103 research outputs found

    Current fidelity susceptibility and conductivity in one-dimensional lattice models with open and periodic boundary conditions

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    We study, both numerically and analytically, the finite size scaling of the fidelity susceptibility \chi_{J} with respect to the charge or spin current in one-dimensional lattice models, and relate it to the low-frequency behavior of the corresponding conductivity. It is shown that in gapless systems with open boundary conditions the leading dependence on the system size L stems from the singular part of the conductivity and is quadratic, with a universal form \chi_{J}= 7KL^2 \zeta(3)/2\pi^4 where K is the Luttinger liquid parameter. In contrast to that, for periodic boundary conditions the leading system size dependence is directly connected with the regular part of the conductivity (giving alternative possibility to study low frequency behavior of the regular part of conductivity) and is subquadratic, \chi_{J} \propto L^\gamma(K), (with a K dependent constant \gamma) in most situations linear, \gamma=1. For open boundary conditions, we also study another current-related quantity, the fidelity susceptibility to the lattice tilt \chi_{P} and show that it scales as the quartic power of the system size, \chi_{P}=31KL^4 \zeta(5)/8 u^2 \pi^6, where u is the sound velocity. We comment on the behavior of the current fidelity susceptibility in gapped phases, particularly in the topologically ordered Haldane state.Comment: 11 pages, 7 eps figure

    Ultra-cold bosons in zig-zag optical lattices

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    Ultra-cold bosons in zig-zag optical lattices present a rich physics due to the interplay between frustration, induced by lattice geometry, two-body interaction and three-body constraint. Unconstrained bosons may develop chiral superfluidity and a Mott-insulator even at vanishingly small interactions. Bosons with a three-body constraint allow for a Haldane-insulator phase in non-polar gases, as well as pair-superfluidity and density wave phases for attractive interactions. These phases may be created and detected within the current state of the art techniques.Comment: 8 pages, 9 figure

    Sustained blood glutamate scavenging enhances protection in ischemic stroke

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    Stroke is a major cause of morbidity, mortality, and disability. During ischemic stroke, a marked and prolonged rise of glutamate concentration in the brain causes neuronal cell death. This study explores the protective effect of a bioconjugate form of glutamate oxaloacetate transaminase (hrGOT), which catalyzes the depletion of blood glutamate in the bloodstream for ~6 days following a single administration. When treated with this bioconjugate, a significant reduction of the infarct volume and a better retention of sensorimotor function was observed for ischemic rats compared to those treated with saline. Moreover, the equivalent dose of native hrGOT yielded similar results to the saline treated group for some tests. Targeting the bioconjugate to the blood-brain-barrier did not improve its performance. The data suggest that the bioconjugates draw glutamate out of the brain by displacing homeostasis between the different glutamate pools of the body

    Unconventional Phases of Attractive Fermi Gases in Synthetic Hall Ribbons

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    An innovative way to produce quantum Hall ribbons in a cold atomic system is to use M hyperfine states of atoms in a one-dimensional optical lattice to mimic an additional “synthetic dimension.” A notable aspect here is that the SU(M) symmetric interaction between atoms manifests as “infinite ranged” along the synthetic dimension. We study the many-body physics of fermions with SU(M) symmetric attractive interactions in this system using a combination of analytical field-theoretic and numerical density-matrix renormalization-group methods. We uncover the rich ground-state phase diagram of the system, including unconventional phases such as squished baryon fluids, shedding light on many-body physics in low dimensions. Remarkably, changing the parameters entails interesting crossovers and transition; e.g., we show that increasing the magnetic field (that produces the Hall effect) converts a “ferrometallic” state at low fields to a “squished baryon superfluid” (with algebraic pairing correlations) at high fields. We also show that this system provides a unique opportunity to study quantum phase separation in a multi flavor ultracold fermionic system

    Reprogramming the assembly of unmodified DNA with a small molecule

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    The ability of DNA to store and encode information arises from base pairing of the four-letter nucleobase code to form a double helix. Expanding this DNA ‘alphabet’ by synthetic incorporation of new bases can introduce new functionalities and enable the formation of novel nucleic acid structures. However, reprogramming the self-assembly of existing nucleobases presents an alternative route to expand the structural space and functionality of nucleic acids. Here we report the discovery that a small molecule, cyanuric acid, with three thymine-like faces reprogrammes the assembly of unmodified poly(adenine) (poly(A)) into stable, long and abundant fibres with a unique internal structure. Poly(A) DNA, RNA and peptide nucleic acid all form these assemblies. Our studies are consistent with the association of adenine and cyanuric acid units into a hexameric rosette, which brings together poly(A) triplexes with a subsequent cooperative polymerization. Fundamentally, this study shows that small hydrogen-bonding molecules can be used to induce the assembly of nucleic acids in water, which leads to new structures from inexpensive and readily available materials

    Encoding of Spatio-Temporal Input Characteristics by a CA1 Pyramidal Neuron Model

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    The in vivo activity of CA1 pyramidal neurons alternates between regular spiking and bursting, but how these changes affect information processing remains unclear. Using a detailed CA1 pyramidal neuron model, we investigate how timing and spatial arrangement variations in synaptic inputs to the distal and proximal dendritic layers influence the information content of model responses. We find that the temporal delay between activation of the two layers acts as a switch between excitability modes: short delays induce bursting while long delays decrease firing. For long delays, the average firing frequency of the model response discriminates spatially clustered from diffused inputs to the distal dendritic tree. For short delays, the onset latency and inter-spike-interval succession of model responses can accurately classify input signals as temporally close or distant and spatially clustered or diffused across different stimulation protocols. These findings suggest that a CA1 pyramidal neuron may be capable of encoding and transmitting presynaptic spatiotemporal information about the activity of the entorhinal cortex-hippocampal network to higher brain regions via the selective use of either a temporal or a rate code

    Coding “What” and “When” in the Archer Fish Retina

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    Traditionally, the information content of the neural response is quantified using statistics of the responses relative to stimulus onset time with the assumption that the brain uses onset time to infer stimulus identity. However, stimulus onset time must also be estimated by the brain, making the utility of such an approach questionable. How can stimulus onset be estimated from the neural responses with sufficient accuracy to ensure reliable stimulus identification? We address this question using the framework of colour coding by the archer fish retinal ganglion cell. We found that stimulus identity, “what”, can be estimated from the responses of best single cells with an accuracy comparable to that of the animal's psychophysical estimation. However, to extract this information, an accurate estimation of stimulus onset is essential. We show that stimulus onset time, “when”, can be estimated using a linear-nonlinear readout mechanism that requires the response of a population of 100 cells. Thus, stimulus onset time can be estimated using a relatively simple readout. However, large nerve cell populations are required to achieve sufficient accuracy
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