2,404 research outputs found

    The magnetic exchange parameters and anisotropy of the quasi-two dimensional antiferromagnet NiPS3_3

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    Neutron inelastic scattering has been used to measure the magnetic excitations in powdered NiPS3_3, a quasi-two dimensional antiferromagnet with spin S=1S = 1 on a honeycomb lattice. The spectra show clear, dispersive magnons with a ∼7\sim 7 meV gap at the Brillouin zone center. The data were fitted using a Heisenberg Hamiltonian with a single-ion anisotropy assuming no magnetic exchange between the honeycomb planes. Magnetic exchange interactions up to the third intraplanar nearest-neighbour were required. The fits show robustly that NiPS3_3 has an easy axis anisotropy with Δ=0.3\Delta = 0.3 meV and that the third nearest-neighbour has a strong antiferromagnetic exchange of J3=−6.90J_3 = -6.90 meV. The data can be fitted reasonably well with either J1<0J_1 < 0 or J1>0J_1 > 0, however the best quantitative agreement with high-resolution data indicate that the nearest-neighbour interaction is ferromagnetic with J1=1.9J_1 = 1.9 meV and that the second nearest-neighbour exchange is small and antiferromagnetic with J2=−0.1J_2 = -0.1 meV. The dispersion has a minimum in the Brillouin zone corner that is slightly larger than that at the Brillouin zone center, indicating that the magnetic structure of NiPS3_3 is close to being unstable.Comment: 21 pages, 7 figures, 33 reference

    Robustness assessment approaches for steel framed structures under catastrophic events

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    The current study deals with the robustness assessment methods of steel framed buildings under catastrophic events. Two steel framed buildings, designed according to old and new seismic Italian codes, have been herein analysed, by considering the uncertainties of both the material strength and the applied loads, through two investigation methods. First, within the methodologies used for robustness assessment under seismic loads, a deterministic method, framed within the Performance Based Seismic Design (PBSD), has been applied. Later on, the robustness of studied structures under different column-removed conditions, related to different catastrophic events (blast, impact, fire and so on), has been assessed by means of two forcebased analysis techniques (a literature approach and a more advanced procedure) in order to estimate their resistance against progressive collapse. The application of the two methods has allowed to calculate the robustness index of examined structures, by taking into account the influence of both the catenary effect phenomenon and different beam-to-column joints, with the final aim to show their behavioural difference in terms of robustness

    Independent component analysis of interictal fMRI in focal epilepsy: comparison with general linear model-based EEG-correlated fMRI

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    The general linear model (GLM) has been used to analyze simultaneous EEG–fMRI to reveal BOLD changes linked to interictal epileptic discharges (IED) identified on scalp EEG. This approach is ineffective when IED are not evident in the EEG. Data-driven fMRI analysis techniques that do not require an EEG derived model may offer a solution in these circumstances. We compared the findings of independent components analysis (ICA) and EEG-based GLM analyses of fMRI data from eight patients with focal epilepsy. Spatial ICA was used to extract independent components (IC) which were automatically classified as either BOLD-related, motion artefacts, EPI-susceptibility artefacts, large blood vessels, noise at high spatial or temporal frequency. The classifier reduced the number of candidate IC by 78%, with an average of 16 BOLD-related IC. Concordance between the ICA and GLM-derived results was assessed based on spatio-temporal criteria. In each patient, one of the IC satisfied the criteria to correspond to IED-based GLM result. The remaining IC were consistent with BOLD patterns of spontaneous brain activity and may include epileptic activity that was not evident on the scalp EEG. In conclusion, ICA of fMRI is capable of revealing areas of epileptic activity in patients with focal epilepsy and may be useful for the analysis of EEG–fMRI data in which abnormalities are not apparent on scalp EEG

    Thermal stability and aggregation of sulfolobus solfataricus b-glycosidase are dependent upon the N-e-methylation of specific lysyl residues: critical role of in vivo post-translational modifications.

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    Methylation in vivo is a post-translational modification observed in several organisms belonging to eucarya, bacteria, and archaea. Although important implications of this modification have been demonstrated in several eucaryotes, its biological role in hyperthermophilic archaea is far from being understood. The aim of this work is to clarify some effects of methylation on the properties of β-glycosidase from Sulfolobus solfataricus, by a structural comparison between the native, methylated protein and its unmethylated counterpart, recombinantly expressed in Escherichia coli. Analysis by Fourier transform infrared spectroscopy indicated similar secondary structure contents for the two forms of the protein. However, the study of temperature perturbation by Fourier transform infrared spectroscopy and turbidimetry evidenced denaturation and aggregation events more pronounced in recombinant than in native β-glycosidase. Red Nile fluorescence analysis revealed significant differences of surface hydrophobicity between the two forms of the protein. Unlike the native enzyme, which dissociated into SDS-resistant dimers upon exposure to the detergent, the recombinant enzyme partially dissociated into monomers. By electrospray mapping, the methylation sites of the native protein were identified. A computational analysis of β-glycosidase three-dimensional structure and comparisons with other proteins from S. solfataricus revealed analogies in the localization of methylation sites in terms of secondary structural elements and overall topology. These observations suggest a role for the methylation of lysyl residues, located in selected domains, in the thermal stabilization of β-glycosidase from S. solfataricu
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