MiniBooNE and LSND data: non-standard neutrino interactions in a (3+1) scheme versus (3+2) oscillations

The recently observed event excess in MiniBooNE anti-neutrino data is in agreement with the LSND evidence for electron anti-neutrino appearance. We propose an explanation of these data in terms of a (3+1) scheme with a sterile neutrino including non-standard neutrino interactions (NSI) at neutrino production and detection. The interference between oscillations and NSI provides a source for CP violation which we use to reconcile different results from neutrino and anti-neutrino data. Our best fit results imply NSI at the level of a few percent relative to the standard weak interaction, in agreement with current bounds. We compare the quality of the NSI fit to the one obtained within the (3+1) and (3+2) pure oscillation frameworks. We also briefly comment on using NSI (in an effective two-flavour framework) to address a possible difference in neutrino and anti-neutrino results from the MINOS experiment.Comment: 28 pages, 9 figures, discussion improved, new appendix added, conclusions unchange

Minimal models with light sterile neutrinos

We study the constraints imposed by neutrino oscillation experiments on the minimal extensions of the Standard Model (SM) with $n_R$ gauge singlet fermions ("right-handed neutrinos"), that can account for neutrino masses. We consider the most general coupling to SM fields of the new fields, in particular those that break lepton number and we do not assume any a priori hierarchy in the mass parameters. We proceed to analyze these models starting from the lowest level of complexity, defined by the number of extra fermionic degrees of freedom. The simplest choice that has enough free parameters in principle (i.e. two mass differences and two angles) to explain the confirmed solar and atmospheric oscillations corresponds to $n_R=1$. This minimal choice is shown to be excluded by data. The next-to-minimal choice corresponds to $n_R=2$. We perform a systematic study of the full parameter space in the limit of degenerate Majorana masses by requiring that at least two neutrino mass differences correspond to those established by solar and atmospheric oscillations. We identify several types of spectra that can fit long-baseline reactor and accelerator neutrino oscillation data, but fail in explaining solar and/or atmospheric data. The only two solutions that survive are the expected seesaw and quasi-Dirac regions, for which we set lower and upper bounds respectively on the Majorana mass scale. Solar data from neutral current measurements provide essential information to constrain the quasi-Dirac region. The possibility to accommodate the LSND/MiniBoone and reactor anomalies, and the implications for neutrinoless double-beta decay and tritium beta decay are briefly discussed.Comment: 32 pages, 15 figures. Misprints and a small error corrected, references added. Conclusions unchange

Neutrinoless Double Beta Decay in the Presence of Light Sterile Neutrinos

We investigate the predictions for neutrinoless double beta ((\u3b2\u3b2)0\u3bd -) decay effective Majorana mass |\u3008m\u3009| in the 3 + 1 and 3 + 2 schemes with one and two additional sterile neutrinos with masses at the eV scale. The two schemes are suggested by the neutrino oscillation interpretation of the reactor neutrino and Gallium \u201canomalies\u201d and of the data of the LSND and MiniBooNE experiments. We analyse in detail the possibility of a complete or partial cancellation between the different terms in |\u3008m\u3009|, leading to a strong suppression of |\u3008m\u3009|. We determine the regions of the relevant parameter spaces where such a suppression can occure. This allows us to derive the conditions under which the effective Majorana mass satisfies |\u3008m\u3009| > 0.01 eV, which is the range planned to be exploited by the next generation of (\u3b2\u3b2)0\u3bd -experiments. \ua9 SISSA 2013

Lepton Number Violation from Colored States at the LHC

The possibility to search for lepton number violating signals at the Large Hadron Collider (LHC) in the colored seesaw scenario is investigated. In this context the fields that generate neutrino masses at the one-loop level are scalar and Majorana fermionic color-octets of SU(3). Due to the QCD strong interaction these states may be produced at the LHC with a favorable rate. We study the production mechanisms and decays relevant to search for lepton number violation signals in the channels with same-sign dileptons. In the simplest case when the two fermionic color-octets are degenerate in mass, one could use their decays to distinguish between the neutrino spectra. We find that for fermionic octets with mass up to about 1 TeV the number of same-sign dilepton events is larger than the standard model background indicating a promising signal for new physics.Comment: minor corrections, added reference

Prevalence, concordance and determinants of human papillomavirus infection among heterosexual partners in a rural region in central Mexico

Background: Although human papillomavirus (HPV) infection in heterosexual couples has been sparsely studied, it is relevant to understand disease burden and transmission mechanisms. The present study determined the prevalence and concordance of type-specific HPV infection as well as the determinants of infection in heterosexual couples in a rural area of Mexico. Methods: A cross-sectional study was conducted in 504 clinically healthy heterosexual couples from four municipalities in the State of Mexico, Mexico. HPV testing was performed using biotinylated L1 consensus primers and reverse line blot in cervical samples from women and in genital samples from men. Thirty-seven HPV types were detected, including high-risk oncogenic types and low-risk types. Multivariate logistic regression models were utilized to evaluate factors associated with HPV. Results: The prevalence of HPV infection was 20.5% in external male genitals and 13.7% in cervical samples. In 504 sexual couples participating in the study, concordance of HPV status was 79%; 34 partners (6.7%) were concurrently infected, and 21 out of 34 partners where both were HPV positive (61.8%) showed concordance for one or more HPV types. The principal risk factor associated with HPV DNA detection in men as well as women was the presence of HPV DNA in the respective regular sexual partner (OR = 5.15, 95% CI 3.01-8.82). In men, having a history of 10 or more sexual partners over their lifetime (OR 2.5, 95% CI 1.3 - 4.8) and having had sexual relations with prostitutes (OR 1.7, 95% CI 1.01 - 2.8) increased the likelihood of detecting HPV DNA. Conclusions: In heterosexual couples in rural regions in Mexico, the prevalence of HPV infection and type-specific concordance is high. High-risk sexual behaviors are strong determinants of HPV infection in men

Clinical trial to assess the effect of physical exercise on endothelial function and insulin resistance in pregnant women

<p>Abstract</p> <p>Background</p> <p>Preeclampsia (PE) is a common maternal disease that complicates 5 to 10% of pregnancies and remains as the major cause of maternal and neonatal mortality. Cost-effective interventions aimed at preventing the development of preeclampsia are urgently needed. However, the pathogenesis of PE is not well known. Multiple mechanisms such as oxidative stress, endothelial dysfunction and insulin resistance may contribute to its development. Regular aerobic exercise recovers endothelial function; improves insulin resistance and decreases oxidative stress. Therefore the purpose of this clinical trial is to determine the effect of regular aerobic exercise on endothelial function, on insulin resistance and on pregnancy outcome.</p> <p>Methods and design</p> <p>64 pregnant women will be included in a blind, randomized clinical trial, and parallel assignment. The exercise group will do regular aerobic physical exercise: walking (10 minutes), aerobic exercise (30 minutes), stretching (10 minutes) and relaxation exercise (10 minutes) in three sessions per week. Control group will do the activities of daily living (bathing, dressing, eating, and walking) without counselling from a physical therapist.</p> <p>Trial registration</p> <p>NCT00741312.</p