state of the outflow tract in modern actinopterygians.

Le premier et unique géoparc mondial UNESCO est situé dans le Cariri du Ceará (géoparc Araripe), dans l'intérieur semi-aride de la région Nordeste, Brésil. Reference: Maldanis et al. (2016) Heart fossilization is possible and informs the evolution of cardiac outflow tract in vertebrates.

SONGS OF THE CETACEAN

A mother humpback and her young charge. Mothers show a tremendous amount of affection and love to their young, often swimming so close together they touch noses.

The calves nurse for almost a year, growing slowly. Once nursed, they keep growing for another 8-10 years before reaching their full adult length. They grow up to 19 metres long and can weigh up to 40 tons (36 metric tons). 

Male humpbacks are known for their singing. They produce some of the most complex “songs” in the animal kingdom. We have recorded many of their high-pitched squeals, whistles and low, rumbling gurgles. Perhaps the males believe that those with the best vocal abilities attract the best mates. They certainly increase the connectedness of those living in their pod.

Humpback whales, Megaptera novaeangliae, are a species of baleen whale for whom I hold a special place in my heart. 

Baleens are whales who feed on plankton and other wee oceanic tasties that they consume through their baleens, a specialised filter of keratin that frames their mouths. There are fifteen species of baleen whales. They inhabit all major oceans, in a wide band running from the Antarctic ice edge to 81°N latitude.

In the Kwak̓wala language of the Kwakiutl or Kwakwaka'wakw, speakers of Kwak'wala, of the Pacific Northwest, whales are known as g̱wa̱'ya̱m. Both the California grey and the Humpback whale live on the coast. Only a small number of individuals in First Nation society had the right to harpoon a whale. It was generally only the Chief who was bestowed this great honour. 

Humpback whales like to feed close to shore and enter the local inlets. Around Vancouver Island and along the coast of British Columbia, this made them a welcome food source as the long days of winter passed into Spring.

Humpback whales are rorquals, members of the Balaenopteridae family that includes the blue, fin, Bryde's, sei and minke whales. The rorquals are believed to have diverged from the other families of the suborder Mysticeti during the middle Miocene. While cetaceans were historically thought to have descended from mesonychids— which would place them outside the order Artiodactyla— molecular evidence supports them as a clade of even-toed ungulates — our dear Artiodactyla. Baleen whales split from toothed whales, the Odontoceti, around 34 million years ago.

CETACEANS OF WASHINGTON STATE

Fossil Whale Bone

Oligocene Fossil Whale vertebrae from Majestic Beach, Olympic Peninsula, Washington State, USA.

These lovely water-worn specimens are difficult to ID to species with certainty but they likely hail from an early baleen whale. Found amongst the beach pebbles on the Olympic Peninsula, they are definitely cetacean and very likely baleen as this area is home to some of the earliest baleen whales in the Pacific Northwest.

In 1993, a twenty-seven million-year-old specimen was discovered in deposits nearby that represents a new species of early baleen whale. It is especially interesting as it is from a stage in the group’s evolutionary history when baleen whales transitioned from having teeth to filtering food with baleen bristles. Visiting researcher Carlos Mauricio Peredo studied the fossil whale remains, publishing his research to solidify Sitsqwayk cornishorum (pronounced sits-quake) in the annals of history.

Baby Gray Whale Eschrichtius robustus showing his baleen

The earliest baleen whales clearly had teeth, and clearly still used them. Modern baleen whales have no teeth and have instead evolved baleen plates for filter feeding. I've included a rather good close-up of a baby Gray Whale here that shows the baleen to good effect.

The baleen is the comb-like strainer that sits on the upper jaw of baleen whales and is used to filter food.

We have to ponder when this evolutionary change —moving from teeth to baleen — occurred and what factors might have caused it. Traditionally, we have sought answers about the evolution of baleen whales by turning to two extinct groups: the aetiocetids and the eomysticetids.

The aetiocetids are small baleen whales that still have teeth, but they are very small, and it remains uncertain whether or not they used their teeth. In contrast, the eomysticetids are about the size of an adult Minke Whale and seem to have been much more akin to modern baleen whales; though it’s not certain if they had baleen. Baleen typically does not preserve in the fossil record being soft tissue; generally, only hard tissue, bones & teeth, are fossilized.

UNLIKELY RHINOCEROS

The Miocene pillow basalts from the Lake Roosevelt National Recreation Area of central Washington hold an unlikely fossil mould of a small rhinoceros, preserved by sheer chance as it's bloated carcass sunk to the bottom of a shallow lake just prior to a volcanic explosion.

We've known about this gem for a long while now. The fossil was discovered by hikers back in 1935 and later cast by the University of California paleontologists in 1948. These were the Dirty Thirties and those living in Washington state were experiencing the Great Depression along with the rest of the country and the world. Franklin D. Roosevelt was President of the United States, navigating the States away from laissez-faire economics. Charmingly, Roosevelt would have his good name honoured by this same park in April of 1946, a few years before researchers at Berkeley would rekindle interest in the site.

Both hiking and fossil collecting was a fine answer to these hard economic times and came with all the delights of discovery with no cost for natural entertainment. And so it was that two fossil enthusiast couples were out looking for petrified wood just south of Dry Falls on Blue Lake in Washington State. While searching the pillow basalt, the Frieles and Peabodys came across a large hole high up in a cave that had the distinctive shape of an upside-down rhinoceros.

This fossil is interesting in all sorts of ways. First, we so rarely see fossils in igneous rocks. As you might suspect, both magma and lava are very hot. Magma, or molten rock, glows a bright red/orange as it simmers at a toasty 700 °C to 1300 °C (or 1300 °F to 2400 °F) in hot chambers beneath the Earth's surface.

During the late Miocene and early Pliocene, repeated basaltic lava floods engulfed about 63,000 square miles of the Pacific Northwest over a period of ten to fifteen million years. After these repeated bathings the residual lava accumulated to more than 6,000 feet.

As the magma pushes up to the surface becoming lava, it cools to a nice deep black. In the case of our rhino friend, this is how this unlikely fellow became a fossil. Instead of vaporizing his remains, the lava cooled relatively quickly preserving his outline as a trace fossil and remarkably, a few of his teeth, jaw and bones. The lava was eventually buried then waters from the Spokane Floods eroded enough of the overburden to reveal the remains once more.

Diceratherium tridactylum (Marsh, 1875)

Diceratherium (Marsh, 1875) is known from over a hundred paleontological occurrences from eighty-seven collections.

While there are likely many more, we've found fossil remains of Diceratherium, an extinct genus of rhinoceros, in the Miocene of Canada in Saskatchewan, China, France, Portugal, Switzerland, and multiple sites in the United States.

He's also been found in the Oligocene of Canada in Saskatchewan, and twenty-five localities in the US, specifically in Arizona, Colorado, Florida, Nebraska, North Dakota, Oregon,  South Dakota, Washington and Wyoming. We know a bit about him. He roamed a much warmer, wetter Washington state some 15 million years ago. By then, the Cascades had arrived and we'd yet to see the volcanic eruptions that would entomb whole forests up near Vantage in the Takama Canyon of Washington state. Diceratherium was a scansorial insectivore with two horns and a fair bit of girth. He was a chunky fellow, weighing in at about one tonne (or 2,200 lbs).

You are welcome to go see his final resting site beside the lake but it is difficult to reach and comes with its own risks. Head to the north end of Blue Lake in Washington. Take a boat and search for openings in the cliff face. You'll know you're in the right place if you see a white "R" a couple hundred feed up inside the cliff. Inside the cave, look for a cache left by those who've explored here before you. Once you find the cache, look straight up. That hole above you is the outline of the rhino.

If you don't relish the thought of basalt caving, you can visit a cast of the rhino at the Burke Museum in Seattle, Washington. They have a great museum and are pretty sporting as they've built the cast hardy enough to let folk climb inside. The Burke Museum recently underwent a rather massive facelift and has re-opened its doors to the public. You can now explore their collections in the New Burke, a 113,000 sq.ft. building at 4300 15th Ave NE, Seattle, WA 98105, United States. Or visit them virtually, at https://www.burkemuseum.org/

Photo: Robert Bruce Horsfall - https://archive.org/details/ahistorylandmam00scotgoog, Public Domain, https://commons.wikimedia.org/w/index.php?curid=12805514

Reference: Prothero, Donald R. (2005). The Evolution of North American Rhinoceroses. Cambridge University Press. p. 228. ISBN 9780521832403.

Reference: O. C. Marsh. 1875. Notice of new Tertiary mammals, IV. American Journal of Science 9(51):239-250

FOSSIL FAUNAS OF THE PACIFIC NORTHWEST

Some water-worn samples of the fossil bivalve Vertipecten fucanus from Lower Miocene deposits in the Clallam Formation.

These were collected on the foreshore near Clallam Bay, Olympic Peninsula, northwestern Washington. Range zones of pectinid bivalves provide a principal means of age determination and correlation of shallow-water, inshore facies for Washington state. Until Addicott's study from 1976, the area was considered middle Miocene. The new Lower Miocene designation can be credited in large part to the restricted stratigraphic range of Vertipecten fucanus (Dall) and the restricted and overlapping ranges of several other fossil mollusks collected from Alaska to California.

Neogene marine sediments of the West Coast of North America were deposited in a series of widely spaced basins that extended geographically from the western and northern Gulf of Alaska (60°N) to southern California (33°N). Rich molluscan faunas occur extensively throughout these deposits and form the basis for biostratigraphic schemes that are useful for correlating within and between individual basins.

Early biostratigraphic work was concerned with faunas from particular horizons and with the stratigraphic range of diverse taxa, such as Pecten and Turritella, without reference to other fossil groups. Succeeding work increasingly dealt with the relationships of molluscan zones to benthic and, later, planktonic foraminiferal stages. In recent years the age limits of Neogene molluscan stages have become better documented by reference to planktonic microfossils from dated DSDP cores and onshore faunas.

Neogene molluscan faunas from California, the Pacific Northwest states (Oregon and Washington), and southern Alaska have been treated separately due to differences in faunal composition and geographic isolation. As a result, a different biostratigraphic sequence has been described for each region.

Pacific Northwest stages have been formally named and defined, and their names are also used informally for Alaskan faunas. California Neogene stages were proposed early in this century, are in need of redescription, and their usage is informal. Precise correlations between the three regional sequences have not yet been achieved, due to the low number of co-occurring species and the general lack of planktonic microfossils in these largely shallow-water faunas. The objectives of ongoing research include the documentation of the faunas of California and Pacific Northwest stages; formal description of California stages; an improved correlation between regional stage sequences; refinement of age estimates for stage boundaries; and, the establishment of Neogene stages for Alaskan faunas.

PANOPEA ABRUPTA OF CLALLAM

This lovely large fossil bivalve is Panopea abrupta (Conrad) an extinct species of marine mollusc in the family Hiatellidae, subclass Heterodonta.

This specimen was collected from lower Miocene deposits in the Clallam Formation on the foreshore bordering the Strait of Juan de Fuca near Clallam Bay, Olympic Peninsula, northwestern Washington.

Clallam Bay is a sleepy little town on the northwestern edge of the Olympic Peninsula. It was founded back in the 1880s as a steamboat stop and later served as a Mill town. If you are planning to visit the fossil exposures, head to the edge of town where it meets the sea.

Once at the water's edge, head east along the shore until you can go no further. You'll find marine fossils in the sandstone on the shore and cliffs. Mind the tide as access to the fossil site is only possible at low or mid-tide. You'll have to swim for it if you time it poorly. Clallam Bay: 48°15′17″N 124°15′30″W. Near this site, there are many additional fossil localities to explore. In Sequim Bay, you can find Pleistocene vertebrates as well as Miocene cetacean bones near Slip Point. Near the Twin Post Office, you can find Oligocene nautiloids and bivalves (2.5km west in the bluff); You can find crabs including, Branchioplax in the Eocene limestone concretions from Neah Bay.

References: Addicott, Warren. Molluscan paleontology of the lower Miocene Clallam Formation, northwestern Washington, Geological Survey Paper 976.