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| Lytoceras sp. Photo: Craig Chivers |
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| The concretion prior to prep |
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| Lytoceras sp. Photo: Craig Chivers |
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| The concretion prior to prep |
Interestingly, we have recently found fossil evidence for manatees along the Texas coast dating back to the most recent ice age.
The discovery raises questions about whether manatees have been visiting for thousands of years, or if an ancient population of ice age manatees once called Texas home.
The findings were published in Palaeontologia Electronica by lead author Christopher Bell, a professor at the UT Jackson School of Geosciences with co-authors Sam Houston State University Natural History Collections curator William Godwin and SHSU alumna Kelsey Jenkins — now a graduate student at Yale University — and SHSU Professor Patrick Lewis.
The eight fossils described in the paper include manatee jawbones and rib fragments from the Pleistocene, the geological epoch of the last ice age. Most of the bones were collected from McFaddin Beach near Port Arthur and Caplen Beach near Galveston during the past 50 years by amateur fossil collectors who donated their finds to the SHSU collections.
The Jackson Museum of Earth History at UT holds two of the specimens. A lower jawbone fossil, which was donated to the SHSU collections by amateur collector Joe Liggio, jumpstarted the research.
Manatee jawbones have a distinct S-shaped curve that immediately caught Godwin's eye. But Godwin said he was met with scepticism when he sought other manatee fossils for comparison. He recalls reaching out to a local fossil enthusiast who told him point-blank, "there are no Pleistocene manatees in Texas."
But an examination of the fossils by Bell and Lewis proved otherwise. The bones belonged to the same species of manatee that visits the Texas coast today, Trichechus manatus. An upper jawbone donated by U.S. Rep. Brian Babin was found to belong to an extinct form of the manatee, Trichechus manatus bakerorum.
The age of the manatee fossils is based on their association with better-known ice age fossils and paleo-Indian artefacts that have been found on the same beaches.
It is assumed that the cooler ice age climate would have made Texas waters even less hospitable to manatees than they are today. But the fact that manatees were in Texas — whether as visitors or residents — raises questions about the ancient environment and ancient manatees. The Texas coast stretched much farther into the Gulf of Mexico and hosted wider river outlets during the ice age than it does today. Either the coastal climate was warmer than is generally thought, or ice age manatees were more resilient to cooler temperatures than manatees of today.
Subsurface imaging of the now flooded modern continental shelf reveals both a greater number of coastal embayments and the presence of significantly wider channels during ice age times.
If there was a population of ice age manatees in Texas, it is entirely plausible that they would have ridden out winters in these warmer river outlets similar to how they do today in Florida and Mexico.
Reference: Christopher Bell, William Godwin, Kelsey Jenkins, Patrick Lewis. First fossil manatees in Texas: Trichechus manatus bakerorum in the Pleistocene fauna from beach deposits along the Texas Coast of the Gulf of Mexico. Palaeontologia Electronica, 2020; DOI: 10.26879/1006
As a member of the subfamily Caprinae of the family Bovidae, the muskox is more closely related to sheep and goats than to oxen. It has been placed in its own genus, Ovibos — Latin for sheep-ox. It is one of the two largest extant members of Caprinae, along with the similarly sized takin.
While the takin and muskox were once considered possibly closely related, the takin lacks common ovibovine features, such as the muskox's specialized horn morphology, and genetic analysis shows that their lineages actually separated early in caprine evolution.
Instead, the muskox's closest living relatives appear to be the gorals of the genus Naemorhedus, nowadays common in many countries of central and east Asia. The vague similarity between takin and muskox must therefore be considered an example of convergent evolution.
The modern muskox is the last member of a line of ovibovines that first evolved in temperate regions of Asia and adapted to a cold tundra environment late in its evolutionary history. They lived alongside our lovely Mammoths and would have competed for the same plant resources as those much larger beasts.
Muskox ancestors with sheep-like high-positioned horns — horn cores being mostly over the plane of the frontal bones, rather than below them as in modern muskoxen — first left the temperate forests for the developing grasslands of Central Asia during the Pliocene, expanding into Siberia and the rest of northern Eurasia.
Later migration waves of Asian ungulates, including the high-horned muskox, reached Europe and North America during the first half of the Pleistocene. The first well-known muskox, the "shrub-ox" Euceratherium, crossed to North America over an early version of the Bering Land Bridge two million years ago and prospered in the American southwest and Mexico. Euceratherium was larger yet more lightly built than modern muskoxen, resembling a giant sheep with massive horns, and preferred hilly grasslands.
A genus with intermediate horns, Soergelia, inhabited Eurasia in the early Pleistocene, from Spain to Siberia, and crossed to North America during the Irvingtonian (1.8 million years to 240,000 years ago), soon after Euceratherium. Unlike Euceratherium, which survived in America until the Pleistocene-Holocene extinction event, Soergelia was a lowland dweller that disappeared fairly early, displaced by more advanced ungulates, such as the "giant muskox" Praeovibos (literally "before Ovibos").
The low-horned Praeovibos was present in Europe and the Mediterranean 1.5 million years ago, colonized Alaska and the Yukon one million years ago and disappeared half a million years ago. Praeovibos was a highly adaptable animal that appears associated with cold tundra (reindeer) and temperate woodland (red deer) faunas alike.
During the Mindel glaciation 500,000 years ago, Praeovibos was present in the Kolyma river area in eastern Siberia in association with many Ice Age megafauna that would later coexist with Ovibos, in the Kolyma itself and elsewhere, including wild horses, reindeer, woolly mammoth and stag-moose.
It is debated, however, if Praeovibos was directly ancestral to Ovibos, or both genera descended from a common ancestor since the two occurred together during the middle Pleistocene. Defenders of ancestry from Praeovibos have proposed that Praeovibos evolved into Ovibos in one region during a period of isolation and expanded later, replacing the remaining populations of Praeovibos.
Two more Praeovibos-like genera were named in America in the 19th century, Bootherium and Symbos, which are now identified as the male and female forms of a single, sexually dimorphic species, the "woodland muskox", Bootherium bombifrons. Bootherium inhabited open woodland areas of North America during the Late Pleistocene, from Alaska to Texas and maybe even Mexico, but was most common in the Southern United States, while Ovibos replaced it in the tundra-steppe to the north, immediately south of the Laurentian ice sheet.
Modern Ovibos appeared in Germany almost one million years ago and were common in the region through the Pleistocene. Muskoxen had also reached the British Isles. Both Germany and Britain were just south of the Scandinavian ice sheet and covered in the tundra during cold periods, but Pleistocene muskoxen are also rarely recorded in more benign and wooded areas to the south like France and Green Spain, where they coexisted with temperate ungulates like red deer and aurochs. Likewise, the muskox is known to have survived in Britain during warm interglacial periods.
Today's muskoxen are descended from others believed to have migrated from Siberia to North America between 200,000 and 90,000 years ago, having previously occupied Alaska (at the time united to Siberia and isolated periodically from the rest of North America by the union of the Laurentide and Cordilleran Ice Sheets during colder periods) between 250,000 and 150,000 years ago.
After migrating south during one of the warmer periods of the Illinoian glaciation, non-Alaskan American muskoxen would be isolated from the rest in the colder periods. The muskox was already present in its current stronghold of Banks Island 34,000 years ago, but the existence of other ice-free areas in the Canadian Arctic Archipelago at the time is disputed.
Along with the bison and the pronghorn, the muskox was one of a few species of Pleistocene megafauna in North America to survive the Pleistocene/Holocene extinction event and live to the present day. The muskox is thought to have been able to survive the last glacial period by finding ice-free areas (refugia) away from prehistoric peoples.
Fossil DNA evidence suggests that muskoxen were not only more geographically widespread during the Pleistocene, but also more genetically diverse. During that time, other populations of muskoxen lived across the Arctic, from the Ural Mountains to Greenland. By contrast, the current genetic makeup of the species is more homogenous. Climate fluctuation may have affected this shift in genetic diversity: research indicates colder periods in Earth's history are correlated with more diversity and warmer periods with more homogeneity.
It is one of four living species of the order Sirenia, which also includes three species of manatees — their large, fully aquatic, mostly herbivorous marine mammal cousins.
The closest living relatives of sirenians are elephants. Manatees evolved from the same land animals as elephants over 50 million years ago.
If not for natural selection, we might have a much more diverse showing of the Sirenia as their fossil lineage shows a much more diverse group of sirenians back in the Eocene than we have today. It is the only living representative of the once-diverse family Dugongidae; its closest modern relative, Steller's sea cow, was hunted to extinction in the 18th century.
While only one species of the dugong is alive today – a second, the Steller's sea cow only left this Earth a few years ago. Sadly, it was hunted to extinction within 27 years of its discovery – about 30 species have been recovered in the fossil record
The first appearance of sirenians in the fossil record was during the early Eocene, and by the late Eocene, sirenians had significantly diversified. Inhabitants of rivers, estuaries, and nearshore marine waters, they were able to spread rapidly.
The most primitive sirenian known to date, Prorastomus, was found in Jamaica, not the Old World; however, more recently the contemporary Sobrarbesiren has been recovered from Spain. The first known quadrupedal sirenian was Pezosiren from the early Eocene.The earliest known sea cows, of the families Prorastomidae and Protosirenidae, are both confined to the Eocene and were about the size of a pig, four-legged amphibious creatures.
By the time the Eocene drew to a close, the Dugongidae had arrived; sirenians had acquired their familiar fully aquatic streamlined body with flipper-like front legs with no hind limbs, powerful tail with horizontal caudal fin, with up and down movements which move them through the water, like cetaceans.
The last of the sirenian families to appear, Trichechidae, apparently arose from early dugongids in the late Eocene or early Oligocene. The current fossil record documents all major stages in hindlimb and pelvic reduction to the extreme reduction in the modern manatee pelvis, providing an example of dramatic morphological change among fossil vertebrates.
Since sirenians first evolved, they have been herbivores, depending on seagrasses and aquatic angiosperms, tasty flowering plants of the sea, for food. To the present, almost all have remained tropical — with the notable exception of Steller's Sea Cow — marine, and angiosperm consumers. Sea cows are shallow divers with large lungs. They have heavy skeletons to help them stay submerged; the bones are pachyostotic (swollen) and osteosclerotic (dense), especially the ribs which are often found as fossils.
Eocene sirenians, like Mesozoic mammals but in contrast to other Cenozoic ones, have five instead of four premolars, giving them a 3.1.5.3 dental formula. Whether this condition is truly primitive retention in sirenians is still under debate.
Although cheek teeth are relied on for identifying species in other mammals, they do not vary to a significant degree among sirenians in their morphology but are almost always low-crowned —brachyodont — with two rows of large, rounded cusps — bunobilophodont. The most easily identifiable parts of sirenian skeletons are the skull and mandible, especially the frontal and other skull bones. With the exception of a pair of tusk-like first upper incisors present in most species, front teeth — incisors and canines — are lacking in all, except the earliest sirenians.
At first glance, they look like beautiful and delicate marine flowers. If you have discovered them in tidepools, you will know that they retract or pull into themselves with the lightest touch. These would-be flowers are predatory marine animals of the order Actiniaria that have graced our oceans for over half a billion years.
They are named after anemones — Anemonastrum, a genus of flowering plants in the family Ranunculaceae — because of their colourful flower-like appearance. Sea anemones are classified in the phylum Cnidaria, class Anthozoa, subclass Hexacorallia.
As cnidarians, sea anemones are related to corals, jellyfish, tube-dwelling anemones, and Hydra. Jellyfish have a complex life cycle that includes both sexual and asexual phases, with the medusa being the sexual stage in most instances.
A typical sea anemone is a single polyp attached to a hard surface by its base, but some species live in soft sediment and a few float near the surface of the water. The polyp has a columnar trunk topped by an oral disc with a ring of sticky tentacles that fold in towards its central mouth. If they have stung and paralyzed a tasty snack, it is pulled towards the gaping mouth to be consumed.
The tentacles can be retracted or pulled back inside the body cavity or stretched out and expanded to catch passing prey. They are armed with cnidocytes or stinging cells. In many species, nourishment comes from a symbiotic relationship with single-celled dinoflagellates — zooxanthellae or with green algae, zoochlorellae, that live within the cells. Some species of sea anemone live in association with hermit crabs, small fish or other animals to their mutual benefit.
Most actinarians are sessile — that is, they live attached to rocks or other substrates and do not move, or move only very slowly by contractions of the pedal disk.Sea anemones breed by releasing sperm and eggs through their mouth into the surrounding ocean. The fertilized eggs develop into wee planula larvae that live as tiny planktonic bits floating in the sea. Eventually, they settle on the seafloor and develop directly into juvenile polyps. Sea anemones can also breed asexually. They do this by breaking in half or into smaller pieces that regenerate into polyps.
We sometimes see these beauties kept in saltwater aquariums. I can understand the appeal but it comes with a price. The global trade in marine ornamentals threatens our lovely sea anemone populations.
Most Actiniaria do not form hard parts that can be recognized as fossils, but a few fossils of sea anemones have been found. The bag-like — almost sea cucumber-like — Mackenzia, from the Middle Cambrian, Stephen Formation in the Canadian Rockies of British Columbia and Alberta, is the oldest fossil identified as a sea anemone. These ancient sea anemones attached themselves to hard surfaces, such as brachiopod shells in a similar fashion to their modern sessile cousins.
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| Mackenzia costalis, Walcott 1911 |
Some fossil sea anemones have also been found from the Lower Cambrian of China. The new find lends support to genetic data that suggests anthozoans — anemones, corals, octocorals and their kin — were one the first Cnidarian groups to diversify. We will likely find more of these rare fossils over time and perhaps get a better view of their long lineage.
Photo: Charles Doolittle Walcott - Charles D. Walcott: Middle Cambrian Holothurians and Medusae. Smithsonian Miscellaneous Collections Volume 57, Number 3 (Publication 2011). City of Washington. Published by the Smithsonian Institution. June 13, 1911.
References:
Caron, Jean-Bernard; Jackson, Donald A. (October 2006). "Taphonomy of the Greater Phyllopod Bed community, Burgess Shale". PALAIOS. 21 (5): 451–65. doi:10.2110/palo.2003.P05-070R. JSTOR 20173022.
Durham, J. W. (1974). "Systematic Position of Eldonia ludwigi Walcott". Journal of Paleontology. 48 (4): 750–755. JSTOR 1303225.
Conway Morris, S. (1993). "Ediacaran-like fossils in Cambrian Burgess Shale–type faunas of North America". Palaeontology. 36 (31–0239): 593–635.
This remarkable fellow is Dimorphodon — a genus of medium-sized pterosaur from the Early Jurassic. He is another favourite of mine for his charming awkwardness.
Mary's specimen was acquired by William Buckland and reported in a meeting of the Geological Society on 5 February 1829. Six years later, in 1835, William Clift and William John Broderip built upon the work by Buckland to publish in the Transactions of the Geological Society, describing and naming the fossil as a new species.
As was the case with most early pterosaur finds, Buckland classified the remains in the genus Pterodactylus, coining the new species Pterodactylus macronyx. The specific name is derived from Greek makros, "large" and onyx, "claw", in reference to the large claws of the hand. The specimen, presently NHMUK PV R 1034, consisted of a partial and disarticulated skeleton on a slab — notably lacking the skull. Buckland in 1835 also assigned a piece of the jaw from the collection of Elizabeth Philpot to P. macronyx.
Later, the many putative species assigned to Pterodactylus had become so anatomically diverse that they began to be broken into separate genera.
In 1858, Richard Owen reported finding two new specimens, NHMUK PV OR 41212 and NHMUK PV R 1035, again partial skeletons but this time including the skulls. Having found the skull to be very different from that of Pterodactylus, Owen assigned Pterodactylus macronyx its own genus, which he named Dimorphodon.
His first report contained no description and the name remained a nomen nudum. In 1859, however, a subsequent publication by Owen provided a description. After several studies highlighting aspects of Dimorphodon's anatomy, Owen finally made NHMUK PV R 1034 the holotype in 1874 — 185 million years after cruising our skies the Dimorphodon had finally fully arrived.
They left many beautifully preserved examples of their three-lobed exoskeletons in the fossil record.
Trilobites — in all their many wonderful forms — lived in our ancient oceans for more than 270 million years. The last of their lineage went extinct at the end of the Permian, 252 million years ago.
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| Dan Bowen, Chair, VIPS, Trent River |
The Pacific Plate is an oceanic tectonic plate that lies beneath the Pacific Ocean. And it is massive. At 103 million km2 (40 million sq mi), it is the largest tectonic plate and continues to grow fed by volcanic eruptions that piggyback onto its trailing edge.
This relentless expansion pushes the Pacific Plate into the North American Plate. The pressure subducts it beneath our continent where it then melts back into the earth. Plate tectonics are slow but powerful forces.
The island chains that rode the plates across the Pacific smashed into our coastline and slowly built the province of British Columbia. And because each of those islands had a different origin, they create pockets of interesting and diverse geology.
It is these islands that make up the Insular Belt — a physio-geological region on the northwestern North American coast. It consists of three major island groups — and many smaller islands — that stretches from southern British Columbia up into Alaska and the Yukon. These bits of islands on the move arrived from the Late Cretaceous through the Eocene — and continues to this day.
The rocks that form the Insular Superterrane are allochthonous, meaning they are not related to the rest of the North American continent. The rocks we walk over along the Trent River are distinct from those we find throughout the rest of Vancouver Island, Haida Gwaii, the rest of the province of British Columbia and completely foreign to those we find next door in Alberta.
To discover what we do find on the Trent takes only a wee stroll, a bit of digging and time to put all the pieces of the puzzle together. The first geological forays to Vancouver Island were to look for coal deposits, the profitable remains of ancient forests that could be burned to the power industry.
Jim Monger and Charlie Ross of the Geological Survey of Canada both worked to further our knowledge of the complex geology of the Comox Basin. They were at the cutting edge of west coast geology in the 1970s. It was their work that helped tease out how and where the rocks we see along the Trent today were formed and made their way north.We know from their work that by 85 million years ago, the Insular Superterrane had made its way to what is now British Columbia.
The lands were forested much as they are now but by extinct genera and families. The fossil remains of trees similar to oak, poplar, maple and ash can be found along the Trent and Vancouver Island. We also see the lovely remains of flowering plants such as Cupanities crenularis, figs and breadfruit.
Heading up the river, you come to a delineation zone that clearly marks the contact between the dark grey marine shales and mudstones of the Haslam Formation where they meet the sandstones of the Comox Formation. Fossilized material is less abundant in the Comox sandstones but still contains some interesting specimens. Here you begin to see fossilized wood and identifiable fossil plant material.
Further upstream, there is a small tributary, Idle Creek, where you can find more of this terrestrial material in the sandy shales. As you walk up, you see identifiable fossil plants beneath your feet and jungle-like, overgrown moss-covered, snarly trees all around you.
Walking west from the Trent River Falls at the bottom, you pass the infamous Ammonite Alley, where you can find Mesopuzosia sp. and Kitchinites sp. of the Upper Cretaceous (Santonian), Haslam Formation. Minding the slippery green algae covering some of the river rocks, you can see the first of the Polytychoceras vancouverense zone.
Continuing west, you reach the first of two fossil turtle sites on the river — amazingly, one terrestrial and one marine. If you continue, you come to the Inland Island Highway.
The Trent River has yielded some very interesting marine specimens, and significant terrestrial finds. We have found a wonderful terrestrial helochelydrid turtle, Naomichelys speciosa, and the caudal vertebrae of a Hadrosauroid dinosaur. Walking down from the Hadrosaur site you come to the site of the fossil ratfish find — one of the ocean's oddest fish.
Ratfish, Hydrolagus Collie, are chimaera found in the north-eastern Pacific Ocean today. The fossil specimen from the Trent would be considered large by modern standards as it is a bruiser in comparison to his modern counterparts.This robust fellow had exceptionally large eyes and sex organs that dangled enticingly between them. You mock, but there are many ratfish who would differ. While inherently sexy by ratfish standards, this fellow was not particularly tasty to their ancient marine brethren (or humans today) — so not hugely sought after as a food source or prey.
A little further again from the ratfish site we reach the contact of the two Formations. The rocks here have travelled a long way to their current location. With them, we peel away the layers of the geologic history of both the Comox Valley and the province of British Columbia.
The Trent River is not far from the Puntledge, a river whose banks have also revealed many wonderful fossil specimens. The Puntledge is also the name used by the K'ómoks First Nation to describe themselves. They have lived here since time immemorial. Along with Puntledge, they refer to themselves as Sahtloot, Sasitla and Ieeksun.
References: Note on the occurrence of the marine turtle Desmatochelys (Reptilia: Chelonioidea) from the Upper Cretaceous of Vancouver Island Elizabeth L. Nicholls Canadian Journal of Earth Sciences (1992) 29 (2): 377–380. https://doi.org/10.1139/e92-033; References: Chimaeras - The Neglected Chondrichthyans". Elasmo-research.org. Retrieved 2017-07-01.
Directions: If you're keen to explore the area, park on the side of Highway 19 about three kilometres south of Courtenay and hike up to the Trent River. Begin to look for parking about three kilometres south of the Cumberland Interchange. There is a trail that leads from the highway down beneath the bridge which will bring you to the Trent River's north side.
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| Collishaw Point, known locally as Boulder Point, Hornby Island |
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| Upper Cretaceous Nanaimo Group Fossil Concretion |
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| Dan Bowen, Chair, VIPS. Photo: Deanna Steptoe Graham |
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| Diplomoceras sp. |
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| Yorkshire Coast |
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| Fashion in Medieval Livonia (1521): Albrecht Dürer |
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| 16th Century Fashion / Ruff Collars and Finery |
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| Alum House, Photo: Joyce Dobson and Keith Bowers |
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| Alum House. Photo: Ann Wedgewood and Keith Bowers |
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| The Dream Team at Fossil Site #15, East Kootenays, August 2, 2020 |
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| Chris New, pleased as punch atop Upper Cambrian Exposures |