Equilibria in Sequential Allocation

Sequential allocation is a simple mechanism for sharing multiple indivisible items. We study strategic behavior in sequential allocation. In particular, we consider Nash dynamics, as well as the computation and Pareto optimality of pure equilibria, and Stackelberg strategies. We first demonstrate that, even for two agents, better responses can cycle. We then present a linear-time algorithm that returns a profile (which we call the "bluff profile") that is in pure Nash equilibrium. Interestingly, the outcome of the bluff profile is the same as that of the truthful profile and the profile is in pure Nash equilibrium for \emph{all} cardinal utilities consistent with the ordinal preferences. We show that the outcome of the bluff profile is Pareto optimal with respect to pairwise comparisons. In contrast, we show that an assignment may not be Pareto optimal with respect to pairwise comparisons even if it is a result of a preference profile that is in pure Nash equilibrium for all utilities consistent with ordinal preferences. Finally, we present a dynamic program to compute an optimal Stackelberg strategy for two agents, where the second agent has a constant number of distinct values for the items

Relationship between membrane phosphatidylinositol-4,5-bisphosphate and receptor-mediated inhibition of native neuronal M channels

The relationship between receptor-induced membrane phosphatidylinositol-4'5'-bisphosphate (PIP2) hydrolysis and M-current inhibition was assessed in single-dissociated rat sympathetic neurons by simultaneous or parallel recording of membrane current and membrane-to-cytosol translocation of the fluorescent PIP2/inositol 1,4,5-trisphosphate (IP3)-binding peptide green fluorescent protein-tagged pleckstrin homology domain of phospholipase C (GFP-PLC delta-PH). The muscarinic receptor agonist oxotremorine-M produced parallel time- and concentration-dependent M-current inhibition and GFP-PLC delta-PH translocation; bradykinin also produced parallel time- dependent inhibition and translocation. Phosphatidylinositol-4-phosphate-5-kinase (PI5-K) overexpression reduced both M-current inhibition and GFP-PLC delta-PH translocation by both oxotremorine-M and bradykinin. These effects were partly reversed by wortmannin, which inhibits phosphatidylinositol-4-kinase (PI4-K). PI5-K overexpression also reduced the inhibitory action of oxotremorine-M on PIP2-gated G-protein-gated inward rectifier (Kir3.1/3.2) channels; bradykinin did not inhibit these channels. Overexpression of neuronal calcium sensor-1 protein (NCS-1), which increases PI4-K activity, did not affect responses to oxotremorine-M but reduced both fluorescence translocation and M-current inhibition by bradykinin. Using an intracellular IP3 membrane fluorescence-displacement assay, initial mean concentrations of membrane [PIP2] were estimated at 261 mu M (95% confidence limit; 192-381 mu M), rising to 693 mu M (417-1153 mu M) in neurons overexpressing PI5-K. Changes in membrane [PIP2] during application of oxotremorine-M were calculated from fluorescence data. The results, taken in conjunction with previous data for KCNQ2/3 (Kv7.2/Kv7.3) channel gating by PIP2 (Zhang et al., 2003), accorded with the hypothesis that the inhibitory action of oxotremorine-M on M current resulted from depletion of PIP2. The effects of bradykinin require additional components of action, which might involve IP3-induced Ca2+ release and consequent M-channel inhibition (as proposed previously) and stimulation of PIP2 synthesis by Ca2+-dependent activation of NCS-1

KCNQ/M currents in sensory neurons: Significance for pain therapy

Neuronal hyperexcitability is a feature of epilepsy and both inflammatory and neuropathic pain. M currents [I-K(M)] play a key role in regulating neuronal excitability, and mutations in neuronal KCNQ2/3 subunits, the molecular correlates of I-K(M), have previously been linked to benign familial neonatal epilepsy. Here, we demonstrate that KCNQ/M channels are also present in nociceptive sensory systems. I-K(M) was identified, on the basis of biophysical and pharmacological properties, in cultured neurons isolated from dorsal root ganglia (DRGs) from 17-d-old rats. Currents were inhibited by the M-channel blockers linopirdine (IC50, 2.1 muM) and XE991 (IC50, 0.26 muM) and enhanced by retigabine (10 muM). The expression of neuronal KCNQ subunits in DRG neurons was confirmed using reverse transcription-PCR and single-cell PCR analysis and by immunofluorescence. Retigabine, applied to the dorsal spinal cord, inhibited C and Adelta fiber-mediated responses of dorsal horn neurons evoked by natural or electrical afferent stimulation and the progressive "windup" discharge with repetitive stimulation in normal rats and in rats subjected to spinal nerve ligation. Retigabine also inhibited responses to intrapaw application of carrageenan in a rat model of chronic pain; this was reversed by XE991. It is suggested that I-K(M) plays a key role in controlling the excitability of nociceptors and may represent a novel analgesic target

A descriptive ecology of the vegetation in the lower Gordon River basin, Tasmania

The vegetation of the Lower Gordon Ri vel' Basin consists of rainforest, sclerophyll forest, scrub and sedgeland-heath, each of which is composed of a number of plant communities forming an intricate mosaic. Field studies conducted over three summer seasons suggest that differential fire regimes are the primary determinants of the composition, structure and distribution of the major vegetation types. Climatic, topographic and edaphic factors play a relatively minor role except through their interaction with the fire regime. The observed patterns and processes in the major vegetation types can be interpreted readily in terms of vegetation succession and ecological drift, but the ubiquity of diffuse ecotones argues against the occurrence of stable fire cycles

Expanding The Living Architecture In Australia

This final report sets out the findings of the business case analysis of whether a voluntary or mandatory approach to green roofs and walls would work best in Australia It uses Sydney and Melbourne as examples to model data

Tissue resolved, gene structure refined equine transcriptome.

BackgroundTranscriptome interpretation relies on a good-quality reference transcriptome for accurate quantification of gene expression as well as functional analysis of genetic variants. The current annotation of the horse genome lacks the specificity and sensitivity necessary to assess gene expression especially at the isoform level, and suffers from insufficient annotation of untranslated regions (UTR) usage. We built an annotation pipeline for horse and used it to integrate 1.9 billion reads from multiple RNA-seq data sets into a new refined transcriptome.ResultsThis equine transcriptome integrates eight different tissues from 59 individuals and improves gene structure and isoform resolution, while providing considerable tissue-specific information. We utilized four levels of transcript filtration in our pipeline, aimed at producing several transcriptome versions that are suitable for different downstream analyses. Our most refined transcriptome includes 36,876 genes and 76,125 isoforms, with 6474 candidate transcriptional loci novel to the equine transcriptome.ConclusionsWe have employed a variety of descriptive statistics and figures that demonstrate the quality and content of the transcriptome. The equine transcriptomes that are provided by this pipeline show the best tissue-specific resolution of any equine transcriptome to date and are flexible for several downstream analyses. We encourage the integration of further equine transcriptomes with our annotation pipeline to continue and improve the equine transcriptome

Molecular footprints of the Holocene retreat of dwarf birch in Britain

© 2014 The Authors. Molecular Ecology Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited

The Structure of Turbulence and mixed-phase Cloud Microphysics in a Highly Supercooled Altocumulus Cloud

Observations of vertically resolved turbulence and cloud microphysics in a mixed-phase altocumulus cloud are presented using in situ measurements from an instrumented aircraft. The turbulence spectrum is observed to have an increasingly negative skewness with distance below cloud top, confirming that longwave radiative cooling from the liquid layer cloud is the source of turbulence kinetic energy. Turbulence data are presented from both the liquid cloud layer and ice virga below. Vertical profiles of both bulk and microphysical liquid and ice cloud properties indicate that ice is produced within the liquid cloud layer at a temperature of -30° C. These high resolution in situ measurements support previous remotely-sensed observations from both ground based and space borne instruments, and could be used to evaluate numerical model simulations of altocumulus clouds at all scales from eddy resolving to climate