This well-preserved partial ichthyosaur was found in the Blue Lias shales by Lewis Winchester-Ellis in 2018. An exciting find to be sure. The vertebrae you see are from the tail section of this marine reptile.
The find includes stomach contents which tell us a little about how this particular fellow liked to dine.
As with most of his brethren, he enjoyed fish and cephalopods. Lewis found fishbone and squid tentacle hooklets in his belly. Oh yes, these ancient cephies had grasping hooklets on their tentacles. I'm picturing them wiggling all ominously. The hooklets were the only hard parts of the animal preserved in this case as the softer parts of this ancient calamari were fully or partially digested before this ichthyosaur met his end.
Ichthyosaurus was an extinct marine reptile first described from fossil fragments found in 1699 in Wales. Shortly thereafter, fossil vertebrae were published in 1708 from the Lower Jurassic and the first member of the order Ichthyosauria to be discovered.
To give that a bit of historical significance, this was the age of James Stuart, Jacobite hopeful to the British throne. While scientific journals of the day were publishing the first vertebrae ichthyosaur finds, he was avoiding the French fleet in the Firth of Forth off Scotland. This wasn’t Bonnie Prince Charlie, this was his Dad. Yes, that far back.
The first complete skeleton was discovered in the early 19th century by Mary Anning and her brother Joseph along the Dorset Jurassic Coast. Joseph had mistakenly, but quite reasonably, taken the find for an ancient crocodile. Mary excavated the specimen a year later and it was this and others that she found that would supply the research base others would soon publish on.
Mary's find was described by a British surgeon, Sir Everard Home, an elected Fellow of the Royal Society, in 1814. The specimen is now on display at the Natural History Museum in London bearing the name Temnodontosaurus platyodon, or “cutting-tooth lizard.”
In 1821, William Conybeare and Henry De La Beche, a friend of Mary's, published a paper describing three new species of unknown marine reptiles based on the Anning's finds.
The Rev. William Buckland would go on to describe two small ichthyosaurs from the Lias of Lyme Regis, Ichthyosaurus communis and Ichthyosaurus intermedius, in 1837.
Remarkable, you'll recall that he was a theologian, geologist, palaeontologist AND Dean of Westminster. It was Buckland who published the first full account of a dinosaur in 1824, coining the name, "Megalosaurus."
The Age of Dinosaurs and Era of the Mighty Marine Reptile had begun.
Ichthyosaurs 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.
Ichthyosaurs ranged from quite small, just a foot or two, to well over twenty-six metres in length and resembled both modern fish and dolphins.
Dean Lomax and Sven Sachs, both active (and delightful) vertebrate paleontologists, have described a colossal beast, Shonisaurus sikanniensis from the Upper Triassic (Norian) Pardonet Formation of northeastern British Columbia, Canada, measuring 3-3.5 meters in length. The specimen is now on display in the Royal Tyrrell Museum of Palaeontology in Alberta, Canada. It was this discovery that tipped the balance in the vote, making it British Columbia's Official Fossil. Ichthyosaurs have been found at other sites in British Columbia, on Vancouver Island and the Queen Charlotte Islands (Haida Gwaii) but Shoni tipped the ballot.
The first specimens of Shonisaurus were found in the 1990s by Peter Langham at Doniford Bay on the Somerset coast of England.
Dr. Betsy Nicholls, Rolex Laureate Vertebrate Palaeontologist from the Royal Tyrrell Museum, excavated the type specimen of Shonisaurus sikanniensis over three field sessions in one of the most ambitious fossil excavations ever ventured. Her efforts from 1999 through 2001, both in the field and lobbying back at home, paid off. Betsy published on this new species in 2004, the culmination of her life’s work and her last paper as we lost her to cancer in autumn of that year.
Charmingly, Betsy had a mail correspondence with Roy Chapman Andrews, former director of the American Museum of Natural History, going back to the late 1950s as she explored her potential career in palaeontology. Do you recall the AMNH’s sexy paleo photos of expeditions to the Gobi Desert in southern Mongolia in China in the early 20th century? You’d remember if you’d seen them. Roy Chapman Andrews was the lead on that trip. His photos are what fueled the flames of my own interest in paleo.
We've found at least 37 specimens of Shonisaurus in Triassic outcrops of the Luning Formation in the Shoshone Mountains of Nevada, USA. The finds go back to the 1920s. The specimens that may it to publication were collected by M. Wheat and C. L. Camp in the 1950s. The aptly named Shonisaurus popularis became the Nevada State Fossil in 1984. Our Shoni got around. Isolated remains have been found in a section of sandstone in Belluno, in the Eastern Dolomites, Veneto region of northeastern Italy. The specimens were published by Vecchia et al. in 2002.
For a time, Shonisaurus was the largest ichthyosaurus known.
Move over, Shoni, as a new marine reptile find competes with the Green Anaconda (Eunectes murinus) and the Blue Whale (Balaenoptera musculus) for size at a whopping twenty-six (26) metres.
The find is the prize of fossil collector turned co-author, Paul de la Salle, who (you guessed it) found it in the lower part of the intertidal area that outcrops strata from the latest Triassic Westbury Mudstone Formation of Lilstock on the Somerset coast. He contacted Dean Lomax and Judy Massare who became co-authors on the paper.
The find and conclusions from their paper put "dinosaur" bones from the historic Westbury Mudstone Formation of Aust Cliff, Gloucestershire, UK site into full reinterpretation.
And remember that ichthyosaur the good Reverend Buckland described back in 1837, the Ichthyosaurus communis? Dean Lomax was the first to describe a wee baby. A wee baby ichthyosaur! Awe. I know, right? He and paleontologist Nigel Larkin published this adorable first in the journal of Historical Biology in 2017.
They had teamed up previously on another first back in 2014 when they completed the reconstruction of an entire large marine reptile skull and mandible in 3-D, then graciously making it available to fellow researchers and the public. The skull and braincase in question were from an Early Jurassic, and relatively rare, Protoichthyosaurus prostaxalis. The specimen had been unearthed in Warwickshire back in the 1950's. Unlike most ichthyosaur finds of this age it was not compressed and allowed the team to look at a 3-D specimen through the lens of computerised tomography (CT) scanning.
Another superb 3-D ichthyosaur skull was found near Lyme Regis by fossil hunter-turned-entrepreneur-local David Sole and prepped by the late David Costain. I'm rather hoping it went into a museum collection as it would be wonderful to see the specimen studied, imaged, scanned and 3-D printed for all to share. Here's hoping.
Lomax and Sven Sachs also published on an embryo from one of the largest ichthyosaurs known, a new species named Ichthyosaurus somersetensis. Their paper in the ACTA Palaeontologica Polonica from 2017, describes the third embryo known for Ichthyosaurus and the first to be positively identified to species level. The specimen was the collected from the Lower Jurassic strata (lower Hettangian, Blue Lias Formation) of Doniford Bay, Somerset, UK and is housed in the collection of the Niedersächsisches Landesmuseum (Lower Saxony State Museum) in Hannover, Germany.
We've learned a lot about them in the time we've been studying them. We now have thousands of specimens, some whole, some as bits and pieces. Many specimens that have been collected are only just now being studied and the tools we are using to study them are getting better and better.
While they resembled fish and dolphins, Ichthyosaurs were large marine reptiles belonging to the order known as Ichthyosauria or Ichthyopterygia. In 2018, Benjamin Kear and his team were able to study ichthyosaur remains at the molecular level, Their findings suggest ichthyosaurs had skin and blubber quite similar to our modern dolphins.
While ichthyosaurs evolved from land-dwelling, lung-breathing reptiles, they returned to our ancient seas and evolved into the fish-shaped creatures we find in the fossil record today.
Their limbs fully transformed into flippers, sometimes containing a very large number of digits and phalanges. Their flippers tell us they were entirely aquatic as they were not well-designed for use on land. And it was their flippers that first gave us the clue that they gave birth to live young; a find later confirmed by fossil embryo and wee baby ichy finds.
They thrived during much of the Mesozoic era; based on fossil evidence, they first appeared around 250 million years ago (Ma) and at least one species survived until about 90 million years ago into the Late Cretaceous.
During the early Triassic period, ichthyosaurs evolved from a group of unidentified land reptiles that returned to the sea. They were particularly abundant in the later Triassic and early Jurassic periods before being replaced as premier aquatic predator by another marine reptilian group, the Plesiosauria, in the later Jurassic and Cretaceous periods.
In the Late Cretaceous, ichthyosaurs were hard hit by the Cenomanian-Turonian anoxic event. As the deepest benthos layers of the seas became anoxic, poisoned by hydrogen sulphide, deep water marine life died off. This caused a cascade that wreaked havoc all the way up the food chain. At the end of that chain were our mighty predaceous marine reptiles.
Bounty turned to scarcity and a race for survival began. The ichthyosaurs lost that race as the last lineage became extinct. It may have been their conservative evolution as a genus when faced with a need for adaptation to the world in which they found themselves and/or being outcompeted by early mosasaurs.
There are promising discoveries coming out of strata from the Cretaceous epeiric seas of Texas, USA from Nathan E. Van Vranken
His published paper from 2017, "An overview of ichthyosaurian remains from the Cretaceous of Texas, USA," looks at ichthyosaurian taxa from the mid-Cretaceous (Albian–Cenomanian) time interval in North America with an eye to ichthyosaurian distribution and demise.
The find and photos are all credited to Lewis Winchester-Ellis. Thank you for sharing your tremendous specimen with us. Lewis did much of the preparation of the specimen, removing the majority of the matrix. The spectacular final prep is credited to Lizzie Hingley, Stonebarrow Fossils, Oxfordshire. Her skill with an air scribe is unparalleled.
Link to Lomax Paper: https://journals.plos.org/plosone/article…
Link to Nathan's Paper: https://www.tandfonline.com/…/10.1080/03115518.2018.1523462…
Nicholls Paper: E. L. Nicholls and M. Manabe. 2004. Giant ichthyosaurs of the Triassic - a new species of Shonisaurus from the Pardonet Formation (Norian: Late Triassic) of British Columbia. Journal of Vertebrate Paleontology 24(4):838-849 [M. Carrano/H. Street]
Tuesday, 30 April 2019
Monday, 29 April 2019
DARING LOVELIES: COLEMAN SHRIMP
Coleman Shrimp / Periclimenes colemani |
The female of the Coleman pair in this photo is the slightly larger beauty on the left. She's looking poised and ready to catch something tasty with her open claws. Coleman shrimp and several other fish and invertebrates were named after the Australian naturalist and underwater nature photographer, Neville Coleman. It was his life's mission to document all of the sea life of Australia.
Sunday, 28 April 2019
Saturday, 27 April 2019
TROPITACEA
Superfamilia Tropitaceae Mojsisovics, 1875. Familia Tropitidae Mojsisovics, 1893. Genus Discotropites Hyatt & Smith, 1925. Type: Discotropites sandlingensis (Fr.v.Hauer) Karn/Tuval 2, Subbulatus-Schichten, Raschberg, Mojs. Plate 130.
The picture shows Discotropites cf. sandlingensis. It was found at the classic Mons Tuval site situated at the Austrian /Bavarian border region south of Salzburg. Size of the ammonoid is about 7cm. This area of the world boasts one of the richest deposits of Triassic ammonite units — more than five hundred magnificent ammonite species are found here along with a diversified selection of cephalopod fauna — orthoceratids, nautiloids, ammonoids — we also see gastropods, bivalves (esp. halobiids), brachiopods, crinoids and a few corals. For microfauna, we see conodonts, foraminifera, sponge spicules, radiolaria, floating crinoids and holothurian sclerites — polyp-like, soft-bodied "wormy" invertebrate echinozoans.
The picture shows Discotropites cf. sandlingensis. It was found at the classic Mons Tuval site situated at the Austrian /Bavarian border region south of Salzburg. Size of the ammonoid is about 7cm. This area of the world boasts one of the richest deposits of Triassic ammonite units — more than five hundred magnificent ammonite species are found here along with a diversified selection of cephalopod fauna — orthoceratids, nautiloids, ammonoids — we also see gastropods, bivalves (esp. halobiids), brachiopods, crinoids and a few corals. For microfauna, we see conodonts, foraminifera, sponge spicules, radiolaria, floating crinoids and holothurian sclerites — polyp-like, soft-bodied "wormy" invertebrate echinozoans.
Friday, 26 April 2019
CERATIOCARIS, YE KEN
This braw fellow is Ceratiocaris papilio (Salter in Murchison, 1859) a pod Shrimp from the Silurian mudstones of the Kip Burn Formation in the Midland Valley of Scotland. He would have swam in rising seas filled with crinoids, coral reefs, brachiopods, trilobites and new and exotic fish -- some sporting jaws for the first time.
Ceratiocaris is a genus of extinct paleozoic phyllocarid crustacean whose fossils are found in marine strata from the Upper Ordovician through to the Silurian.
They are typified by eight short thoracic segments, seven longer abdominal somites and an elongated pretelson somite. Their carapace is slightly oval shaped; they have many ridges parallel to the ventral margin and possess a horn at the anterior end.
This tidy specimen is from the Silurian mudstones that characterise the Kip Burn Formation with it's dark laminated silty bands. The lower part of the Kip Burn houses the highly fossiliferous ‘Ceratiocaris beds’, that yield the arthropods Ceratiocaris, Dictyocaris, Pterygotus, Slimonia and the fish Birkenia and Thelodus.
The upper part of the formation, the ‘Pterygotus beds’, contain abundant eurypterid fauna together with the brachiopods Lingula and Ceratiocaris. The faunas in the Kip Burn Formation reflect the start of the transition from marine to quasi- or non-marine conditions in the group.
Ceratiocaris are also well known from the Silurian Eramosa Formation of Ontario, Canada (which also has rather nice eurypterids). Photo credit / collection of: York Yuxi Wang and Tianyi Zhang
Joseph H. Collette; David M. Rudkin (2010). "Phyllocarid crustaceans from the Silurian Eramosa Lagerstätte (Ontario, Canada): taxonomy and functional morphology". Journal of Paleontology. 84 (1): 118–127. doi:10.1666/08-174.1.
M. Copeland; T. E. Bolton (1985). Fossils of Ontario part 3: the eurypterids and phyllocarids. Volume 48 of Life Sciences Miscellaneous Publications. Royal Ontario Museum. ISBN 0-88854-314-X.
Ceratiocaris is a genus of extinct paleozoic phyllocarid crustacean whose fossils are found in marine strata from the Upper Ordovician through to the Silurian.
They are typified by eight short thoracic segments, seven longer abdominal somites and an elongated pretelson somite. Their carapace is slightly oval shaped; they have many ridges parallel to the ventral margin and possess a horn at the anterior end.
This tidy specimen is from the Silurian mudstones that characterise the Kip Burn Formation with it's dark laminated silty bands. The lower part of the Kip Burn houses the highly fossiliferous ‘Ceratiocaris beds’, that yield the arthropods Ceratiocaris, Dictyocaris, Pterygotus, Slimonia and the fish Birkenia and Thelodus.
The upper part of the formation, the ‘Pterygotus beds’, contain abundant eurypterid fauna together with the brachiopods Lingula and Ceratiocaris. The faunas in the Kip Burn Formation reflect the start of the transition from marine to quasi- or non-marine conditions in the group.
Ceratiocaris are also well known from the Silurian Eramosa Formation of Ontario, Canada (which also has rather nice eurypterids). Photo credit / collection of: York Yuxi Wang and Tianyi Zhang
Joseph H. Collette; David M. Rudkin (2010). "Phyllocarid crustaceans from the Silurian Eramosa Lagerstätte (Ontario, Canada): taxonomy and functional morphology". Journal of Paleontology. 84 (1): 118–127. doi:10.1666/08-174.1.
M. Copeland; T. E. Bolton (1985). Fossils of Ontario part 3: the eurypterids and phyllocarids. Volume 48 of Life Sciences Miscellaneous Publications. Royal Ontario Museum. ISBN 0-88854-314-X.
Thursday, 25 April 2019
SOLAR POWERED: TABANIDAE
Horsefly / Diptera / Tabanidae; Latreille, 1802 |
It's the female horseflies that do the chomping, preferring livestock and the occasional human as they hike or enjoy the great outdoors.
Horseflies are sun lovers, they are out in force on nice sunny days and set a healthy bedtime as they become inactive and rest when the sun goes down.
Wednesday, 24 April 2019
VICTORASPIS LONGICORNUALIS
This lovely specimen is an armoured agnatha jawless bony fish, Victoraspis longicornualis, from Lower Devonian deposits of Podolia, Ukraine. The specimen shows both the positive and negative of the fossil in high relief.
Victoraspis longicornualis was named by Anders Carlsson and Henning Bloom back in 2008. The new osteostracan genus and species were described based on material from Rakovets' present-day Ukraine. This new taxon shares characteristics with the two genera Stensiopelta (Denison, 1951) and Zychaspis (Javier, 1985).
Agnatha is a superclass of vertebrates. This fellow looks quite different from our modern Agnatha, which include lamprey and hagfish. Ironically, hagfish are vertebrates who do not have vertebrae. Sometime in their evolution they lost them as they adapted to their environment. Photo: Fossilero Fisherman
Victoraspis longicornualis was named by Anders Carlsson and Henning Bloom back in 2008. The new osteostracan genus and species were described based on material from Rakovets' present-day Ukraine. This new taxon shares characteristics with the two genera Stensiopelta (Denison, 1951) and Zychaspis (Javier, 1985).
Agnatha is a superclass of vertebrates. This fellow looks quite different from our modern Agnatha, which include lamprey and hagfish. Ironically, hagfish are vertebrates who do not have vertebrae. Sometime in their evolution they lost them as they adapted to their environment. Photo: Fossilero Fisherman
Tuesday, 23 April 2019
JOHN DAY FOSSIL BEDS
Dogs, cats, swine and horses are common. Oreodonts, camels, rhinoceros and rodents have also been found in this ancient deciduous forested area.
Here my talented young paleontologist cousin Spencer is holding a well preserved Oreodont skull.Many sites in Oregon yield beautifully preserved fossil shells laid down over 60 million years.
The asteroid that hit the Gulf of Mexico at the end of the Cretaceous caused a seafloor rift that split ancient Oregon. The massive hole left behind as the coastal lands slid northward filled in with sediment, refilling the basin.
These marine sediments were uplifted around the time of the birth of Oregon's Coastal Range. Easily collected and identified, as they look very similar to their modern cousins, you can dig for marine fossils all along Oregon's beachfront. I'll post some photos when I return from collecting later this year.
Sunday, 21 April 2019
MUMMIFIED BRANCHIOSTEGUS
An amazing mummified tilefish, Branchiostegus japonicus (Houttuyn, 1782) from Holocene deposits near Shizuoka, Japan. This specimen shows remarkable detail right down to the scales. Quite spectacular, truly.
Modern cousins of this fellow live as far south as the Arafura Sea today. Collection and photos from the deeply awesome Takashi Ito. サンさん、ありがとうございました
Modern cousins of this fellow live as far south as the Arafura Sea today. Collection and photos from the deeply awesome Takashi Ito. サンさん、ありがとうございました
Saturday, 20 April 2019
DEEPLY GROOVED DECAPOD
A beautiful example of the "deeply groovy" decapod, Dorippe sinica, from Holocene deposits near Shizuoka, Japan. This regal fellow has a strongly sculptured carapace. He looks like he would have been quite the bruiser moving about on the seafloor looking for tasty snacks. He likely enjoyed just about any form of meat, potentially dining on fish, worms, eggs, squid, starfish or even a few of his slow-moving cousins.
The carapace is deeply grooved with conspicuous wart-like tubercles; anterolateral margin, between the base of the exorbital tooth and cervical groove, smooth, without tubercles or denticles.
The teeth on the lower orbital margin in the cluster. Carpus of cheliped distinctly granulated on the upper surface and with a conspicuous row of granules along the anterior margin. Though missing here, the merus of second and third pereiopods are almost cylindrical. (Türkay 1995). This specimen was collected and is the collection of the deeply awesome Takashi Ito of Japan
The carapace is deeply grooved with conspicuous wart-like tubercles; anterolateral margin, between the base of the exorbital tooth and cervical groove, smooth, without tubercles or denticles.
The teeth on the lower orbital margin in the cluster. Carpus of cheliped distinctly granulated on the upper surface and with a conspicuous row of granules along the anterior margin. Though missing here, the merus of second and third pereiopods are almost cylindrical. (Türkay 1995). This specimen was collected and is the collection of the deeply awesome Takashi Ito of Japan
Friday, 19 April 2019
FRENCHMAN MOUNTAIN TRILOBITE: BRISTOLIA INSOLENS
Bristolia insolens |
The mountain provides an example of the Great unconformity with the tilted Paleozoic Tapeats Sandstone underlain by Paleoproterozoic Vishnu Schist. An unconformity is a buried erosional or non-depositional surface separating two strata of different ages. We know when we find these that the sediment was not laid down in a continuous deposition. The range also boasts some of the oldest rock on the North American continent, at about two billion years old.
This spectacular specimen is in the collection of York Yuxi Wang. It is about 4-5cm long; 3-4cm wide.
Thursday, 18 April 2019
Wednesday, 17 April 2019
MOLLUSCA GASTROPODA
Gastropods, or univalves, are the largest and most successful class of molluscs. They started as exclusively marine but have adapted well and now their rank spend more time in freshwater than in salty marine environments.
Many are marine, but two thirds off all living species live in freshwater or on land. Their entry into the fossil record goes all the way back to the Cambrian.
Slugs and snails, abalones, limpets, cowries, conches, top shells, whelks, and sea slugs are all gastropods. They are the second largest class of animals with over 60,000–75,000 known living species.
The gastropods are originally sea-floor predators, though they have evolved to live happily in many other habitats. Many lines living today evolved in the Mesozoic. The first gastropods were exclusively marine and appeared in the Upper Cambrian (Chippewaella, Strepsodiscus).
By the Ordovician, gastropods were a varied group present in a variety of aquatic habitats. Commonly, fossil gastropods from the rocks of the early Palaeozoic era are too poorly preserved for accurate identification. Still, the Silurian genus Poleumita contains fifteen identified species.
Most of the gastropods of the Palaeozoic era belong to primitive groups, a few of which still survive today. By the Carboniferous period many of the shapes we see in living gastropods can be matched in the fossil record, but despite these similarities in appearance the majority of these older forms are not directly related to living forms. It was during the Mesozoic era that the ancestors of many of the living gastropods evolved.
In rocks of the Mesozoic era gastropods are more common as fossils and their shell often very well preserved. While not all gastropods have shells, the ones that do fossilize more easily and consequently, we know a lot more about them. We find them in fossil beds from both freshwater and marine environments, in ancient building materials and as modern guests of our gardens.
Many are marine, but two thirds off all living species live in freshwater or on land. Their entry into the fossil record goes all the way back to the Cambrian.
Slugs and snails, abalones, limpets, cowries, conches, top shells, whelks, and sea slugs are all gastropods. They are the second largest class of animals with over 60,000–75,000 known living species.
The gastropods are originally sea-floor predators, though they have evolved to live happily in many other habitats. Many lines living today evolved in the Mesozoic. The first gastropods were exclusively marine and appeared in the Upper Cambrian (Chippewaella, Strepsodiscus).
By the Ordovician, gastropods were a varied group present in a variety of aquatic habitats. Commonly, fossil gastropods from the rocks of the early Palaeozoic era are too poorly preserved for accurate identification. Still, the Silurian genus Poleumita contains fifteen identified species.
Most of the gastropods of the Palaeozoic era belong to primitive groups, a few of which still survive today. By the Carboniferous period many of the shapes we see in living gastropods can be matched in the fossil record, but despite these similarities in appearance the majority of these older forms are not directly related to living forms. It was during the Mesozoic era that the ancestors of many of the living gastropods evolved.
In rocks of the Mesozoic era gastropods are more common as fossils and their shell often very well preserved. While not all gastropods have shells, the ones that do fossilize more easily and consequently, we know a lot more about them. We find them in fossil beds from both freshwater and marine environments, in ancient building materials and as modern guests of our gardens.
Tuesday, 16 April 2019
Monday, 15 April 2019
IDENTIFYING FOSSIL BONE
If you’re wondering if you have Fossil Bone, you’ll want to look for the telltale texture on the surface. It’s best to take the specimen outside and photograph it in natural light.
With fossil bone, you will be able to see the different canals and webbed structure of the bone, sure signs that the object was of biological origin.
As my good friend Mike Boyd notes, without going into the distinction between dermal bone and endochondral bone — which relates to how they form - or ossify — it's worth noting that bones such as the one illustrated here will usually have a layer of smooth — periosteal — bone on the outer surface and spongy — or trabecular — bone inside.
The distinction can be well seen in the photograph. The partial weathering away of the smooth external bone has resulted in the exposure of the spongy bone interiors. Geographic context is important, so knowing where it was found is very helpful for an ID. Knowing the geologic context of your find can help you to figure out if you've perhaps found a terrestrial or marine fossil. Did you find any other fossils nearby? Can you see pieces of fossil shells or remnants of fossil leaves? Things get tricky with erratics. That's when something has deposited a rock or fossil far from the place it originated. We see this with glaciers. The ice can act like a plow, lifting up and pushing a rock to a new location, then melting away to leave something out of context.
With fossil bone, you will be able to see the different canals and webbed structure of the bone, sure signs that the object was of biological origin.
As my good friend Mike Boyd notes, without going into the distinction between dermal bone and endochondral bone — which relates to how they form - or ossify — it's worth noting that bones such as the one illustrated here will usually have a layer of smooth — periosteal — bone on the outer surface and spongy — or trabecular — bone inside.
The distinction can be well seen in the photograph. The partial weathering away of the smooth external bone has resulted in the exposure of the spongy bone interiors. Geographic context is important, so knowing where it was found is very helpful for an ID. Knowing the geologic context of your find can help you to figure out if you've perhaps found a terrestrial or marine fossil. Did you find any other fossils nearby? Can you see pieces of fossil shells or remnants of fossil leaves? Things get tricky with erratics. That's when something has deposited a rock or fossil far from the place it originated. We see this with glaciers. The ice can act like a plow, lifting up and pushing a rock to a new location, then melting away to leave something out of context.
Sunday, 14 April 2019
ZEACRINITES 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 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 with 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 this same cirri that allows crinoids to latch to surfaces on the sea floor.
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.
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 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 with 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 this same cirri that allows crinoids to latch to surfaces on the sea floor.
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.
Saturday, 13 April 2019
CROCODILIAN UPSTARTS: THE CRUROTARSANS
Dinosaurs, long hailed as the rulers of the Triassic almost lost the title belt to a group of crocodilian upstarts, the crurotarsans. In a short-lived battle for survival, geologically speaking, the two groups ran head-to-head for about thirty million years.
The Crurotarsi or "cross-ankles" as they are affectionately known, are a group of archosaurs - formerly known as Pseudosuchians when paleontologist Paul Serono, the darling of National Geographic, renamed them for their node-based clade in 1991. Image: By Nobu Tamura (http://spinops.blogspot.com) - Own work, CC BY 2.5, https://commons.wikimedia.org/w/index.php?curid=19459679
The Crurotarsi or "cross-ankles" as they are affectionately known, are a group of archosaurs - formerly known as Pseudosuchians when paleontologist Paul Serono, the darling of National Geographic, renamed them for their node-based clade in 1991. Image: By Nobu Tamura (http://spinops.blogspot.com) - Own work, CC BY 2.5, https://commons.wikimedia.org/w/index.php?curid=19459679
Thursday, 11 April 2019
HEXACORALLIA
Hexacorallia is a subclass of Anthozoa comprising approximately 4,300 species of aquatic organisms formed of polyps, generally with six-fold symmetry. Their temporal range is from the Fortunian to the Holocene. The subclass includes all of the stony corals, most of which are colonial and reef-forming, as well as all sea anemones, and zoanthids, arranged within five extant orders.
The hexacorallia are distinguished from another subclass of Anthozoa, Octocorallia, in having six or fewer axes of symmetry in their body structure; the tentacles are simple and unbranched and normally number more than eight. These organisms are formed of individual soft polyps which in some species live in colonies and can secrete a calcite skeleton. As with all Cnidarians, these organisms have a complex life cycle including a motile planktonic phase and a later characteristic sessile phase. Hexacorallia also includes the significant extinct order of rugose corals.
The hexacorallia are distinguished from another subclass of Anthozoa, Octocorallia, in having six or fewer axes of symmetry in their body structure; the tentacles are simple and unbranched and normally number more than eight. These organisms are formed of individual soft polyps which in some species live in colonies and can secrete a calcite skeleton. As with all Cnidarians, these organisms have a complex life cycle including a motile planktonic phase and a later characteristic sessile phase. Hexacorallia also includes the significant extinct order of rugose corals.
Wednesday, 10 April 2019
AURELIA AURITA: MOON DANCERS
Moon Jelly Fish / Aurelia Aurita |
The genus Aurelia is found throughout most of the world's oceans, from the tropics to as far north as latitude 70° north and as far south as 40° south. The species Aurelia aurita is found along the eastern Atlantic coast of Northern Europe and the western Atlantic coast of North America in New England and Eastern Canada. In general, Aurelia is an inshore genus that can be found in estuaries and harbours.
The genus Aurelia is found throughout most of the world's oceans, from the tropics to as far north as latitude 70° north and as far south as 40° south. The species Aurelia aurita is found along the eastern Atlantic coast of Northern Europe and the western Atlantic coast of North America in New England and Eastern Canada. In general, Aurelia is an inshore genus that can be found in estuaries and harbours.
Tuesday, 9 April 2019
OH MAXIMUS: ISOTELUS REX
This lovely big fella is Isotelus rex from Churchill, Manitoba, Canada. He was found along the Hudson Bay and is the largest complete trilobite ever found. Isotelus is a genus of asaphid trilobites, an extinct group of arthropods, from the middle and upper Ordovician
Discovered by a paleo dream team, including the deeply awesome, Dave Rudkin, assistant curator of paleobiology at the Royal Ontario Museum, along with Robert Elias (Project Lead), University of Manitoba, Graham Young (Project Lead), associate curator of geology at the Manitoba Museum of Man and Nature (and adjunct professor at the University of Manitoba) and Edward Dobrzanski, Manitoba Museum during a long-term field project in 1998-1999.
The specimen measures in at a whopping 28 inches in length and is 70 percent larger than the previous record holder and warranted a new species name. The image here shows one of several replicas (casts), not the actual holotype specimen which is on exhibit at the Manitoba Museum.
There is a second complete specimen (430 mm in length) of Isotelus rex in the collections of the Geological Survey of Canada (GSC 85292 - a designated paratype). As with many such projects, financial contributions make field work and research possible. A nod to the Natural Sciences and Engineering Research Council of Canada, the University of Manitoba, the Manitoba Museum Foundation nd the Royal Ontario Museum Foundation.
Kudos as well to field crew, David Wright, Curtis Moffat and Janis Klapecki. You arrived four hundred and forty-five million years too late for sunscreen and tropical weather.
In the prophetic words of Eddard Stark, "Winter is Coming." And so it did to the Canadian prairies. Thank you to everyone involved for enduring the frozen cold, wind, rains and hail of northern Manitoba. For those who haven't had the pleasure, dear Manitoba gets blasted by cold Arctic high-pressure that drops it to a frigid -47.2 Celsius. That's a sweet, sweet -52 with wind chill.
Paper: Rudkin, D.A.; Young, G.A.; Elias, R.J.; Dobrzanski, E.P. (2003). "The World's biggest Trilobite: Isotelus rex new species from the Upper Ordovician of northern Manitoba, Canada". Palaeontology. 70 (1): 99–112. doi:10.1666/0022-3360(2003)077<0099:twbtir>2.0.CO;2. ISSN 0022-3360.0099:twbtir>
Photo credit: Mike Beauregard from Nunavut, Canada. Cast of Isotelus rex. Churchill Manitoba. 2 foot long replica housed at the University of Manitoba. Original specimen is in the Manitoba Museum. The original specimen was recovered the intertidal zone of Hudson Bay.
Discovered by a paleo dream team, including the deeply awesome, Dave Rudkin, assistant curator of paleobiology at the Royal Ontario Museum, along with Robert Elias (Project Lead), University of Manitoba, Graham Young (Project Lead), associate curator of geology at the Manitoba Museum of Man and Nature (and adjunct professor at the University of Manitoba) and Edward Dobrzanski, Manitoba Museum during a long-term field project in 1998-1999.
The specimen measures in at a whopping 28 inches in length and is 70 percent larger than the previous record holder and warranted a new species name. The image here shows one of several replicas (casts), not the actual holotype specimen which is on exhibit at the Manitoba Museum.
There is a second complete specimen (430 mm in length) of Isotelus rex in the collections of the Geological Survey of Canada (GSC 85292 - a designated paratype). As with many such projects, financial contributions make field work and research possible. A nod to the Natural Sciences and Engineering Research Council of Canada, the University of Manitoba, the Manitoba Museum Foundation nd the Royal Ontario Museum Foundation.
Kudos as well to field crew, David Wright, Curtis Moffat and Janis Klapecki. You arrived four hundred and forty-five million years too late for sunscreen and tropical weather.
In the prophetic words of Eddard Stark, "Winter is Coming." And so it did to the Canadian prairies. Thank you to everyone involved for enduring the frozen cold, wind, rains and hail of northern Manitoba. For those who haven't had the pleasure, dear Manitoba gets blasted by cold Arctic high-pressure that drops it to a frigid -47.2 Celsius. That's a sweet, sweet -52 with wind chill.
Paper: Rudkin, D.A.; Young, G.A.; Elias, R.J.; Dobrzanski, E.P. (2003). "The World's biggest Trilobite: Isotelus rex new species from the Upper Ordovician of northern Manitoba, Canada". Palaeontology. 70 (1): 99–112. doi:10.1666/0022-3360(2003)077<0099:twbtir>2.0.CO;2. ISSN 0022-3360.0099:twbtir>
Photo credit: Mike Beauregard from Nunavut, Canada. Cast of Isotelus rex. Churchill Manitoba. 2 foot long replica housed at the University of Manitoba. Original specimen is in the Manitoba Museum. The original specimen was recovered the intertidal zone of Hudson Bay.
Monday, 8 April 2019
OREGON PALEONTOLOGY
Driving down the Oregon coast, you see large basalt sentinels left stranded on the beaches. The surf rubs at them slowly eroding a story that extends into our geologic past.
The rugged landscape of Oregon was shaped over millions of years. Fire, floods, earthquakes and volcanic eruptions — driven by the collision of an oceanic and continental plate — each had a hand in helping to shape this beautiful part of the world. The ground here has been moving and shifting on a steady northeast direction for several hundred million years and continues today.
Oregon's geologic record extends back to the Devonian. Oregon had been mostly submerged hidden beneath the depths of an ancient ocean. The centre of the state boasts the oldest rocks. Near Suplee, Oregon snuggled up against the Malheur National Forest you can find Devonian limestones with a lovely of shallow-water marine invertebrates. Look for corals and brachiopod who made a living in Devonian seas far from where they rest today.
In the Carboniferous period, a series of volcanic archipelagos formed in Oregon. The islands enjoyed a warm, wet, terrestrial environments. Think of the Mississipi today. Fossils in Oregon's oldest floral assemblage, dating to the Late Carboniferous, were built on a lagoon ecosystem. The fossil fauna here include horsetails, ferns, scale trees, and conifer tree seeds. Formations of similar age also include shallow-water invertebrates telling us that Oregon's volcanic islands were surrounded by coral reefs.
Oregon remained mostly submerged until the Paleocene. Oregon was covered by seaways and volcanic islands during the Mesozoic. We find marine plants, invertebrates, ichthyosaurs, pterosaurs, and traces such as invertebrate burrows.
During the Cenozoic, Oregon's climate gradually cooled and eventually yielded the environments now found in the state. The era's fossils include marine and terrestrial plants, invertebrates, fish, amphibians, turtles, birds, mammals, and traces such as eggs and animal tracks.
Sediment records show that Oregon remained mostly submerged until the Paleocene period. The state's earliest fossil record includes plants, corals, and conodonts.
Oregon was covered by seaways and volcanic islands during the Mesozoic era. Fossils from this period include marine plants, invertebrates, ichthyosaurs, pterosaurs, and traces such as invertebrate burrows.
During the Cenozoic, Oregon's climate gradually cooled and eventually yielded the environments now found in the state. The era's fossils include marine and terrestrial plants, invertebrates, fish, amphibians, turtles, birds, mammals, and traces such as eggs and animal tracks.
Reference: https://www.oregongeology.org/pubs/ims/ims-028/index.htm
The rugged landscape of Oregon was shaped over millions of years. Fire, floods, earthquakes and volcanic eruptions — driven by the collision of an oceanic and continental plate — each had a hand in helping to shape this beautiful part of the world. The ground here has been moving and shifting on a steady northeast direction for several hundred million years and continues today.
Oregon's geologic record extends back to the Devonian. Oregon had been mostly submerged hidden beneath the depths of an ancient ocean. The centre of the state boasts the oldest rocks. Near Suplee, Oregon snuggled up against the Malheur National Forest you can find Devonian limestones with a lovely of shallow-water marine invertebrates. Look for corals and brachiopod who made a living in Devonian seas far from where they rest today.
In the Carboniferous period, a series of volcanic archipelagos formed in Oregon. The islands enjoyed a warm, wet, terrestrial environments. Think of the Mississipi today. Fossils in Oregon's oldest floral assemblage, dating to the Late Carboniferous, were built on a lagoon ecosystem. The fossil fauna here include horsetails, ferns, scale trees, and conifer tree seeds. Formations of similar age also include shallow-water invertebrates telling us that Oregon's volcanic islands were surrounded by coral reefs.
Oregon remained mostly submerged until the Paleocene. Oregon was covered by seaways and volcanic islands during the Mesozoic. We find marine plants, invertebrates, ichthyosaurs, pterosaurs, and traces such as invertebrate burrows.
During the Cenozoic, Oregon's climate gradually cooled and eventually yielded the environments now found in the state. The era's fossils include marine and terrestrial plants, invertebrates, fish, amphibians, turtles, birds, mammals, and traces such as eggs and animal tracks.
Sediment records show that Oregon remained mostly submerged until the Paleocene period. The state's earliest fossil record includes plants, corals, and conodonts.
Oregon was covered by seaways and volcanic islands during the Mesozoic era. Fossils from this period include marine plants, invertebrates, ichthyosaurs, pterosaurs, and traces such as invertebrate burrows.
During the Cenozoic, Oregon's climate gradually cooled and eventually yielded the environments now found in the state. The era's fossils include marine and terrestrial plants, invertebrates, fish, amphibians, turtles, birds, mammals, and traces such as eggs and animal tracks.
Reference: https://www.oregongeology.org/pubs/ims/ims-028/index.htm
Tuesday, 2 April 2019
CROCUTA CROCUTA
Female Spotted Hyena / Sub-Saharan Africa |
Like all her kin, she's a wonderful hunter either with her pack or out solo. While portrayed as scavengers, those who've seen them in the wild know that she's a good little hunter and not a picky eater. Hyenas snack on a varied selection of birds, lizards, snakes, fish and insects over their long lives. Most live about 25 years and are quite social animals. They live in large groups called clans, some up to 75-80 individuals. They eat larger game as well, often hunting with their clan packs to take down zebra, antelope, wildebeest and even young hippos.
Spotted hyenas are mammals in the Family Hyaenidae. They roam the tropical grasslands, woodlands and savanna of Africa. The females are the larger of the species, weighing up to 82 kg and growing up to 2 metres long and are the leaders of the group. Each clan is led by one alpha female who rules the roost and still takes time out to have one ot cubs a year. They are the original working moms.
Monday, 1 April 2019
PALEO PARENTING: NOTHOSAURS
In Sauropterygia, a diverse group of Mesozoic marine reptiles, fossil evidence of viviparity (live‐bearing) only exists for Pachypleurosauria and Plesiosauria, and was assumed to also be the case for nothosaurs.
Previous studies have successfully applied an extant squamate model to sauropterygian life‐history traits. In extant squamates, oviparity and viviparity are associated with differences in life‐history trait combinations.
A paper released in March 2019, in the journal Palaeontology, sheds light on this view. Griebeler et al. have establish growth curves for Nothosaurus specimens based on their humeral histology.
They analyzed life‐history traits derived from these curves and compared inferred traits to those of modern squamates and pachypleurosaurs to assess their reproduction mode.
Their data shows birth to adult size ratios (i.e. birth size divided by the mother's size) provides a good estimate of clutch sizes in extant squamates and in viviparous extinct marine reptiles, but these ratios cannot discriminate viviparous and oviparous squamates.
Thus, large ratios do not indicate viviparity in fossil taxa to which the extant squamate model is applicable.
Applying differences in birth size, age at maturation, and maximum longevity that are observed between extant viviparous and oviparous squamates to our Nothosaurus sample, they identified 7 out of 24 specimens as being potentially viviparous.
Conversely, they suggested oviparity for many nothosaurs but also for many pachypleurosaur samples.
Under the assumption that the entire clade Pachypleurosauria was viviparous, the majority of nothosaurs would also have been viviparous as they comprised trait combinations similar to those seen in pachypleurosaurs.
Overall, this suggests that within nothosaurs and pachypleurosaurs both reproduction modes existed in different taxa.
Previous studies have successfully applied an extant squamate model to sauropterygian life‐history traits. In extant squamates, oviparity and viviparity are associated with differences in life‐history trait combinations.
A paper released in March 2019, in the journal Palaeontology, sheds light on this view. Griebeler et al. have establish growth curves for Nothosaurus specimens based on their humeral histology.
They analyzed life‐history traits derived from these curves and compared inferred traits to those of modern squamates and pachypleurosaurs to assess their reproduction mode.
Their data shows birth to adult size ratios (i.e. birth size divided by the mother's size) provides a good estimate of clutch sizes in extant squamates and in viviparous extinct marine reptiles, but these ratios cannot discriminate viviparous and oviparous squamates.
Thus, large ratios do not indicate viviparity in fossil taxa to which the extant squamate model is applicable.
Applying differences in birth size, age at maturation, and maximum longevity that are observed between extant viviparous and oviparous squamates to our Nothosaurus sample, they identified 7 out of 24 specimens as being potentially viviparous.
Conversely, they suggested oviparity for many nothosaurs but also for many pachypleurosaur samples.
Under the assumption that the entire clade Pachypleurosauria was viviparous, the majority of nothosaurs would also have been viviparous as they comprised trait combinations similar to those seen in pachypleurosaurs.
Overall, this suggests that within nothosaurs and pachypleurosaurs both reproduction modes existed in different taxa.