245 research outputs found
On the Formation Age of the First Planetary System
Recently, it has been observed the extreme metal-poor stars in the Galactic
halo, which must be formed just after Pop III objects. On the other hand, the
first gas clouds of mass are supposed to be formed at 10, 20, and 30 for the , and , where the
density perturbations are assumed of the standard CDM cosmology. If we
could apply this gaussian distribution to the extreme small probability, the
gas clouds would be formed at 40, 60, and 80 for the ,
, and . The first gas clouds within our galaxy must be formed
around . Even if the gas cloud is metal poor, there is a lot of
possibility to form the planets around such stars. The first planetary systems
could be formed within years after the Big Bang in the
universe. Even in our galaxies, it could be formed within
years. It is interesting to wait the observations of planets around metal-poor
stars. For the panspermia theory, the origin of life could be expected in such
systems.Comment: 5 pages,Proceedings IAU Symposium No. 249, 2007, Exoplanets:Y-S. Sun,
S. Ferraz-Mello and J.-L, Zhou, eds. (p325
Comparative Visual Function in Predatory Fishes from the Indian River Lagoon
Visual temporal resolution and spectral sensitivity of three coastal teleost species (common snook [Centropomus undecimalis], gray snapper [Lutjanus griseus], and pinfish [Lagodon rhomboides]) were investigated by electroretinogram. Temporal resolution was quantified under photopic and scotopic conditions using response waveform dynamics and maximum critical flicker fusion frequency (CFFmax). Photopic CFFmax was significantly higher than scotopic CFFmax in all species. The snapper had the shortest photoreceptor response latency time (26.7 ms) and the highest CFFmax (47 Hz), suggesting that its eyes are adapted for a brighter photic environment. In contrast, the snook had the longest response latency time (36.8 ms) and lowest CFFmax (40 Hz), indicating that its eyes are adapted for a dimmer environment or nocturnal lifestyle. Species spectral responses ranged from 360 to 620 nm and revealed the presence of rods sensitive to dim and twilight conditions, as well as multiple cone visual pigments providing the basis for color and contrast discrimination. Collectively, our results demonstrate differences in visual function among species inhabiting the Indian River Lagoon system, representative of their unique ecology and life histories
A Physiological Analysis of Color Vision in Batoid Elasmobranchs
The potential for color vision in elasmobranchs has been studied in detail; however, a high degree of variation exists among the group. Evidence for ultraviolet (UV) vision is lacking, despite the presence of UV vision in every other vertebrate class. An integrative physiological approach was used to investigate color and ultraviolet vision in cownose rays and yellow stingrays, two batoids that inhabit different spectral environments. Both species had peaks in UV, short, medium, and long wavelength spectral regions in dark-, light-, and chromatic-adapted electroretinograms. Although no UV cones were found with microspectrophotometric analysis, both rays had multiple cone visual pigments with λmax at 470 and 551 nm in cownose rays (Rhinoptera bonasus) and 475, 533, and 562 nm in yellow stingrays (Urobatis jamaicensis). The same analysis demonstrated that both species had rod λmax at 500 and 499 nm, respectively. The lens and cornea of cownose rays maximally transmitted wavelengths greater than 350 nm and greater than 376 nm in yellow stingrays. These results support the potential for color vision in these species and future investigations should reveal the extent to which color discrimination is significant in a behavioral context
Fuzzy sphere bimodule, ABS construction to the exact soliton solutions
In this paper, we set up the bi-module of the algebra on fuzzy
sphere. Based on the differential operators in moving frame, we generalize the
ABS construction into fuzzy sphere case. The applications of ABS construction
are investigated in various physical systems.Comment: Latex file without figure, 13 page
On open-closed extension of boundary string field theory
We investigate a classical open-closed string field theory whose open string
sector is given by boundary string field theory. The open-closed interaction is
introduced by the overlap of a boundary state with a closed string field. With
the help of the Batalin-Vilkovisky formalism, the closed string sector is
determined to be the HIKKO closed string field theory. We also discuss the
gauge invariance of this theory in both open and closed string sides.Comment: 25 pages, 2 figures, comments and a reference added, typos correcte
Boundary states, matrix factorisations and correlation functions for the E-models
The open string spectra of the B-type D-branes of the N=2 E-models are
calculated. Using these results we match the boundary states to the matrix
factorisations of the corresponding Landau-Ginzburg models. The identification
allows us to calculate specific terms in the effective brane superpotential of
E_6 using conformal field theory methods, thereby enabling us to test results
recently obtained in this context.Comment: 20 pages, no figure
Solitons on Noncommutative Torus as Elliptic Calogero Gaudin Models, Branes and Laughlin Wave Functions
For the noncommutative torus , in case of the N.C. parameter
, we construct the basis of Hilbert space {\caH}_n\thetaz_in{\cal A}_nZ_n
\times Z_n\thetagsu(n)transform covariantly by the global gauge
transformation of By acting on we establish the
isomorphism of . We embed this into the -matrix of the
elliptic Gaudin andsu_n({\cal T})D(k, u)spectral curve
describes the brane configuration, with the dynamical
variables of N.C. solitons asT^{\otimes n} / S_nthe N.C. cotangent bundle with marked points. The
eigenfunction of the Gaudin differential -operators as the
Laughli$wavefunction is solved by Bethe ansatz.Comment: 25 pages, plain latex, no figure
Cohomology Groups of Deformations of Line Bundles on Complex Tori
The cohomology groups of line bundles over complex tori (or abelian
varieties) are classically studied invariants of these spaces. In this article,
we compute the cohomology groups of line bundles over various holomorphic,
non-commutative deformations of complex tori. Our analysis interpolates between
two extreme cases. The first case is a calculation of the space of
(cohomological) theta functions for line bundles over constant, commutative
deformations. The second case is a calculation of the cohomologies of
non-commutative deformations of degree-zero line bundles.Comment: 24 pages, exposition improved, typos fixe
Tachyon Condensation on Noncommutative Torus
We discuss noncommutative solitons on a noncommutative torus and their
application to tachyon condensation. In the large B limit, they can be exactly
described by the Powers-Rieffel projection operators known in the mathematical
literature. The resulting soliton spectrum is consistent with T-duality and is
surprisingly interesting. It is shown that an instability arises for any
D-branes, leading to the decay into many smaller D-branes. This phenomenon is
the consequence of the fact that K-homology for type II von Neumann factor is
labeled by R.Comment: LaTeX, 17 pages, 1 figur
Rigidity and defect actions in Landau-Ginzburg models
Studying two-dimensional field theories in the presence of defect lines
naturally gives rise to monoidal categories: their objects are the different
(topological) defect conditions, their morphisms are junction fields, and their
tensor product describes the fusion of defects. These categories should be
equipped with a duality operation corresponding to reversing the orientation of
the defect line, providing a rigid and pivotal structure. We make this
structure explicit in topological Landau-Ginzburg models with potential x^d,
where defects are described by matrix factorisations of x^d-y^d. The duality
allows to compute an action of defects on bulk fields, which we compare to the
corresponding N=2 conformal field theories. We find that the two actions differ
by phases.Comment: 53 pages; v2: clarified exposition of pivotal structures, corrected
proof of theorem 2.13, added remark 3.9; version to appear in CM
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