Detection of variable frequency signals using a fast chirp transform

The detection of signals with varying frequency is important in many areas of physics and astrophysics. The current work was motivated by a desire to detect gravitational waves from the binary inspiral of neutron stars and black holes, a topic of significant interest for the new generation of interferometric gravitational wave detectors such as LIGO. However, this work has significant generality beyond gravitational wave signal detection. We define a Fast Chirp Transform (FCT) analogous to the Fast Fourier Transform (FFT). Use of the FCT provides a simple and powerful formalism for detection of signals with variable frequency just as Fourier transform techniques provide a formalism for the detection of signals of constant frequency. In particular, use of the FCT can alleviate the requirement of generating complicated families of filter functions typically required in the conventional matched filtering process. We briefly discuss the application of the FCT to several signal detection problems of current interest

Timing analysis of low-energy gamma ray emission from galactic compact objects using the Gamma Ray Observatory

The principal goal of our phase 1 investigation was the development of techniques and data analysis tools for pulsar searches and timing. After the launch of the Compton Observatory, we received from the Burst and Transient Source Experiment (BATSE) team one day of discriminator large area (DISCLA) data for use in the development and testing of data analysis techniques. Using this first day of data for testing and optimizing our timing tools we detected four x-ray binary pulsars, Vela X-1, Cen X-3, 4U 0115+63, and GX 301-2. Subsequently, we received four more days of data, allowing us to test our timing tools with data from a variety of days. In summary, using the tools we developed based on the first day of data that we received, we have detected 8 pulsars in 5 days of data, or roughly one quarter of the approximately 30 known x-ray binary pulsars. In addition to the pulsars listed above, we detected GX 1+4, 4U 1626-67, OAO 1657-415, and Her X-1. Many of the data analysis tools that we developed have been ported to MSFC and are being used for the analysis of BATSE data. This appendix describes some of the timing tools and presents preliminary pulse period and phase profile results

Lorentz Symmetry Breaking in N=2\mathcal{N} =2 Superspace

In this paper, we will study the deformation of a three dimensional theory with $\mathcal{N} =2$ supersymmetry. This theory will be deformed by the presence of a constant vector field. This deformation will break the Lorentz symmetry. So, we will analyse this theory using $\mathcal{N} =2$ aether superspace. The $\mathcal{N} =2$ aether superspace will be obtained from a deformation of the usual $\mathcal{N} =2$ superspace. This will be done by deforming the generators of the three dimensional $\mathcal{N} =2$ supersymmetry. After analysing this deformed superalgebra, we will derive an explicit expression for the superspace propagators in this deformed superspace. Finally, we will use these propagators for performing perturbative calculations.Comment: 9 pages, 0 figures, Accepted for publication in EP

XSIL: Extensible Scientific Interchange Language

We motivate and define the XSIL language as a flexible, hierarchical, extensible transport language for scientific data objects. The entire object may be represented in the file, or there may be metadata in the XSIL file, with a powerful, fault-tolerant linking mechanism to external data. The language is based on XML, and is designed not only for parsing and processing by machines, but also for presentation to humans through web browsers and web-database technology. There is a natural mapping between the elements of the XSIL language and the object model into which they are translated by the parser. As well as common objects (Parameter, Array, Time, Table), we have extended XSIL to include the IGWDFrame, used by gravitational-wave observatories

Research in cosmic and gamma ray astrophysics

Discussed here is research in cosmic ray and gamma ray astrophysics at the Space Radiation Laboratory (SRL) of the California Institute of Technology. The primary activities discussed involve the development of new instrumentation and techniques for future space flight. In many cases these instrumentation developments were tested in balloon flight instruments designed to conduct new investigations in cosmic ray and gamma ray astrophysics. The results of these investigations are briefly summarized. Specific topics include a quantitative investigation of the solar modulation of cosmic ray protons and helium nuclei, a study of cosmic ray positron and electron spectra in interplanetary and interstellar space, the solar modulation of cosmic rays, an investigation of techniques for the measurement and interpretation of cosmic ray isotopic abundances, and a balloon measurement of the isotopic composition of galactic cosmic ray boron, carbon, and nitrogen

Andersen-Tawil Syndrome

Andersen-Tawil syndrome (ATS) is a rare condition consisting of ventricular arrhythmias, periodic paralysis, and dysmorphic features. In 2001, mutations in KCNJ2, which encodes the α subunit of the potassium channel Kir2.1, were identified in patients with ATS. To date, KCNJ2 is the only gene implicated in ATS, accounting for approximately 60% of cases. ATS is a unique channelopathy, and represents the first link between cardiac and skeletal muscle excitability. The arrhythmias observed in ATS are distinctive; patients may be asymptomatic, or minimally symptomatic despite a high arrhythmia burden with frequent ventricular ectopy and bidirectional ventricular tachycardia. However, patients remain at risk for life-threatening arrhythmias, including torsades de pointes and ventricular fibrillation, albeit less commonly than observed in other genetic arrhythmia syndromes. The characteristic heterogeneity at both the genotypic and phenotypic levels contribute to the continued difficulties with appropriate diagnosis, risk stratification, and effective therapy. The initial recognition of a syndromic association of clinically diverse symptoms, and the subsequent identification of the underlying molecular genetic basis of ATS has enhanced both clinical care, and our understanding of the critical function of Kir2.1 on skeletal muscle excitability and cardiac action potentia