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Soft Substrates (soft + substrate)
Selected AbstractsEffect of Flaw State on the Strength of Brittle Coatings on Soft SubstratesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2001Hae-Won Kim A study is made of the role of flaw state on the strength properties of brittle ceramic coating layers bonded to soft polycarbonate substrates. We introduce Vickers radial cracks at prescribed loads into the coating undersurfaces prior to bonding to control the sizes and locations of the starting flaws. A spherical indenter is then loaded on the top bilayer surfaces, directly above the Vickers indentation sites, subjecting the radial cracks to flexural tensile stress. Radial crack responses are monitored in situ, using a camera located below the transparent substrate. Critical loads to cause radial crack instability, and ensuing growth of the arrested cracks, are recorded. Conventional biaxial flexure tests on corresponding monolith coating materials provide a baseline for data comparison. Relative to the monolith flexure specimens, the bilayers show higher strengths, the more so the larger the flaw, indicating enhanced flaw tolerance. A simple fracture mechanics analysis of the radial crack evolution in the concentrated-load field, with due account for distribution of flexural tensile stresses at the coating undersurface, is unable to account completely for the enhanced bilayer strengths for the larger Vickers flaws. It is hypothesized that the epoxy used to bond the bilayer components enters the cracks, causing crack-wall adherence and providing an increased resistance to radial crack instability. The fracture mechanics are nevertheless able to account for the arrest and subsequent stable extension of the radial cracks beyond the critical loads once this extraneous adherence has been overcome. [source] GENETIC DIVERGENCE CORRELATES WITH MORPHOLOGICAL AND ECOLOGICAL SUBDIVISION IN THE DEEP-WATER ELK KELP, PELAGOPHYCUS PORRA (PHAEOPHYCEAE)JOURNAL OF PHYCOLOGY, Issue 5 2000Kathy Ann Miller Pelagophycus porra (Leman) Setchell has a narrow distribution confined to deep water from the Channel Islands off the southern California coast to central Baja California, Mexico. Distinct morphotypes are consistently correlated with distinctive habitats, that is, windward exposures characterized by strong water motion and rocky substrates, and sheltered areas with soft substrates found on the lee sides of the islands. We tested the hypothesis that morphologically and ecologically distinct forms reflect genetically distinct stands. Individuals representing populations from three islands and the mainland were compared using RFLP analyses of the nuclear rDNA internal transcribed spacers (ITS1 and ITS2), chloroplast trnL (UAA) intron sequences, and random amplified polymorphic DNA (RAPDs). No variation was found in a survey of 20 restriction sites of ITS1 (ca. 320 base pair [bp]) and ITS2 (ca. 360 bp) among individuals from six populations. Likewise, comparisons of trnL intron (241 bp) sequences among nine individuals from seven populations were identical with the exception of a CATAGT insert in two adjacent stands. A RAPD analysis of 24 individuals from nine populations (4 windward and 5 leeward) using 16 primers generated 166 bands. Thirty-eight percent of the bands did not vary, 16% were unique to a given individual, and 46% were variable. Neighbor joining analysis produced a well-resolved tree with moderately high bootstrap support in which windward and leeward populations were easily distinguished. The lack of divergence in both the fast evolving nuclear rDNA-ITS and the chloroplast trnL intron does not support the morphotypes as different species. However, the compartmentalized differentiation shown in the RAPD data clearly points to isolation. This, and previous ecological studies that demonstrate habitat specificity suggest that leeward stands probably comprise a species in statu nascendi. [source] Complex behavioural pattern as an aid to identify the producer of Zoophycos from the Middle Permian of OmanLETHAIA, Issue 2 2009DIRK KNAUST The trace fossil Zoophycos is abundant in transgressive, shallow marine carbonates in the Middle Permian (Wordian) Khuff Formation of the Huqf-Haushi Uplift of Interior Oman. It often occurs as part of a complex (compound) trace fossil that comprises two integrated elements: (i) irregular galleries with straight to gently curved tunnels and interconnected shafts, and (ii) simple planar to complex spreiten structures with a marginal tube (Zoophycos). The galleries are characterized by irregularly winding, dichotomous branching, large variation in shape and size and circular to elliptical vertical cross-sections. Zoophycos consists of spreiten with a marginal tube, either originating as a simple lobe from the convex segment of a curved tunnel, or forming more complex, subcircular, spreiten systems parallel to bedding. The spreiten were formed by simple strip mining, where the animal defecated without producing faecal pellets. U-shaped marginal tubes indicate that the burrows were well aerated. The complex trace fossil points to combined dwelling and deposit-feeding behaviour, with irregular galleries in the firm substrate and Zoophycos spreiten in the softground below it. It can be assumed that the animal used the open tunnel system mainly for dwelling (domichnion) and possibly suspension feeding, but occasionally changed to deposit feeding while creating the spreiten (fodinichnion). The integration of the irregular galleries (tunnels and interconnected shafts) with the marginal tubes of Zoophycos suggests the same producer for this compound trace fossil. Many modern polychaetes produce very similar galleries within firm and soft substrates, and polychaetes are therefore interpreted as the most likely producers. Similarities between Permian and Triassic Zoophycos suggest comparable trace making behaviour before and after the end-Permian mass extinction. [source] Role of polymers in CVD growth of nanocrystalline diamond films on foreign substratesPHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 11-12 2009A. Kromka Abstract Spin coating of PVA polymer with fine grained diamond powder is used as the nucleation treatment for achieving growth of nanocrystalline diamond (NCD) thin films. The growth is realized by standard microwave plasma chemical vapor deposition (CVD). The morphology and character of deposited NCD film is strongly related to the growth temperature. The low temperature process (430°C) results in a growth of well-faceted continuous films. The high temperature process (830,°C) results in voids and openings in the layer. Addition of PVA as the interlayer between the substrate and the seeding polymer composite leads to more openings. The effect is the most pronounced at 830,°C. This is assigned to thermal instability of PVA and oxygen chemistry present in the early beginning of the CVD growth. An optimized seeding process based on the polymer composite procedure at low substrate temperature and low PVA amount allows the diamond growth on extremely soft substrates. [source] Influence of different substrates on the evolution of morphology and life-history traits of azooxanthellate solitary corals (Scleractinia: Flabellidae)BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, Issue 1 2010YUKI TOKUDA Sessile organisms are influenced considerably by their substrate conditions, and their adaptive strategies are key to understanding their morphologic evolution and traits of life history. The family Flabellidae (Cnidaria: Scleractinia) is composed of the representative azooxanthellate solitary corals that live on both soft and hard substrates using various adaptive strategies. We reconstructed the phylogenetic tree and ancestral character states of this family from the mitochondrial 16S and nuclear 28S ribosomal DNA sequences of ten flabellids aiming to infer the evolution of their adaptive strategies. The Javania lineage branched off first and adapted to hard substrates by using a tectura-reinforced base. The extant free-living flabellids, including Flabellum and Truncatoflabellum, invaded soft substrates and acquired the flabellate corallum morphology of their common ancestor, followed by a remarkable radiation with the exploitation of adaptive strategies, such as external soft tissue [e.g. Flabellum (Ulocyathus)], thecal edge spine, and transverse division (e.g. Placotrochus and Truncatoflabellum). Subsequently, the free-living ancestors of two genera (Rhizotrochus and Monomyces) invaded hard substrates independently by exploiting distinct attachment apparatuses such as tube-like and massive rootlets, respectively. In conclusion, flabellids developed various morphology and life-history traits according to the differences in substrate conditions during the course of their evolution. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 101, 184,192. [source] Individual feeding specialisation in shorebirds: population consequences and conservation implicationsBIOLOGICAL REVIEWS, Issue 4 2000SARAH E. A. LE V. DIT DURELL ABSTRACT Individual feeding specialisation in shorebirds is reviewed, and the possible mechanisms involved in such specialisations. Any specialisation can be seen as an individual strategy, and the optimum strategy for any given individual will be conditional upon its specific priorities and constraints. Some specialisations are related to social status and some to individual skills. Some are also probably frequency-dependent. However, most shorebird specialisations are constrained to a large extent by individual morphology, particularly bill morphology. For example, larger birds are able to handle larger prey, and birds with longer bills are able to feed on more deeply buried prey. Sex differences in bill length are uncommon in the Charardriidae, which are surface peckers, but are common in the Scolopacidae, which feed by probing in soft substrates. Sex differences in bill morphology are frequently associated with sex differences in feeding specialisation. There is evidence that different feeding specialisations are associated with different payoffs, in which case the probability of failing to reproduce or of dying will not be distributed equally throughout the population. I consider the population consequences of such feeding specialisations, particularly the different risks and benefits associated with different habitats or diets. I also consider the way in which individuals may differ in their response to habitat loss or change. I suggest that population models designed to predict the effect of habitat loss or change on shorebirds should have the ability to investigate the differential response of certain sections of the population, particularly different ages or sexes, that specialise in different diets or feeding methods. [source] | ||||||||||