10,592 research outputs found

    The boundary between the middle Eocene Brussel sand and the Lede sand formations in the Zaventem-Nederokkerzeel area (northeast of Brussels, Belgium)

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    In the Zaventem airport railway cutting, to the north-east of Brussels, the upper part of the Brussel Sand Formation consists of two major units, both attributable to calcareous nannofossil zone NP14a. The lower predomi­nantly sandy unit ZB1 (including subunits A, B and C, belonging to NP14al) is built up of sparsely glauconitic, relatively coarse tidal current deposits with nodule levels cemented by carbonate and silica, of which one shows slump­ing structures and is interpreted as a seismite. The uppermost unit ZB2 (also labelled D, belonging to NP14a2), com­posed of alternating thin fine sandstone bands and silty marls, represents the fill of a large channel. In the Berg-Nederokkerzeel sandpit the carbonate-rich Brussel Sand Formation is finer grained and more homogeneous. Here, the basal sand (unit A) is attributable to NP14a3 and consequently, younger than the section exposed at Zaventem. It is incised at its the top by a rather narrow erosive gully, filled in with well-sorted fine sand rich in washed-in molluscs (unit B), some of which seem to point to a brackish influence. The extreme top is made up of half a meter of sand with abundant Callianassa burrows and echinid fragments (unit C). From the nannofossil data it appears that, east of Brus­sels, at least two generations of tidal channel systems seem to have occurred within the Brussel Sand Formation, followed by a partial emersion at the end of the filling of the uppermost channel (Nederokkerzeel B). This was suc­ceeded by a relative sea-level rise, as shown by unit C and the remains of a completely eroded fully marine deposit, reworked in the base of the overlying Lede Sand Formation. The lowest relative sea level, with at least partial emer­gence of the Brussels area, occurred during middle to late Biochron NP14b. In both outcrops the Lede Sand Formation displays its characteristic pale grey relatively fine-grained homogeneous nature with a stone layer near its base. It can be concluded that, at the beginning of the "Lede transgression", an erosion of older deposits, containing already lifhified stone layers, occurred. This was, apparently, at least locally, caused by storms, which could redistribute, imbricate and turn over the stones, explaining their bio-perforation on both sides. Afterwards the stones have been above water for a relatively long time, enough to allow the dissolution of the perforating organisms and consequently an important oxidation of their surfaces. These stones have subsequently been colonised by a new marine fauna. Part of the shark teeth and calcareous nannofossil assemblages found in the coarse base of the Lede Sand is definitely older than the taxa normally found in the Lede Sand Formation. These fossils are the remains of a sediment package, believed to represent the formerly "Laekenian" stage

    Measuring the mixing efficiency in a simple model of stirring:some analytical results and a quantitative study via Frequency Map Analysis

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    We prove the existence of invariant curves for a TT--periodic Hamiltonian system which models a fluid stirring in a cylindrical tank, when TT is small and the assigned stirring protocol is piecewise constant. Furthermore, using the Numerical Analysis of the Fundamental Frequency of Laskar, we investigate numerically the break down of invariant curves as TT increases and we give a quantitative estimate of the efficiency of the mixing.Comment: 10 figure

    Impact of ultrafast electronic damage in single particle x-ray imaging experiments

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    In single particle coherent x-ray diffraction imaging experiments, performed at x-ray free-electron lasers (XFELs), samples are exposed to intense x-ray pulses to obtain single-shot diffraction patterns. The high intensity induces electronic dynamics on the femtosecond time scale in the system, which can reduce the contrast of the obtained diffraction patterns and adds an isotropic background. We quantify the degradation of the diffraction pattern from ultrafast electronic damage by performing simulations on a biological sample exposed to x-ray pulses with different parameters. We find that the contrast is substantially reduced and the background is considerably strong only if almost all electrons are removed from their parent atoms. This happens at fluences of at least one order of magnitude larger than provided at currently available XFEL sources.Comment: 15 pages, 3 figures submitted to PR

    Observation of Pure Spin Transport in a Diamond Spin Wire

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    Spin transport electronics - spintronics - focuses on utilizing electron spin as a state variable for quantum and classical information processing and storage. Some insulating materials, such as diamond, offer defect centers whose associated spins are well-isolated from their environment giving them long coherence times; however, spin interactions are important for transport, entanglement, and read-out. Here, we report direct measurement of pure spin transport - free of any charge motion - within a nanoscale quasi 1D 'spin wire', and find a spin diffusion length ~ 700 nm. We exploit the statistical fluctuations of a small number of spins (N\sqrt{N} < 100 net spins) which are in thermal equilibrium and have no imposed polarization gradient. The spin transport proceeds by means of magnetic dipole interactions that induce flip-flop transitions, a mechanism that can enable highly efficient, even reversible, pure spin currents. To further study the dynamics within the spin wire, we implement a magnetic resonance protocol that improves spatial resolution and provides nanoscale spectroscopic information which confirms the observed spin transport. This spectroscopic tool opens a potential route for spatially encoding spin information in long-lived nuclear spin states. Our measurements probe intrinsic spin dynamics at the nanometre scale, providing detailed insight needed for practical devices which seek to control spin.Comment: 7 pages, 2 figures, under consideration at Nature Nanotechnolog

    Surface scattering velocities in III-nitride quantum well laser structures via the emission of hybrid phonons

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    We have theoretically and numerically studied nitride-based quantum well (QW) laser structures. More specifically, we have used a QW made with III-nitride where the width of the barrier region is large relative to the electron mean free path, and we have calculated the electron surface capture velocities by considering an electron flux which is captured into the well region. The process is assisted by the emission of the longitudinal optical phonons as predicted by the hybrid (HB) model. The results of surface capture velocities via the emission of HB phonons are compared to the emission of the dielectric continuum phonons (Zakhleniuk et al 1999 Phys. Status Solidi a 176 79). Our investigation shows that the two different phonon models predict almost the same results for the non-retarded limit. Furthermore, the surface capture velocities strongly depend on the size of the structure and the heterostructure materials. Lastly, a comparison to the recent experimental values shows that our model could accurately describe the experimentally measured parameters of the quantum capture processes

    2-Thiabicyclo[3.2.0]hepta-3,6-Dienes. 1. Aluminum Chloride Catalyzed Thermal [2 + 2] Cycloaddition of 2-Butynedinitrile with Alkyl-Substituted Thiophenes

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    Tetra- and Trialkylthiophenes 4–6 React with 2-Butynedinitrile in the Presence of 1 Equiv of Aluminum Chloride in Dichloromethane at 0 °C Via [2 + 2] Cycloaddition to 2-3.2.0] hepta-3,6-Diene-6,7-Dicarbonitriles 7–10 as the Major Products. Reaction of 4 and 5 Also Gave Small Amounts (4% and 6%) of 1,2-Benzenedicarbonitriles 11 and 12 Which Result from [4 + 2] Cycloaddition and Subsequent Extrusion of Sulfur. 4,5,6,7-Tetrahydro-1,3-Dimethylbenzo[C]thiophene (6) Reacts with 2-Butynedinitrile under the Same Conditions to Give an Ene Adduct (13) in Addition to the [2 + 2] Cycloadduct 10. 2,5-Dimethylthiophene (3) Gave a 2:1 Reaction Product 14, the Formation of Which Can Be Explained Via Friedel-Crafts Alkylation of 3 by the Initially Formed [2 + 2] Cycloadduct. the 2-3.2.0] hepta-3,6-Dienes 7–10 and the Ene Adduct 13 Show Intramolecular Charge-Transfer Absorptions in the UV Spectra. © 1982, American Chemical Society. All Rights Reserved
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