Mosasaur tooth marks on the ammonite Placenticeras from the Upper Cretaceous of Alberta, Canada

1990 ◽  
Vol 27 (3) ◽  
pp. 469-472 ◽  
Author(s):  
R. A. Hewitt ◽  
G. E. G. Westermann

Mosasaur tooth marks were found in the body chamber and phragmocone of the Campanian ammonite Placenticeras meeki Boehm from the Bearpaw Formation of the St. Mary River area near Lethbridge. They imply that the shell wall of the ammonite buckled around point loads and did not break into fragments like the shell of Nautilus. The complex septal sutures provided a strong but marginally flexible support for the shell wall. The shells were probably attacked near the surface, perhaps during initial postmortem drift of corpses.

1989 ◽  
Vol 63 (5) ◽  
pp. 626-636 ◽  
Author(s):  
Eduardo B. Olivero ◽  
William J. Zinsmeister

Two species of the heteromorph ammonite genus Diplomoceras Hyatt are described from the Upper Cretaceous of the James Ross–Seymour Islands area, Antarctica. The late Campanian–early Maastrichtian D. lambi Spath has a relatively high rib density, whereas D. maximum n. sp. has a lower rib density and is known only from the uppermost Maastrichtian of the Lopez de Bertodano Formation on Seymour Island. Both species attain an exceptionally large size with the body chamber of D. maximum n. sp. attaining a length in excess of one meter. The structure of the shell wall in Diplomoceras is characterized by the thickening of the nacreous layer below the ribs. The shell thickening results in an inner flat surface and a smooth phragmocone. Reconstruction of the shell suggests at least four parallel shafts and three U-connectives. Estimates of the total density, center of buoyancy, and center of mass in this reconstructed shell indicate a slightly positive buoyant shell with a relatively unstable floating position.


1900 ◽  
Vol 7 (12) ◽  
pp. 560-561
Author(s):  
G. C. Crick

The name Nautilus clitellarius was given by J. de C. Sowerby to a Nautiloid from the Coal-measures, Coalbrookdale, Shropshire, and the description was accompanied by three figures, each representing a different specimen. In 1884 the species was included by Professor Hyatt in his new genus Ephippioceras. In 1891 Dr. A. H. Foord found a new species, Ephippioceras costatum, which was said to be “distinguished from E. clitellarium (to which it is, however, very closely related) by the character of the septa and by the surface ornaments. The septa in E. costatum do not form such an acute lobe upon the periphery as do those of E. clitellarium, and they are also a little wider apart in the former species than they are in the latter. Moreover, E. costatum is provided with prominent transverse costæ, which are strongest upon the sides of the shell where they swell out into heavy folds. These costæ are directed obliquely backwards, and cross the septa at an acute angle, passing across the periphery and forming a shallow sinus in the middle. None of the specimens in the British Museum have the test preserved, so that the ribbing has only been observed upon casts. The costæ are equally well developed upon the body-chamber and upon the septate part of the shell in the adult, but they were either very feeble or altogether absent in the young.” A re-examination of the specimens in the Museum collection shows that the separation of the two forms is quite justifiable.


1995 ◽  
Vol 69 (4) ◽  
pp. 703-707 ◽  
Author(s):  
Kazushige Tanabe ◽  
Royal H. Mapes

A well-preserved mouth apparatus consisting of jaws and a radula was found in situ within the body chamber of the goniatite Cravenoceras fayettevillae Gordon, 1965 (Neoglyphiocerataceae: Cravenoceratidae), from the middle Chesterian (Upper Mississippian) of Arkansas. Both upper and lower jaws consist of a black material. The lower jaw is characterized by a widely opened larger outer lamella and a shorter inner lamella. The upper jaw is fragmental. The radula is preserved in the anterior portion of the buccal space and comprises a series of tooth elements. Each transverse tooth row consists of seven teeth (a rhachidian and pairs of two lateral and one marginal teeth), with a pair of marginal plates. This arrangement is typical of radulae of other ammonoids of Carboniferous to Cretaceous age, coleoids, and the orthoconic “nautiloid” Michelinoceras (Silurian, Michelinocerida), suggesting a phylogenetic affinity among them.


Paleobiology ◽  
1977 ◽  
Vol 3 (3) ◽  
pp. 300-321 ◽  
Author(s):  
G. E. G. Westermann

Models of “ideal” orthoconic shells having simple concave septa with minimal weight and maximal strength and analysis of 72 species of fossil orthocones and cyrtocones yield important insights into the physical principles underlying cephalopod shell design. The ideal septum is a spherical cap weighing only 77% of a hemispherical septum of equal strength. The septa of most longicones approximate this ideal shape while those of brevicones are less curved, probably owing to buoyancy problems. Increase in septal strength leads to weight increase unless the shell becomes more logiconic or septal spacing increases or both. However, increased spacing requires more cameral liquid for septum formation, thus reducing buoyancy. In ideal longicones, septal spacing resembles the cone radius for thick, strong septa but declines to half of the cone radius for thin, weak septa. In ideal intermediates and brevicones, spacings are respectively reduced by factors of about 2 and 4, with similar additional dependence on septal thickness. Most real septa resemble these ideal models.The relative length of the body chamber to the phragmocone varies greatly between about 0.2 and 1.5, depending mainly on the wall thickness and to a lesser degree on the septal thickness, apical angle and body density. Removal of cameral liquid in the adult must be compensated for by additional growth to retain neutral buoyancy. The conditions for neutral equilibrium calculated for longicones with different “counterweights” indicate that: (1) cameral liquid only is least feasible; (2) half-and-half calcium carbonate and liquid results in one-third length and one-quarter volume reduction of the body chamber; (3) with calcium carbonate only, body chamber reduction is minimal. Real ‘counterweights’ appear to be intermediate between (2) and (3), providing the animal with horizontal stability, which is missing in (3). Most uncalcified siphuncles reduce the body chamber only slightly although they improve horizontal stability. If the wall attains full thickness only at the apical end of body chamber, the liquid-only ‘counterweight’ becomes feasible.


2004 ◽  
Vol 41 (8) ◽  
pp. 961-986 ◽  
Author(s):  
Kenneth Carpenter

The armor-plated dinosaur Ankylosaurus magniventris is redescribed based on specimens from the Hell Creek Formation of northeastern Montana, USA., Lance Formation of Wyoming, USA., and from the Scollard Formation of south-central Alberta, Canada. Except for brief descriptions, most of these specimens have not been described in detail. Ankylosaurus is one of the largest known ankylosaurids, having an estimated length of up to 6.25 m (20.5 ft). It is characterized by a long, low skull having very prominent cranial “horns” that project laterally or dorsolaterally. The body armor includes a large half-ring that sat across the base of the neck and shoulders and a large, low tail club.


2017 ◽  
Vol 92 (2) ◽  
pp. 146-156 ◽  
Author(s):  
Royal H. Mapes ◽  
Larisa A. Doguzhaeva

AbstractFour rare Pennsylvanian (Stark Shale: Pennsylvanian, Missourian [=Kasimovian]) coleoids from Nebraska and Iowa, which are preserved as flattened partial phragmocones and body chambers associated with three-dimensionally fossilized ink sacs, are herein described as Pabianiconus starkensis new genus new species, Nebraskaconus whitei new genus new species, and Starkites compressus new genus new species. One specimen that is missing most of the phragmocone, is provisionally assigned to Donovaniconus. The fossils are assigned to the Coleoidea because of the presence of ink-filled sacs in the body chamber region of the conch. Additionally, eight fragmented and flattened phragmocones and body-chamber clusters with similar morphologies, including some with ink fragments and arm hooks, are assigned to the Coleoidea, but are not named because of their fragmentary condition. On most of the eight specimens, the shell material is associated with other unidentified finely macerated material, which suggests these fossils are probably either ejectoid masses or coprolites from coleoid predators and/or scavengers. However, the new genera named above appear to have been deposited as complete animals, based on the presence of the ink-filled sacs that are in the body chambers. With their body chamber and phragmocone morphologies, these rare coleoid taxa provide valuable information about conch variability within the Carboniferous evolutionary radiation of coleoids.


2008 ◽  
Vol 27 (2) ◽  
pp. 103-110 ◽  
Author(s):  
Michael A. Kaminski ◽  
Alfred Uchman ◽  
Theodor Neagu ◽  
Claudia G. Cetean

Abstract. The large, agglutinated foraminiferal genus Aschemocella Vialov, 1966 (type species Aschemonella carpathica Neagu, 1964) and the body fossil Halysium Świdziński, 1934 (type species Halysium problematicum Świdziński, 1934) are herein synonymized with the genus Arthrodendron Ulrich, 1904 (type species A. diffusum Ulrich, 1904), a form originally described as a marine alga from Upper Cretaceous (Maastrichtian) flysch sediments of the Kodiak Formation of the Yakutat Group (formerly Yakutat Formation) on Pogibshi Island, Alaska. The species Aschemonella carpathica Neagu is regarded as a subjective junior synonym of Arthrodendron diffusum Ulrich, which is herein lectotypified and transferred to the Foraminifera.


1889 ◽  
Vol 6 (5) ◽  
pp. 200-203 ◽  
Author(s):  
S. S. Buckman

In a former communication (Geol. Mag. Dec. III. Vol. IV. No. 9, p. 396, 1887), when pointing out how Reinecke's Amm. serpentinus had been misunderstood, I gave as a synonym, but with a query, Sowerby's Amm. Strangewaysi. As I have, since then, examined the type-specimen of the latter species contained in the collection of the Natural History Museum, and as Mr. E. Walford kindly forwarded me for my determination a capital specimen from Byfield, I have been able to satisfactorily settle the identity of these forms. Except being evolute carinate Ammonites, the two species have hardly a feature in common.Discoidal, compressed, hollow-carinate. Whorls flattened, ornamented with genuine sickle-shaped ribs, which, though less conspicuous in size on the body-chamber, are there more distinctly bent. Ventral area marked by the prolonged forward sweep of the ribs, and surmounted by a well-marked hollow-carina.


2020 ◽  
Vol 57 (5) ◽  
pp. 617-629
Author(s):  
James A. Campbell ◽  
Michael J. Ryan ◽  
Jason S. Anderson

Scabby Butte is an isolated exposure of Upper Cretaceous (uppermost Campanian to lowermost Maastrichtian) strata of the St. Mary River Formation. These rocks have produced a diverse assemblage of both terrestrial and aquatic vertebrates, although hadrosaurid and ceratopsid dinosaurs represent the largest component by volume. Almost all of these dinosaur remains were collected from a single bonebed (Site 2) at Scabby Butte and have been referred to the hadrosaurid Edmontosaurus regalis Lambe, 1917 and the ceratopsid Pachyrhinosaurus canadensis Sternberg, 1950. This study presents a quantitative taphonomic reanalysis of the originally published data, providing new information previously overlooked and important information about the age-class structure of the dinosaur fauna preserved at the site. Site 2 is a lag deposit with a minimum number of 11 individuals (two ceratopsid, nine hadrosaurid), with three-quarters of the material being adult-sized based on size-class analysis. Most elements have undergone moderate to severe breakage and abrasion, and are completely disarticulated, suggesting that they were transported from where they died; post-mortem scavenging is also a possibility, as evidenced by the presence of tooth marks and trample marks on several elements. Burial took place soon after scavenging, as there is little evidence of subaerial weathering.


Sign in / Sign up

Export Citation Format

Share Document