Probing the CP nature of the Higgs coupling in tt¯h events at the LHC

The determination of the CP nature of the Higgs coupling to top quarks is addressed in this paper, using t¯th events produced in √s=13  TeV proton-proton collisions at the LHC. Dileptonic final states are employed, with two oppositely charged leptons and four jets, corresponding to the decays t→bW+→bℓ+νℓ, ¯t→¯bW−→¯bℓ−¯νℓ, and h→b¯b. Pure scalar (h=H), pure pseudoscalar (h=A), and CP-violating Higgs boson signal events, generated with MadGraph5_aMC@NLO, are fully reconstructed through a kinematic fit. We furthermore generate samples that have both a CP-even and a CP-odd component in the t¯th coupling in order to probe the ratio of the two components. New angular distributions of the decay products, as well as CP angular asymmetries, are explored in order to separate the scalar from the pseudoscalar components of the Higgs boson and reduce the contribution from the dominant irreducible background, t¯tb¯b. Significant differences between the angular distributions and asymmetries are observed, even after the full kinematic fit reconstruction of the events, allowing to define the best observables for a global fit of the Higgs couplings parameters.info:eu-repo/semantics/publishedVersio

Angular distributions in tt¯H(H→bb¯) reconstructed events at the LHC

The associated production of a Higgs boson and a top-quark pair, tt¯H, in proton-proton collisions is addressed in this paper for a center of mass energy of 13TeV at the LHC. Dileptonic final states of tt¯H events with two oppositely charged leptons and four jets from the decays t→bW+→bℓ+νℓ, t¯→b¯W−→b¯ℓ−ν¯ℓ and h→bb¯, are used. Signal events, generated with MadGraph5_aMC@NLO, are fully reconstructed by applying a kinematic fit. New angular distributions of the decay products as well as angular asymmetries are explored in order to improve discrimination of tt¯H signal events over the dominant irreducible background contribution, tt¯bb¯. Even after the full kinematic fit reconstruction of the events, the proposed angular distributions and asymmetries are still quite different in the tt¯H signal and the dominant background (tt¯bb¯).This work was partially supported by Fundação para a Ciência e Tecnologia, FCT (projects CERN/FP/123619/2011 and EXPL/FIS-NUC/1705/2013, grants SFRH/BI/52524/2014 and SFRH/BD/73438/2010, and contracts IF/00050/2013 and IF/00014/2012). The work of M.C.N. Fiolhais was supported by LIP-Laboratório de Instrumentação e Física Experimental de Partículas, Portugal (grant PestIC/FIS/LA007/2013). The work of R.S. is supported in part by FCT under contract PTDC/FIS/117951/2010. Special thanks go to Juan Antonio Aguilar-Saavedra for all the fruitful discussions and a long term collaboration

A comparative study on the use of microscopy in pharmacology and cell biology research.

Microscopy is the main technique to visualize and study the structure and function of cells. The impact of optical and electron microscopy techniques is enormous in all fields of biomedical research. It is possible that different research areas rely on microscopy in diverse ways. Here, we analyzed comparatively the use of microscopy in pharmacology and cell biology, among other biomedical sciences fields. We collected data from articles published in several major journals in these fields. We analyzed the frequency of use of different optical and electron microscopy techniques: bright field, phase contrast, differential interference contrast, polarization, conventional fluorescence, confocal, live cell imaging, super resolution, transmission and scanning electron microscopy, and cryoelectron microscopy. Our analysis showed that the use of microscopy has a distinctive pattern in each research area, and that nearly half of the articles from pharmacology journals did not use any microscopy method, compared to the use of microscopy in almost all the articles from cell biology journals. The most frequent microscopy methods in all the journals in all areas were bright field and fluorescence (conventional and confocal). Again, the pattern of use was different: while the most used microscopy methods in pharmacology were bright field and conventional fluorescence, in cell biology the most used methods were conventional and confocal fluorescence, and live cell imaging. We observed that the combination of different microscopy techniques was more frequent in cell biology, with up to 6 methods in the same article. To correlate the use of microscopy with the research theme of each article, we analyzed the proportion of microscopy figures with the use of cell culture. We analyzed comparatively the vocabulary of each biomedical sciences field, by the identification of the most frequent words in the articles. The collection of data described here shows a vast difference in the use of microscopy among different fields of biomedical sciences. The data presented here could be valuable in other scientific and educational contexts

Angular distributions in tt‾H(H→bb‾)t \overline{t}H(H → b \overline{b}) reconstructed events at the LHC

The associated production of a Higgs boson and a top-quark pair, $t{\bar t} H$, in proton-proton collisions is addressed in this paper for a center of mass energy of 13TeV at the LHC. Dileptonic final states of $t{\bar t}H$ events with two oppositely charged leptons and four jets from the decays $t\rightarrow bW^+ \rightarrow b \ell^+\nu_\ell$, $\bar{t}\rightarrow \bar{b}W^- \rightarrow \bar{b} \ell^-\bar{\nu}_\ell$ and $h\rightarrow b\bar{b}$, are used. Signal events, generated with MadGraph5_aMC@NLO, are fully reconstructed by applying a kinematic fit. New angular distributions of the decay products as well as angular asymmetries are explored in order to improve discrimination of $t{\bar t} H$ signal events over the dominant irreducible background contribution, $t{\bar t}b{\bar b}$. Even after the full kinematic fit reconstruction of the events, the proposed angular distributions and asymmetries are still quite different in the $t\bar{t}H$ signal and the dominant background ($t\bar{t}b\bar{b}$).Peer Reviewe