383 research outputs found

    Particle relabelling transformations in elastodynamics

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    The motion of a self-gravitating hyperelastic body is described through a time-dependent mapping from a reference body into physical space, and its material properties are determined by a referential density and strain-energy function defined relative to the reference body. Points within the reference body do not have a direct physical meaning, but instead act as particle labels that could be assigned in different ways. We use Hamilton’s principle to determine how the referential density and strain-energy functions transform when the particle labels are changed, and describe an associated “particle relabelling symmetry”. We apply these results to linearised elastic wave propagation, and discuss their implications for seismological inverse problems. In particular, we show that the effects of boundary topography on elastic wave propagation can be mapped exactly into volumetric heterogeneity while preserving the form of the equations of motion. Several numerical calculations are presented to illustrate our results.O.C. is supported through a NERC PhD studentship.This is the final version of the article. It first appeared from Oxford University Press via http://dx.doi.org/10.1093/gji/ggw03

    Intrinsic non-uniqueness of the acoustic full waveform inverse problem

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    SUMMARY In the context of seismic imaging, full waveform inversion (FWI) is increasingly popular. Because of its lower numerical cost, the acoustic approximation is often used, especially at the exploration geophysics scale, both for tests and for real data. Moreover, some research domains such as helioseismology face true acoustic media for which FWI can be useful. In this work, an argument that combines particle relabelling and homogenization is used to show that the general acoustic inverse problem based on band-limited data is intrinsically non-unique. It follows that the results of such inversions should be interpreted with caution. To illustrate these ideas, we consider 2-D numerical FWI examples based on a Gauss–Newton iterative inversion scheme and demonstrate effects of this non-uniqueness in the local optimization context.</jats:p

    Quantitative and qualitative differences in subcutaneous adipose tissue stores across lipodystrophy types shown by magnetic resonance imaging

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    BACKGROUND: Lipodystrophies are characterized by redistributed subcutaneous fat stores. We previously quantified subcutaneous fat by magnetic resonance imaging (MRI) in the legs of two patients with familial partial lipodystrophy subtypes 2 and 3 (FPLD2 and FPLD3, respectively). We now extend the MRI analysis across the whole body of patients with different forms of lipodystrophy. METHODS: We studied five subcutaneous fat stores (supraclavicular, abdominal, gluteal, thigh and calf) and the abdominal visceral fat stores in 10, 2, 1, 1 and 2 female subjects with, respectively, FPLD2, FPLD3, HIV-related partial lipodystrophy (HIVPL), acquired partial lipodystrophy (APL), congenital generalized lipodystrophy (CGL) and in six normal control subjects. RESULTS: Compared with normal controls, FPLD2 subjects had significantly increased supraclavicular fat, with decreased abdominal, gluteal, thigh and calf subcutaneous fat. FPLD3 subjects had increased supraclavicular and abdominal subcutaneous fat, with less severe reductions in gluteal, thigh and calf fat compared to FPLD2 subjects. The repartitioning of fat in the HIVPL subject closely resembled that of FPLD3 subjects. APL and CGL subjects had reduced upper body, gluteal and thigh subcutaneous fat; the APL subject had increased, while CGL subjects had decreased subcutaneous calf fat. Visceral fat was markedly increased in FPLD2 and APL subjects. CONCLUSION: Semi-automated MRI-based adipose tissue quantification indicates differences between various lipodystrophy types in these studied clinical cases and is a potentially useful tool for extended quantitative phenomic analysis of genetic metabolic disorders. Further studies with a larger sample size are essential for confirming these preliminary findings

    Dimensional accuracy of Electron Beam Melting (EBM) additive manufacture with regard to weight optimized truss structures

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    The Electron Beam (EBM) additive manufacturing process is well suited to fabricating complex structural designs in Ti–6Al–4V because of the design freedoms it offers combined with strong and consistent material properties. However it has been observed that complications may arise when manufacturing truss-like structures (such as those produced via structural topology optimization) in the form of undersized features on the finished part. The issue appears to affect truss members that are not aligned with the vertical build direction, with an apparent lack of material on the negative surfaces. This effect appears to worsen with a greater angle between the truss member and the build direction, even with the use of support structures. This investigation has characterized and measured the dimensional errors that result from this issue through 3D scanning techniques. Process modifications have then been made which result in significant improvements in dimensional accuracy. This investigation highlights the importance of heat management at features with negative surfaces to yield parts that are dimensionally accurate without introducing excessive internal melt defects in the form of voids and porosity

    How the other half lives: CRISPR-Cas's influence on bacteriophages

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    CRISPR-Cas is a genetic adaptive immune system unique to prokaryotic cells used to combat phage and plasmid threats. The host cell adapts by incorporating DNA sequences from invading phages or plasmids into its CRISPR locus as spacers. These spacers are expressed as mobile surveillance RNAs that direct CRISPR-associated (Cas) proteins to protect against subsequent attack by the same phages or plasmids. The threat from mobile genetic elements inevitably shapes the CRISPR loci of archaea and bacteria, and simultaneously the CRISPR-Cas immune system drives evolution of these invaders. Here we highlight our recent work, as well as that of others, that seeks to understand phage mechanisms of CRISPR-Cas evasion and conditions for population coexistence of phages with CRISPR-protected prokaryotes.Comment: 24 pages, 8 figure
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