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Skeletons of Bonatitan and Austroraptor at the Museo Argentino de Ciencias Naturales Bernardino Rivadavia

Reconstructed skeleton of Daxiatitan binglingi.

Identifier: waterreptilesofp1914will Title: Water reptiles of the past and present Year: 1914 (1910s) Authors: Williston, Samuel Wendell, 1851-1918 Subjects: Aquatic reptiles Publisher: Chicago, Ill., The University of Chicago Press Contributing Library: Boston Public Library Digitizing Sponsor: Boston Public Library View Book Page: Book Viewer About This Book: Catalog Entry View All Images: All Images From Book Click here to view book online to see this illustration in context in a browseable online version of this book. Text Appearing Before Image: served and very complete skeletons ofdifferent species of ichthyosaurs from the Jurassic deposits ofWiirtemberg, in which remains of these animals occur in great 112 WATER REPTILES OF THE PAST AND PRESENT profusion. His researches, and those of several authors since then,supplementing and confirming or disproving those of the manyobservers made during the preceding seventy years, have finallydetermined almost perfectly the complete structure of the moretypical ichthyosaurs, enabling us to infer not a little as to theirhabits and distribution in the old Jurassic oceans. Within thepast few years the discoveries of Professor J. C. Merriam of Cali-fornia have likewise added greatly to our knowledge of the earlierichthyosaurs. It may now truthfully be said that of no group ofextinct reptiles do we have a more complete and satisfactory knowl-edge than of the ichthyosaurs. Nevertheless we have yet very much more to learn about theorder Ichthyosauria as a whole—whence they came and how they Text Appearing After Image: Fig. 52.—Ichthyosaurus quadricissus.museum, from Dr. Dreverman. Photograph of specimen in Senckenberg originated; what their nearest kin were among other reptiles; andespecially, more about the connecting links between them andterrestrial reptiles. They have, as an order, so isolated a position,are so widely separated from all other reptiles in structure, that theyhave long been a puzzle to paleontologists. Like the whales andother cetaceans among mammals, we know the ichthyosaurs wellin the plenitude of their power and the fulness of their development,but have yet only an imperfect knowledge of their earlier history,and none whatever of their earliest. However, as will be seenfarther on, the recent discoveries by Merriam have shed much lighton some of the stages of their evolution. So nearly perfectly wereall the later ichthyosaurs adapted to their life in the water that itwas believed by nearly all paleontologists until about a score of years ICHTHYOSAURIA 3 ago that they had desc Note About Images Please note that these images are extracted from scanned page images that may have been digitally enhanced for readability - coloration and appearance of these illustrations may not perfectly resemble the original work.

Identifier: annalsofmedicalh01pack (find matches) Title: Annals of medical history Year: 1917 (1910s) Authors: Packard, Francis R. (Francis Randolph), 1870-1950 Subjects: Medicine Publisher: New York P.B. Hoeber Contributing Library: Gerstein - University of Toronto Digitizing Sponsor: University of Toronto View Book Page: Book Viewer About This Book: Catalog Entry View All Images: All Images From Book Click here to view book online to see this illustration in context in a browseable online version of this book. Text Appearing Before Image: ail strongly Hexed, and the toescontracted and appressed. The whole atti-tude strongly suggests a spastic distress,possibly brought on by some form ofpoisoning of the central nervous system,from infection or the deglutition of somepoisonous substance. 14. Osteomalacia is evidently the causeof the hypertrophy of the bones of Lim-nocyron potens, an early carnivore from theWashakie Eocene of Wyoming, nearly3,000,000 years old. MATERIALS AND METHODS The material described in the presentpaper has been loaned the writer lor de-scription by the Field Museum of Chii Osborn: Hull. Amcr. \lus. Natl. Hist., 1917,vol. 35. !>• 733. P>- 28. Studies in Paleopathology 393 by the American Museum of Natural His-tory of New York City, by Walker Museumof the University of Chicago, and by the Uni-versity of Kansas Natural History Museum. made by the well-known petrographic meth-ods so common in all geological labora-tories. The diagnoses, where they are at-tempted, arc made from comparisons of the Text Appearing After Image: Fig. 20. The skeleton of Strutbiomimus altus, a small dinosaur from the BeliyRiver series (Cretaceous), Red Deer River, Alberta, Canada, now regarded as ofapproximately the same age as the Judith River series. The unique feature ofthe skull is the total absence of teeth, with a size of skull one-third larger thanthe ostrich and a length of body of about fifteen feet. The position of the skeletonis decidedly that of the opisthotonos which may be regarded as an indication ofdisease. (After Osborn). A beautiful specimen of an osteoma, theonly one known so far, on the vertebra of aKansas Cretaceous mosasaur, was given thewriter by Dr. J. M. Armstrong of St. Paul.The writer expresses his obligations to thegentlemen connected with the above-men-tioned institutions and to Dr. Armstrong.The methods used are a combination ofprocedures in the various lines involved.Microscopic sections, which can be madethin enough for immersion lens study, are material with similar lesions in recent hu-man mat Note About Images Please note that these images are extracted from scanned page images that may have been digitally enhanced for readability - coloration and appearance of these illustrations may not perfectly resemble the original work.

Photo of the partial holotype skeleton of the ornithomimosaur Garudimimus brevipes, as mounted in the Mongolian Natural History Museum. Scan of physical photograph.

Selected elements used in the diagnosis of Saltriovenator zanellai n. gen. n. sp. Right humerus in medial (A), frontal (B) and distal (C) views; (D) left scapula, medial view; (E) right scapular glenoid and coracoid, lateral view; (F) furcula, ventral view; tooth, labial (G) and apical (H) views; (I) left humerus, medial view; right second metacarpal in dorsal (J), lateral (L) and distal (N) views; first phalanx of the right second digit in dorsal (K), lateral (M) and proximal (O) views; (P–T) right third digit in proximal, dorsal and lateral views; (U) right distal tarsal IV, proximal view; third right metatarsal in proximal (V) and frontal (X) views; second right metatarsal, proximal (W) and frontal (Y) views; (Z) reconstructed skeleton showing identified elements (red). Abbreviations as in text, asterisks mark autapomorphic traits. Scale bars: 10 cm in (A)–(E), (I), and (U)–(Y); two cm in (F), and (J)–(T); one cm in (G).

(a) Photograph. (b) Highly schematic outline shows general layout of the skeleton (illustrated by Zhaochuang). Scale bar, 5 cm. d, dentary; f, femur; fi, fibula; fr, frontal; lj, lower jaw; or, orbit; ti, tibia.

Skeleton of Henodus at the American Museum of Natural History

Photograph and outline drawing of the skeleton of Chuanqilong chaoyangensis. A, photograph; B, outline drawing. Abbreviations: ca, caudal vertebrae; cb, cervical band; da, dermal armor; dr, dorsal rib; lfe, left femur; lfi, left fibula; lhu, left humerus; lil, left ilium; lis, left ischium; lma, left maxilla; lmd, left mandible; lmt, left metatarsal; lra, left radius; lsc, left scapula; lti, left tibia; lul, left ulna; mc, metacarpals; orb, orbital; pl, plates; q, quadrate; rfe, right femur; rfi, right fibula; rhu, right humerus; ril, right ilium; rma, right maxilla; rmd, right mandible; rmt, right metatarsals; rra, right radius; rsc, right scapula; rti, right tibia; rul, right ulna; sar, sacral rib; te, tendons. [planned for page width].

Holotype skeleton of Wukongopterus lii on display at the Paleozoological Museum of China.

Fig 3. Skeletal map of Keilhauia nui (PMO 222.655) viewed from the side stratigraphically down, i.e. the prepared side. Vertebrae numbers (“x#”) indicate position relative to the anterior end of the preserved skeleton and do not correspond to their actual position in the column. Dashed lines show three faults. Scale bar equals 50 cm. Modified from Delsett et al. 2016.

Reconstructed skeleton of a megaraptoran highlighting the known bones of Joaquinraptor casali in blue. Reconstruction by TK Robinson and Andrew McAfee. Scale bar=1 m.

Composite skeleton on display at the Perot Museum of Nature and Science. Scale bar equals 10 cm.

The holotype skeleton of Kamuysaurus japonicus gen. et sp. nov. (b) Reconstructed skeleton, showing recovered elements. Selected postcranial elements: cervical vertebrae (atlas, axis, and fourth and twelfth cervicals) in left lateral view (c), dorsal vertebrae (first, seventh, and sixteenth dorsals) in left lateral view (d), caudal vertebrae (anterior, middle, and posterior caudals) in left lateral view (e), left scapula (f) and coracoid (g) in lateral view, right sternum in ventral view (h), left humerus in anterior view (i), right ulna and radius in medial view (j), right manus in dorsal view (k), right pelvis in lateral view (l), right femur in anterior view (m), right tibia in anterior view (n), right fibula in lateral view (o), right astragalus and calcaneum, articulated positioned with tibia (p), and right pes in dorsal view (q). All scales are 10 cm except 1 m scale for (b). Abbreviations; ac, acromion process; ast, astragalus; cal, calcaneum; dpc, deltopectoral crest; fi, fibula; icg, intercondylar groove; il, ilium; is, ischium; ltr, lesser trochanter; mc2, metacarpal II; mc5, metacarpal V; mt2, metatarsal II; mt4, metatarsal IV; nc, neurocentrum; od, odontoid; olp, olecranon process; pc, pleurocentrum; pu, pubis; ra, radius; ti, tibia; ul, ulna; vp, ventral process.

Skeleton of Thililua longicollis. Exhibit in the National Museum of Nature and Science, Tokyo, Japan.

Reconstruction of the Bravoceratops skeleton with known bones marked in white. Specimen: TMM 46015-1 (holotype). Scale bar=2 m. Total length along centra=6.97 m.