28 research outputs found

    The morphological evolution of the Adephaga (Coleoptera)

    No full text
    The evolution of the coleopteran suborder Adephaga is discussed based on a robust phylogenetic background. Analyses of morphological characters yield results nearly identical to recent molecular phylogenies, with the highly specialized Gyrinidae placed as sister to the remaining families, which form two large, reciprocally monophyletic subunits, the aquatic Haliplidae + Dytiscoidea (Meruidae, Noteridae, Aspidytidae, Amphizoidae, Hygrobiidae, Dytiscidae) on one hand, and the terrestrial Geadephaga (Trachypachidae + Carabidae) on the other. The ancestral habitat of Adephaga, either terrestrial or aquatic, remains ambiguous. The former option would imply two or three independent invasions of aquatic habitats, with very different structural adaptations in larvae of Gyrinidae, Haliplidae and Dytiscoidea.Deutsche Forschungsgemeinschaft. Grant Number: BE 1789/11‐

    Circadian misalignment and health

    No full text

    The Morphology And Phylogeny Of Dionychan Spiders (Araneae: Araneomorphae)

    No full text

    Measurements of branching fractions and CP-violating charge asymmetries in multibody charmless BB decays reconstructed in 2019-2020 Belle II data

    No full text
    We report on measurements of branching fractions (B\mathcal{B}) and CP-violating charge asymmetries (ACP\mathcal{A}_{\rm CP}) of multibody charmless BB decays reconstructed by the Belle II experiment at the SuperKEKB electron-positron collider. We use a sample of collisions collected in 2019 and 2020 at the ΄(4S)\Upsilon(4S) resonance and corresponding to 62.862.8 fb−1^{-1} of integrated luminosity. We use simulation to determine optimized event selections. The ΔE\Delta E and MbcM_{\rm bc} distributions of the resulting samples are fit to determine signal yields of approximately 690, 840, and 380 decays for the channels B+→K+K−K+B^+ \to K^+K^-K^+, B+→K+π−π+B^+ \to K^+\pi^-\pi^+, and B0→K+π−π0B^0 \to K^+\pi^-\pi^0, respectively. These yields are corrected for efficiencies determined from simulation and control data samples to obtain B(B+→K+K−K+)=[35.8±1.6(stat)±1.4(syst)]×10−6\mathcal{B}(B^+ \to K^+K^-K^+) = [35.8 \pm 1.6(\rm stat) \pm 1.4 (\rm syst)]\times 10^{-6}, B(B+→K+π−π+)=[67.0±3.3(stat)±2.3(syst)]×10−6\mathcal{B}(B^+ \to K^+\pi^-\pi^+) = [67.0 \pm 3.3 (\rm stat)\pm 2.3 (\rm syst)]\times 10^{-6}, B(B0→K+π−π0)=[38.1±3.5(stat)±3.9(syst)]×10−6\mathcal{B}(B^0 \to K^+\pi^-\pi^0) = [38.1 \pm 3.5 (\rm stat)\pm 3.9 (\rm syst)]\times 10^{-6}, ACP(B+→K+K−K+)=−0.103±0.042(stat)±0.020(syst)\mathcal{A}_{\rm CP}(B^+ \to K^+K^-K^+) = -0.103 \pm 0.042(\rm stat) \pm 0.020 (\rm syst), ACP(B+→K+π−π+)=−0.010±0.050(stat)±0.021(syst)\mathcal{A}_{\rm CP}(B^+ \to K^+\pi^-\pi^+) = -0.010 \pm 0.050 (\rm stat)\pm 0.021(\rm syst), and ACP(B0→K+π−π0)=0.207±0.088(stat)±0.011(syst)\mathcal{A}_{\rm CP}(B^0 \to K^+\pi^-\pi^0) = 0.207 \pm 0.088 (\rm stat)\pm 0.011(\rm syst). Results are consistent with previous measurements and demonstrate detector performance comparable with the best Belle results
    corecore