Temporal range: Middle-Early Cretaceous, 170–136.4Ma
|Diplodocus carnegii skeleton cast, Berlin Hauptbahnhof|
Diplodocids, or members of the family Diplodocidae ("double beams"), are a group of sauropod dinosaurs. The family includes some of the longest creatures ever to walk the Earth, including Diplodocus and Supersaurus, which may have reached lengths of up to 34 metres (112 ft).
While still massive, when compared to the titanosaurids and brachiosaurs, the diplodocids were relatively slender but extremely long. They had short legs, making them the "dachshund" of giant dinosaurs; and their rear legs were longer than front legs, giving their back a distinctive downward slope towards the neck.
In 1992, a fragmentary diplodocid specimen was described with associated keratinous (horny, not bony) spines. Their arrangement suggests that in life the spines formed a continuous line down the diplodocid's back. Since dermal tissue is rarely preserved in the fossil record it is not known how widespread the feature is, but spines may have been a common feature among diplodocids or among sauropods as a whole.
Their necks were also extremely long, and according to recent computer simulations they may not have been able to lift their necks like other sauropods. However these simulations do not take vertebral cartilage into account, which would likely allow a greater range of motion. Instead of reaching up into trees, they may have used their necks to graze over a broad area. They may also have used their necks to reach into dense stands of conifers, or over marshy ground.
Their heads, like those of other sauropods, were tiny with the nasal openings on the top of the head (though in life the nostrils themselves would have been close to the tip of the snout). Their teeth were only present in the front of the mouth, and looked like pencils or pegs. They probably used their teeth to crop off food, without chewing, and relied on gastroliths (gizzard stones) to break down tough plant fibers (similar to modern birds).
Diplodocids also had long, whip-like tails, which were thick at the base and tapered off to be very thin at the end. Computer simulations have shown that the diplodocids could have easily snapped their tails, like a bullwhip. This could generate a sonic boom in excess of 200 decibels, and may have been used in mating displays, or to drive off predators. There is some circumstantial evidence supporting this as well: A number of diplodocids have been found with fused or damaged tail vertebrae, which may be a symptom of cracking their tails.
Few skin impressions of diplodocids have been found. However, at least one significant find first reported by Stephen Czerkas in 1992 preserved portions of the skin from around the tip of the tail, or "whiplash". Czerkas noted that the skin preserved a sequence of conical spines, and that other, larger spines were found scattered around larger tail vertebrae. The spines appeared to be oriented in a single row along the mid-line of the tail, and Czerkas speculated that this midline row may have continued over the animal's entire back and neck.
Long-bone histology enables researchers to estimate the age that a specific individual reached. A study by Griebeler et al. (2013) examined long bone histological data and concluded that the diplodocid MfN.R.2625 weighed 4,753 kilograms (5.2 short tons), reached sexual maturity at 23 years and died at age 24. The same growth model indicated that the diplodocid MfN.R.NW4 weighed 18,463 kilograms (20.4 short tons), and died at age 23, prior to reaching sexual maturity.
Diplodocidae was the third name given to what is now recognized as the single family of long-necked, whip-tailed sauropods. Edward Drinker Cope named the family Amphicoeliidae in 1878 for his genus Amphicoelias, sometimes considered a diplodocid. However, the name Amphicoeliidae did not come into wider use and was not used in the scientific literature after 1899, making it a nomen oblitum ("forgotten name") according to the ICZN, preventing it from displacing the name Diplodocidae as a senior synonym. More recent studies have also shown that Amphicoelias itself does not belong to this family, but is instead a more primitive diplodocoid. A similar situation occurred for the family name Atlantosauridae, named by Othniel Charles Marsh in 1877, and which Hay argued had priority over Amphicoelidae. George Olshevsky declared Atlantosauridae a nomen oblitum in 1991, though scientists such as Steel and Nowinski had treated Atlantosauridae as a valid name as late as 1971, and the former even added a subfamily, Atlantosaurinae.
Some dinosaurs have been considered diplodocids in the past but have not been found to be members of that group in later, larger analyses of the family's relationships. Australodocus, for example, was initially described as a diplodocid, but may actually have been a Macronarian. Amphicoelias was traditionally been considered a diplodocid due to its similar anatomy, but phylogenetic studies showed it to be a more basal member of the Diplodocoidea.
The relationships of species within diplodocidae has also been subject to frequent revision. A study by Lovelace, Hartman and Wahl in 2008 found that Suuwassea and Supersaurus were relatives of Apatosaurus, within the subfamily Apatosaurinae. However, subsequent analysis by Whitlock in 2011 showed that Supersaurus is slightly closer to Diplodocus than to Apatosaurus, and that Suuwassea is actually a primitive dicraeosaurid.
The subfamily Diplodocinae, was erected to include Diplodocus and its closest relatives, including Barosaurus. The Portuguese Dinheirosaurus and the African Tornieria have also been identified as close relatives of Diplodocus by some authors.
Distinguishing anatomical features
A diagnosis is a statement of the anatomical features of an organism (or group) that collectively distinguish it from all other organisms. Some, but not all, of the features in a diagnosis are also autapomorphies. An autapomorphy is a distinctive anatomical feature that is unique to a given organism or group.
The clade Diplodocidae is distinguished based on the following characteristics:
- nares: the external nares face dorsally; and the internarial bar is absent
- jugal: the jugal forms a substantial part of the caudoventral margin of the antorbital fenestra
- quadratojugal processes: the angle between the rostral quadratojugal process and the dorsal quadratojugal process is approximately 130°
- paroccipital process: the distal end of the paroccipital process is rounded and tongue-like in shape
- parasphenoid: the parasphenoid rostrum is a laterally compressed, thin spike and is lacking the longitudinal dorsal groove
- pterygoid: the ectopterygoid process of the pterygoid is located below the antorbital fenestra, and is reduced, such that it is not visible below the ventral margin of the skull when examined in lateral view; also the breadth of the main body of the pterygoid at least 33% of the length of the pterygoid
- teeth: at least 5-6 replacement teeth occur per alveolus (as observed in Nigersaurus)
- dorsal vertebrae: no more than 10 dorsal vertebrae are present
- caudal vertebrae: 70-80 caudal vertebrae are present
- pedal phalanges: pedal phalanx I-1 has a proximoventral margin drawn out into a thin plate or heel that underlies the distal end of metatarsal I; also pedal phalanx II-2 is reduced in craniocaudal length and has an irregular shape
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