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Rebbachisauridae is a clade of sauropod dinosaurs whose maximum diversification and abundance are known from the Cretaceous of South America. We describe an anterior caudal vertebra, MDPA-Pv 007, from the Upper Cretaceous of Argentine Patagonia, whose characters allow it to be referred to this clade. Also, two phylogenetic analyses reinforce the referral of the new material more exclusively to Rebbachisaurinae. We analyze pneumatic structures using the first CT scans of a caudal element of a rebbachisaurid. The excellent preservation of MDPA-Pv 007, combined with CT images, allows us to document external fossae and foramina that connect to larger internal chambers, constituting unambiguous evidence of pneumaticity. The centrum of MDPA-Pv 007 is camerate, with large interconnected internal chambers; this is accompanied by a neural arch with wide and deep fossae. Caudal pneumaticity has a complex phylogenetic distribution among neosauropods. This feature may have evolved independently in diplodocoids and titanosauriforms, or it could be ancestral for Neosauropoda but secondarily lost in a few lineages. Future investigations, taking advantage of new technologies, will provide insights into the phylogenetic distribution and paleobiological implications of pneumaticity in sauropod dinosaurs and other fossil archosaurs. [ABSTRACT FROM AUTHOR]

Tooth-marked bones provide important evidence for feeding choices made by extinct carnivorous animals. In the case of the dinosaurs, most bite traces are attributed to the large and robust osteophagous tyrannosaurs, but those of other large carnivores remain underreported. Here we report on an extensive survey of the literature and some fossil collections cataloging a large number of sauropod bones (68) from the Upper Jurassic Morrison Formation of the USA that bear bite traces that can be attributed to theropods. We find that such bites on large sauropods, although less common than in tyrannosaur-dominated faunas, are known in large numbers from the Morrison Formation, and that none of the observed traces showed evidence of healing. The presence of tooth wear in non-tyrannosaur theropods further shows that they were biting into bone, but it remains difficult to assign individual bite traces to theropod taxa in the presence of multiple credible candidate biters. The widespread occurrence of bite traces without evidence of perimortem bites or healed bite traces, and of theropod tooth wear in Morrison Formation taxa suggests preferential feeding by theropods on juvenile sauropods, and likely scavenging of large-sized sauropod carcasses. [ABSTRACT FROM AUTHOR]

Pneumatic dorsal ribs are known for many sauropods, but to date costal pneumaticity has received relatively little attention. In particular, the pneumatic ribs of the holotype specimen of Brachiosaurus altithorax have been largely overlooked, although they present a unique configuration of pneumatic features. One rib, with a pneumatic foramen some distance down the shaft, was briefly described and illustrated in the early 20th century by Elmer S. Riggs. A second rib with a pneumatic foramen in the tuberculum of the rib has not previously been described or illustrated. This previously undescribed foramen is similar in location to those in some dorsal ribs of Brontosaurus excelsus and Giraffatitan brancai, but differs from them in both size and shape. The contrasting sites of costal pneumaticity in the holotype individual of Brachiosaurus altithorax emphasize the generally opportunistic mode of postcranial pneumatization, in both sauropods and other ornithodirans, but conform to models of pneumatization following vascularization. [ABSTRACT FROM AUTHOR]

The origin of the air sac system present in birds has been an enigma for decades. Skeletal pneumaticity related to an air sac system is present in both derived non-avian dinosaurs and pterosaurs. But the question remained open whether this was a shared trait present in the common avemetatarsalian ancestor. We analyzed three taxa from the Late Triassic of South Brazil, which are some of the oldest representatives of this clade (233.23 ± 0.73 Ma), including two sauropodomorphs and one herrerasaurid. All three taxa present shallow lateral fossae in the centra of their presacral vertebrae. Foramina are present in many of the fossae but at diminutive sizes consistent with neurovascular rather than pneumatic origin. Micro-tomography reveals a chaotic architecture of dense apneumatic bone tissue in all three taxa. The early sauropodomorphs showed more complex vascularity, which possibly served as the framework for the future camerate and camellate pneumatic structures of more derived saurischians. Finally, the evidence of the absence of postcranial skeletal pneumaticity in the oldest dinosaurs contradicts the homology hypothesis for an invasive diverticula system and suggests that this trait evolved independently at least 3 times in pterosaurs, theropods, and sauropodomorphs. [ABSTRACT FROM AUTHOR]

Skeletal pneumaticity is found in the presacral vertebrae of most sauropod dinosaurs, but pneumaticity is much less common in the vertebrae of the tail. We describe previously unrecognized pneumatic fossae in the mid-caudal vertebrae of specimens of Giraffatitan and Apatosaurus. In both taxa, the most distal pneumatic vertebrae are separated from other pneumatic vertebrae by sequences of three to seven apneumatic vertebrae. Caudal pneumaticity is not prominent in most individuals of either of these taxa, and its unpredictable development means that it may be more widespread than previously recognised within Sauropoda and elsewhere in Saurischia. The erratic patterns of caudal pneumatization in Giraffatitan and Apatosaurus, including the pneumatic hiatuses, show that pneumatic diverticula were more broadly distributed in the bodies of the living animals than are their traces in the skeleton. Together with recently published evidence of cryptic diverticula—those that leave few or no skeletal traces—in basal sauropodomorphs and in pterosaurs, this is further evidence that pneumatic diverticula were widespread in ornithodirans, both across phylogeny and throughout anatomy. [ABSTRACT FROM AUTHOR]

The necks of sauropod dinosaurs were a key factor in their evolution. The habitual posture and range of motion of these necks has been controversial, and computer-aided studies have argued for an obligatory sub-horizontal pose. However, such studies are compromised by their failure to take into account the important role of intervertebral cartilage. This cartilage takes very different forms in different animals. Mammals and crocodilians have intervertebral discs, while birds have synovial joints in their necks. The form and thickness of cartilage varies significantly even among closely related taxa. We cannot yet tell whether the neck joints of sauropods more closely resembled those of birds or mammals. Inspection of CT scans showed cartilage:bone ratios of 4.5% for Sauroposeidon and about 20% and 15% for two juvenile Apatosaurus individuals. In extant animals, this ratio varied from 2.59% for the rhea to 24% for a juvenile giraffe. It is not yet possible to disentangle ontogenetic and taxonomic signals, but mammal cartilage is generally three times as thick as that of birds. Our most detailed work, on a turkey, yielded a cartilage:bone ratio of 4.56%. Articular cartilage also added 11% to the length of the turkey's zygapophyseal facets. Simple image manipulation suggests that incorporating 4.56% of neck cartilage into an intervertebral joint of a turkey raises neutral posture by 15°. If this were also true of sauropods, the true neutral pose of the neck would be much higher than has been depicted. An additional 11% of zygapophyseal facet length translates to 11% more range of motion at each joint. More precise quantitative results must await detailed modelling. In summary, including cartilage in our models of sauropod necks shows that they were longer, more elevated and more flexible than previously recognised. [ABSTRACT FROM AUTHOR]

Skeletal pneumaticity is found in the presacral vertebrae of most sauropod dinosaurs, but pneumaticity is much less common in the vertebrae of the tail. We describe previously unrecognized pneumatic fossae in the mid-caudal vertebrae of specimens of Giraffatitan and Apatosaurus. In both taxa, the most distal pneumatic vertebrae are separated from other pneumatic vertebrae by sequences of three to seven apneumatic vertebrae. Caudal pneumaticity is not prominent in most individuals of either of these taxa, and its unpredictable development means that it may be more widespread than previously recognised within Sauropoda and elsewhere in Saurischia. The erratic patterns of caudal pneumatization in Giraffatitan and Apatosaurus, including the pneumatic hiatuses, show that pneumatic diverticula were more broadly distributed in the bodies of the living animals than are their traces in the skeleton. Together with recently published evidence of cryptic diverticula—those that leave few or no skeletal traces—in basal sauropodomorphs and in pterosaurs, this is further evidence that pneumatic diverticula were widespread in ornithodirans, both across phylogeny and throughout anatomy. [ABSTRACT FROM AUTHOR]

It has recently been argued that neural spine bifurcation increases through ontogeny in several Morrison Formation sauropods, that recognition of ontogenetic transformation in this 'key character' will have sweeping implications for sauropod phylogeny, and that Suuwassea and Haplocanthosaurus in particular are likely to be juveniles of known diplodocids. However, we find that serial variation in sauropod vertebrae can mimic ontogenetic change and is therefore a powerful confounding factor, especially when dealing with isolated elements whose serial position cannot be determined. When serial position is taken into account, there is no evidence that neural spine bifurcation increased over ontogeny in Morrison Formation diplodocids. Through phylogenetic analysis we show that neural spine bifurcation is not a key character in sauropod phylogeny and that Suuwassea and Haplocanthosaurus are almost certainly not juveniles of known diplodocids. Skeletochronology based on the sequence of skeletal fusions during ontogeny can provide relative ontogenetic ages for some sauropods. Although such data are sparsely available to date and often inconsistent among sauropod genera they provide another line of evidence for testing hypotheses of ontogenetic synonymy. Data from skeletal fusions suggest that Suuwassea and Haplocanthosaurus are both valid taxa and that neither is an ontogenetic morph of a known diplodocid. [ABSTRACT FROM AUTHOR]

The recurrent laryngeal nerve is an often cited example of "unintelligent design" in biology, especially in the giraffe. The nerve appears early in embryonic development, before the pharyngeal and aortic arches are separated by the development of the neck. The recurrent course of the nerve from the brain, around the great vessels, to the larynx, is shared by all extant tetrapods. Therefore we may infer that the recurrent laryngeal nerve was present in extinct tetrapods, had the same developmental origin, and followed the same course. The longest-necked animals of all time were the extinct sauropod dinosaurs, some of which had necks 14 meters long. In these animals, the neurons that comprised the recurrent laryngeal nerve were at least 28 meters long. Still longer neurons may have spanned the distance from the end of the tail to the brainstem, as in all extant vertebrates. In the longest sauropods these neurons may have been 40-50 meters long, probably the longest cells in the history of life. [ABSTRACT FROM AUTHOR]

Postcranial skeletal pneumaticity (PSP) is present in a range of basal sauropodomorphs spanning the basal sauropodomorph-sauropod transition. We describe the PSP of five taxa, Plateosaurus engelhardti, Eucnemesaurus fortis, Aardonyx celestae, Antetonitrus ingenipes, and an unnamed basal sauropod from Spion Kop, South Africa (hereafter referred to as the Spion Kop sauropod). The PSP of Plateosaurus is apparently sporadic in its occurrence and has only been observed in very few specimens, in which it is of very limited extent, affecting only the posterior cervical vertebrae and possibly the mid dorsals in one specimen. The PSP of Eucnemesaurus, Aardonyx, Antetonitrus, and the Spion Kop sauropod consists of subfossae (fossa-within-fossa structures) that excavate the vertices of the posterior infradiapophyseal fossae of the posterior dorsal vertebrae. These subfossae range from simple shallow depressions (Eucnemesaurus) to deep, steepsided, internally subdivided and asymmetrically developed chambers (Antetonitrus). The middle and anterior dorsal vertebrae of these taxa lack PSP, demonstrating that abdominal air sacs were the source of the invasive diverticula. The presence of pneumatic features within the infradiapophyseal fossae suggest that the homologous fossae of more basal saurischians and dinosauriforms were receptacles that housed pneumatic diverticula. We suggest that it is probable that rigid non-compliant lungs ventilated by compliant posterior air sacs evolved prior to the origination of Dinosauria. [ABSTRACT FROM AUTHOR]

The article focuses on the evidence for bird-like air sacs in Saurischian dinosaurs. The documentation of the origin and evolution of postcanial skeletal pneumaticity (PSP) in sauropodomorphs provides information that help to phylogenetically constrain inferences about the evolution of PSP and presence of air sacs in Saurischia. It accounts that the cervical vertebrae of most sauropods and therapods have invasive pneumatic features. Pneumatic furculae are present in the dromaeosaur Buitreraptor and the basal tetanuran Aerosteon suggests clavicular air sac was present. Moreover, the posterior dorsal, sacral, and anterior caudal vertebrae are pneumatic in many sauropods and nonavian therapods.