530 research outputs found
Phenomenological Scaling of Rapidity Dependence for Anisotropic Flows in 25 MeV/nucleon Ca + Ca by Quantum Molecular Dynamics Model
Anisotropic flows (, , and ) of light fragments up till
the mass number 4 as a function of rapidity have been studied for 25
MeV/nucleon Ca + Ca at large impact parameters by Quantum
Molecular Dynamics model. A phenomenological scaling behavior of rapidity
dependent flow parameters (n = 1, 2, 3 and 4) has been found as a
function of mass number plus a constant term, which may arise from the
interplay of collective and random motions. In addition, keeps
almost independent of rapidity and remains a rough constant of 1/2 for all
light fragments.Comment: 4 pages, 5 figure
Strong quantum fluctuation of vortices in the new superconductor
By using transport and magnetic measurement, the upper critical field
and the irreversibility line has been determined. A
big separation between and has been found showing the
existence of a quantum vortex liquid state induced by quantum fluctuation of
vortices in the new superconductor . Further investigation on the
magnetic relaxation shows that both the quantum tunneling and the thermally
activated flux creep weakly depends on temperature. But when the melting field
is approached, a drastic rising of the relaxation rate is observed.
This may imply that the melting of the vortex matter at a finite temperature is
also induced by the quantum fluctuation of vortices.Comment: 4 pages, 4 figure
Edge states and topological orders in the spin liquid phases of star lattice
A group of novel materials can be mapped to the star lattice, which exhibits
some novel physical properties. We give the bulk-edge correspondence theory of
the star lattice and study the edge states and their topological orders in
different spin liquid phases. The bulk and edge-state energy structures and
Chern number depend on the spin liquid phases and hopping parameters because
the local spontaneous magnetic flux in the spin liquid phase breaks the time
reversal and space inversion symmetries. We give the characteristics of bulk
and edge energy structures and their corresponding Chern numbers in the
uniform, nematic and chiral spin liquids. In particular, we obtain analytically
the phase diagram of the topological orders for the chiral spin liquid states
SL[\phi,\phi,-2\phi], where \phi is the magnetic flux in two triangles and a
dodecagon in the unit cell. Moreover, we find the topological invariance for
the spin liquid phases, SL[\phi_{1},\phi_{2},-(\phi_{1}+\phi_{2})] and
SL[\phi_{2},\phi_{1},-(\phi_{1}+\phi_{2})]. The results reveal the relationship
between the energy-band and edge-state structures and their topological orders
of the star lattice.Comment: 7 pages, 8 figures, 1 tabl
Charmed hadron chemistry in relativistic heavy-ion collisions
We develop for charmed hadron production in relativistic heavy-ion collisions
a comprehensive coalescence model that includes an extensive set of and
-wave hadronic states as well as the strict energy-momentum conservation,
which ensures the boost invariance of the coalescence probability and the
thermal limit of the produced hadron spectrum. By combining our hadronization
scheme with an advanced Langevin-hydrodynamics model that incorporates both
elastic and inelastic energy loss of heavy quarks inside the dynamical
quark-gluon plasma, we obtain a successful description of the
-integrated and differential and ratios
measured at RHIC and the LHC. We find that including the effect of radial flow
of the medium is essential for describing the enhanced ratio
observed in relativistic heavy-ion collisions. We also find that the puzzling
larger ratio observed in Au+Au collisions at RHIC than in Pb+Pb
collisions at the LHC is due to the interplay between the effects of the QGP
radial flow and the charm quark transverse momentum spectrum at hadronization.
Our study further suggests that charmed hadrons have larger sizes in medium
than in vacuum.Comment: 6 pages, 5 figure
A Novel p.Leu(381)Phe Mutation in Presenilin 1 is Associated with Very Early Onset and Unusually Fast Progressing Dementia as well as Lysosomal Inclusions Typically Seen in Kufs Disease
Whole exome sequencing in a family with suspected dominant Kufs disease identified a novel Presenilin 1 mutation p.Leu(381)Phe in three brothers who, along with their father, developed progressive dementia and motor deficits in their early 30s. All affected relatives had unusually rapid disease progression (on average 3.6 years from disease onset to death). In silico analysis of mutation p.Leu(381)Phe predicted more detrimental effects when compared to the common Presenilin 1 mutation p.Glu(280)Ala. Electron microscopy study of peripheral fibroblast cells of the proband showed lysosomal inclusions typical for Kufs disease. However his brain autopsy demonstrated typical changes of Alzheimer disease
A Nonaqueous Approach to the Preparation of Iron Phosphide Nanowires
Previous preparation of iron phosphide nanowires usually employed toxic and unstable iron carbonyl compounds as precursor. In this study, we demonstrate that iron phosphide nanowires can be synthesized via a facile nonaqueous chemical route that utilizes a commonly available iron precursor, iron (III) acetylacetonate. In the synthesis, trioctylphosphine (TOP) and trioctylphosphine oxide (TOPO) have been used as surfactants, and oleylamine has been used as solvent. The crystalline structure and morphology of the as-synthesized products were characterized by powder X-ray diffraction (XRD) and transmission electron microscopy (TEM). The obtained iron phosphide nanowires have a typical width of ~16 nm and a length of several hundred nanometers. Structural and compositional characterization reveals a hexagonal Fe2P crystalline phase. The morphology of as-synthesized products is greatly influenced by the ratio of TOP/TOPO. The presence of TOPO has been found to be essential for the growth of high-quality iron phosphide nanowires. Magnetic measurements reveal ferromagnetic characteristics, and hysteresis behaviors below the blocking temperature have been observed
Three-dimensional conceptual model for service-oriented simulation
In this letter, we propose a novel three-dimensional conceptual model for an
emerging service-oriented simulation paradigm. The model can be used as a
guideline or an analytic means to find the potential and possible future
directions of the current simulation frameworks. In particular, the model
inspects the crossover between the disciplines of modeling and simulation,
service-orientation, and software/systems engineering. Finally, two specific
simulation frameworks are studied as examples.Comment: 7 pages, 1 figures, 3 table, Journal of Zhejiang University SCIENCE
A, 2009, 10(8): 1075-108
Mutations in the Gene DNAJC5 Cause Autosomal Dominant Kufs Disease in a Proportion of Cases: Study of the Parry Family and 8 Other Families
Background: The Neuronal Ceroid Lipofuscinoses (NCL) comprise at least nine progressive neurodegenerative genetic disorders. Kufs disease, an adult-onset form of NCL may be recessively or dominantly inherited. Our study aimed to identify genetic mutations associated with autosomal dominant Kufs disease (ADKD). Methodology and Principal Findings We have studied the family first reported with this phenotype in the 1970s, the Parry family. The proband had progressive psychiatric manifestations, seizures and cognitive decline starting in her mid 20s. Similarly affected relatives were observed in seven generations. Several of the affected individuals had post-mortem neuropathological brain study confirmatory for NCL disease. We conducted whole exome sequencing of three affected family members and identified a pLeu116del mutation in the gene DNAJC5, which segregated with the disease phenotype. An additional eight unrelated affected individuals with documented autosomal dominant or sporadic inheritance were studied. All had diagnostic confirmation with neuropathological studies of brain tissue. Among them we identified an additional individual with a p.Leu115Arg mutation in DNAJC5. In addition, a pAsn477Ser change in the neighboring gene PRPF6, a gene previously found to be associated with retinitis pigmentosa, segregated with the ADKD phenotype. Interestingly, two individuals of the Parry family did report visual impairment. Conclusions: Our study confirmed the recently reported association of DNAJC5 mutations with ADKD in two out of nine well-defined families. Sequence changes in PRPF6 have not been identified in other unrelated cases. The association of vision impairment with the expected PRPF6 dysfunction remains possible but would need further clinical studies in order to confirm the co-segregation of the visual impairment with this sequence change
Common Features in Electronic Structure of the Fe-Based Layered Superconductors from Photoemission Spectroscopy
High resolution photoemission measurements have been carried out on
non-superconducting LaOFeAs parent compound and various superconducting
R(O1-xFx)FeAs (R=La, Ce and Pr) compounds. We found that the parent LaOFeAs
compound shows a metallic character. Through extensive measurements, we have
identified several common features in the electronic structure of these
Fe-based compounds: (1). 0.2 eV feature in the valence band; (2). A universal
13~16 meV feature; (3). A clear Fermi cutoff showing zero leading-edge shift in
the superconducting state;(4). Lack of superconducting coherence peak(s); (5).
Near EF spectral weight suppression with decreasing temperature. These
universal features can provide important information about band structure,
superconducting gap and pseudogap in these Fe-based materials.Comment: 5 pages,4 figure
- …