25,157 research outputs found
Composite fermion theory of rapidly rotating two-dimensional bosons
Ultracold neutral bosons in a rapidly rotating atomic trap have been
predicted to exhibit fractional quantum Hall-like states. We describe how the
composite fermion theory, used in the description of the fractional quantum
Hall effect for electrons, can be applied to interacting bosons. Numerical
evidence supporting the formation of composite fermions, each being the bound
state of a boson and one flux quantum, is shown for filling fractions of the
type nu=p/(p+1), both by spectral analysis and by direct comparison with trial
wave functions. The rapidly rotating system of two-dimensional bosons thus
constitutes an interesting example of "statistical transmutation," with bosons
behaving like composite fermions. We also describe the difference between the
electronic and the bosonic cases when p approaches infinity. Residual
interactions between composite fermions are attractive in this limit, resulting
in a paired composite-fermion state described by the Moore-Read wave function.Comment: 12 pages, 9 figures. Conference proceeding. BEC 2005 Ital
Prediction of a non-Abelian fractional quantum Hall state with -wave pairing of composite fermions in wide quantum wells
We theoretically investigate the nature of the state at quarter filled lowest
Landau level and predict that, as the quantum well width is increased, a
transition occurs from the composite fermion Fermi sea into a novel non-Abelian
fractional quantum Hall state that is topologically equivalent to -wave
pairing of composite fermions. This state is topologically distinct from the
familiar -wave paired Pfaffian state. We compare our calculated phase
diagram with experiments and make predictions for many observable quantities
Evolutionary dynamics of the most populated genotype on rugged fitness landscapes
We consider an asexual population evolving on rugged fitness landscapes which
are defined on the multi-dimensional genotypic space and have many local
optima. We track the most populated genotype as it changes when the population
jumps from a fitness peak to a better one during the process of adaptation.
This is done using the dynamics of the shell model which is a simplified
version of the quasispecies model for infinite populations and standard
Wright-Fisher dynamics for large finite populations. We show that the
population fraction of a genotype obtained within the quasispecies model and
the shell model match for fit genotypes and at short times, but the dynamics of
the two models are identical for questions related to the most populated
genotype. We calculate exactly several properties of the jumps in infinite
populations some of which were obtained numerically in previous works. We also
present our preliminary simulation results for finite populations. In
particular, we measure the jump distribution in time and find that it decays as
as in the quasispecies problem.Comment: Minor changes. To appear in Phys Rev
Excitation spectrum and effective mass of the even-fraction quantum Hall liquid
To probe the nature of the even-fraction quantum Hall system, we have
investigated the low-lying excitation spectrum by means of exact
diagonalization for finite systems. We have found (i) a striking one-to-one
correspondence (i.e., a shell structure) between the spectrum and those for
free (composite) fermions, (ii) a surprisingly straight scaling plot for the
excitation energy that gives a zero gap (metal) in the thermodynamic limit,
(iii) the effective mass evaluated from the scaling becoming heavier for
filling factor = 1/2, 1/4, 1/6, but (iv) some deviations from the single-mode
or the Hartree-Fock composite fermion approximation as well.Comment: 4 pages, REVTeX format, 4 eps-figure
Opioids Delay Healing of Spinal Fusion: A Rabbit Posterolateral Lumbar Fusion Model
Background Context Opioid use is prevalent in the management of pre- and postoperative pain in patients undergoing spinal fusion. There is evidence that opioids downregulate osteoblasts in vitro, and a previous study found that morphine delays the maturation and remodeling of callus in a rat femur fracture model. However, the effect of opioids on healing of spinal fusion has not been investigated before. Isolating the effect of opioid exposure in humans would be limited by the numerous confounding factors that affect fusion healing. Therefore, we have used a well-established rabbit model to study the process of spinal fusion healing that closely mimics humans. Purpose The objective of this work was to study the effect of systemic opioids on the process of healing of spinal fusion in a rabbit posterolateral spinal fusion model. Study Design/Setting This is a preclinical animal study. Materials and Methods Twenty-four adult New Zealand white rabbits were studied in two groups after approval from the Institutional Animal Care and Use Committee (IACUC). The opioid group (n=12) received 4 weeks\u27 preoperative and 6 weeks\u27 postoperative transdermal fentanyl. Serum fentanyl levels were measured just before surgery and 4 weeks postoperatively to ensure adequate levels. The control group (n=12) received only perioperative pain control as necessary. All animals underwent a bilateral L5âL6 posterolateral spinal fusion using iliac crest autograft. Animals were euthanized at the 6-week postoperative time point, and assessment of fusion was done by manual palpation, plain radiographs, microcomputed tomography (microCT), and histology. Results Twelve animals in the control group and 11 animals in the opioid group were available for analysis at the end of 6 weeks. The fusion scores on manual palpation, radiographs, and microCT were not statistically different. Three-dimensional microCT morphometry found that the fusion mass in the opioid group had a lower bone volume (p=.09), a lower trabecular number (p=.02), and a higher trabecular separation (p=.02) compared with the control group. Histologic analysis found areas of incorporation of autograft and unincorporated graft fragments in both groups. In the control group, there was remodeling of de novo woven bone to lamellar organization with incorporation of osteocytes, formation of mature marrow, and relative paucity of hypertrophied osteoblasts lining new bone. Sections from the opioid group showed formation of de novo woven bone, and hypertrophied osteoblasts were seen lining the new bone. There were no sections showing lamellar organization and development of mature marrow elements in the opioid group. Less dense trabeculae on microCT correlated with histologic findings of relatively immature fusion mass in the opioid group. Conclusions Systemic opioids led to an inferior quality fusion mass with delay in maturation and remodeling at 6 weeks in this rabbit spinal fusion model. These preliminary results lay the foundation for further research to investigate underlying cellular mechanisms, the temporal fusion process, and the dose-duration relationship of opioids responsible for our findings
Persistence in the Zero-Temperature Dynamics of the Diluted Ising Ferromagnet in Two Dimensions
The non-equilibrium dynamics of the strongly diluted random-bond Ising model
in two-dimensions (2d) is investigated numerically.
The persistence probability, P(t), of spins which do not flip by time t is
found to decay to a non-zero, dilution-dependent, value . We find
that decays exponentially to zero at large times.
Furthermore, the fraction of spins which never flip is a monotonically
increasing function over the range of bond-dilution considered. Our findings,
which are consistent with a recent result of Newman and Stein, suggest that
persistence in disordered and pure systems falls into different classes.
Furthermore, its behaviour would also appear to depend crucially on the
strength of the dilution present.Comment: some minor changes to the text, one additional referenc
Exact solution of a model of time-dependent evolutionary dynamics in a rugged fitness landscape
A simplified form of the time dependent evolutionary dynamics of a
quasispecies model with a rugged fitness landscape is solved via a mapping onto
a random flux model whose asymptotic behavior can be described in terms of a
random walk. The statistics of the number of changes of the dominant genotype
from a finite set of genotypes are exactly obtained confirming existing
conjectures based on numerics.Comment: 5 pages RevTex 2 figures .ep
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Complex macrocycle exploration: parallel, heuristic, and constraint-based conformer generation using ForceGen.
ForceGen is a template-free, non-stochastic approach for 2D to 3D structure generation and conformational elaboration for small molecules, including both non-macrocycles and macrocycles. For conformational search of non-macrocycles, ForceGen is both faster and more accurate than the best of all tested methods on a very large, independently curated benchmark of 2859 PDB ligands. In this study, the primary results are on macrocycles, including results for 431 unique examples from four separate benchmarks. These include complex peptide and peptide-like cases that can form networks of internal hydrogen bonds. By making use of new physical movements ("flips" of near-linear sub-cycles and explicit formation of hydrogen bonds), ForceGen exhibited statistically significantly better performance for overall RMS deviation from experimental coordinates than all other approaches. The algorithmic approach offers natural parallelization across multiple computing-cores. On a modest multi-core workstation, for all but the most complex macrocycles, median wall-clock times were generally under a minute in fast search mode and under 2 min using thorough search. On the most complex cases (roughly cyclic decapeptides and larger) explicit exploration of likely hydrogen bonding networks yielded marked improvements, but with calculation times increasing to several minutes and in some cases to roughly an hour for fast search. In complex cases, utilization of NMR data to constrain conformational search produces accurate conformational ensembles representative of solution state macrocycle behavior. On macrocycles of typical complexity (up to 21 rotatable macrocyclic and exocyclic bonds), design-focused macrocycle optimization can be practically supported by computational chemistry at interactive time-scales, with conformational ensemble accuracy equaling what is seen with non-macrocyclic ligands. For more complex macrocycles, inclusion of sparse biophysical data is a helpful adjunct to computation
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