236 research outputs found

    Strain analysis of a seismically imaged mass‐transport complex, offshore Uruguay

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    Strain style, magnitude and distribution within mass‐transport complexes (MTCs) are important for understanding the process evolution of submarine mass flows and for estimating their runout distances. Structural restoration and quantification of strain in gravitationally driven passive margins have been shown to approximately balance between updip extensional and downdip contractional domains; such an exercise has not yet been attempted for MTCs. We here interpret and structurally restore a shallowly buried (c. 1,500 mbsf) and well‐imaged MTC, offshore Uruguay using a high‐resolution (12.5 m vertical and 15 × 12.5 m horizontal resolution) three‐dimensional seismic‐reflection survey. This allows us to characterise and quantify vertical and lateral strain distribution within the deposit. Detailed seismic mapping and attribute analysis shows that the MTC is characterised by a complicated array of kinematic indicators, which vary spatially in style and concentration. Seismic‐attribute extractions reveal several previously undocumented fabrics preserved in the MTC, including internal shearing in the form of sub‐orthogonal shear zones, and fold‐thrust systems within the basal shear zone beneath rafted‐blocks. These features suggest multiple transport directions and phases of flow during emplacement. The MTC is characterised by a broadly tripartite strain distribution, with extensional (e.g. normal faults), translational and contractional (e.g. folds and thrusts) domains, along with a radial frontally emergent zone. We also show how strain is preferentially concentrated around intra‐MTC rafted‐blocks due to their kinematic interactions with the underlying basal shear zone. Overall, and even when volume loss within the frontally emergent zone is included, a strain deficit between the extensional and contractional domains (c. 3%–14%) is calculated. We attribute this to a combination of distributed, sub‐seismic, ‘cryptic’ strain, likely related to de‐watering, grain‐scale deformation and related changes in bulk sediment volume. This work has implications for assessing MTCs strain distribution and provides a practical approach for evaluating structural interpretations within such deposits

    Pulmonary Arterial Stent Implantation in an Adult with Williams Syndrome

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    We report a 38-year-old patient who presented with pulmonary hypertension and right ventricular dysfunction due to pulmonary artery stenoses as a manifestation of Williams syndrome, mimicking chronic thromboembolic pulmonary hypertension. The patient was treated with balloon angioplasty and stent implantation. Short-term follow-up showed a good clinical result with excellent patency of the stents but early restenosis of the segments in which only balloon angioplasty was performed. These stenoses were subsequently also treated successfully by stent implantation. Stent patency was observed 3 years after the first procedure

    Determination of Membrane Protein Transporter Oligomerization in Native Tissue Using Spatial Fluorescence Intensity Fluctuation Analysis

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    Membrane transporter proteins exist in a complex dynamic equilibrium between various oligomeric states that include monomers, dimers, dimer of dimers and higher order oligomers. Given their sub-optical microscopic resolution size, the oligomerization state of membrane transporters is difficult to quantify without requiring tissue disruption and indirect biochemical methods. Here we present the application of a fluorescence measurement technique which combines fluorescence image moment analysis and spatial intensity distribution analysis (SpIDA) to determine the oligomerization state of membrane proteins in situ. As a model system we analyzed the oligomeric state(s) of the electrogenic sodium bicarbonate cotransporter NBCe1-A in cultured cells and in rat kidney. The approaches that we describe offer for the first time the ability to investigate the oligomeric state of membrane transporter proteins in their native state

    Structural Organization of DNA in Chlorella Viruses

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    Chlorella viruses have icosahedral capsids with an internal membrane enclosing their large dsDNA genomes and associated proteins. Their genomes are packaged in the particles with a predicted DNA density of ca. 0.2 bp nm−3. Occasionally infection of an algal cell by an individual particle fails and the viral DNA is dynamically ejected from the capsid. This shows that the release of the DNA generates a force, which can aid in the transfer of the genome into the host in a successful infection. Imaging of ejected viral DNA indicates that it is intimately associated with proteins in a periodic fashion. The bulk of the protein particles detected by atomic force microscopy have a size of ∌60 kDa and two proteins (A278L and A282L) of about this size are among 6 basic putative DNA binding proteins found in a proteomic analysis of DNA binding proteins packaged in the virion. A combination of fluorescence images of ejected DNA and a bioinformatics analysis of the DNA reveal periodic patterns in the viral DNA. The periodic distribution of GC rich regions in the genome provides potential binding sites for basic proteins. This DNA/protein aggregation could be responsible for the periodic concentration of fluorescently labeled DNA observed in ejected viral DNA. Collectively the data indicate that the large chlorella viruses have a DNA packaging strategy that differs from bacteriophages; it involves proteins and share similarities to that of chromatin structure in eukaryotes

    Learning From History About Reducing Infant Mortality: Contrasting the Centrality of Structural Interventions to Early 20th‐Century Successes in the United States to Their Neglect in Current Global Initiatives

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    Movement characteristics, physiological and perceptual responses of elite standard youth football players to different high intensity running drills

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    This is an Accepted Manuscript of an article published by Taylor & Francis in Science and Medicine in Football on 06/04/2018, available online: https://doi.org/10.1080/24733938.2018.1461235Purpose: To examine responses to high intensity running drills in youth football players. Methods: Seventeen players completed the YoYo Intermittent Recovery test level one (YYIR1) and a 15 m maximal sprint to quantify target running speeds. Players performed three conditions on separate occasions comprising: 12 x 15 s high intensity runs at 100% of the final YYIRT1 speed, 12 x ~4 s repeated sprints with ~26 s recovery, and combination running using both modalities. Heart rate was monitored continuously with PlayerLoadTM and movement characteristics using microtechnology. Ratings of perceived exertion and blood lactate responses were measured 2 min after the final repetition. The ratio of Flight:contraction time was calculated from a countermovement jump before and at 2 min and 14 hours after each condition. Data analysis used magnitude based inferences and effect sizes statistics. Results: Peak speed (1.1%; ES 0.23 ± 0.44) and mean speed over the initial 4s (6.3%; ES 0.45 ± 0.46) were possibly faster during combination compared to high intensity running with unclear differences when compared to repeated sprinting. This was despite most likely (21.6%; ES 7.65 ± 1.02) differences in prescribed speeds between conditions. There were likely reductions in F:C at 14 hours ratio after high intensity (-5.6%; ES –0.44 ± 0.32) and combination running (-6.8%; ES -0.53 ± 0.47). Changes in the repeated sprinting condition were unclear. Conclusions: Actual movement characteristics of high intensity running drills may not reflect those used to prescribe them whilst reductions in F:C ratio are still evident 14 hours after their completion
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