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Figure 4 in Phylogenetic relationships of the Cretaceous Gondwanan theropods Megaraptor and Australovenator: the evidence afforded by their manual anatomy
Figure 4. Left manus of (A,C), Allosaurus fragilis, and (B,D), Australovenator wintonensis in (A,B) dorsal, and (C,D) ventral views. Not to scale. B,D, mofied from White et al. (2012).
Figure 2 in Phylogenetic relationships of the Cretaceous Gondwanan theropods Megaraptor and Australovenator: the evidence afforded by their manual anatomy
Figure 2. Distal end of humerus in anterior (A,C,E,G,I,K,) and distal (B,D,F,H,J,L) views of Australovenator (A,B), Allosaurus (C,D), Xuanhanosaurus (E,F), Chilantaisaurus (G,H), Guanlong (I,J), and Coelurus (K,L). Not to scale. A,B, modified from White et al. (2012). G,H, modified from Benson and Xu (2008).
Figure 1 in Phylogenetic relationships of the Cretaceous Gondwanan theropods Megaraptor and Australovenator: the evidence afforded by their manual anatomy
Figure 1. Humerus in lateral (C-I) and medial (A-B,J) views of: A, Megaraptor (MUCPv 341), B, Australovenator, C, Allosaurus, D, Acrocanthosaurus, E, Coelurus, F, Ornitholestes, G, Xuanhanosaurus, H, Torvosaurus, and I, Baryonyx. J, Fukuiraptor. B, modified from White et al. (2012). D, modified from Currie and Carpenter (2000). H, modified from Galton and Jensen (1979). I, modified from Charing and Milner (1997). Scale bar: 5cm. Abbreviations: it, internal tuberosity; lf, longitudinal furrow.
FIGURE 7 in A new name for old bones: A reassessment of Early Jurassic theropod remains from Dorset, England
FIGURE 7. Life reconstruction of Dornraptor normani. Credit for this artwork is owed to Megan Williams.
FIGURE 5 in A new name for old bones: A reassessment of Early Jurassic theropod remains from Dorset, England
FIGURE 5. Results of phylogenetic analyses (simplified) that utilised the dataset of Zahner and Brinkmann (2019) – Dornraptor normani again recovered within Averostra.
FIGURE 3 in A new name for old bones: A reassessment of Early Jurassic theropod remains from Dorset, England
FIGURE 3. Holotype (BMNH 39496) and referred material (GSM 109560) of Dornraptor normani. BMNH 39496 – distal end of right femur in (A) anterior; (B) posterior; and (B) lateral views. GSM 109560 – partial femur in (d) medial; and (e) anterior views (adapted from Benson, 2010). BMNH 39496 – proximal portion of right tibia, in (f) lateral view. Abr. a.t., anterior trochanter; bulb., bulbous expansion of fibular crest; cn.c. cnemial crest; ct.c, crista tibiofibularis; f.t., fourth trochanter; lat.c., lateral condyle of distal end of femur; lat.r. I, lateral ridge I, or fibular crest; lat.r. II, second lateral ridge; sc., scarring on anterior surface.
FIGURE 1 in A new name for old bones: A reassessment of Early Jurassic theropod remains from Dorset, England
FIGURE 1. Artist's rendering of BMNH 39496 from the Early Jurassic of England (adapted from Lydekker, 1888). The specimen comprises a distal end of right femur, articulated with a proximal portion of the right tibia and fibula (now lost). (A) medial view; (B) posterior; (C) lateral view.
FIGURE 2 in A new name for old bones: A reassessment of Early Jurassic theropod remains from Dorset, England
FIGURE 2. Artist's rendering of GSM 109560 (adapted from Lydekker, 1888). (a) anterior view; (b) lateral view; (c) posterior view.
FIGURE 4 in A new name for old bones: A reassessment of Early Jurassic theropod remains from Dorset, England
FIGURE 4. Results of phylogenetic analyses that utilised the dataset of Baron et al. (2017a), as modified by Langer et al. (2017) and Baron et al. (2017b). Dornraptor normani is recovered nested within Averostra (blue, bold). Also included in these analyses, the only two contemporaneous theropodan taxa Sarcosaurus woodi and Dracorptor hanigani (blue).
FIGURE 6 in A new name for old bones: A reassessment of Early Jurassic theropod remains from Dorset, England
FIGURE 6. Results of phylogenetic analyses (simplified) that utilised the dataset of Smith et al. (2010), as modified by Novas et al. (2015), and then Baron (2024) – Dornraptor normani again recovered within Averostra.
Fig. 1 in Macroevolutionary and morphofunctional patterns in theropod skulls: A morphometric approach
Fig. 1. Diversity of skull shapes in theropod dinosaurs. A. Basal theropod Herrerasaurus. B. Coelophysid Syntarsus. C. Generalized spinosaurid. D. Abelisaurid Carnotaurus. E. Allosaurid Allosaurus. F. Ornithomimosaur Ornithomimus. G. Unnamed oviraptorid (originally referred to Oviraptor). H. Dromaeosaurid Velociraptor. I. Basal bird (avialian) Archaeopteryx. Modified from Rauhut (2003).
Fig. 3 in The systematics of Late Jurassic tyrannosauroid theropods from Europe and North America
Fig. 3. Autapomorphies of tyrannosauroids Juratyrant langhami Benson, 2008, Kimmeridge Clay, Dorset England, Late Jurassic (early Tithonian) (A, B) and Stokesosaurus clevelandi Madsen, 1974, Morrison Formation, Utah, USA, Late Jurassic (early Tithonian) (C). A. Right pubis (OUMNH J.3311−22) in lateral view, with the autapomorphic lateral fossa denoted. B. Left ischium (OUMNH J.3311−25) in lateral (B1) and anterior (B2) views, with an inset close up (2.5× magnification) of the autapomorphic folded proximal region of the ischial apron (B3). The autapomorphic convex ischial tubercle is also denoted. C. Pubic peduncle of the left ilium (UMNH 2938) in medial view, with the autapomorphic swollen rim indicated.
Fig. 5 in Macroevolutionary and morphofunctional patterns in theropod skulls: A morphometric approach
Fig. 5. Two−dimensional morphospace of the theropod skull shape and CVA plot with distribution of the carnivorous (black triangle), omnivorous (grey squares) and herbivorous (white diamonds) taxa (non−theropod taxa are not shown). A. PC 1 vs. PC 2. B. PC 2 vs. PC 3. In both diagrams herbivorous and omnivorous taxa overlap one another strongly, whereas carnivorous taxa overlap only marginally with herbivorous forms, but moderately with omnivorous forms. C. CVA plot with oviraptorids. D. CVA plot with oviraptorids excluded.
Fig. 2 in The systematics of Late Jurassic tyrannosauroid theropods from Europe and North America
Fig. 2. The phylogenetic relationships of tyrannosauroids, based on a revised analysis of the Brusatte et al. (2010) dataset. Details of the analysis are described in the text and the dataset is presented in SOM. The cladogram shown here is the single most parsimonious tree recovered by the analysis, with the wildcard taxon Aviatyrannis excluded (570 steps, CI = 0.640, RI = 0.835). Numbers next to nodes denote bootstrap percentages (based on 1000 replicates) and Bremer support. Note that Stokesosaurus clevelandi and "S." langhami (here referred to by its new genus name, Juratyrant) are not found as sister taxa, and therefore a monophyletic Stokesosaurus is not recovered. When Aviatyrannis is included in the analysis, the strict consensus of nine most parsimonious trees (not figured) shows identical and fully resolved relationships among Xiongguanlong and all more derived taxa. However, Stokesosaurus clevelandi, "S." langhami, and Eotyrannus, form a polytomy. This clade, in turn, is part of a large basal polytomy that also includes the Xiongguanlong + more derived clade, Dilong, Aviatyrannis, Guanlong, Kileskus, Proceratosaurus, and Sinotyrannus. On the figured cladogram, the following unambiguous synapomorphies support major clades, with character numbering following that in the character list of Brusatte et al. (2010) and SOM: all tyrannosauroids more derived than Dilong (33, 41, 49, 80, 180, 181, 196, 198, 221, 239, 241, 244, 257, 274, 281, 289, 290); the clade of S. clevelandi, Juratyrant, and Eotyrannus (258, 310, 311, 313); the clade of Juratyrant and Eotyrannus (no unambiguous synapomorphies).
Fig. 3 in Macroevolutionary and morphofunctional patterns in theropod skulls: A morphometric approach
Fig. 3. Two−dimensional morphospace of the theropod skull shape (large data set) with distribution of the different theropod clades, based on the first two PC axes. The most derived taxa with respect to the first two components are visualized with relative warps. Shape changes along PC 1 reflect changes in the length and height of the snout and the anteroposterior dimensions of the lateral temporal fenestra. Changes along PC 2 reflect the height of the postorbital region, the size of the orbit and the position of the jaw joint.
Fig. 1 in The systematics of Late Jurassic tyrannosauroid theropods from Europe and North America
Fig. 1. Ilia of basal non−tyrannosaurid tyrannosauroids with a posterodorsally inclined ridge on the lateral surface of the ilium. A. Right ilium (reversed) of Juratyrant langhami Benson, 2008 (OUMNH J.3311−21), Kimmeridge Clay, Dorset England, Late Jurassic (early Tithonian). B. Left ilium of Stokesosaurus clevelandi, Madsen 1974 (UMNH VP 7473), Morrison Formation, Utah, USA, Late Jurassic (early Tithonian). C. Left ilium of Eotyrannus lengi Hutt, Naish, Martill, Barker, and Newberry, 2001 (MIWG 1997.550), Wessex Formation, Isle of Wight, England, Early Cretaceous (Barremian). All in lateral view. Arrows denote the lateral ridge.
Fig. 2 in Macroevolutionary and morphofunctional patterns in theropod skulls: A morphometric approach
Fig. 2. Position of the landmarks on theropod skulls. A. 20 landmarks used for the large data set plotted on the skull of Ceratosaurus (modified from Sampson and Witmer 2007). B. 15 landmarks used for the small data set plotted on the skull of Anchiornis (modified from Hu et al. 2009). The description of landmark positions is given in the SOM at http://app.pan.pl/ SOM/app58−Foth_Rauhut_SOM.pdf.
Fig. 1 in Large theropod dinosaur footprint associations in western Gondwana: Behavioural and palaeogeographic implications
Fig. 1. Location of the large theropod trackbeds: track 1 indicates the Querulpa Chico locality while track 2 indicates the Chacarilla locality.
Fig. 3 in A reassessment of Kelmayisaurus petrolicus, a large theropod dinosaur from the Early Cretaceous of China
Fig. 3. The phylogenetic relationships of Kelmayisaurus and other basal tetanuran theropods. Strict consensus of 1728 most parsimonious trees (639 steps) recovered by the cladistic analysis (CI = 0.44; RI = 0.64). "Derived carcharodontosaurids" include Shaochilong, Tyrannotitan, Carcharodontosaurus, Giganotosaurus, and Mapusaurus. Kelmayisaurus is recovered as a basal member of Carcharodontosauridae.
Fig. 5 in Large theropod dinosaur footprint associations in western Gondwana: Behavioural and palaeogeographic implications
Fig. 5. Photographs of Early Cretaceous theropod footprints from the Querulpa Chico tracksite, Peru. A–I refer to the individual trackways in Fig. 4, and the number to the particular print in the trackway. Arrows point to hallux impressions. Scale bars 0.5 m.
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
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.
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.
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.