2,983 research outputs found
Rotons in interacting ultracold Bose gases
In three dimensions, non-interacting bosons undergo Bose-Einstein
condensation at a critical temperature, , which is slightly shifted by
, if the particles interact. We calculate the excitation
spectrum of interacting Bose-systems, \sup{4}He and \sup{87}Rb, and show that a
roton minimum emerges in the spectrum above a threshold value of the gas
parameter. We provide a general theoretical argument for why the roton minimum
and the maximal upward critical temperature shift are related. We also suggest
two experimental avenues to observe rotons in condensates. These results, based
upon a Path-Integral Monte-Carlo approach, provide a microscopic explanation of
the shift in the critical temperature and also show that a roton minimum does
emerge in the excitation spectrum of particles with a structureless,
short-range, two-body interaction.Comment: 5 pages, 6 figure
Is there a "native" band gap in ion conducting glasses?
It is suggested that the spectrum of ion site energies in glasses exhibits a
band gap, establishing an analogy between ion conducting glasses and intrinsic
semiconductors. This implies that ion conduction in glasses takes place via
vacancies and interstitial ions (as in crystals).Comment: 3 page
Integrated Power/Attitude Control System (IPACS) study. Volume 2: Conceptual designs
For abstract, see N74-22706
The effect of continuous interscalene nerve blockade on hospital length of stay following shoulder surgery
Continuous macroscopic limit of a discrete stochastic model for interaction of living cells
In the development of multiscale biological models it is crucial to establish
a connection between discrete microscopic or mesoscopic stochastic models and
macroscopic continuous descriptions based on cellular density. In this paper a
continuous limit of a two-dimensional Cellular Potts Model (CPM) with excluded
volume is derived, describing cells moving in a medium and reacting to each
other through both direct contact and long range chemotaxis. The continuous
macroscopic model is obtained as a Fokker-Planck equation describing evolution
of the cell probability density function. All coefficients of the general
macroscopic model are derived from parameters of the CPM and a very good
agreement is demonstrated between CPM Monte Carlo simulations and numerical
solution of the macroscopic model. It is also shown that in the absence of
contact cell-cell interactions, the obtained model reduces to the classical
macroscopic Keller-Segel model. General multiscale approach is demonstrated by
simulating spongy bone formation from loosely packed mesenchyme via the
intramembranous route suggesting that self-organizing physical mechanisms can
account for this developmental process.Comment: 4 pages, 3 figure
Computationally designed libraries of fluorescent proteins evaluated by preservation and diversity of function
To determine which of seven library design algorithms best introduces new protein function without destroying it altogether, seven combinatorial libraries of green fluorescent protein variants were designed and synthesized. Each was evaluated by distributions of emission intensity and color compiled from measurements made in vivo. Additional comparisons were made with a library constructed by error-prone PCR. Among the designed libraries, fluorescent function was preserved for the greatest fraction of samples in a library designed by using a structure-based computational method developed and described here. A trend was observed toward greater diversity of color in designed libraries that better preserved fluorescence. Contrary to trends observed among libraries constructed by error-prone PCR, preservation of function was observed to increase with a library's average mutation level among the four libraries designed with structure-based computational methods
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The martyrdom effect : when pain and effort increase prosocial contributions
Most theories of motivation and behavior (and lay intuitions alike) consider pain and effort to be deterrents. In contrast to this widely held view, we provide evidence that the prospect of enduring pain and exerting effort for a prosocial cause can promote contributions to the cause. Specifically, we show that willingness to contribute to a charitable or collective cause increases when the contribution process is expected to be painful and effortful rather than easy and enjoyable. Across five experiments, we document this “martyrdom effect,” show that the observed patterns defy standard economic and psychological accounts, and identify a mediator and moderator of the effect. Experiment 1 showed that people are willing to donate more to charity when they anticipate having to suffer to raise money. Experiment 2 extended these findings to a non-charity laboratory context that involved real money and actual pain. Experiment 3 demonstrated that the martyrdom effect is not the result of an attribute substitution strategy (whereby people use the amount of pain and effort involved in fundraising to determine donation worthiness). Experiment 4 showed that perceptions of meaningfulness partially mediate the martyrdom effect. Finally, Experiment 5 demonstrated that the nature of the prosocial cause moderates the martyrdom effect: the effect is strongest for causes associated with human suffering. We propose that anticipated pain and effort lead people to ascribe greater meaning to their contributions and to the experience of contributing, thereby motivating higher prosocial contributions. We conclude by considering some implications of this puzzling phenomenon. Copyright © 2011 John Wiley & Sons, Ltd
Fermi Surface as the Driving Mechanism for Helical Antiferromagnetic Ordering in Gd-Y Alloys
The first direct experimental evidence for the Fermi surface (FS) driving the
helical antiferromagnetic ordering in a gadolinium-yttrium alloy is reported.
The presence of a FS sheet capable of nesting is revealed, and the nesting
vector associated with the sheet is found to be in excellent agreement with the
periodicity of the helical ordering.Comment: 4 pages, 4 figure
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