1,268 research outputs found
Robust Ferroelectric State in Multiferroic MnZnWO
We report the remarkably robust ferroelectric state in the multiferroic
compound MnZnWO. The substitution of the magnetic Mn
with nonmagnetic Zn reduces the magnetic exchange and provides control
of the various magnetic and multiferroic states of MnWO. Only 5 % of Zn
substitution results in a complete suppression of the frustrated collinear
(paraelectric) low temperature phase. The helical magnetic and ferroelectric
phase develops as the ground state. The multiferroic state is stable up to a
high level of substitution of more than 50 %. The magnetic, thermodynamic, and
dielectric properties as well as the ferroelectric polarization of single
crystals of MnZnWO are studied for different substitutions up
to x=0.5. The magnetic phases have been identified in single crystal neutron
scattering experiments. The ferroelectric polarization scales with the neutron
intensity of the incommensurate peak of the helical phase.Comment: 6 pages, 8 figure
Theoretical analysis of neutron scattering results for quasi-two dimensional ferromagnets
A theoretical study has been carried out to analyse the available results
from the inelastic neutron scattering experiment performed on a quasi-two
dimensional spin-1/2 ferromagnetic material . Our formalism is based
on a conventional semi-classical like treatment involving a model of an ideal
gas of vortices/anti-vortices corresponding to an anisotropic XY Heisenberg
ferromagnet on a square lattice. The results for dynamical structure functions
for our model corresponding to spin-1/2, show occurrence of negative values in
a large range of energy transfer even encompassing the experimental range, when
convoluted with a realistic spectral window function. This result indicates
failure of the conventional theoretical framework to be applicable to the
experimental situation corresponding to low spin systems. A full quantum
formalism seems essential for treating such systems.Comment: 16 pages, 6 figures, 1 Table Submitted for publicatio
EFX Allocations: Simplifications and Improvements
The existence of EFX allocations is a fundamental open problem in discretefair division. Given a set of agents and indivisible goods, the goal is todetermine the existence of an allocation where no agent envies anotherfollowing the removal of any single good from the other agent's bundle. Sincethe general problem has been illusive, progress is made on two fronts: proving existence when the number of agents is small, proving existenceof relaxations of EFX. In this paper, we improve results on both fronts (andsimplify in one of the cases). We prove the existence of EFX allocations with three agents, restricting onlyone agent to have an MMS-feasible valuation function (a strict generalizationof nice-cancelable valuation functions introduced by Berger et al. whichsubsumes additive, budget-additive and unit demand valuation functions). Theother agents may have any monotone valuation functions. Our proof technique issignificantly simpler and shorter than the proof by Chaudhury et al. onexistence of EFX allocations when there are three agents with additivevaluation functions and therefore more accessible. Secondly, we consider relaxations of EFX allocations, namely, approximate-EFXallocations and EFX allocations with few unallocated goods (charity). Chaudhuryet al. showed the existence of -EFX allocation with charity by establishing a connection to aproblem in extremal combinatorics. We improve their result and prove theexistence of -EFX allocations with charity. In fact, some of our techniques can be usedto prove improved upper-bounds on a problem in zero-sum combinatoricsintroduced by Alon and Krivelevich.<br
Magnetic Field resulting from non-linear electrical transport in single crystals of charge-ordered Pr Ca MnO}
In this letter we report that the current induced destabilization of the
charge ordered (CO) state in a rare-earth manganite gives rise to regions with
ferromagnetic correlation. We did this experiment by measurement of the I-V
curves in single crystal of the CO system
PrCaMnO and simultanously measuring the magnetization
of the current carrying conductor using a high T SQUID working at T = 77K.
We have found that the current induced destabilization of the CO state leads to
a regime of negative differential resistance which leads to a small enhancement
of the magnetization of the sample, indicating ferromagnetically aligned
moments.Comment: 4 pages LateX, 4 eps figure
Optical Flow Estimation in the Deep Learning Age
Akin to many subareas of computer vision, the recent advances in deep
learning have also significantly influenced the literature on optical flow.
Previously, the literature had been dominated by classical energy-based models,
which formulate optical flow estimation as an energy minimization problem.
However, as the practical benefits of Convolutional Neural Networks (CNNs) over
conventional methods have become apparent in numerous areas of computer vision
and beyond, they have also seen increased adoption in the context of motion
estimation to the point where the current state of the art in terms of accuracy
is set by CNN approaches. We first review this transition as well as the
developments from early work to the current state of CNNs for optical flow
estimation. Alongside, we discuss some of their technical details and compare
them to recapitulate which technical contribution led to the most significant
accuracy improvements. Then we provide an overview of the various optical flow
approaches introduced in the deep learning age, including those based on
alternative learning paradigms (e.g., unsupervised and semi-supervised methods)
as well as the extension to the multi-frame case, which is able to yield
further accuracy improvements.Comment: To appear as a book chapter in Modelling Human Motion, N. Noceti, A.
Sciutti and F. Rea, Eds., Springer, 202
Developmentally regulated HEART STOPPER, a mitochondrially targeted L18 ribosomal protein gene, is required for cell division, differentiation, and seed development in Arabidopsis.
Evidence is presented for the role of a mitochondrial ribosomal (mitoribosomal) L18 protein in cell division, differentiation, and seed development after the characterization of a recessive mutant, heart stopper (hes). The hes mutant produced uncellularized endosperm and embryos arrested at the late globular stage. The mutant embryos differentiated partially on rescue medium with some forming callus. HES (At1g08845) encodes a mitochondrially targeted member of a highly diverged L18 ribosomal protein family. The substitution of a conserved amino residue in the hes mutant potentially perturbs mitoribosomal function via altered binding of 5S rRNA and/or influences the stability of the 50S ribosomal subunit, affecting mRNA binding and translation. Consistent with this, marker genes for mitochondrial dysfunction were up-regulated in the mutant. The slow growth of the endosperm and embryo indicates a defect in cell cycle progression, which is evidenced by the down-regulation of cell cycle genes. The down-regulation of other genes such as EMBRYO DEFECTIVE genes links the mitochondria to the regulation of many aspects of seed development. HES expression is developmentally regulated, being preferentially expressed in tissues with active cell division and differentiation, including developing embryos and the root tips. The divergence of the L18 family, the tissue type restricted expression of HES, and the failure of other L18 members to complement the hes phenotype suggest that the L18 proteins are involved in modulating development. This is likely via heterogeneous mitoribosomes containing different L18 members, which may result in differential mitochondrial functions in response to different physiological situations during development.Hongyu Zhang, Ming Luo, Robert C. Day, Mark J. Talbot, Aneta Ivanova, Anthony R. Ashton, Abed M. Chaudhury, Richard C. Macknight, Maria Hrmova, and Anna M. Koltuno
Dynamic Disorder in Quasi-Equilibrium Enzymatic Systems
Conformations and catalytic rates of enzymes fluctuate over a wide range of timescales. Despite these fluctuations, there exist some limiting cases in which the enzymatic catalytic rate follows the macroscopic rate equation such as the Michaelis-Menten law. In this paper we investigate the applicability of macroscopic rate laws for fluctuating enzyme systems in which catalytic transitions are slower than ligand binding-dissociation reactions. In this quasi-equilibrium limit, for an arbitrary reaction scheme we show that the catalytic rate has the same dependence on ligand concentrations as obtained from mass-action kinetics even in the presence of slow conformational fluctuations. These results indicate that the timescale of conformational dynamics – no matter how slow – will not affect the enzymatic rate in quasi-equilibrium limit. Our numerical results for two enzyme-catalyzed reaction schemes involving multiple substrates and inhibitors further support our general theory
Benchmarking and Analysis of Protein Docking Performance in Rosetta v3.2
RosettaDock has been increasingly used in protein docking and design strategies in order to predict the structure of protein-protein interfaces. Here we test capabilities of RosettaDock 3.2, part of the newly developed Rosetta v3.2 modeling suite, against Docking Benchmark 3.0, and compare it with RosettaDock v2.3, the latest version of the previous Rosetta software package. The benchmark contains a diverse set of 116 docking targets including 22 antibody-antigen complexes, 33 enzyme-inhibitor complexes, and 60 ‘other’ complexes. These targets were further classified by expected docking difficulty into 84 rigid-body targets, 17 medium targets, and 14 difficult targets. We carried out local docking perturbations for each target, using the unbound structures when available, in both RosettaDock v2.3 and v3.2. Overall the performances of RosettaDock v2.3 and v3.2 were similar. RosettaDock v3.2 achieved 56 docking funnels, compared to 49 in v2.3. A breakdown of docking performance by protein complex type shows that RosettaDock v3.2 achieved docking funnels for 63% of antibody-antigen targets, 62% of enzyme-inhibitor targets, and 35% of ‘other’ targets. In terms of docking difficulty, RosettaDock v3.2 achieved funnels for 58% of rigid-body targets, 30% of medium targets, and 14% of difficult targets. For targets that failed, we carry out additional analyses to identify the cause of failure, which showed that binding-induced backbone conformation changes account for a majority of failures. We also present a bootstrap statistical analysis that quantifies the reliability of the stochastic docking results. Finally, we demonstrate the additional functionality available in RosettaDock v3.2 by incorporating small-molecules and non-protein co-factors in docking of a smaller target set. This study marks the most extensive benchmarking of the RosettaDock module to date and establishes a baseline for future research in protein interface modeling and structure prediction
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