On right conjugacy closed loops of twice prime order

The right conjugacy closed loops of order 2p, where p is an odd prime, are classified up to isomorphism.Comment: Clarified definitions, added some remarks and a tabl

WILLINGNESS TO PAY FOR LOCAL COHO SALMON ENHANCEMENT IN COASTAL COMMUNITIES

Salmon restoration and enhancement are dominant environmental policy issues in Oregon and Washington. In response to salmon species listings under the Endangered Species Act, salmon protection and recovery actions are being implemented throughout the Pacific Northwest at substantial opportunity costs. In this paper, we examine the willingness to pay (WTP) of coastal residents for local coho salmon enhancement programs. A contingent valuation study is completed using survey responses from five rural, coastal communities of Oregon and Washington, where coho salmon are prevalent. Our empirical results indicate that coastal residents are willing to pay for local coho salmon enhancement and that WTP varies considerably with individual opinions of the merit of the enhancement program.Resource /Energy Economics and Policy,

Dynamics of fingering convection II: The formation of thermohaline staircases

Regions of the ocean's thermocline unstable to salt fingering are often observed to host thermohaline staircases, stacks of deep well-mixed convective layers separated by thin stably-stratified interfaces. Decades after their discovery, however, their origin remains controversial. In this paper we use 3D direct numerical simulations to shed light on the problem. We study the evolution of an analogous double-diffusive system, starting from an initial statistically homogeneous fingering state and find that it spontaneously transforms into a layered state. By analysing our results in the light of the mean-field theory developed in Paper I, a clear picture of the sequence of events resulting in the staircase formation emerges. A collective instability of homogeneous fingering convection first excites a field of gravity waves, with a well-defined vertical wavelength. However, the waves saturate early through regular but localized breaking events, and are not directly responsible for the formation of the staircase. Meanwhile, slower-growing, horizontally invariant but vertically quasi-periodic gamma-modes are also excited and grow according to the gamma-instability mechanism. Our results suggest that the nonlinear interaction between these various mean-field modes of instability leads to the selection of one particular gamma-mode as the staircase progenitor. Upon reaching a critical amplitude, this progenitor overturns into a fully-formed staircase. We conclude by extending the results of our simulations to real oceanic parameter values, and find that the progenitor gamma-mode is expected to grow on a timescale of a few hours, and leads to the formation of a thermohaline staircase in about one day with an initial spacing of the order of one to two metres.Comment: 18 pages, 9 figures, associated mpeg file at http://earth.uni-muenster.de/~stellma/movie_small.mp4, submitted to JF

A 16-channel Digital TDC Chip with internal buffering and selective readout for the DIRC Cherenkov counter of the BABAR experiment

A 16-channel digital TDC chip has been built for the DIRC Cherenkov counter of the BaBar experiment at the SLAC B-factory (Stanford, USA). The binning is 0.5 ns, the conversion time 32 ns and the full-scale 32 mus. The data driven architecture integrates channel buffering and selective readout of data falling within a programmable time window. The time measuring scale is constantly locked to the phase of the (external) clock. The linearity is better than 80 ps rms. The dead time loss is less than 0.1% for incoherent random input at a rate of 100 khz on each channel. At such a rate the power dissipation is less than 100 mw. The die size is 36 mm2.Comment: Latex, 18 pages, 13 figures (14 .eps files), submitted to NIM

Simple classical groups of Lie type are determined by their character degrees

In this paper, we will show that nonabelian simple classical groups of Lie type are uniquely determined by the structure of their complex group algebras.Comment: 10 pages, to appear in Journal of Algebr

Symmetric groups are determined by their character degrees

Let $G$ be a finite group. Let $X_1(G)$ be the first column of the ordinary character table of $G.$ In this paper, we will show that if $X_1(G)=X_1(S_n),$ then $G\cong S_n.$ As a consequence, we show that $S_n$ is uniquely determined by the structure of the complex group algebra \C S_n.Comment: 12 pages, to appear in Journal of Algebr

Identification of multiple genomic DNA sequences which form i-motif structures at neutral pH

i-Motifs are alternative DNA secondary structures formed in cytosine-rich sequences. Particular examples of these structures, traditionally assumed to be stable only at acidic pH, have been found to form under near-physiological conditions. To determine the potential impact of these structures on physiological processes, investigation of sequences with the capacity to fold under physiological conditions is required. Here we describe a systematic study of cytosine-rich DNA sequences, with varying numbers of consecutive cytosines, to gain insights into i-motif DNA sequence and structure stability. i-Motif formation was assessed using ultraviolet spectroscopy, circular dichroism and native gel electrophoresis. We found that increasing cytosine tract lengths resulted in increased thermal stability; sequences with at least five cytosines per tract folded into i-motif at room temperature and neutral pH. Using these results, we postulated a folding rule for i-motif formation, analogous to (but different from) that for G-quadruplexes. This indicated that thousands of cytosine-rich sequences in the human genome may fold into i-motif structures under physiological conditions. Many of these were found in locations where structure formation is likely to influence gene expression. Characterization of a selection of these identified i-motif forming sequences uncovered 17 genomic i-motif forming sequence examples which were stable at neutral pH

Identification of multiple genomic DNA sequences which form i-motif structures at neutral pH

i-Motifs are alternative DNA secondary structures formed in cytosine-rich sequences. Particular examples of these structures, traditionally assumed to be stable only at acidic pH, have been found to form under near-physiological conditions. To determine the potential impact of these structures on physiological processes, investigation of sequences with the capacity to fold under physiological conditions is required. Here we describe a systematic study of cytosine-rich DNA sequences, with varying numbers of consecutive cytosines, to gain insights into i-motif DNA sequence and structure stability. i-Motif formation was assessed using ultraviolet spectroscopy, circular dichroism and native gel electrophoresis. We found that increasing cytosine tract lengths resulted in increased thermal stability; sequences with at least five cytosines per tract folded into i-motif at room temperature and neutral pH. Using these results, we postulated a folding rule for i-motif formation, analogous to (but different from) that for G-quadruplexes. This indicated that thousands of cytosine-rich sequences in the human genome may fold into i-motif structures under physiological conditions. Many of these were found in locations where structure formation is likely to influence gene expression. Characterization of a selection of these identified i-motif forming sequences uncovered 17 genomic i-motif forming sequence examples which were stable at neutral pH

The Simple Ree groups 2F4(q2){}^2F_4(q^2) are determined by the set of their character degrees

Let $G$ be a finite group. Let ${\rm{cd}}(G)$ be the set of all complex irreducible character degrees of $G.$ In this paper, we will show that if ${\rm{cd}}(G)={\rm{cd}}(H),$ where $H$ is the simple Ree group ${}^2F_4(q^2),q^2\geq 8,$ then $G\cong H\times A,$ where $A$ is an abelian group. This verifies Huppert's Conjecture for the simple Ree groups ${}^2F_4(q^2)$ when $q^2\geq 8.$Comment: 14 pages, to appear in Journal of Algebr