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144 results for “Sauropodomorph”

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Fig. 6 in The early evolution of postcranial skeletal pneumaticity in sauropodomorph dinosaurs

Fig. 6. Neural arch of posterior cervical vertebra,?C7 of the basal sauropodomorph Aardonyx celestae Yates, Bonnan, Neveling, Chinsamy, and Blackbeard, 2010, BP/1/6615 from the Elliot Formation of Spion Kop, South Africa, in left lateral view.

opencc-by-4.0Mar 2011View details →
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Fig. 9 in The early evolution of postcranial skeletal pneumaticity in sauropodomorph dinosaurs

Fig. 9. Middle posterior dorsal vertebra of the basal sauropod Antetonitrus ingenipes Yates and Kitching, 2003, BP/1/4952 from the Upper Triassic Elliot Formation of Ladybrand, South Africa, in right lateral (A) and posterior (B) views. Left (C) and right (D) posterior infradiapophyseal fossa in oblique posterolateral and slightly ventral views. Close up of invasive left posterior infradiapophyseal subfossa (E).

opencc-by-4.0Mar 2011View details →
zenodo40/100

Fig. 1 in The early evolution of postcranial skeletal pneumaticity in sauropodomorph dinosaurs

Fig. 1. The pneumaticity profile of O'Connor (2006: fig. 12). The osteological correlate with the lowest specificity is at the bottom of the profile, while the correlate that specifies only pneumatic diverticula is at the top. The profile has been modified to indicate that pneumatic diverticula can form simple vertebral fossae.

opencc-by-4.0Mar 2011View details →
zenodo40/100

Fig. 8 in The early evolution of postcranial skeletal pneumaticity in sauropodomorph dinosaurs

Fig. 8. Sacral elements of the basal sauropodomorph Aardonyx celestae Yates, Bonnan, Neveling, Chinsamy, and Blackbeard, 2010, from the Lower Jurassic Elliot Formation of Spion Kop, South Africa. A. Incomplete neural arch of first sacral vertebra, BP/1/5379 in left lateral (A1) and posterior (A2) views. Close−up of left posterior fossa in posteroventral view (A3). Note the subfossae separated by a ridge (arrowed). B. First sacral centrum, BP/1/6241 in left lateral (B1) and oblique posterolateral and slightly ventral (B2) views. Close−up of the dorsolateral fossa (B3) developed behind the sutural scar for the attachment of the sacral rib.

opencc-by-4.0Mar 2011View details →
zenodo40/100

Fig. 5 in The early evolution of postcranial skeletal pneumaticity in sauropodomorph dinosaurs

Fig. 5. Dorsal vertebrae of the basal sauropodomorph Eucnemesaurus fortis Van Hoepen, 1920, from the Upper Triassic Elliot Formation of South Africa. A. Posterior dorsal BP/1/6107 in posterior (A1) and right posterolateral (A2) views. Close−up of the right posterior infradiapophyseal fossa in posterolateral view (A3). B. Neural arch of middle dorsal TM 119 in right lateral view.

opencc-by-4.0Mar 2011View details →
zenodo40/100

Fig. 4 in The early evolution of postcranial skeletal pneumaticity in sauropodomorph dinosaurs

Fig. 4. Cervico−dorsal transition of the vertebral column of the basal sauropodomorph Plateosaurus engelhardti Meyer, 1837, AMNH 6810 from the Upper Triassic Loewenstein Formation of the Trossingen Quarry, Germany. A. The posterior cervical vertebrae, C9 and 10 (left and middle) and the first dorsal vertebra, D1 (right) in left lateral view. B. Close−up of the pneumatic fossa on the dorsal surface of C10.

opencc-by-4.0Mar 2011View details →
zenodo40/100

Fig. 12. A in The early evolution of postcranial skeletal pneumaticity in sauropodomorph dinosaurs

Fig. 12. A phylogenetic diagram showing the distribution of invasive PSP along the vertebral column (the caudal series is truncated) in Sauropodomorpha. Black boxes indicate the presence of pneumatic fossae or invasive infradiapophyseal subfossae. Note that in the case of Plateosaurus PSP is presently known in a single specimen whereas other specimens of same taxon lack it. The phylogeny is based on Yates (2010), with the modification that Eucnemesaurus is placed closer to Anchisauria than Massospondylus is. The position of the Spion Kop sauropod is based on an unpublished analysis (AMY unpublished data). The distributions of PSP in the taxa not directly examined in this study were gleaned from the following sources: Pantydraco (Yates 2003; Wedel 2007), Tazoudasaurus (Allain and Aquesbi 2008), Shunosaurus (Zhang 1988), Jobaria (Sereno et al. 1999), Haplocanthosaurus (Hatcher 1903).

opencc-by-4.0Mar 2011View details →
zenodo40/100

Fig. 1 in Anatomy of a basal sauropodomorph dinosaur from the Early Jurassic Hanson Formation of Antarctica

Fig. 1. Map of Antarctica (A), with inset maps showing the Central Transantarctic Mountains (B), and the Beardmore Glacier area where the Mount Kirkpatrick dinosaur site is located (C). Age and generalized stratigraphy of Triassic and Jurassic portions of the Beacon Supergroup in the Beardmore Glacier area, with relative positions of Mesozoic vertebrate faunas indicated at right (D). Abbreviations: FM, Formation; L, lower member; M, middle member; U, upper member.

opencc-by-4.0Dec 2007View details →
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Fig. 5 in Anatomy of a basal sauropodomorph dinosaur from the Early Jurassic Hanson Formation of Antarctica

Fig. 5. Sauropodomorph dinosaur Glacialisaurus hammeri gen. et sp. nov. from the Early Jurassic Hanson Formation at Mt. Kirkpatrick, Beardmore Glacier region, Antarcticac. Right pes (FMNH PR1823) in anterior (A), medial (B), and posterior (C) views. Astragalus and distal tarsals have been digitally removed in B.

opencc-by-4.0Dec 2007View details →
zenodo40/100

Fig. 2 in Anatomy of a basal sauropodomorph dinosaur from the Early Jurassic Hanson Formation of Antarctica

Fig. 2. Sauropodomorph dinosaur Glacialisaurus hammeri gen. et sp. nov. from the Early Jurassic Hanson Formation at Mt. Kirkpatrick, Beardmore Glacier region, Antarcticac. Distal left femur (FMNH PR1822) in anterior (A), lateral (B), posterior (C), and medial (D) views.

opencc-by-4.0Dec 2007View details →
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Fig. 4 in Anatomy of a basal sauropodomorph dinosaur from the Early Jurassic Hanson Formation of Antarctica

Fig. 4. Sauropodomorph dinosaur Glacialisaurus hammeri gen. et sp. nov. from the Early Jurassic Hanson Formation at Mt. Kirkpatrick, Beardmore Glacier region, Antarcticac. Right astragalus (FMNH PR1823) in dorsal (A), and posterior (B) views. Right distal tarsals and metatarsus have been digitally removed in A.

opencc-by-4.0Dec 2007View details →
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Fig. 7 in Anatomy of a basal sauropodomorph dinosaur from the Early Jurassic Hanson Formation of Antarctica

Fig. 7. Phylogenetic analysis of basal sauropodomorph dinosaurs based on Yates (2007a, b), and including Glacialisaurus and several novel characters (see Appendix 1). Bootstrap values greater than 50% are listed above nodes, and Bremer decay indices greater than 1 are listed below nodes. Relationships among non−sauropodomorph taxa (here collapsed into an "outgroup" lineage) are identical to those recovered in Yates (2007a, b). Several taxon labels (in bold) follow Yates (2007b).

opencc-by-4.0Dec 2007View details →
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Fig. 6 in Anatomy of a basal sauropodomorph dinosaur from the Early Jurassic Hanson Formation of Antarctica

Fig. 6. Sauropodomorph dinosaur Glacialisaurus hammeri gen. et sp. nov. from the Early Jurassic Hanson Formation at Mt. Kirkpatrick, Beardmore Glacier region, Antarcticac. Right metatarsal II (FMNH PR1823) in distal view. Anterior is toward the top of the page. Note the medial twisting of the distal articular end, and the more robust development of the medial condyle.

opencc-by-4.0Dec 2007View details →
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Fig. 3 in Anatomy of a basal sauropodomorph dinosaur from the Early Jurassic Hanson Formation of Antarctica

Fig. 3. Sauropodomorph dinosaur Glacialisaurus hammeri gen. et sp. nov. from the Early Jurassic Hanson Formation at Mt. Kirkpatrick, Beardmore Glacier region, Antarcticac. Distal left femur (FMNH PR1822) in distal view.

opencc-by-4.0Dec 2007View details →
dryad36/100

Data from: Ten more years of discovery: revisiting the quality of the sauropodomorph dinosaur fossil record

<p>Spatiotemporal changes in fossil specimen completeness can bias our understanding of a group's evolutionary history. The quality of the sauropodomorph fossil record was assessed a decade ago, but the number of valid species has since increased by 60%, and 17% of the taxa from that study have since undergone taxonomic revision. Here, we assess how 10 years of additional research has changed our outlook on the group's fossil record. We quantified the completeness of all 307 sauropodomorph species currently considered valid, using the skeletal completeness metric, which calculates the proportion of a complete skeleton preserved for each taxon. Taxonomic and stratigraphic age revisions, rather than new species, are the drivers of the most significant differences between the current results and those of the previous assessment. No statistical differences are found when we use our new dataset to generate temporal completeness curves based on only the taxa known in 2009 or 1999. We now observe a severe drop in mean completeness values across the Jurassic/Cretaceous boundary that never recover to pre-Cretaceous levels. Explaining this pattern is difficult, as we find no convincing evidence it is related to environmental preferences or body size changes. Instead, it might result from: (1) reduction of terrestrial fossil preservation space due to sea level rise; (2) ecological specificities and relatively high diagnosability of Cretaceous species; and/or (3) increased sampling of newly explored sites with many previously unknown taxa. Revisiting patterns in this manner allows us to test the longevity of conclusions made in previous quantitative studies.</p>

opencc-zeroJul 2020View details →
dryad36/100

Data from: Ten more years of discovery: revisiting the quality of the sauropodomorph dinosaur fossil record

Open the record for dataset details and reuse information.

publicJul 2020View details →
dryad32/100

Data from: Ontogeny of the Massospondylus labyrinth: implications for locomotory shifts in a basal sauropodomorph dinosaur

Ontogeny is a vital aspect of life history sometimes overlooked in palaeontological studies. However, the changing geometry of anatomical structures during growth can be informative regarding ecological and functional reconstructions. The inner ear, or labyrinth, is an ideal ontogenetic study system because it has a strong functional signal in its morphology that is linked to locomotor mode. Yet almost nothing is known about labyrinth development in dinosaurs. We quantified labyrinth scale and geometry through ontogeny in the Early Jurassic dinosaur Massospondylus carinatus, which has an exceptional fossil record and is hypothesized to have undergone a gait change, from quadrupedal juvenile to bipedal adult. To test whether this putative locomotor shift is reflected in labyrinth morphology, computed microtomography (μCT) and propagation phase‐contrast synchrotron radiation microtomography (PPC‐SRμCT) were used to obtain labyrinths from eight specimens, ranging from near‐hatchling to adult. Labyrinths grow substantially but scale with slight negative allometry compared to skull length throughout ontogeny, the first time this has been documented in dinosaurs. Geometric morphometric analysis of the labyrinth using a sliding semilandmark approach shows some morphological change through ontogeny, but little evidence supporting a locomotor shift. These results have implications for our understanding of sauropodomorph development and provide a better understanding of dinosaur locomotory evolution.

opencc-zeroDec 2017View details →
zenodo32/100

Figure 15 in A new basal sauropodiform from South Africa and the phylogenetic relationships of basal sauropodomorphs

Figure 15. Sefapanosaurus zastronensis gen. et sp. nov., incomplete left fibula (BP/1/7447), photographs and interpretative drawings. Medial (A, G), caudal (B, H), cranial (C, I), lateral (D, J), proximal (E, K, lateral towards top), and distal (F, L, medial towards top) views. Abbreviations: cmp, craniomedial projection; ltu, lateral tuberosity. Numbers indicate character.character state, respectively. Scale bar = 5 cm.

opennotspecifiedJun 2015View details →
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Figure 14 in A new basal sauropodiform from South Africa and the phylogenetic relationships of basal sauropodomorphs

Figure 14. Sefapanosaurus zastronensis gen. et sp. nov., incomplete right tibia (BP/1/7445), photographs and interpretative drawings. Lateral (A, D), medial (B, E), and proximal (C, F, lateral towards top), views. Numbers indicate character.character state, respectively. Abbreviation: cc, cnemial crest. Scale bar = 5 cm.

opennotspecifiedJun 2015View details →
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Figure 12 in A new basal sauropodiform from South Africa and the phylogenetic relationships of basal sauropodomorphs

Figure 12. Sefapanosaurus zastronensis gen. et sp. nov., incomplete left manus (BP/1/7438), photographs and interpretative drawings. Incomplete digits one and two in dorsal (A, E), palmar (B, F), and proximal (C, G, palmar towards top) views. Digit five in medial (D, H) view. Numbers indicate character.character state, respectively. Abbreviations: dc1, distal carpal 1; dc2, distal carpal 2; mcI, metacarpal I; mcII, metacarpal II; mcV, metacarpal V; pI.1, phalanx I.1; pV.1, phalanx V.1; pV.2, phalanx V.2. Scale bar = 5 cm.

opennotspecifiedJun 2015View details →

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Allen Brain Atlas

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Annotated Behaviour and Observability Dataset (ABODe)

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DANDI Archive for NWB datasets

DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.

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electrophysiologyopenPublished Dandiset metadata and archive endpoints are available through the production DANDI API.
Last verified 2026-04-30Open record

International Brain Laboratory public data

The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.

ibl
behavioral-neuroscienceopenPublic sessions can be searched and loaded from the IBL public data server through ONE.
Last verified 2026-04-29Open record

OpenNeuro

OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.

openneuro
neuroscienceopenPublished datasets are available on demand over the internet.
Last verified 2026-04-29Open record