Some aspects of floor spectra of 1DOF nonlinear primary structures

In this paper the influence of the nonlinear behaviour of the primary structure on floor spectra is investigated by means of simple models. The general trends of floor spectra for different types of nonlinear behaviour of one degree of freedom (1DOF) primary structure are shown and we point out their common futures and their differences. A special attention is given to the cases of elastoplastic and nonlinear elastic behaviours and methods to determine an equivalent linear oscillator are proposed. The properties (frequency and damping) of this equivalent linear oscillator are quite different from the properties of equivalent linear oscillators commonly considered in practice. In particular, in the case of elastoplastic behaviour, there is no frequency shift and damping is smaller than assumed by other methods commonly used. In the case of nonlinear elastic behaviour, the concept of an equivalent frequency which is a random variable is used. Finally, a design floor spectrum of primary structures, exhibiting energy dissipating nonlinear behaviour is proposed. Copyright © 2006 John Wiley & Sons, Ltd.     

A study of dells in the new forest,Hampshire, England

Dells in the New Forest are described as amphitheatre-shaped hollows, perched on valley sides, sometimes singly, in other places in groups tributary to small dry valleys. They have steep rear walls and sides, flatfish floors, and convex lips, usually without any water-worn channels. The slopes on which they occur, cut in Eocene sands and clays, have been subjected to solifluction, and this has produced wide gently sloping terraces at the foot of the hillside. Superficial deposits within the New Forest dells are divided into two groups by process: a lower head of fragmented flints in a sandy or clayey matrix, assigned to Zone III; overlying colluvial deposits including slumped material and slope wash, dated by reference to a buried soil to Zone VIIa. Although scoured by solifluction, other processes probably account for the initial formation of the hollows, and nivation is suggested. The dells are compared with the chalk coombes of southern England and the dellen of European and other writers. A possible chronology is suggested for the New Forest dells.     

Extraction of amino acids from soils and sediments with superheated water

A method of extraction for amino acids from soils and sediments involving superheated water has been investigated. About 75–97 per cent of the amino acids contained in four soils of a soil profile from Illinois were extracted by this method. Deep penetration of water into soil aggregates and partial hydrolysis of peptide bonds during this extraction by water at high temperature are likely mechanisms responsible for the release of amino acids from samples. This extraction method does not require subsequent desalting treatments when analyses are carried out with an ion-exchange amino acid analyzer.     

Hydrogen partitioning between melt,clinopyroxene, and garnet at 3 GPa in a hydrous MORB with 6 wt.% H<Subscript>2</Subscript>O

To understand partitioning of hydrogen between hydrous basaltic and andesitic liquids and coexisting clinopyroxene and garnet, experiments using a mid-ocean ridge basalt (MORB) + 6 wt.% H₂O were conducted at 3 GPa and 1,150–1,325°C. These included both isothermal and controlled cooling rate crystallization experiments, as crystals from the former were too small for ion microprobe (SIMS) analyses. Three runs at lower bulk water content are also reported. H₂O was measured in minerals by SIMS and in glasses by SIMS, Fourier Transform infrared spectroscopy (FTIR), and from oxide totals of electron microprobe (EMP) analyses. At 3 GPa, the liquidus for MORB with 6 wt.% H₂O is between 1,300 and 1,325°C. In the temperature interval investigated, the melt proportion varies from 100 to 45% and the modes of garnet and clinopyroxene are nearly equal. Liquid composition varies from basaltic to andesitic. The crystallization experiments starting from above the liquidus failed to nucleate garnets, but those starting from below the liquidus crystallized both garnet and clinopyroxene. SIMS analyses of glasses with >7 wt.% H₂O yield spuriously low concentrations, perhaps owing to hydrogen degassing in the ultra-high vacuum of the ion microprobe sample chamber. FTIR and EMP analyses show that the glasses have 3.4 to 11.9 wt.% water, whilst SIMS analyses indicate that clinopyroxenes have 1,340–2,330 ppm and garnets have 98–209 ppm H₂O. D _H ^cpx−gt is 11 ± 3, D _H ^cpx−melt is 0.023 ± 0.005 and D _H ^gt−melt is 0.0018 ± 0.0006. Most garnet/melt pairs have low values of D _H ^gt−melt, but D _H ^gt−melt increases with TiO₂ in the garnet. As also found by previous studies, values of D _H ^cpx−melt increase with Al₂O₃ of the crystal. For garnet pyroxenite, estimated values of D _H ^{pyroxenite−melt} decrease from 0.015 at 2.5 GPa to 0.0089 at 5 GPa. Hydration will increase the depth interval between pyroxenite and peridotite solidi for mantle upwelling beneath ridges or oceanic islands. This is partly because the greater pyroxene/olivine ratio in pyroxenite will tend to enhance the H₂O concentration of pyroxenite, assuming that neighboring pyroxenite and peridotite bodies have similar H₂O in their pyroxenes. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Fine-scale rainfall over New Caledonia under climate change

Climate Dynamics - Global climate models projections indicate no clear future rainfall changes over the Southwestern Pacific islands in response to anthropogenic forcing. Yet, these models have low...     

Study on the cross-correlation of GNSS signals and typical approximations

In global navigation satellite system (GNSS) receivers, the first signal processing stage is the acquisition, which consists of detecting the received GNSS signals and determining the associated code delay and Doppler frequency by means of correlations with a code and carrier replicas. These codes, as part of the GNSS signal, were chosen to have very good correlation properties without considering the effect of a potential received Doppler frequency. In the literature, it is often admitted that the maximum GPS L1 C/A code cross-correlation is about ?24 dB. We show that this maximum can be as high as ?19.2 dB when considering a Doppler frequency in a typical range of [?5, 5] kHz. We also show the positive impact of the coherent integration time on the cross-correlation and that even a satellite with Doppler outside the frequency search space of a receiver impacts the cross-correlation. In addition, the expression of the correlation is often provided in the continuous time domain, while its implementation is typically made in the discrete domain. It is then legitimate to ask the validity of this approximation. Therefore, the purpose of this research is twofold: First, we discuss typical approximations and evaluate their regions of validity, and second, we provide characteristic values such as maximums and quantiles of the auto- and cross-correlation of the GPS L1 C/A and Galileo E1 OS codes in the presence of Doppler, for frequency ranges up to 50 kHz and for different integration times.     

Abundance of organic compounds photochemically produced in the atmospheres of the outer planets

Organic photochemical syntheses in the Jovian atmosphere were simulated by irradiating, at 147 nm, gaseous mixtures of methane and ammonia with varying quantities of hydrogen. An excess of H₂ did not eliminate organic synthesis but did affect the yields quantitatively and qualitatively.     

Change in carbon flux (1960–2015) of the Red River (Vietnam)

Global riverine carbon concentrations and fluxes have been impacted by climate and human-induced changes for many decades. This paper aims to reconstruct the longterm carbon concentrations and carbon fluxes of the Red River, a system under the coupled pressures of environmental change and human activity. Based on (1) the relationships between particulate and dissolved organic carbon (POC, DOC) or dissolved inorganic carbon (DIC), and suspended sediments (TSS) or river water discharge and on (2) the available detailed historical records of river discharge and TSS concentration, the variations of the Red River carbon concentration and flux were estimated for the period 1960–2015. The results show that total carbon flux of the Red River averaged 2555?±?639 kton C year^?1. DIC fluxes dominated total carbon fluxes, representing 64% of total, reflecting a strong weathering process from carbonate rocks in the upstream basin. Total carbon fluxes significantly decreased from 2816 kton C year^?1 during the 1960s to 1372 kton C year^?1 during the 2010s and showed clear seasonal and spatial variations. Organic carbon flux decreased in both quantity and proportion of the total carbon flux from 40.9% in 1960s to 14.9% in 2010s, reflecting the important impact of dam impoundment. DIC flux was also reduced over this period potentially as a consequence of carbonate precipitation in the irrigated, agricultural land and the reduction of the Red River water discharge toward the sea. These decreases in TSS and carbon fluxes are probably partially responsible for different negatives impacts observed in the coastal zone.