44 research outputs found

    Relationship between Density and Biogenic Opal in Sediments from Sites 658 and 660

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    At Site 658, and especially at Site 660, sediments rich in biogenic opal were recovered. The fractions of biogenic silica, biogenic carbonate, and terrigenous material vary throughout the entire sequence at these sites (see chapters for Sites 658 and 660, this volume). At Site 660, biogenic-opal contents up to 100% are common in Eocene sediments. In studying these opal-rich sediments, a rapid method for estimating biogenic opal published by Mann and Muller (1980) was found useful. These authors applied an X-ray method which measures the height of a broad, diffuse reflection band of opal extending from about 15° to 32° 20, with a maximum at about 22° 20 (i.e., 4.04A) (Fig. 1, IB). Furthermore, this paper describes another method for estimating variations in the biogenic-opal content by using grain density. Grain density (p) can easily be determined by measuring the weight (G) and the volume (V) of the dry sediment, where p = G/P7g/cm3)

    Pattern recognition with a magnon-scattering reservoir

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    Magnons are elementary excitations in magnetic materials and undergo nonlinear multimode scattering processes at large input powers. In experiments and simulations, we show that the interaction between magnon modes of a confined magnetic vortex can be harnessed for pattern recognition. We study the magnetic response to signals comprising sine wave pulses with frequencies corresponding to radial mode excitations. Three-magnon scattering results in the excitation of different azimuthal modes, whose amplitudes depend strongly on the input sequences. We show that recognition rates above 95\% can be attained for four-symbol sequences using the scattered modes, with strong performance maintained with the presence of amplitude noise in the inputs

    Tailoring crosstalk between localized 1D spin-wave nanochannels using focused ion beams

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    1D spin-wave conduits are envisioned as nanoscale components of magnonics-based logic and computing schemes for future generation electronics. `A-la-carte methods of versatile control of the local magnetization dynamics in such nanochannels are highly desired for efficient steering of the spin waves in magnonic devices. Here, we present a study of localized dynamical modes in 1-μ\mum-wide Permalloy conduits probed by microresonator ferromagnetic resonance technique. We clearly observe the lowest-energy edge mode in the microstrip after its edges were finely trimmed by means of focused Ne+^+ ion irradiation. Furthermore, after milling the microstrip along its long axis by focused ion beams, creating consecutively \sim50 and \sim100 nm gaps, additional resonances emerge and are attributed to modes localized at the inner edges of the separated strips. To visualize the mode distribution, spatially resolved Brillouin light scattering microscopy was used showing an excellent agreement with the ferromagnetic resonance data and confirming the mode localization at the outer/inner edges of the strips depending on the magnitude of the applied magnetic field. Micromagnetic simulations confirm that the lowest-energy modes are localized within \sim15-nm-wide regions at the edges of the strips and their frequencies can be tuned in a wide range (up to 5 GHz) by changing the magnetostatic coupling (i.e. spatial separation) between the microstrips.Comment: 10 pages, 4 figure

    Genetic polymorphisms of manganese-superoxide dismutase and glutathione-S-transferase in chronic alcoholic pancreatitis

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    Chronic alcohol consumption is a major risk factor for the development of chronic pancreatitis. However, chronic pancreatitis occurs only in a minority of heavy drinkers. This variability may be due to yet unidentified genetic factors. Several enzymes involved in the degradation of reactive oxidants and xenobiotics, such as glutathione-S-transferase P1 (GSTP1) and manganese-superoxide dismutase (MnSOD) reveal functional polymorphisms that affect the antioxidative capacity and may therefore modulate the development of chronic pancreatitis and long-term complications like endocrine and exocrine pancreatic insufficiency. Two functional polymorphisms of the MnSOD and the GSTP1 gene were assessed by polymerase chain reaction and restriction fragment length polymorphism in 165 patients with chronic alcoholic pancreatitis, 140 alcoholics without evidence of pancreatic disease and 160 healthy control subjects. The distribution of GSTP1 and MnSOD genotypes were in Hardy-Weinberg equilibrium in the total cohort. Genotype and allele frequencies for both genes were not statistically different between the three groups. Although genotype MnSOD Ala/Val was seemingly associated with the presence of exocrine pancreatic insufficiency, this subgroup was too small and the association statistically underpowered. None of the tested genotypes affected the development of endocrine pancreatic insufficiency. Polymorphisms of MnSOD and GSTP1 are not associated with chronic alcoholic pancreatitis. The present data emphasize the need for stringently designed candidate gene association studies with well-characterized cases and controls and sufficient statistical power to exclude chance observation
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