Using Subsystem MT2 for Complete Mass Determinations in Decay Chains with Missing Energy at Hadron Colliders

We propose to use the MT2 concept to measure the masses of all particles in SUSY-like events with two unobservable, identical particles. To this end we generalize the usual notion of MT2 and define a new MT2(n,p,c) variable, which can be applied to various subsystem topologies, as well as the full event topology. We derive analytic formulas for its endpoint MT2{max}(n,p,c) as a function of the unknown test mass Mc of the final particle in the subchain and the transverse momentum pT due to radiation from the initial state. We show that the endpoint functions MT2{max}(n,p,c)(Mc,pT) may exhibit three different types of kinks and discuss the origin of each type. We prove that the subsystem MT2(n,p,c) variables by themselves already yield a sufficient number of measurements for a complete determination of the mass spectrum (including the overall mass scale). As an illustration, we consider the simple case of a decay chain with up to three heavy particles, X2 -> X1 -> X0, which is rather problematic for all other mass measurement methods. We propose three different MT2-based methods, each of which allows a complete determination of the masses of particles X0, X1 and X2. The first method only uses MT2(n,p,c) endpoint measurements at a single fixed value of the test mass Mc. In the second method the unknown mass spectrum is fitted to one or more endpoint functions MT2{max}(n,p,c)(Mc,pT) exhibiting a kink. The third method is hybrid, combining MT2 endpoints with measurements of kinematic edges in invariant mass distributions. As a practical application of our methods, we show that the dilepton W+W- and tt-bar samples at the Tevatron can be used for an independent determination of the masses of the top quark, the W boson and the neutrino, without any prior assumptions.Comment: 47 pages, 9 figures. revised version, published in JHEP. Major addition: a new appendix with the complete set of formulas for the MT2 endpoints as functions of the upstream transverse momentum pT and test mass M

Supersymmetric particle mass measurement with invariant mass correlations

The kinematic end-point technique for measuring the masses of supersymmetric particles in R-Parity conserving models at hadron colliders is re-examined with a focus on exploiting additional constraints arising from correlations in invariant mass observables. The use of such correlations is shown to potentially resolve the ambiguity in the interpretation of quark+lepton end-points and enable discrimination between sequential two-body and three-body lepton-producing decays. The use of these techniques is shown to improve the SUSY particle mass measurement precision for the SPS1a benchmark model by at least 20-30% compared to the conventional end-point technique.Comment: 29 pages, 23 .eps figures, JHEP3 style; v2 adds some references and small clarifications to text; v3 adds some more clarifications to the tex

On Measuring Split-SUSY Neutralino and Chargino Masses at the LHC

In Split-Supersymmetry models, where the only non-Standard Model states produceable at LHC-energies consist of a gluino plus neutralinos and charginos, it is conventionally accepted that only mass differences among these latter are measureable at the LHC. The present work shows that application of a simple `Kinematic Selection' technique allows full reconstruction of neutralino and chargino masses from one event, in principle. A Monte Carlo simulation demonstrates the feasibilty of using this technique at the LHC.Comment: 17 pages, 4 figures; EPJC versio

\sqrt{s}_min: a global inclusive variable for determining the mass scale of new physics in events with missing energy at hadron colliders

We propose a new global and fully inclusive variable \sqrt{s}_{min} for determining the mass scale of new particles in events with missing energy at hadron colliders. We define \sqrt{s}_{min} as the minimum center-of-mass parton level energy consistent with the measured values of the total calorimeter energy E and the total visible momentum \vec{P}. We prove that for an arbitrary event, \sqrt{s}_{min} is simply given by the formula \sqrt{s}_{min}=\sqrt{E^2-P_z^2}+\sqrt{\met^2+M_{inv}^2}, where M_{inv} is the total mass of all invisible particles produced in the event. We use t\bar{t} production and several supersymmetry examples to argue that the peak in the \sqrt{s}_{min} distribution is correlated with the mass threshold of the parent particles originally produced in the event. This conjecture allows a determination of the heavy superpartner mass scale (as a function of the LSP mass) in a completely general and model-independent way, and without the need for any exclusive event reconstruction. In our SUSY examples of several multijet plus missing energy signals, the accuracy of the mass measurement based on \sqrt{s}_{min} is typically at the percent level, and never worse than 10%. After including the effects of initial state radiation and multiple parton interactions, the precision gets worse, but for heavy SUSY mass spectra remains 10%.Comment: 33 pages, 36 figures, discussion on effect of ISR and MPI adde

Sparticle masses in deflected mirage mediation

We discuss the sparticle mass patterns that can be realized in deflected mirage mediation scenario of supersymmetry breaking, in which the moduli, anomaly, and gauge mediations all contribute to the MSSM soft parameters. Analytic expression of low energy soft parameters and also the sfermion mass sum rules are derived, which can be used to interpret the experimentally measured sparticle masses within the framework of the most general mixed moduli-gauge-anomaly mediation. Phenomenological aspects of some specific examples are also discussed.Comment: 43 pages, 17 figures, references adde

Myristoylated CIL-7 regulates ciliary extracellular vesicle biogenesis

The cilium both releases and binds to extracellular vesicles (EVs). EVs may be used by cells as a form of intercellular communication and mediate a broad range of physiological and pathological processes. The mammalian polycystins (PCs) localize to cilia, as well as to urinary EVs released from renal epithelial cells. PC ciliary trafficking defects may be an underlying cause of autosomal dominant polycystic kidney disease (PKD), and ciliary–EV interactions have been proposed to play a central role in the biology of PKD. In Caenorhabditis elegans and mammals, PC1 and PC2 act in the same genetic pathway, act in a sensory capacity, localize to cilia, and are contained in secreted EVs, suggesting ancient conservation. However, the relationship between cilia and EVs and the mechanisms generating PC-containing EVs remain an enigma. In a forward genetic screen for regulators of C. elegans PKD-2 ciliary localization, we identified CIL-7, a myristoylated protein that regulates EV biogenesis. Loss of CIL-7 results in male mating behavioral defects, excessive accumulation of EVs in the lumen of the cephalic sensory organ, and failure to release PKD-2::GFP-containing EVs to the environment. Fatty acylation, such as myristoylation and palmitoylation, targets proteins to cilia and flagella. The CIL-7 myristoylation motif is essential for CIL-7 function and for targeting CIL-7 to EVs. C. elegans is a powerful model with which to study ciliary EV biogenesis in vivo and identify cis-targeting motifs such as myristoylation that are necessary for EV–cargo association and function

Using kinematic boundary lines for particle mass measurements and disambiguation in SUSY-like events with missing energy

We revisit the method of kinematical endpoints for particle mass determination, applied to the popular SUSY decay chain squark -> neutralino -> slepton -> LSP. We analyze the uniqueness of the solutions for the mass spectrum in terms of the measured endpoints in the observable invariant mass distributions. We provide simple analytical inversion formulas for the masses in terms of the measured endpoints. We show that in a sizable portion of the SUSY mass parameter space the solutions always suffer from a two-fold ambiguity, due to the fact that the original relations between the masses and the endpoints are piecewise-defined functions. The ambiguity persists even in the ideal case of a perfect detector and infinite statistics. We delineate the corresponding dangerous regions of parameter space and identify the sets of "twin" mass spectra. In order to resolve the ambiguity, we propose a generalization of the endpoint method, from single-variable distributions to two-variable distributions. In particular, we study analytically the boundaries of the (m_{jl(lo)}, m_{jl(hi)}) and (m_{ll}, m_{jll}) distributions and prove that their shapes are in principle sufficient to resolve the ambiguity in the mass determination. We identify several additional independent measurements which can be obtained from the boundary lines of these bivariate distributions. The purely kinematical nature of our method makes it generally applicable to any model that exhibits a SUSY-like cascade decay.Comment: 47 pages, 19 figure

Central obesity as a precursor to the metabolic syndrome in the AusDiab study and Mauritius

Evidence from epidemiologic studies that central obesity precedes future metabolic change and does not occur concurrently with the appearance of the blood pressure, glucose, and lipid abnormalities that characterize the metabolic syndrome (MetS) has been lacking. Longitudinal surveys were conducted in Mauritius in 1987, 1992, and 1998, and in Australia in 2000 and 2005 (AusDiab). This analysis included men and women (aged 25 years) in three cohorts: AusDiab 2000&ndash;2005 (n = 5,039), Mauritius 1987&ndash;1992 (n = 2,849), and Mauritius 1987&ndash;1998 (n = 1,999). MetS components included waist circumference, systolic blood pressure, fasting and 2-h postload plasma glucose, high-density lipoprotein (HDL) cholesterol, triglycerides, and homeostasis model assessment of insulin sensitivity (HOMA-S) (representing insulin sensitivity). Linear regression was used to determine which baseline components predicted deterioration in other MetS components over 5 years in AusDiab and 5 and 11 years in Mauritius, adjusted for age, sex, and ethnic group. Baseline waist circumference predicted deterioration (P &lt; 0.01) in four of the other six MetS variables tested in AusDiab, five of six in Mauritius 1987&ndash;1992, and four of six in Mauritius 1987&ndash;1998. In contrast, an increase in waist circumference between baseline and follow-up was only predicted by insulin sensitivity (HOMA-S) at baseline, and only in one of the three cohorts. These results suggest that central obesity plays a central role in the development of the MetS and appears to precede the appearance of the other MetS components.<br /

Precise reconstruction of sparticle masses without ambiguities

We critically reexamine the standard applications of the method of kinematical endpoints for sparticle mass determination. We consider the typical decay chain in supersymmetry (SUSY) squark -> neutralino -> slepton -> LSP, which yields a jet j and two leptons ln and lf. The conventional approaches use the upper kinematical endpoints of the individual distributions m_{jll}, m_{jl(lo)} and m_{jl(hi)}, all three of which suffer from parameter space region ambiguities and may lead to multiple solutions for the SUSY mass spectrum. In contrast, we do not use m_{jll}, m_{jl(lo)} and m_{jl(hi)}, and instead propose a new set of (infinitely many) variables whose upper kinematic endpoints exhibit reduced sensitivity to the parameter space region. We then outline an alternative, much simplified procedure for obtaining the SUSY mass spectrum. In particular, we show that the four endpoints observed in the three distributions m^2_{ll}, m^2_{jln} U m^2_{jlf} and m^2_{jln}+m^2_{jlf} are sufficient to completely pin down the squark mass and the two neutralino masses, leaving only a discrete 2-fold ambiguity for the slepton mass. This remaining ambiguity can be easily resolved in a number of different ways: for example, by a single additional measurement of the kinematic endpoint of any one out of the many remaining 1-dimensional distributions at our disposal, or by exploring the correlations in the 2-dimensional distribution of m^2_{jln} U m^2_{jlf} versus m^2_{ll}. We illustrate our method with two examples: the LM1 and LM6 CMS study points. An additional advantage of our method is the expected improvement in the accuracy of the SUSY mass determination, due to the multitude and variety of available measurements.Comment: 37 pages, added a new figure in the Appendix, published versio

Phyllosticta citricarpa and sister species of global importance to Citrus.

Several Phyllosticta species are known as pathogens of Citrus spp., and are responsible for various disease symptoms including leaf and fruit spots. One of the most important species is P. citricarpa, which causes a foliar and fruit disease called citrus black spot. The Phyllosticta species occurring on citrus can most effectively be distinguished from P. citricarpa by means of multilocus DNA sequence data. Recent studies also demonstrated P. citricarpa to be heterothallic, and reported successful mating in the laboratory. Since the domestication of citrus, different clones of P. citricarpa have escaped Asia to other continents via trade routes, with obvious disease management consequences. This pathogen profile represents a comprehensive literature review of this pathogen and allied taxa associated with citrus, focusing on identification, distribution, genomics, epidemiology and disease management. This review also considers the knowledge emerging from seven genomes of Phyllosticta spp., demonstrating unknown aspects of these species, including their mating behaviour.TaxonomyPhyllosticta citricarpa (McAlpine) Aa, 1973. Kingdom Fungi, Phylum Ascomycota, Class Dothideomycetes, Order Botryosphaeriales, Family Phyllostictaceae, Genus Phyllosticta, Species citricarpa.Host rangeConfirmed on more than 12 Citrus species, Phyllosticta citricarpa has only been found on plant species in the Rutaceae.Disease symptomsP. citricarpa causes diverse symptoms such as hard spot, virulent spot, false melanose and freckle spot on fruit, and necrotic lesions on leaves and twigs.Useful websitesDOE Joint Genome Institute MycoCosm portals for the Phyllosticta capitalensis (https://genome.jgi.doe.gov/Phycap1), P. citriasiana (https://genome.jgi.doe.gov/Phycit1), P. citribraziliensis (https://genome.jgi.doe.gov/Phcit1), P. citrichinaensis (https://genome.jgi.doe.gov/Phcitr1), P. citricarpa (https://genome.jgi.doe.gov/Phycitr1, https://genome.jgi.doe.gov/Phycpc1), P. paracitricarpa (https://genome.jgi.doe.gov/Phy27169) genomes. All available Phyllosticta genomes on MycoCosm can be viewed at https://genome.jgi.doe.gov/Phyllosticta