CONLINOCERAS TARRANTENSE

Previously Calycoceras Tarrantense, this ammonite is now called Conlinoceras tarrantense after J.P. Conlin, a famous early 20th-century fossil collector from Texas, USA.

Ammonite expert Bill Cobban used this collection to describe many Texas Cretaceous ammonites species including this species from Tarrant County, Arlington, Texas.

He was a surveyor by training and kept incredibly detailed notes on the context of his fossils.

Conlin donated his collection to the USGS and we have learned much by studying it along with other specimens from the Lone Star State. Almost a quarter of Texas is covered by Cretaceous strata, much of it fossiliferous. If we stepped back 95 million years, the world and what we now call Texas was a very different place.

95 million years ago, during the Late Cretaceous, a shallow seaway separated North America into separate eastern and western landmasses. We have a pretty complete picture in the fossil record of the western groups of species but relatively little in comparison to their cohorts in the east.

At the time this fellow was swimming our ancient seas, he was sharing the Earth with carnivorous dinosaurs, duck-billed dinosaurs, mammals, crocodilians, turtles, a variety of amphibians, prehistoric bony fish, oddly prolific sea cucumbers, various invertebrates and plants. Many of these sites are just being written up now and contain new species just being discovered.

During the Late Cretaceous Period, a shallow seaway separated North America into separate eastern and western landmasses. The Woodbine Formation in Texas preserves a rare fossil record of this time for the east, but many of these fossils are isolated and incomplete, making interpretations more difficult. Preliminary excavations at the Arlington Archosaur Site (AAS) are providing hints at a more complete ecosystem, preserving similar patterns of change to what we see in the west.

The Arlington Archosaur site contains an extraordinary diversity, abundance, and quality of fossil material, preserving one of the most complete terrestrial ecosystems known for this time period and area.

These outcrops and the fossils they contain have a lot to tell us about Late Cretaceous life in the east. Over 2200 individual specimens have been found belonging to numerous groups including carnivorous dinosaurs, duck-billed dinosaurs, crocodilians, turtles, mammals, amphibians, sharks, bony fish, invertebrates, and plants.

Many of the fossils found here represent brand new species and studying these fossils will help to establish the geographic and environmental forces that shaped Cretaceous ecosystems in North America by providing a necessary comparison to the fossil record of the west.

VOAY ROBUSTUS

This big beastie is Voay robustus. You likely met him first as Crocodylus‭ (‬C.‭ ‬robustus‭) from his original naming by Grandidier and Vaillant in‭ 1872. 

Looking more closely at his remains revealed that he is nearer in design to the dwarf crocodile Osteolaemus. 

The type series cannot be identified, but the original description includes details consistent with known specimens that almost certainly pertain to the same species. 

It had a prominent triangular ‘horn’ on the posterolateral corner of each squamosal; near-exclusion of the nasals from the external naris; constricted supratemporal fenestral rims; a dorsoventrally deep snout; a constricted external mandibular fenestra in which the surangular–angular suture emerges from the posterior rather than posteroventral margin; and robust limb and limb-girdle elements. 

It shares with Osteolaemus, and with several extinct crocodylids from the Neogene of Africa, a depressed surface of the pterygoid around the internal choana forming a choanal ‘neck’. It cannot be referred to as Crocodylus and a new praenomen, Voay, was established for its reception. 

In 2007, Christopher‭ ‬A.‭ ‬Brochu created a new genus, Voay, and this fellow became Voay robustus. Christopher published his work in the Zoological Journal of the Linnean Society in Volume 150, Issue 4, August 2007, Pages 835-863. Voay lived into the Holocene of Madagasgar, perhaps meeting some of our relatives 2,000 years ago. Voay was replaced by Crocodylus niloticus in Madagascar as they moved into the niche left by Voay's ultimate demise. 

https://doi.org/10.1111/j.1096-3642.2007.00315.x

WHALER

 

INKY BEAUTY: AMMONITE OF PONGO DE MANSERICHE

This inky beauty is Prolyelliceras ulrichi (Knechtel, 1947) a fast-moving nektonic carnivorous ammonite from Cretaceous lithified, black, carbonaceous limestone outcrops in the Pongo de Manseriche gorge in northwest Peru. 

If you look closely, you can see that this specimen shows a pathology, a slight deviation to the side of the siphonal of the ammonite. We see Prolyelliceras from the Albian to Middle Albian from five localities in Peru.

The canyons of the Amazon River system in the eastern ranges of the Andes of Peru are known by the Indian name pongo. 

The most famous of these is the Pongo de Manseriche, cut by the Marañon River through the eastern range of the Andes, where it emerges from the cordillera into the flat terrane of the Amazon Basin. The fossil exposures here are best explored by boat. The reality of the collecting is similar to the imagined. I was chatting with Betty Franklin, VIPS, about this. They float along and pick up amazing specimen after amazing specimen. When the water rises, the ammonites are aided in their erosion out of the cliffs.  

The Pongo de Manseriche lies nearly 500 miles upstream from Iquitos, and consequently nearly 3,000 miles above the mouth of the Amazon River. It is situated in the heart of the montaña, in a vast region the ownership of which has long been in dispute between Peru and Ecuador, but over which neither country exercises any police or other governmental control. There is an ancient tradition of the indigenous people of the vicinity that one of their gods descended the Marañón and another ascended the Amazon to communicate with him. Together they opened the pass called the Pongo de Manseriche.

Reference: M. M. Knechtel. 1947. Cephalopoda. In: Mesozoic fossils of the Peruvian Andes, Johns Hopkins University Studies in Geology 15:81-139

W. J. Kennedy and H. C. Klinger. 2008. Cretaceous faunas from Zululand and Natal, South Africa. The ammonite subfamily Lyelliceratinae Spath, 1921. African Natural History 4:57-111. The beauty you see here is in the collection of the deeply awesome José Juárez Ruiz.

FOSSILIZED SEA URCHIN: AM'DA'MA

This lovely little biscuit is a Holectypus sea urchin from 120 million-year-old deposits from the Lagniro Formation of Madagascar.

The specimen you see here is in the collections of my beautiful friend Ileana. She and I were blessed to meet in China many years ago and formed an unbreakable bond that happens so few times in one's life. 

Holectypus are a genus of extinct echinoids related to modern sea urchins and sand dollars. They were abundant from the Jurassic to the Cretaceous (between 200 million and 65.5 million years ago).

This specimen is typical of Holectypus with his delicate five-star pattern adorning a slightly rounded test and flattened bottom. The specimen has been polished and was harvested both for its scientific and aesthetic value. 

I have many wonderful memories of collecting their modern cousins that live on the north end of Vancouver Island and along the beaches of Balaklava Island. In the Kwak̓wala language of the Kwakiutl or Kwakwaka'wakw, speakers of Kwak'wala, of the Pacific Northwest, sea urchins are known as a̱m'da̱'ma and it is this name that I hear in my head when I think of them.

In echinoids, the skeleton is almost always made up of tightly interlocking plates that form a rigid structure or test — in contrast with the more flexible skeletal arrangements of starfish, brittle stars, and sea cucumbers. Test shapes range from nearly globular, as in some sea urchins, to highly flattened, as in sand dollars. 

Sea Urchin Detail

Living echinoids are covered with spines, which are movable and anchored in sockets in the test. These spines may be long and prominent, as in typical sea urchins and most have lovely raised patterns on their surface. 

In sand dollars and heart urchins, however, the spines are very short and form an almost felt-like covering. The mouth of most echinoids is provided with five hard teeth arranged in a circle, forming an apparatus known as Aristotle’s lantern.

Echinoids are classified by the symmetry of the test, the number and arrangement of plate rows making up the test, and the number and arrangement of respiratory pore rows called petals. Echinoids are divided into two subgroups: regular echinoids, with nearly perfect pentameral (five-part) symmetry; and irregular echinoids with altered symmetry.

Because most echinoids have rigid tests, their ability to fossilize is greater than that of more delicate echinoderms such as starfish, and they are common fossils in many deposits. The oldest echinoids belong to an extinct regular taxon called the Echinocystitoidea. 

They first appeared in the fossil record in the Late Ordovician. Cidaroids or pencil urchins appear in the Mississippian (Early Carboniferous) and were the only echinoids to survive the mass extinction at the Permo-Triassic boundary. Echinoids did not become particularly diverse until well after the Permo-Triassic mass extinction event, evolving the diverse forms we find them in today. 

True sea urchins first appear in the Late Triassic, cassiduloids in the Jurassic, and spatangoids or heart urchins in the Cretaceous. Sand dollars, a common and diverse group today, do not make an appearance in the fossil record until the Paleocene. They remain one of my favourite echinoderms and stand tall amongst the most pleasing of the invertebrates.

AMMONITE TRACE FOSSIL

This is a particularly fetching trace fossil of an ammonite.

Trace fossils or ichnofossils are burrows, footprints, tracks or even faeces left behind by plants and animals that lived long ago. 

Animals may have scurried across a muddy exposure or sea bottom, perhaps eaten a tasty meal then pooped it out — leaving behind clues to how they lived, what they ate and what the environment was like at the time. These are wonderfully informative clues to our ancient world.

OPABINIA REGALIS

Opabinia regalis is an extinct stem-group arthropod found in the Greater Phyllopod Bed, Middle Cambrian Burgess Shale Lagerstätte of British Columbia, Canada. 

These marine arthropods flourished from 505 million years ago to 487 million years ago.

Charles Doolittle Walcott found nine partially complete fossils of Opabinia regalis and a few of what he classified as Opabinia media, that he published in 1912. 

The bizarre arthropod's name is derived from the Opabin pass between Mount Hungabee and Mount Biddle, southeast of Lake O'Hara, British Columbia, Canada. 

In 1966–1967, Harry B. Whittington found a rather good specimen which he published in 1975. He provided a detailed description based on a very thorough dissection of some specimens and photographs of these specimens lit from a variety of angles. Harry was a very thorough fellow.

But he was still ridiculed. Opabinia looked so strange that the audience at the first presentation of Whittington's analysis laughed.

Earth's ancient seas teemed with new life 541 - 485 Million Years Ago. The Cambrian Explosion had arrived. Weird and wonderful life forms like Hallucigenia and Anomalocaris are found in the fossil record giving us a peek at ancient life half a billion years ago.

THE DUDLEY BUG: CALYMENE BLUMENBACHII

A lovely rolled trilobite, Calymene blumenbachii,  from outcrops in the UK. This wee beauty is in the collections of the deeply awesome Theresa Paul Spink Dunn — or perhaps in her daughter Layla's collections as she is quite the budding palaeontologist. This Silurian beauty is from the Homerian, Wenlock Series, Wrens Nest, Dudley, UK.

Calymene blumenbachii, sometimes erroneously spelled blumenbachi, is a species of trilobite found in the limestone quarries of the Wren's Nest in Dudley, England.

Nicknamed the Dudley Bug or Dudley Locust by an 18th-century quarryman, it became a symbol of the town and featured on the Dudley County Borough Council coat-of-arms. Calymene blumenbachii is commonly found in Silurian rocks (422.5-427.5 million years ago) and is thought to have lived in the shallow waters of the Silurian, in low energy reefs.

This particular species of Calymene — a fairly common genus in the Ordovician-Silurian — is unique to the Wenlock series in England and comes from the Wenlock Limestone Formation in Much Wenlock and the Wren's Nest in Dudley. These sites seem to yield trilobites more readily than any other areas on the Wenlock Edge, and the rock here is dark grey as opposed to yellowish or whitish as it appears on other parts of the Edge, just a few miles away, in Church Stretton and elsewhere. This suggests local changes in the environment in which the rock was deposited. The Wenlock Edge quarry is closed now to further collecting but may be open to future research projects. We shall have to see.

PIKAIA GRACILIENS: MIDDLE CAMBRIAN GRACE

Pikaia graciliens is an extinct, primative chordate animals from the Middle Cambrian Burgess Shale Lagerstätte of British Columbia, Canada. 

These lovelies swam by moving their bodies in a series of zigzag curves similar to the movement of eels, all the while filtering particles from the water.

Although primitive, Pikaia shows the essential prerequisites for vertebrates. When alive, Pikaia was a compressed, leaf-shaped animal with an expanded tail fin; the flattened body is divided into pairs of segmented muscle blocks, seen as faint vertical lines. 

The muscles lie on either side of a flexible structure resembling a rod that runs from the tip of the head to the tip of the tail. It swam by throwing its body into a series of S-shaped undulating movements that mimicked the movement of eels. Fish inherited this same swimming movement, but they generally have stiffer backbones so it does not quite have the same visual effect. 

Pikaia was likely a slow swimmer since it lacked the fast-twitch fibres that we associate with rapid swimming in modern chordates. Still, even that form of movement in the Middle Cambrian is impressive in terms of mobility and design.

Conway Morris and Caron (2012) published an exhaustive description based on more than one hundred known fossil specimens. Through their deeper look at this primitive marine mystery, they discovered new and unexpected characteristics that they recognized as primitive features of the first chordate animals. On the basis of these findings, they constructed a new scenario for chordate evolution. 

Subsequently, Mallatt and Holland reconsidered Conway Morris and Caron's description and concluded that many of the newly recognized characters are unique, already-divergent specializations that would not be helpful for establishing Pikaia as a basal chordate.

PTEROSAURS: SOARING ANCIENT SKIES

If you could travel through time and go back to observe our ancient skies, you would see massive pterosaurs — huge, winged flying reptiles of the extinct order Pterosauria — cruising along with you. 

They soared our skies during most of the Mesozoic — from the late Triassic to the end of the Cretaceous (228 to 66 million years ago). 

By the end of the Cretaceous, they had grown to giants and one of their brethren, Quetzalcoatlus, a member of the family Azhdarchidae, boasts being the largest known flying animal that ever lived. 

They were the earliest vertebrates known to have evolved powered flight. Their wings were formed by a membrane of skin, muscle, and other tissues stretching from the ankles to a dramatically lengthened fourth finger.

PISTA DE BAILE JURÁSICA

This busy slate grey dinosaur trackway from the Iberian Peninsula looks more like a dance floor than the thoroughfare it is. 

The numerous theropod dinosaur tracks — with a few enormous sauropod tracks thrown in for good measure — cover the entire surface. 

The local soil has a bit of rusty iron ore in it that highlights each print nicely when the soil is blown into the depressions the tracks left. 

The dinosaurs crossed this muddy area en masse sometime back in the Jurassic.

The Iberian Peninsula is the westernmost of the three major southern European peninsulas — the Iberian, Italian, and Balkan. It is bordered on the southeast and east by the Mediterranean Sea, and on the north, west, and southwest by the Atlantic Ocean. The Pyrenees mountains are situated along the northeast edge of the peninsula, where it adjoins the rest of Europe. Its southern tip is very close to the northwest coast of Africa, separated from it by the Strait of Gibraltar and the Mediterranean Sea.

The Iberian Peninsula contains rocks of every geological period from the Ediacaran to the recent, and almost every kind of rock is represented. To date, there are 127 localities of theropod fossil finds ranging from the Callovian-Oxfordian — Middle-Upper Jurassic — to the Maastrichtian (Upper Cretaceous), with most of the localities concentrated in the Kimmeridgian-Tithonian interval and the Barremian and Campanian stages. The stratigraphic distribution is interesting and suggests the existence of ecological and/or taphonomic biases and palaeogeographical events that warrant additional time and attention.

As well as theropods, we also find their plant-eating brethren. This was the part of the world where the last of the hadrosaurs, the duck-billed dinosaurs, lived then disappeared in the Latest Cretaceous K/T extinction event 65.5 million years ago.

The core of the Iberian Peninsula is made up of a Hercynian cratonic block known as the Iberian Massif. On the northeast, this is bounded by the Pyrenean fold belt, and on the southeast, it is bounded by the Baetic System. These twofold chains are part of the Alpine belt. To the west, the peninsula is delimited by the continental boundary formed by the magma-poor opening of the Atlantic Ocean. The Hercynian Foldbelt is mostly buried by Mesozoic and Tertiary cover rocks to the east but nevertheless outcrops through the Sistema Ibérico and the Catalan Mediterranean System. The photo you see here is care of the awesome Pedro Marrecas from Lisbon, Portugal. Hola, Pista de baile jurásica!

Pereda-Suberbiola, Xabier; Canudo, José Ignacio; Company, Julio; Cruzado-Caballero, Penélope; Ruiz-Omenaca, José Ignacio. "Hadrosauroid dinosaurs from the latest Cretaceous of the Iberian Peninsula" Journal of Vertebrate Paleontology 29(3): 946-951, 12 de septiembre de 2009.

Pereda-Suberbiola, Xabier; Canudo, José Ignacio; Cruzado-Caballero, Penélope; Barco, José Luis; López-Martínez, Nieves; Oms, Oriol; Ruíz-Omenaca, José Ignacio. Comptes Rendus Palevol 8(6): 559-572 septiembre de 2009.

SNOWY TREE CRICKET: CHIRPING THERMOMETERS

About 250 million years ago, our once silent world became a cacophony of diverse animal sounds. 

One of the most lyrical of those voices to join the Earth's chorus were the true crickets. We can count them as some of the earliest musicians on the planet. 

This group evolved and contributed to the nocturnal circumambience of our planet a full 150 million years before our human ancestors would have heard them for the very first time. It is their long lineage that I am mindful of when I am out for an evening stroll and hear their pleasing serenade.

If you find yourself out in the woods and are wondering what the temperature might be, you need only slip closer to the nearest stand of deciduous trees to follow the musical sounds of the wee Snowy Tree Cricket, Oecanthus Fultoni, part of the order orthoptera.

Snowy Tree Crickets and their cousins double as thermometers and wee garden predators, dining on aphids and other wee beasties. Weather conditions, both hot and cold, alter the speed at which they rub the base of their wings together and consequently regulate their rate of chirping.

Listen closely for their tell-tale high pitch triple chirp sound in the early evening. Being in Canada, our crickets chirp in Celsius. To figure out the temperature, we simply count the number of chirps over a seven-second period and add five to learn the local temperature.

If did not happen to bring your calculator and you are still operating in old-school Fahrenheit, you can use this handy conversion — double the temperature in Celsius, add 32 you'll get the approximate temperature in Fahrenheit. And if you are not all that interested in the temperature, enjoy their pleasing serenade as you take your early evening stroll. They've been working on this number for millions of years. 

Daniel Otte from the Academy of Natural Sciences in Philadelphia did up a wonderful piece on the evolution of cricket songs. If you’re a keen bean & want to learn more, I'll attach the journal article for you. https://doi.org/10.2307/3503559. https://www.jstor.org/stable/3503559

DIMORPHODON: TWO TOOTH PTERODACTYLUS

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.

You can see this fellow's interesting teeth within his big, bulky skull. Dimorphodon had two distinct types of teeth in their jaws — an oddity amongst reptiles — and also proportionally short wings for their overall size. 

Just look at him. What an amazing beast. We understand their anatomy quite well today, but can you imagine being the first to study their fossils and try to make sense of them. 

The first fossil remains now attributed to Dimorphodon were found in England by fossil collector Mary Anning, at Lyme Regis in Dorset, United Kingdom in December 1828. While she faced many challenges in her life, she was blessed to live in one of the richest areas in Britain for finding fossils. 

She walked the beaches way back in the early 1800s of what would become the Jurassic Coast UNESCO World Heritage Site. The Jurassic Coast holds some of the most interesting fossils ever found — particularly within the strata of the Blue Lias which date back to the Hettangian-Sinemurian. It is one of the world’s most famous fossil sites. Millions come to explore the eroding coastline looking for treasures that provide delight and inspiration to young and old.

 

These fossil treasures provide us with tremendous insights into our world 185 million years ago when amazing animals like Dimorphodon ruled the skies. 

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.