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Predatory shell breakage is known to occur occasionally on the ventrolateral portion of the body chamber in Mesozoic ammonoids. Here we report, for the first time, quantitative data of shell breakage in large ammonoid samples that were recovered from the lower Toarcian (Lower Jurassic) strata in the Toyora area, western Japan. The strata yielding the ammonoid samples consisted mostly of well-laminated, bituminous black shale that was deposited in an oxygen-depleted shelf basin of the northwestern Panthalassa, under the influence of the early Toarcian oceanic anoxic event. Among a total of 1305 specimens from 18 localities, apparent shell breakage was recognised in 35 specimens belonging to 7 genera, resulting in only a 2.7% frequency of occurrence relative to the total number of specimens. The breakage occurs mostly on the ventrolateral side of the body chamber with a complete shell aperture. This fact, as well as the low energy bottom condition suggested for the ammonoid-bearing shale, indicate that the shell breaks observed in the examined ammonoids were not produced by non-biological, post-mortem biostratinomical processes but were lethal injuries inflicted by nek-tonic predators such as reptiles, jawed fishes, coleoids, nautiloids, and carnivorous ammonoids with calcified rostral tips in their upper and lower jaws. Similar predatory shell breaks on the ventrolateral side of the body chamber have been found in contemporaneous ammonoid assemblages of the Tethys Realm, with a much higher frequency of occurrence than in the examined samples from the northwestern Panthalassa, suggesting a weaker durophagous predation pressure on ammonoids in the latter bioprovince.
The most distinctive and important element of the hydrostatic organ of ammonoids and nautiloids is the siphuncular tube. It consists of mineral and organic segments (so−called connecting rings). The connecting ring of ammonites never preserves its original organic matter in the mineralized state, usually having undergone diagenetic phosphatisation, more rarely, calcification, or even complete loss. Our knowledge about its original ultrastructure is based upon comparison with Recent Nautilus and phosphatised or calcified ammonite fossils. We show that depending on the taphonomic history, both calcium phosphate and calcite can participate in the diagenesis of the connecting ring wall. Under standard light microscopy, the phosphatised elements are indistinguishable from the calcified ones. Both are dark brown in colour, due to an excess of carbon. The structure of the phosphatised siphuncle does not closely replicate the structure of its organic elements. This casts doubts on conclusions of other authors who described a complex porous structure in ammonite siphuncles, which is completely dissimilar to the siphuncular structure of Recent Nautilus and suggests that this organ functioned differently in ammonites. SEM observations using a BSE detector on the calcified parts of the walls of connecting rings revealed a multilayered structure with perpendicular elements connecting particular layers, resembling the structure of a stacked nacreous layer.
The origin and phylogenetic relationships of most modern coleoid groups have not yet been explained by reliable fossil evidence, in large part because of the reduction or disappearance of a calcified chambered shell during their evolutionary history. Herein we describe two exceptionally large coleoid lower jaws from the Upper Cretaceous strata in Hokkaido, Japan. On the basis of the comparison of gross morphology and morphometric data of the lower jaws of modern and fossil coleoids, we assigned the two lower jaws to the following new taxa: Nanaimoteuthis hikidai sp. nov. of the order Vampyromorpha (superorder Octobrachia) and Haboroteuthis poseidon gen. et sp. nov. of the order Teuthida (superorder Decabrachia). The lower jaw of N. hikidai is distinguished from other species of the same genus from the Upper Cretaceous of Vancouver Island (Canada) and Hokkaido by having a broader, more anteriorly curved hood of the outer lamella. The lower jaw of H. poseidon seemingly exhibits mosaic features like those of modern teuthids and sepiids but is assigned to Teuthida on the basis of the overall shape of the outer lamella and the development of a distinct fold on the lateral wall. Because of the unusually large lower jaws, these new taxa appear to be comparable in body size to modern giant squids (Architeuthis spp.) and the Humboldt squid (Dosidicus gigas). This and other discoveries of large jaws referable to octobrachian and decabrachian coleoids from the Upper Cretaceous strata of the North Pacific fill the gap in the relatively poor fossil record of mainly soft-bodied coleoids.
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Dorsal shell wall in ammonoids

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In ammonoids, a soft body organ (possibly a supracephalicmantle fold), extending from the conch aperture secreted aragonitic wrinkles, forming a layer on the surface of the preceding whorl. The dorsal shell wall consists of the outer and inner components which were deposited sequentially, beginning at the aperture of the living chamber inwards. The dorsal wall attains its full thickness near the last septum. The outer component is visible in the apertural region and is smooth or wrinkled; it is called the wrinkled layer in the latter case. The wrinkles may be continuous, interrupted, or form isolated patches arranged in rows. The wrinkles are usually triangular in cross section. A further stage of dorsal wall development involves filling in the space between the apices of triangles, and then adding one or more inner prismatic layers from the inside of the living chamber. This pattern occurs at least in the postembryonic stage of all genera studied, belonging to five suborders of Ammonoidea ranging from Late Carboniferousto Late Cretaceous. In many genera, the outer component of the dorsal shell wall exhibits remarkable ontogenetic change in its ultrastructure and microornament. It may be compared with the black film of Recent Nautilus shells with respect to place of formation. The outer component of the ammonoid dorsal shell wall is regarded as a product of organic secretion and carbonate precipitation in the area of the supracephalic mantle fold.
Organic membranes preserved in the rear part of the body chamber of the Late Cretaceous phylloceratid ammonite Phyllopachyceras ezoense were examined with scanning electron microscopy (SEM) on the basis of well−preserved specimens from Hokkaido, Japan. SEM observations revealed that the membranes are continuous with the siphuncular tube wall in the phragmocone and consist of two layers, both of which are made of a dark, primarily conchiolin material; namely, a thinner inner homogeneous layer and a thicker outer layer with gently inclined pillar−like units. Hence, they are interpreted as the precursory siphuncular membranes. The precursory siphuncular membranes are not associated with any other organic components such as the siphuncular sheets reported in some Paleozoic and Mesozoic ammonoids. Unlike the tube−like condition in the phragmocone, the precursory siphuncular membranes in the body chamber of the specimens examined do not form a tube shape; on the ventral side the membranes are truncated and directly contact the outer shell wall. These observations suggest that the inner and outer layers of the precursory siphuncular membranes in the body chamber were respectively formed by the siphuncular epithelium from the inner side and by the invaginated septal epithelium from the outer side. It is also postulated that at the initial stage of septal formation, the rear part of the body moved slowly forward, developing a circumsiphonal invagination of the septal epithelium. Because similar conchiolin membranes are occasionally preserved in the body chambers of other phylloceratids, the above morphogenetic process applies to all members of the Phylloceratina. The tube−shaped structure in the rear part of the body chamber of desmoceratid Damesites consists only of nacreous layer. We interpret it as a pathologically overgrown prochoanitic septal neck.
The objective of this report is to document first Mesozoic occurrences of chemosynthesis−based communities developed on large marine reptile carcasses. Micro−grazing provannid gastropods (typical of chemosynthetic communities) are associated with plesiosaurid skeletons in the Upper Cretaceous deposits of Hokkaido, northern Japan. The cancellous bones of the examined plesiosaurid bones contain a ubiquity of iron sulfides within the bone trabeculae, which provides evidence of anaerobic sulfate reduction of the bone lipids. We also report numerous microborings in the bone trabeculae, which might result from the activity of sulfur−oxidizing bacteria. This finding addresses the hotly debated problem of the emergence and radiation of whale bone faunas. We postulate that vertebrate bone environments in the Northwest Pacific region were settled repeatedly by animals from a regional pool of chemosynthesis−based communities that flourished in the methane seeps and/or hot vents that were present during the Late Cretaceous–Miocene.
A new theoretical morphological model is proposed for the analysis of growth, form and morphospace of ammonoid shells. In this model, the shape of a radial cross section through the shell is simulated by “piggybacking” of successive whorls. The “piggyback whorls model” is defined in terms of the enlarging rate of the perimeter and the proportion of the dorsal wall to the whorl periphery, if an isometric relationship is assumed between perimeter and area of the cross−sectioned whorl. Allometric coefficients on these growth parameters determine how compressed and evolute shells are formed. The present model successfully reproduced some correlations among purely geometric variables that have been reported in previous works and were also observed in our biometric analyses. This model yields a hypothesis of “constructional linkages” between aperture shape and coiling geometry that might provide a functional coupling between hydrostatic and hydrodynamic characters. The model may partly explain Buckman’s Law of Covariation between rib features and shell shapes.
Exceptionally well preserved specimens of the bivalve mollusc Modiola major were collected from a Lower Cretaceous (Barremian) hydrocarbon seep deposit in northern California. This material, together with the type series of M. major, and various other specimens from Upper Jurassic to Lower Cretaceous seep localities in California, is redescribed and referred to the hydrocarbon seep−restricted modiomorphid genus Caspiconcha. We include also a description of Myoconcha americana because some previous reports have incorrectly synonymized Myoconcha americana with Caspiconcha major. In addition, we report Caspiconcha sp. from a Lower Cretaceous (Albian) hydrocarbon seep from Hokkaido, Japan, and we review all currently described species of Caspiconcha, and other species that probably belong to this genus. We demonstrate that Caspiconcha had a widespread distribution in Late Jurassic to Early Cretaceous hydrocarbon seeps, but became rare thereafter, with the last representative occurring in Upper Cretaceous strata of Japan. This macroevolutionary pattern is similar to that observed in the seep−restricted brachiopods. After the decline of Caspiconcha at the end of the Early Cretaceous and its last occurrence in the Campanian, the ecological niche of epifaunal to semi−infaunal seep endemic bivalves was largely vacant and not reoccupied until the Eocene with the appearance of the vesicomyid and bathymodiolin bivalves. The formal placement of M. major into the genus Caspiconcha restricts the fossil record of mytilids at seeps to post−Mesozoic times, and thus there is less discrepancy between the fossil record of chemosynthetic mytilids and their divergence age estimates from molecular data.
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