15,093 research outputs found

    Quantum phase transition in a three-level atom-molecule system

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    We adopt a three-level bosonic model to investigate the quantum phase transition in an ultracold atom-molecule conversion system which includes one atomic mode and two molecular modes. Through thoroughly exploring the properties of energy level structure, fidelity, and adiabatical geometric phase, we confirm that the system exists a second-order phase transition from an atommolecule mixture phase to a pure molecule phase. We give the explicit expression of the critical point and obtain two scaling laws to characterize this transition. In particular we find that both the critical exponents and the behaviors of ground-state geometric phase change obviously in contrast to a similar two-level model. Our analytical calculations show that the ground-state geometric phase jumps from zero to ?pi/3 at the critical point. This discontinuous behavior has been checked by numerical simulations and it can be used to identify the phase transition in the system.Comment: 8 pages,8 figure

    Bs0βˆ’BΛ‰s0B_s^0-\bar{B}_s^0 mixing within minimal flavor-violating two-Higgs-doublet models

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    In the "Higgs basis" for a generic 2HDM, only one scalar doublet gets a nonzero vacuum expectation value and, under the criterion of minimal flavor violation, the other one is fixed to be either color-singlet or color-octet, which are named as the type-III and type-C models, respectively. In this paper, the charged-Higgs effects of these two models on Bs0βˆ’BΛ‰s0B_s^0-\bar{B}_s^0 mixing are studied. Firstly, we perform a complete one-loop computation of the electro-weak corrections to the amplitudes of Bs0βˆ’BΛ‰s0B_s^0-\bar{B}_s^0 mixing. Together with the up-to-date experimental measurements, a detailed phenomenological analysis is then performed in the cases of both real and complex Yukawa couplings of charged scalars to quarks. The spaces of model parameters allowed by the current experimental data on Bs0βˆ’BΛ‰s0B_s^0-\bar{B}_s^0 mixing are obtained and the differences between type-III and type-C models are investigated, which is helpful to distinguish between these two models.Comment: 19 pages, 3 figures, 2 tables; More references and discussions added, final version published in the journa

    RAG-1 Mutations Associated with B-Cell-Negative SCID Dissociate the Nicking and Transesterification Steps of V(D)J Recombination

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    Some patients with B-cell-negative severe combined immune deficiency (SCID) carry mutations in RAG-1 or RAG-2 that impair V(D)J recombination. Two recessive RAG-1 mutations responsible for B-cell-negative SCID, R621H and E719K, impair V(D)J recombination without affecting formation of single-site recombination signal sequence complexes, specific DNA contacts, or perturbation of DNA structure at the heptamer-coding junction. The E719K mutation impairs DNA cleavage by the RAG complex, with a greater effect on nicking than on transesterification; a conservative glutamine substitution exhibits a similar effect. When cysteine is substituted for E719, RAG-1 activity is enhanced in Mn2+ but remains impaired in Mg2+, suggesting an interaction between this residue and an essential metal ion. The R621H mutation partially impairs nicking, with little effect on transesterification. The residual nicking activity of the R621H mutant is reduced at least 10-fold upon a change from pH 7.0 to pH 8.4. Site-specific nicking is severely impaired by an alanine substitution at R621 but is spared by substitution with lysine. These observations are consistent with involvement of a positively charged residue at position 621 in the nicking step of the RAG-mediated cleavage reaction. Our data provide a mechanistic explanation for one form of hereditary SCID. Moreover, while RAG-1 is directly involved in catalysis of both nicking and transesterification, our observations indicate that these two steps have distinct catalytic requirements

    The Formation Stability of a Multi-Robotic Formation Control System

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    Detecting Female Students Transforming Entrepreneurial Competency, Mindset, and Intention into Sustainable Entrepreneurship

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    Entrepreneurship has been viewed as an opportunity for economic development and changing economic scenario in global markets. Women are viewed as a reservoir of entrepreneurial talents, so they can be growth engines in novel markets. Previous studies have considered entrepreneurship as the most effective way towards the economic empowerment of women. Female students engaged in entrepreneurial education have been addressed persistently, while what transforms them in an education process is still unclear. Considering the transforming global economy and its influence on higher education, this study aims to detect female students transforming entrepreneurial competency, mindset, and intention into sustainable entrepreneurship. Using a self-compiled survey, we targeted 752 female students to investigate their entrepreneurial competency, mindset, and intention. SPSS and AMOS were used to transform the data for interpretation. We assumed that the impact of female student’s entrepreneurial competency could be modified by an entrepreneurial mindset and result in entrepreneurial intention. To detect this causal relationship, this study employed reliability, factor, structural equation modeling (SEM), and bootstrapping analyses to verify the evidence. The result of the SEM confirms that the female students’ entrepreneurial competency will, through their entrepreneurial mindset, impact entrepreneurial intention. With bootstrapping, 5000 samples were collected, and it was demonstrated that the measure constructs were still reliable in the model. This study found that there is a mediation effect between entrepreneurial competency and entrepreneurial intention. The entrepreneurial mindset plays a crucial role in the transformation process. Without an entrepreneurial mindset, entrepreneurial competency cannot exert a significant effect on entrepreneurial intention. The findings can help reinvent related entrepreneurial education in higher education
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