Barosaurus

Description

Barosaurus was an enormous animal, with some adults measuring about 25 - in length and weighing about 12–20 metric tons (13–22 short tons). The estimated tail length of Barosaurus makes up about half the total body length. According to Mike Taylor, the 1.37 m long vertebra BYU 9024, previously identified as part of the type individual of Supersaurus vivianae, In 2020 Molina-Perez and Larramendi estimated it to be slightly smaller at 45 m and 60 t. However, research presented by Brian Curtice at the Society of Vertebrate Paleontology conference has supported the previous interpretation of BYU 9024 as a Supersaurus vertebra. Despite this, there are other specimens that provide evidence of gigantic Barosaurus individuals which may have been among the longest dinosaurs. One of these is a series of three cervical vertebrae (BYU 3GR/BYU 20815) and the third vertebra is 1110 mm to 1220 mm in length. Dr Mike Taylor and Dr Matt Wedel compared the size of this bone to the same bone in smaller Barosaurus specimens, such as AMNH 6341, and estimated the neck length of the BYU 3GR/20815 Barosaurus at 12.07 -, which would make it one of the longest necks of any dinosaur and indicate a total body length of around 40 m. * Barosaurus* was differently proportioned than its close relative Diplodocus, with a longer neck and shorter tail, but was about the same length overall. It was longer than Apatosaurus, but its skeleton was less robust.

Sauropod skulls are rarely preserved, and scientists have yet to discover a Barosaurus skull. Related diplodocids like Apatosaurus and Diplodocus had long, low skulls with peg-like teeth confined to the front of the jaws.

Most of the distinguishing skeletal features of Barosaurus were in the vertebrae, although a complete vertebral column has never been found. Diplodocus and Apatosaurus both had 15 cervical (neck) and 10 dorsal (trunk) vertebrae, while Barosaurus had only 9 dorsals. A dorsal may have been converted into a cervical vertebra, for a total of 16 vertebrae in the neck. Barosaurus cervicals were similar to those of Diplodocus, but some were up to 50% longer. The neural spines protruding from the top of the vertebrae were neither as tall or as complex in Barosaurus as they were in Diplodocus. In contrast to its neck vertebrae, Barosaurus had shorter caudal (tail) vertebrae than Diplodocus, resulting in a shorter tail. The chevron bones lining the underside of the tail were forked and had a prominent forward spike, much like the closely related Diplodocus. The tail probably ended in a long whiplash, much like Apatosaurus, Diplodocus and other diplodocids, some of which had up to 80 tail vertebrae.

The limb bones of Barosaurus were virtually indistinguishable from those of Diplodocus. Barosaurus feet have never been discovered, but like other sauropods, it would have been digitigrade, with all four feet each bearing five small toes. A large claw adorned the inside digit on the manus (forefoot) while smaller claws tipped the inside three digits of the pes (hindfoot).

In 2008, Lehman and Woodward estimated the minimum and maximum ages of Barosaurus to be at least 21 and at most 39 years, and the average growth rate to be 297 - per year.

Classification and systematics

Barosaurus is a member of the sauropod family Diplodocidae, and sometimes placed with Diplodocus in the subfamily Diplodocinae. Diplodocids are characterized by long tails with over 70 vertebrae, shorter forelimbs than other sauropods, and numerous features of the skull. Diplodocines like Barosaurus and Diplodocus have slenderer builds and longer necks and tails than apatosaurines, the other subfamily of diplodocids.

Below is a cladogram of Diplodocinae after Tschopp, Mateus, and Benson (2015).

The systematics (evolutionary relationships) of Diplodocidae are becoming better established. Diplodocus has long been regarded as the closest relative of Barosaurus. Barosaurus is monospecific, containing only the type species, B. lentus, while at least three species belong to the genus Diplodocus. Tornieria (formerly "Barosaurus" africanus) and Australodocus from the famous Tendaguru Beds of Tanzania in eastern Africa have also been classified as diplodocines. With its elongated neck vertebrae, Tornieria may have been particularly closely related to Barosaurus. Diplodocid fossils are found in North America, Europe, and Africa. More distantly related within Diplodocoidea are the families Dicraeosauridae and Rebbachisauridae, found only on the southern continents.

Discovery, naming, and history

The first Barosaurus remains were discovered in the Morrison Formation of South Dakota by Ms. Isabella R. Ellerman, postmistress of Postville, and excavated by Othniel Charles Marsh and John Bell Hatcher of Yale University in 1889. Only six tail vertebrae were recovered at that time, forming the type specimen (YPM 429) of a new species, which Marsh named Barosaurus lentus, from the Classical Greek words βαρυς (barys) ("heavy") and σαυρος (sauros) ("lizard"), and the Latin word lentus ("slow"). The rest of the type specimen was left in the ground under the protection of the landowner, Ms Rachel Hatch, until it was collected nine years later, in 1898, by Marsh's assistant, George Reber Wieland. These new remains consisted of vertebrae, ribs, and limb bones. In 1896 Marsh had placed Barosaurus in the Atlantosauridae; in 1898 it was classified by him as a diplodocid for the first time. In his last published paper before his death, Marsh named two smaller metatarsals found by Wieland as a second species, Barosaurus affinis, but this has long been considered a junior synonym of B. lentus.

After the turn of the 20th century, Pittsburgh's Carnegie Museum of Natural History sent fossil hunter Earl Douglass to Utah to excavate the Carnegie Quarry in the area now known as Dinosaur National Monument. Four neck vertebrae, each 1 meter (3 feet) long, were collected in 1912 near a specimen of Diplodocus, but a few years later, William Jacob Holland realized they belonged to a different species. Meanwhile, the type specimen of Barosaurus had finally been prepared at Yale in the winter of 1917 and was fully described by Richard Swann Lull in 1919. Based on Lull's description, Holland referred the vertebrae (CM 1198), along with a second partial skeleton found by Douglass in 1918 (CM 11984), to Barosaurus. This second Carnegie specimen remains in the rock wall at Dinosaur National Monument and was not fully prepared until the 1980s.

The most complete specimen of Barosaurus lentus was excavated from the Carnegie Quarry in 1923 by Douglass, now working for the University of Utah after the death of U.S. Steel founder Andrew Carnegie, who had been financing Douglass' earlier work in Pittsburgh. Material from this specimen was originally spread across three institutions. Most of the back vertebrae, ribs, pelvis, hindlimb and most of the tail stayed at the University of Utah, while the neck vertebrae, some back vertebrae, the shoulder girdle and forelimb were shipped to the National Museum of Natural History in Washington D.C., and a small section of tail vertebrae ended up in the Carnegie Museum in Pittsburgh. However, in 1929 Barnum Brown arranged for all of the material to be shipped to the American Museum of Natural History in New York City, where it remains today. A cast of this specimen (AMNH 6341) was controversially mounted in the lobby of the American Museum, rearing up to defend its young (AMNH 7530, now classified as Kaatedocus siberi) from an attacking Allosaurus fragilis.

More recently, more vertebrae and a pelvis were recovered in South Dakota. This material (SDSM 25210 and 25331) is stored in the collection of the South Dakota School of Mines and Technology in Rapid City.

Darren Naish has noted a common error in books of the late 20th century to depict Barosaurus as a kind of brachiosaur-like short tailed sauropod with raphes on its neck and body, and often curving the upper half of its neck downwards into a U-shape, citing it as an example of a Palaeoart meme. This originated with a drawing by Robert Bakker in a 1968 article, in which two Barosaurus appeared to have short tails due to a mix of foreshortening and one obscuring the other.

In 2007, paleontologist David Evans was flying to the U.S. Badlands when he discovered reference to a Barosaurus skeleton (ROM 3670) in the collection of the Royal Ontario Museum in Toronto, where he had recently become a curator. Earl Douglass had excavated this specimen at the Carnegie Quarry in the early 20th century; the ROM acquired it in a 1962 trade with the Carnegie Museum. The specimen was never exhibited and remained in storage until its rediscovery by David Evans 45 years later. He returned to Toronto and searched the storage areas and found many fragments, large and small, of the skeleton. It is now a centrepiece of the ROM's dinosaur exhibit, in the James and Louise Temerty Galleries of the Age of Dinosaurs.{{cite press release |access-date=February 25, 2009}} At almost 27.5 meters (90 feet) long, the specimen is the largest dinosaur ever to be mounted in Canada. The specimen is about 40% complete. As a skull of Barosaurus has never been found, the ROM specimen wears the head of a Diplodocus. Each bone is mounted on a separate armature so that it can be removed from the skeleton for study and then replaced without disturbing the rest of the skeleton. (See video "Dino Workshop" at reference.) The ROM specimen is nicknamed "Gordo" after Gordon Edmunds, the museum curator who arranged for the skeleton to be brought to the ROM, and who had hoped to display it fully but was unable to. John McIntosh believes that the ROM's skeleton is the same individual represented by four neck vertebrae labeled "CM 1198" in the collection of the Carnegie Museum.

Misidentified discoveries in Africa

In 1907, German paleontologist Eberhard Fraas discovered the skeletons of two sauropods on an expedition to the Tendaguru Beds in German East Africa (now Tanzania). He classified both specimens in the new genus Gigantosaurus, with each skeleton representing a new species (G. africanus and G. robustus). |author-link=Harry Govier Seeley |author-link=Werner Janensch In 1991, "Gigantosaurus" robustus was recognized as a titanosaur and placed in a new genus, Janenschia, as J. robusta.

Paleobiology

Feeding

The structure of the cervical vertebrae of Barosaurus allowed for a significant degree of lateral flexibility in the neck, but restricted vertical flexibility. This suggests a different feeding style for this genus when compared to other diplodocids. Barosaurus swept its neck in long arcs at ground level when feeding, which resembled the strategy that was first proposed by John Martin in 1987. The restriction in vertical flexibility suggests that Barosaurus did not primarily feed on vegetation that was high off the ground.

Paleoecology

Barosaurus remains are limited to the Morrison Formation, which is widespread in the western United States between the Great Plains and Rocky Mountains. or approximately 155 to 148 million years ago. Barosaurus fossils are found in late Kimmeridgian to early Tithonian sediments, around 150 million years old.

The Morrison Formation was deposited in floodplains along the edge of the ancient Sundance Sea, an arm of the Arctic Ocean which extended southward to cover the middle of North America as far south as the modern state of Colorado. Due to tectonic uplift to the west, the sea was receding to the north, and had retreated into what is now Canada by the time Barosaurus evolved. The sediments of the Morrison were washed down out of the western highlands, which had been uplifted during the earlier Nevadan orogeny and were now eroding. A more recent study suggested even higher CO2 concentrations of up to 3180 parts per million. Warm temperatures that led to significant evaporation year-round, along with possible rain shadow effect from the mountains to the west, led to a semi-arid climate with only seasonal rainfall. This formation is similar in age to the Solnhofen limestone Formation in Germany and the Tendaguru Formation in Tanzania. In 1877 this formation became the center of the Bone Wars, a fossil-collecting rivalry between early paleontologists Othniel Charles Marsh and Edward Drinker Cope.

The Morrison Formation records an environment and time dominated by gigantic sauropod dinosaurs such as Camarasaurus, Diplodocus, Apatosaurus and Brachiosaurus. Dinosaurs that lived alongside Barosaurus included the herbivorous ornithischians Camptosaurus, Dryosaurus, Stegosaurus and Othnielosaurus, and predators in this paleoenvironment included the theropods Saurophaganax, Allosaurus, Torvosaurus, Ceratosaurus, Marshosaurus, Stokesosaurus and Ornitholestes.{{cite book |last=Foster |first=John R. |title=Jurassic West: The Dinosaurs of the Morrison Formation and Their World (Appendix) |publisher=Indiana University Press. |year=2007 |pages=327–329 |isbn=978-0-253-34870-8

Assistant Curator David Evans mounted the ROM specimen conservatively, with a relatively low head to give the dinosaur moderate blood pressure. The extremely long neck, 10 meters (30 feet) may have developed to enable Barosaurus to feed over a wide area without moving around; it may also have enabled the dinosaurs to radiate excess body heat. Evans suggests that sexual selection might have favored those with longer necks. (See video "Neck Impossible" at reference.)

References

Books:

References

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