The Impact of User Effects on the Performance of Dual Receive Antenna Diversity Systems in Flat Rayleigh Fading Channels

In this paper we study the impact of user effects on the performance of receive antenna diversity systems in flat Rayleigh fading channels. Three diversity combining techniques are compared: maximal ratio combining (MRC), equal gain combining (EGC), and selection combining (SC). User effects are considered in two scenarios: 1) body loss (the reduction of effective antenna gain due to user effects) on a single antenna, and 2) equal body loss on both antennas. The system performance is assessed in terms of mean SNR, link reliability, bit error rate of BPSK, diversity order and ergodic capacity. Our results show that body loss on a single antenna has limited (bounded) impact on system performance. In comparison, body loss on both antennas has unlimited (unbounded) impact and can severely degrade system performance. Our results also show that with increasing body loss on a single antenna the performance of EGC drops faster than that of MRC and SC. When body loss on a single antenna is larger than a certain level, EGC is not a “sub-optimal” method anymore and has worse performance than SC

The non-existence of stable Schottky forms

Let $A_g^S$ be the Satake compactification of the moduli space $A_g$ of principally polarized abelian $g$-folds and $M_g^S$ the closure of the image of the moduli space $M_g$ of genus $g$ curves in $A_g$ under the Jacobian morphism. Then $A_g^S$ lies in the boundary of $A_{g+m}^S$ for any $m$. We prove that $M_{g+m}^S$ and $A_g^S$ do not meet transversely in $A_{g+m}^S$, but rather that their intersection contains the $m$th order infinitesimal neighbourhood of $M_g^S$ in $A_g^S$. We deduce that there is no non-trivial stable Siegel modular form that vanishes on $M_g$ for every $g$. In particular, given two inequivalent positive even unimodular quadratic forms $P$ and $Q$, there is a curve whose period matrix distinguishes between the theta series of $P$ and $Q$.Comment: Corrected version, using Yamada's correct version of Fay's formula for the period matrix of a certain degenerating family of curves. To appear in Compositio Mathematic

Noiseless Quantum Circuits for the Peres Separability Criterion

In this Letter we give a method for constructing sets of simple circuits that can determine the spectrum of a partially transposed density matrix, without requiring either a tomographically complete POVM or the addition of noise to make the spectrum non-negative. These circuits depend only on the dimension of the Hilbert space and are otherwise independent of the state.Comment: 4 pages RevTeX, 7 figures encapsulated postscript. v5: title changed slightly, more-or-less equivalent to the published versio

Probing Hadronic Structure with The Decay Δ→Nl+l−\Delta\rightarrow Nl^+l^-

We compute the branching ratio for $\Delta\rightarrow Ne^+e^-$ and $\Delta\rightarrow N\mu^+\mu^-$ in chiral perturbation theory and find that both decays should be observable at CEBAF. With sufficiently low thresholds on the $e^+e^-$ invariant mass a branching ratio of $\sim 10^{-5}$ may be observed for $\Delta\rightarrow Ne^+e^-$. For the $\Delta\rightarrow N\mu^+\mu^-$ decay mode we predict a branching ratio of $3\times 10^{-7}$. The dependence of the M1 and E2 amplitudes on the momentum transfer will provide a useful test of chiral perturbation theory which predicts $\sim 20\%$ variation over the allowed kinematic range.Comment: 6 pages, 3 figures, UCSD/PTH 93-06, QUSTH-93-02, Duke-TH-93-4

Dynamic Patterns of Transcript Abundance of Transposable Element Families in Maize.

Transposable Elements (TEs) are mobile elements that contribute the majority of DNA sequences in the maize genome. Due to their repetitive nature, genomic studies of TEs are complicated by the difficulty of properly attributing multi-mapped short reads to specific genomic loci. Here, we utilize a method to attribute RNA-seq reads to TE families rather than particular loci in order to characterize transcript abundance for TE families in the maize genome. We applied this method to assess per-family expression of transposable elements in >800 published RNA-seq libraries representing a range of maize development, genotypes, and hybrids. While a relatively small proportion of TE families are transcribed, expression is highly dynamic with most families exhibiting tissue-specific expression. A large number of TE families were specifically detected in pollen and endosperm, consistent with reproductive dynamics that maintain silencing of TEs in the germ line. We find that B73 transcript abundance is a poor predictor of TE expression in other genotypes and that transcript levels can differ even for shared TEs. Finally, by assessing recombinant inbred line and hybrid transcriptomes, complex patterns of TE transcript abundance across genotypes emerged. Taken together, this study reveals a dynamic contribution of TEs to maize transcriptomes

A unified approach on Springer fibers in the hook, two-row and two-column cases

We consider the Springer fiber over a nilpotent endomorphism. Fix a Jordan basis and consider the standard torus relative to this. We deal with the problem to describe the flags fixed by the torus which belong to a given component of the Springer fiber. We solve the problem in the hook, two-row and two-column cases. We provide two main characterizations which are common to the three cases, and which involve dominance relations between Young diagrams and combinatorial algorithms. Then, for these three cases, we deduce topological properties of the components and their intersections.Comment: 42 page

Cohomology of the minimal nilpotent orbit

We compute the integral cohomology of the minimal non-trivial nilpotent orbit in a complex simple (or quasi-simple) Lie algebra. We find by a uniform approach that the middle cohomology group is isomorphic to the fundamental group of the sub-root system generated by the long simple roots. The modulo $\ell$ reduction of the Springer correspondent representation involves the sign representation exactly when $\ell$ divides the order of this cohomology group. The primes dividing the torsion of the rest of the cohomology are bad primes.Comment: 29 pages, v2 : Leray-Serre spectral sequence replaced by Gysin sequence only, corrected typo

On spherical twisted conjugacy classes

Let G be a simple algebraic group over an algebraically closed field of good odd characteristic, and let theta be an automorphism of G arising from an involution of its Dynkin diagram. We show that the spherical theta-twisted conjugacy classes are precisely those intersecting only Bruhat cells corresponding to twisted involutions in the Weyl group. We show how the analogue of this statement fails in the triality case. We generalize to good odd characteristic J-H. Lu's dimension formula for spherical twisted conjugacy classes.Comment: proof of Lemma 6.4 polished. The journal version is available at http://www.springerlink.com/content/k573l88256753640