Search for the Hypothetical pi -> mu x Decay

The KARMEN collaboration has reported the possible observation of a hitherto unknown neutral and weakly interacting particle x, which is produced in the decay pi -> mu + x with a mass m(x) = 33.9 MeV. We have searched for this hypothetical decay branch by studying muons from pion decay in flight with the LEPS spectrometer at the piE3 channel at PSI and find branching ratios BR(pi- to mu- anti-x) < 4e-7 and BR(pi+ to mu+ x) < 7e-8 (95\% C.L.). Together with the limit BR > 2e-8 derived in a recent theoretical paper our result would leave only a narrow region for the existence of x if it is a heavy neutrino.Comment: 10 pages, TeX (uses epsf), 3 Postscript figures uu-encode

Macrophage Migration Inhibitory Factor Is Enhanced in Acute Coronary Syndromes and Is Associated with the Inflammatory Response

Chronic inflammation promotes atherosclerosis in cardiovascular disease and is a major prognostic factor for patients undergoing percutaneous coronary intervention (PCI). Macrophage migration inhibitory factor (MIF) is involved in the progress of atherosclerosis and plaque destabilization and plays a pivotal role in the development of acute coronary syndromes (ACS). Little is known to date about the clinical impact of MIF in patients with symptomatic coronary artery disease (CAD).In a pilot study, 286 patients with symptomatic CAD (n = 119 ACS, n = 167 stable CAD) undergoing PCI were consecutively evaluated. 25 healthy volunteers served as control. Expression of MIF was consecutively measured in patients at the time of PCI. Baseline levels of interleukin 6 (IL-6), “regulated upon activation, normal T-cell expressed, and secreted” (RANTES) and monocyte chemoattractant protein-1 (MCP-1) were measured by Bio-Plex Cytokine assay. C-reactive protein (CRP) was determined by Immunoassay. Patients with ACS showed higher plasma levels of MIF compared to patients with stable CAD and control subjects (median 2.85 ng/mL, interquartile range (IQR) 3.52 versus median 1.22 ng/mL, IQR 2.99, versus median 0.1, IQR 0.09, p<0.001). Increased MIF levels were associated with CRP and IL-6 levels and correlated with troponin I (TnI) release (spearman rank coefficient: 0.31, p<0.001). Patients with ACS due to plaque rupture showed significantly higher plasma levels of MIF than patients with flow limiting stenotic lesions (p = 0.002).To our knowledge this is the first study, demonstrating enhanced expression of MIF in ACS. It is associated with established inflammatory markers, correlates with the extent of cardiac necrosis marker release after PCI and is significantly increased in ACS patients with “culprit” lesions. Further attempts should be undertaken to characterize the role of MIF for risk assessment in the setting of ACS

Modulated structure of nepheline.

The incommensurately modulated structure of a natural nepheline of composition K(0.54)Na(3.24)Ca(0.03)Al(3.84)Si(4.16)O(16) has been determined in superspace. The compound crystallizes in the trigonal centered superspace group X3(00γ)0 with γ = 0.2048 (10), X = (0, 0, 0, 0), (1/3, 2/3, 0, 2/3), (2/3, 1/3, 0, 1/3), a = 17.2889 (8) and c = 8.3622 (10) Å. The structure is characterized by a framework of corner-connected (Al,Si)O(4) tetrahedra. The additional cations are incorporated in two different types of channels of the framework. All atoms in the structure are displacively modulated with amplitudes below 0.1 Å. The modulation can be well described taking into account harmonics of first order only. Atomic positions in the smaller channels of the framework are fully occupied by Na(+). Cationic positions in the larger channel are occupationally modulated, yet the variation of electron density as a function of the internal coordinate t is very small and indicates that the incorporation of different types of cations (K(+), Na(+), Ca(2+)) and vacancies is realised in a highly disordered way. Average T-O distances indicate a nearly complete Al/Si ordering in the tetrahedral framework. A large part of the O atoms are approximated by split-atom positions, which are additionally affected by occupational modulation resulting in a high degree of disorder in the modulated structure. Occupational probabilities for the split-atom positions are complementary. Occupational modulations of the cations in the larger channels and the O atoms of the tetrahedral framework are coupled and correlations between occupational and displacive modulations exist

Exclusive photoproduction of a photon-meson pair: A new class of observables to probe GPDs

11 pages, 3 figures. Presented at 25th International Spin Physics Symposium (SPIN 2023), Durham, NC, USAInternational audienceWe discuss the exclusive photoproduction of a photon-meson pair with large $p_{T}$ as a channel to probe generalised parton distributions (GPDs). Like other $2\to3$ exclusive processes, this channel allows us to better study the $x$-dependence of GPDs, in contrast to $2\to2$ processes such as Deeply Virtual Compton Scattering (DVCS) which give only "moment-type" information. Moreover, it also gives the possibility to access, at leading twist, the chiral-odd GPDs, which are still completely unknown experimentally. In the first part of these proceedings, we present the computation of the amplitude at leading order and leading twist, for charged pions, and rho mesons of any charge and polarisation. These processes are sensitive to quark GPDs only. We also discuss the possibility of measuring such processes at various experiments, namely JLab, COMPASS, future EIC and LHC in ultra-peripheral collisions. In particular, in collider experiments, the dependence of GPDs at small skewness $(<10^{-3})$ can be extracted. For the second part, we report on our recent work on the exclusive photoproduction of $\pi^{0}\gamma$ pair, which, in addition to a quark GPD channel, also has a contribution from gluon GPDs. In the latter case, we demonstrate that a collinear factorisation of the process fails, due to the presence of a Glauber pinch. Our findings also imply that other similar processes, like $\pi ^{0} N \to \gamma \gamma N$ also suffer from the same issue. On the other hand, we stress that the processes discussed earlier, which are sensitive to the quark GPD channels only, are safe from these factorisation breaking effects