Constraints on Parity-Even Time Reversal Violation in the Nucleon-Nucleon System and Its Connection to Charge Symmetry Breaking

Parity-even time reversal violation (TRV) in the nucleon-nucleon interaction is reconsidered. The TRV $\rho$-exchange interaction on which recent analyses of measurements are based is necessarily also charge-symmetry breaking (CSB). Limits on its strength $\bar{g}_\rho$ relative to regular $\rho$-exchange are extracted from recent CSB experiments in neutron-proton scattering. The result $\bar{g}_\rho\le 6.7\times 10^{-3}$ (95% CL) is considerably lower than limits inferred from direct TRV tests in nuclear processes. Properties of $a_1$-exchange and limit imposed by the neutron EDM are briefly discussed.Comment: RevTex, 8 pages. Factor ten error in cited neutron EDM corrected, discussion and two references adde

How the recent BABAR data for P to \gamma\gamma* affect the Standard Model predictions for the rare decays P to l+l-

Measuring the lepton anomalous magnetic moments $(g-2)$ and the rare decays of light pseudoscalar mesons into lepton pairs $P\to l^{+}l^{-}$, serve as important tests of the Standard Model. To reduce the theoretical uncertainty in the standard model predictions, the data on the charge and transition form factors of the light pseudoscalar mesons play a significant role. Recently, new data on the behavior of the transition form factors $P\to\gamma\gamma*$ at large momentum transfer were supplied by the BABAR collaboration. There are several problems with the theoretical interpretation of these data: 1) An unexpectedly slow decrease of the pion transition form factor at high momenta, 2) the qualitative difference in the behavior of the pion form factor and the $\eta$ and $\eta^\prime$ form factors at high momenta, 3) the inconsistency of the measured ratio of the $\eta$ and $\eta^\prime$ form factors with the predicted one. We comment on the influence of the new BABAR data on the rare decay branchings.Comment: 11 pages, 3 figure

A quark model analysis of the charge symmetry breaking in nuclear force

In order to investigate the charge symmetry breaking (CSB) in the short range part of the nuclear force, we calculate the difference of the masses of the neutron and the proton, $\Delta {\rm M}$, the difference of the scattering lengths of the p-p and n-n scatterings, $\Delta a$, and the difference of the analyzing power of the proton and the neutron in the n-p scattering, $\Delta A(\theta)$, by a quark model. In the present model the sources of CSB are the mass difference of the up and down quarks and the electromagnetic interaction. We investigate how much each of them contributes to $\Delta {\rm M}$, $\Delta a$ and $\Delta A(\theta)$. It is found that the contribution of CSB of the short range part in the nuclear force is large enough to explain the observed $\Delta A(\theta)$, while $\Delta a$ is rather underestimated.Comment: 26 pages,6 figure

Selected nucleon form factors and a composite scalar diquark

A covariant, composite scalar diquark, Fadde'ev amplitude model for the nucleon is used to calculate pseudoscalar, isoscalar- and isovector-vector, axial-vector and scalar nucleon form factors. The last yields the nucleon sigma-term and on-shell sigma-nucleon coupling. The calculated form factors are soft, and the couplings are generally in good agreement with experiment and other determinations. Elements in the dressed-quark-axial-vector vertex that are not constrained by the Ward-Takahashi identity contribute ~20% to the magnitude of g_A. The calculation of the nucleon sigma-term elucidates the only unambiguous means of extrapolating meson-nucleon couplings off the meson mass-shell.Comment: 12 pages, REVTEX, 5 figures, epsfi

Characteristic retinal atrophy pattern allows differentiation between pediatric MOGAD and MS after a single optic neuritis episode.

BACKGROUND Optic neuritis (ON) is the most prevalent manifestation of pediatric multiple sclerosis (MSped) and myelin-oligodendrocyte glycoprotein antibody-associated disease (MOGADped) in children > 6 years. In this study, we investigated retinal atrophy patterns and diagnostic accuracy of optical coherence tomography (OCT) in differentiating between both diseases after the first ON episode. METHODS Patients were retrospectively identified in eight tertial referral centers. OCT, VEP and high/low-contrast visual acuity (HCVA/LCVA) have been investigated > 6 months after the first ON. Prevalence of pathological OCT findings was identified based on data of 144 age-matched healthy controls. RESULTS Thirteen MOGADped (10.7 ± 4.2 years, F:M 8:5, 21 ON eyes) and 21 MSped (14.3 ± 2.4 years, F:M 19:2, 24 ON eyes) patients were recruited. We observed a significantly more profound atrophy of both peripapillary and macular retinal nerve fiber layer in MOGADped compared to MSped (pRNFL global: 68.2 ± 16.9 vs. 89.4 ± 12.3 µm, p < 0.001; mRNFL: 0.12 ± 0.01 vs. 0.14 ± 0.01 mm3, p < 0.001). Neither other macular layers nor P100 latency differed. MOGADped developed global atrophy affecting all peripapillary segments, while MSped displayed predominantly temporal thinning. Nasal pRNFL allowed differentiation between both diseases with the highest diagnostic accuracy (AUC = 0.902, cutoff < 62.5 µm, 90.5% sensitivity and 70.8% specificity for MOGADped). OCT was also substantially more sensitive compared to VEP in identification of ON eyes in MOGAD (pathological findings in 90% vs. 14%, p = 0.016). CONCLUSION First MOGAD-ON results in a more severe global peripapillary atrophy compared to predominantly temporal thinning in MS-ON. Nasal pRNFL allows differentiation between both diseases with the highest accuracy, supporting the additional diagnostic value of OCT in children with ON

Anomalous η/η′\eta/\eta^\prime Decays: The Triangle and Box Anomalies

We examine the decay modes \eta/\etp\ra \pi^+ \pi^- \gamma within the context of the Hidden Local Symmetry (HLS) Model. Using numerical information derived in previous fits to $VP\gamma$ and $Ve^+e^-$ decay modes in isolation and the $\rho$ lineshape determined in a previous fit to the pion form factor, we show that all aspects of these decays can be predicted with fair accuracy. Freeing some parameters does not improve the picture. This is interpreted as a strong evidence in favor of the box anomaly in the \eta/\etp decays, which occurs at precisely the level expected. We also construct the set of equations defining the amplitudes for \eta/\etp\ra \pi^+ \pi^- \gamma and \eta/\etp \ra \ggam at the chiral limit, as predicted from the anomalous HLS Lagrangian appropriately broken. This provides a set of four equations depending on only one parameter, instead of three for the traditional set. This is also shown to match the (two--angle, two--decay--constant) \eta-\etp mixing scheme recently proposed and is also fairly well fulfilled by the data. The information returned from fits also matches expectations from previously published fits to the $VP\gamma$ decay modes in isolation.Comment: 47 page

Rare decay \pi^0 \to e^+e^- as a Test of Standard Model

Experimental and theoretical progress concerning the rare decay \pi^0 \to e^+e^- is briefly reviewed. It includes the latest data from KTeV and a new model independent estimate of the decay branching which show the deviation between experiment and theory at the level of $3.3\sigma$. The predictions for \eta and \eta' decays into lepton pair are presented. We also comment on the impact on the pion rare decay estimate of the BABAR collaboration on the pion transition form factor at large momentum transfer.Comment: 11 pages, 2 figures, extended version of the talk given at "New Physics and Quantum Chromodynamics at External Conditions" conference, May 3-6, 2009, Dnipropetrovsk, Ukrain

Native diversity buffers against severity of non-native tree invasions

Determining the drivers of non-native plant invasions is critical for managing native ecosystems and limiting the spread of invasive species$^{1,2}$. Tree invasions in particular have been relatively overlooked, even though they have the potential to transform ecosystems and economies$^{3,4}$. Here, leveraging global tree databases$^{5–7}$, we explore how the phylogenetic and functional diversity of native tree communities, human pressure and the environment influence the establishment of non-native tree species and the subsequent invasion severity. We find that anthropogenic factors are key to predicting whether a location is invaded, but that invasion severity is underpinned by native diversity, with higher diversity predicting lower invasion severity. Temperature and precipitation emerge as strong predictors of invasion strategy, with non-native species invading successfully when they are similar to the native community in cold or dry extremes. Yet, despite the influence of these ecological forces in determining invasion strategy, we find evidence that these patterns can be obscured by human activity, with lower ecological signal in areas with higher proximity to shipping ports. Our global perspective of non-native tree invasion highlights that human drivers influence non-native tree presence, and that native phylogenetic and functional diversity have a critical role in the establishment and spread of subsequent invasions

Evenness mediates the global relationship between forest productivity and richness

1. Biodiversity is an important component of natural ecosystems, with higher species richness often correlating with an increase in ecosystem productivity. Yet, this relationship varies substantially across environments, typically becoming less pronounced at high levels of species richness. However, species richness alone cannot reflect all important properties of a community, including community evenness, which may mediate the relationship between biodiversity and productivity. If the evenness of a community correlates negatively with richness across forests globally, then a greater number of species may not always increase overall diversity and productivity of the system. Theoretical work and local empirical studies have shown that the effect of evenness on ecosystem functioning may be especially strong at high richness levels, yet the consistency of this remains untested at a global scale.2. Here, we used a dataset of forests from across the globe, which includes composition, biomass accumulation and net primary productivity, to explore whether productivity correlates with community evenness and richness in a way that evenness appears to buffer the effect of richness. Specifically, we evaluated whether low levels of evenness in speciose communities correlate with the attenuation of the richness–productivity relationship.3. We found that tree species richness and evenness are negatively correlated across forests globally, with highly speciose forests typically comprising a few dominant and many rare species. Furthermore, we found that the correlation between diversity and productivity changes with evenness: at low richness, uneven communities are more productive, while at high richness, even communities are more productive.4. Synthesis. Collectively, these results demonstrate that evenness is an integral component of the relationship between biodiversity and productivity, and that the attenuating effect of richness on forest productivity might be partly explained by low evenness in speciose communities. Productivity generally increases with species richness, until reduced evenness limits the overall increases in community diversity. Our research suggests that evenness is a fundamental component of biodiversity–ecosystem function relationships, and is of critical importance for guiding conservation and sustainable ecosystem management decisions

The global biogeography of tree leaf form and habit

Understanding what controls global leaf type variation in trees is crucial for comprehending their role in terrestrial ecosystems, including carbon, water and nutrient dynamics. Yet our understanding of the factors influencing forest leaf types remains incomplete, leaving us uncertain about the global proportions of needle-leaved, broadleaved, evergreen and deciduous trees. To address these gaps, we conducted a global, ground-sourced assessment of forest leaf-type variation by integrating forest inventory data with comprehensive leaf form (broadleaf vs needle-leaf) and habit (evergreen vs deciduous) records. We found that global variation in leaf habit is primarily driven by isothermality and soil characteristics, while leaf form is predominantly driven by temperature. Given these relationships, we estimate that 38% of global tree individuals are needle-leaved evergreen, 29% are broadleaved evergreen, 27% are broadleaved deciduous and 5% are needle-leaved deciduous. The aboveground biomass distribution among these tree types is approximately 21% (126.4 Gt), 54% (335.7 Gt), 22% (136.2 Gt) and 3% (18.7 Gt), respectively. We further project that, depending on future emissions pathways, 17–34% of forested areas will experience climate conditions by the end of the century that currently support a different forest type, highlighting the intensification of climatic stress on existing forests. By quantifying the distribution of tree leaf types and their corresponding biomass, and identifying regions where climate change will exert greatest pressure on current leaf types, our results can help improve predictions of future terrestrial ecosystem functioning and carbon cycling