Subcritical Superstrings

We introduce the Liouville mode into the Green-Schwarz superstring. Like massive supersymmetry without central charges, there is no kappa symmetry. However, the second-class constraints (and corresponding Wess-Zumino term) remain, and can be solved by (twisted) chiral superspace in dimensions D=4 and 6. The matter conformal anomaly is c = 4-D < 1. It thus can be canceled for physical dimensions by the usual Liouville methods, unlike the bosonic string (for which the consistency condition is c = D <= 1).Comment: 9 pg., compressed postscript file (.ps.Z), other formats (.dvi, .ps, .ps.Z, 8-bit .tex) available at http://insti.physics.sunysb.edu/~siegel/preprints/ or at ftp://max.physics.sunysb.edu/preprints/siege

Effectively Closed Infinite-Genus Surfaces and the String Coupling

The class of effectively closed infinite-genus surfaces, defining the completion of the domain of string perturbation theory, can be included in the category $O_G$, which is characterized by the vanishing capacity of the ideal boundary. The cardinality of the maximal set of endpoints is shown to be 2^{\mit N}. The product of the coefficient of the genus-g superstring amplitude in four dimensions by $2^g$ in the $g\to \infty$ limit is an exponential function of the genus with a base comparable in magnitude to the unified gauge coupling. The value of the string coupling is consistent with the characteristics of configurations which provide a dominant contribution to a finite vacuum amplitude.Comment: TeX, 33 page

Versatile liquid helium scintillation counter of large volume design

Design and performance of large liquid helium scintillation counter for meson experiment

On Supermultiplet Twisting and Spin-Statistics

Twisting of off-shell supermultiplets in models with 1+1-dimensional spacetime has been discovered in 1984, and was shown to be a generic feature of off-shell representations in worldline supersymmetry two decades later. It is shown herein that in all supersymmetric models with spacetime of four or more dimensions, this off-shell supermultiplet twisting, if non-trivial, necessarily maps regular (non-ghost) supermultiplets to ghost supermultiplets. This feature is shown to be ubiquitous in all fully off-shell supersymmetric models with (BV/BRST-treated) constraints.Comment: Extended version, including a new section on manifestly off-shell and supersymmetric BRST treatment of gauge symmetry; added reference

A new measurement of the lifetime of the positive pion

Digital timing method for measuring positive pion lifetim

Energy and width measurements of low-Z pionic X-ray transitions

High resolution spectrometric measurement of energy and natural line widths of 2p-1s pionic X ray transitions, as well as muonic transition energies in Li, Be, B, and C isotope

New massive supergravity multiplets

We present new off-shell formulations for the massive superspin-3/2 multiplet. In the massless limit, they reduce respectively to the old minimal (n=-1/3) and non-minimal ($n\neq -1/3, 0$) linearized formulations for 4D N=1 supergravity. Duality transformations, which relate the models constructed, are derived.Comment: 18 pages, LaTeX; v2: minor changes, references adde

Efficient and specific oligo-based depletion of rRNA

In most organisms, ribosomal RNA (rRNA) contributes to >85% of total RNA. Thus, to obtain useful information from RNA-sequencing (RNA-seq) analyses at reasonable sequencing depth, typically, mature polyadenylated transcripts are enriched or rRNA molecules are depleted. Targeted depletion of rRNA is particularly useful when studying transcripts lacking a poly(A) tail, such as some non-coding RNAs (ncRNAs), most bacterial RNAs and partially degraded or immature transcripts. While several commercially available kits allow effective rRNA depletion, their efficiency relies on a high degree of sequence homology between oligonucleotide probes and the target RNA. This restricts the use of such kits to a limited number of organisms with conserved rRNA sequences. In this study we describe the use of biotinylated oligos and streptavidin-coated paramagnetic beads for the efficient and specific depletion of trypanosomal rRNA. Our approach reduces the levels of the most abundant rRNA transcripts to less than 5% with minimal off-target effects. By adjusting the sequence of the oligonucleotide probes, our approach can be used to deplete rRNAs or other abundant transcripts independent of species. Thus, our protocol provides a useful alternative for rRNA removal where enrichment of polyadenylated transcripts is not an option and commercial kits for rRNA are not available