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46,474 result(s) for "Shells"
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Why do snails and other animals have shells?
\"Discover how body coverings vary and the different jobs they do in helping animals to survive. This book is all about shells and how they help snails to stay safe and survive. Discover how shells are different on different animals and how they change as animals grow up.\"--Provided by publisher.
Nonlinear forced vibrations of FGM sandwich cylindrical shells with porosities on an elastic substrate
The nonlinear forced vibrations of functionally graded material (FGM) sandwich cylindrical shells with porosities on an elastic substrate are studied. A step function and a porosity volume fraction are introduced to describe the porosities in FGM layers of sandwich shells. Using the Donnell’s nonlinear shallow shell theory and Hamilton’s principle, an energy approach is employed to gain the nonlinear equations of motion. Afterwards, the multi-degree-of-freedom nonlinear ordinary differential equations are carried out by using Galerkin scheme, and subsequently the pseudo-arclength continuation method is utilized to perform the bifurcation analysis. Finally, the effects of the core-to-thickness ratio, porosity volume fraction, power-law exponent, and external excitation on nonlinear forced vibration characteristics of FGM sandwich shells with porosities are investigated in detail.
The beachcomber's companion
\"The Beachcomber's Companion is an illustrated guide to collecting shells and other beach objects and includes basic tips and fun tidbits for shell collectors: how to clean shells, beachcombing commandments, the beachcomber's toolkit, and an identification guide for 40 shells and beach treasures\"-- Provided by publisher.
Nonlinear forced vibration of functionally graded graphene platelet-reinforced metal foam cylindrical shells: internal resonances
In the present study, we analyze the nonlinear forced vibration of thin-walled metal foam cylindrical shells reinforced with functionally graded graphene platelets. Attention is focused on the 1:1:1:2 internal resonances, which is detected to exist in this novel nanocomposite structure. Three kinds of porosity distribution and different kinds of graphene platelet distribution are considered. The equations of motion and the compatibility equation are deduced according to the Donnell’s nonlinear shell theory. The stress function is introduced, and then, the four-degree-of-freedom nonlinear ordinary differential equations (ODEs) are obtained via the Galerkin method. The numerical analysis of nonlinear forced vibration responses is presented by using the pseudo-arclength continuation technique. The present results are validated by comparison with those in existing literature for special cases. Results demonstrate that the amplitude–frequency relations of the system are very complex due to the 1:1:1:2 internal resonances. Porosity distribution and graphene platelet (GPL) distribution influence obviously the nonlinear behavior of the shells. We also found that the inclusion of graphene platelets in the shells weakens the nonlinear coupling effect. Moreover, the effects of the porosity coefficient and GPL weight fraction on the nonlinear dynamical response are strongly related to the porosity distribution as well as graphene platelet distribution.
Dual Gene Repertoires for Larval and Adult Shells Reveal Molecules Essential for Molluscan Shell Formation
Molluscan shells, mainly composed of calcium carbonate, also contain organic components such as proteins and polysaccharides. Shell organic matrices construct frameworks of shell structures and regulate crystallization processes during shell formation. To date, a number of shell matrix proteins (SMPs) have been identified, and their functions in shell formation have been studied. However, previous studies focused only on SMPs extracted from adult shells, secreted after metamorphosis. Using proteomic analyses combined with genomic and transcriptomic analyses, we have identified 31 SMPs from larval shells of the pearl oyster, Pinctada fucata, and 111 from the Pacific oyster, Crassostrea gigas. Larval SMPs are almost entirely different from those of adults in both species. RNA-seq data also confirm that gene expression profiles for larval and adult shell formation are nearly completely different. Therefore, bivalves have two repertoires of SMP genes to construct larval and adult shells. Despite considerable differences in larval and adult SMPs, some functional domains are shared by both SMP repertoires. Conserved domains include von Willebrand factor type A (VWA), chitin-binding (CB), carbonic anhydrase (CA), and acidic domains. These conserved domains are thought to play crucial roles in shell formation. Furthermore, a comprehensive survey of animal genomes revealed that the CA and VWA–CB domain-containing protein families expanded in molluscs after their separation from other Lophotrochozoan linages such as the Brachiopoda. After gene expansion, some family members were co-opted for molluscan SMPs that may have triggered to develop mineralized shells from ancestral, nonmineralized chitinous exoskeletons.
Conches
Conches are sea snails with eyestalks and feet. There are about 50 different species of conches. Underwater photographs show conches in their natural habitats. The life cycle and adaptations of these marine creatures are explained in accessible language.
Static bistability of spherical caps
Depending on its geometry, a spherical shell may exist in one of two stable states without the application of any external force: there are two ‘self-equilibrated’ states, one natural and the other inside out (or ‘everted’). Though this is familiar from everyday life—an umbrella is remarkably stable, yet a contact lens can be easily turned inside out—the precise shell geometries for which bistability is possible are not known. Here, we use experiments and finite-element simulations to determine the threshold between bistability and monostability for shells of different solid angle. We compare these results with the prediction from shallow shell theory, showing that, when appropriately modified, this offers a very good account of bistability even for relatively deep shells. We then investigate the robustness of this bistability against pointwise indentation. We find that indentation provides a continuous route for transition between the two states for shells whose geometry makes them close to the threshold. However, for thinner shells, indentation leads to asymmetrical buckling before snap-through, while also making these shells more ‘robust’ to snap-through. Our work sheds new light on the robustness of the ‘mirror buckling’ symmetry of spherical shell caps.