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The beam-helicity asymmetry was measured, for the first time, in photoproduction of $\pi^{0}\eta$ pairs on carbon, aluminum, and lead, with the A2 experimental setup at MAMI. The results are compared to an earlier measurement on a free proton and to the corresponding theoretical calculations. The Mainz model is used to predict the beam-helicity asymmetry for the nuclear targets. The present results indicate that the photoproduction mechanism for $\pi^{0}\eta$ pairs on nuclei is similar to photoproduction on a free nucleon. This process is dominated by the $D_{33}$ partial wave with the $\eta\Delta(1232)$ intermediate state.

The Anderson-Higgs mechanism provides mass to the photon in a superconductor, resulting in the Meissner effect, representing a one-to-one analogy to high-energy physics. We report on the direct observation of the Higgs excitation in d-wave high-temperature superconductors by developing an innovative technique to study the Higgs mode after a soft quench of the Mexican-hat free-energy potential by light: Non-Equilibrium Anti-Stokes Raman Scattering (NEARS) identifies the Higgs mode by its distinct characteristic symmetry-dependent excitation energy below twice the energy of the superconducting gap of optimally-doped Bi-2212. Disentangling the Higgs mode from different types of superconductivity-induced excitations opens the avenue for Higgs spectroscopy and provides a unique pathway to study exotic forms of superconductivity at interfaces and in transient states.

Electron transport through biomolecules and in biological transport networks is of great importance to bioenergetics and biocatalysis. More generally, it is of crucial importance to understand how the pathways that connect buried metallocofactors to other cofactors, and to protein surfaces, affect the biological chemistry of metalloproteins. In terms of electron transfer (ET), the strongest coupling pathways usually comprise covalent and hydrogen bonded networks, with a limited number of through-space contacts. Herein, we set out to determine the relative roles of hydrogen bonds involved in ET via an established heme-to-surface tunneling pathway in cytochrome (cyt)

Carex (Cyperaceae), with an estimated 2000 species, nearly cosmopolitan distribution and broad range of habitats, is one of the largest angiosperm genera and the largest in the temperate zone. In this article, we provide argument and evidence for a broader circumscription of Carex to add all species currently classified in Cymophyllus (monotypic), Kobresia (c. 60 species), Schoenoxiphium (c. 15 species) and Uncinia (c. 70 species) to those currently classified as Carex. Carex and these genera comprise tribe Cariceae (subfamily Cyperoideae, Cyperaceae) and form a wellsupported monophyletic group in all molecular phylogenetic studies to date. Carex as defined here in the broad sense currently comprises at least four clades. Three are strongly supported (Siderostictae, core Vignea and core Carex), whereas the caricoid clade, which includes all the segregate genera, receives only weak to moderate support. The caricoid clade is most commonly split into two clades, one including a monophyletic Schoenoxiphium and two small clades of species of Carex s.s., and the other comprising Kobresia, Uncinia and mostly unispicate species of Carex s.s. Morphological variation is high in all but the Vignea clade, making it extremely difficult to define consistent synapomorphies for most clades. However, Carex s.l. as newly circumscribed here is clearly differentiated from the sister groups in tribe Scirpeae by the transition from bisexual flowers with a bristle perianth in the sister group to unisexual flowers without a perianth in Carex. The naked female flowers of Carex s.l. are at least partially enclosed in a flask-shaped prophyll, termed a perigynium. Carex s.s. is not only by far the largest genus in the group, but also the earliest published name. As a result, only 72 new combinations and 58 replacement names are required to treat all of tribe Cariceae as a single genus Carex. We present the required transfers here, with synonymy, and we argue that this broader monophyletic circumscription of Carex reflects the close evolutionary relationships in the group and serves the goal of nomenclatural stability better than other possible treatments. We are grateful to the John D. and Catherine T. MacArthur Foundation for funding of the Biodiversity Synthesis Group of the Encyclopedia of Life (EOL) project, which funded our BioSynC Synthesis meeting at the Field Museum in Chicago in September 2011, when the Global Carex Group was formed. We also thank the US National Science Foundation (NSF) for funding our continuing international collaborative work on the phylogeny and classification of Carex under grants DEB 1255901 to ALH and MJW, and DEB 1256033 to EHR. We also acknowledge with thanks funding for nomenclatural research and for attendance at our second meeting during the Monocots V conference in New York in July, 2013, from the Natural Sciences and Engineering Research Council, Canada (NSERC) to MJW and JRS; University of Mainz to BG; JSPS KAKENHI Grant no. 25840136 to OY; Korea National Arboretum to SK; CGL2012- 38744 project from the Spanish Ministry of Economy and Competitiveness to ML; project 30870178 from the National Natural Science Foundation of China to SRZ, and a University of Wisconsin-Madison Raper Travel Grant to DS. The figures were prepared with invaluable technical advice from H. C. Rimmer. Peer reviewed

The ratio of branching fractions $R(D^{*}) = \mathcal{B}(\overline{B} \rightarrow D^{*} \tau^{-} \overline{\nu}_{\tau})$/$\mathcal{B} (\overline{B} \rightarrow D^{*} \ell^{-} \overline{\nu}_{\ell})$, where $\ell$ is an electron or muon, is measured using a Belle~II data sample with an integrated luminosity of $189~\mathrm{fb}^{-1}$ at the SuperKEKB asymmetric-energy $e^{+} e^{-}$ collider. Data is collected at the $\Upsilon(\mathrm{4S})$ resonance, and one $B$ meson in the $\Upsilon(\mathrm{4S})\rightarrow B\overline{B}$ decay is fully reconstructed in hadronic decay modes. The accompanying signal $B$ meson is reconstructed as $\overline{B}\rightarrow D^{*} \tau^{-}\overline{\nu}_{\tau}$ using leptonic $\tau$ decays. The normalization decay, $\overline{B}\rightarrow D^{*} \ell^{-} \overline{\nu}_{\ell}$, where $\ell$ is an electron or muon, produces the same observable final state particles. The ratio of branching fractions is extracted in a simultaneous fit to two signal-discriminating variables in both channels and yields $R(D^{*}) = 0.262~_{-0.039}^{+0.041}(\mathrm{stat})~_{-0.032}^{+0.035}(\mathrm{syst})$. This result is consistent with the current world average and with standard model predictions. Comment: 16 pages, 17 figures, submitted to PRD

Fusarium head blight (FHB), caused principally by the species belonging to the

Bone density diseases such as osteoporosis affect a significant number of people worldwide. Lanthanide ions are functional mimics of calcium ions, able to substitute for Ca2+ in the bone mineral component, hydroxyapatite (HAP). Bone undergoes a continuous remodelling cycle and lanthanides can affect this cycle, exerting a positive influence on bone mineral. We have been engaged in efforts to find new lanthanide containing complexes as active agents for treatment of these diseases and have identified two lead compounds, 3-hydroxy-1,2-dimethylpyridin-4(1H)-one (Hdpp) and a phosphinate-EDTA derivative, bis[[bis(carboxymethyl)amino]-methyl]phosphinate (H5XT). In this paper, we report in vivo data for the first time for the two lead compounds. The pharmacokinetics of La(dpp)3 suggest the complex is rapidly cleared from plasma. We demonstrate that La3+ accumulates in the bone following IV dose of either La(dpp)3 or La(XT) and we have investigated the influence of each chelating ligand on the incorporation of La3+ into HAP using ITC and HAP-binding studies. Lanthanum could act as a preventative measure against bone resorption disorders; two compounds are thoroughly investigated both in vivo and ex vivo as potential oral drug candidates.

Population synthesis consists of generating synthetic but realistic representations of a target population of micro-agents for the purpose of behavioral modeling and simulation. We introduce a new framework based on copulas to generate synthetic data for a target population of which only the empirical marginal distributions are known by using a sample from another population sharing similar marginal dependencies. This makes it possible to include a spatial component in the generation of population synthesis and to combine various sources of information to obtain more realistic population generators. Specifically, we normalize the data and treat them as realizations of a given copula, and train a generative model on the normalized data before injecting the information on the marginals. We compare the copulas framework to IPF and to modern probabilistic approaches such as Bayesian networks, variational auto-encoders, and generative adversarial networks. We also illustrate on American Community Survey data that the method proposed allows to study the structure of the data at different geographical levels in a way that is robust to the peculiarities of the marginal distributions.