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Abstract Ice‐nucleating particles (INPs) play a key role in ice formation and cloud microphysics and thus significantly impact the water cycle and the climate. However, our understanding of atmospheric INPs, particularly their sources, emissions, and spatiotemporal variability, is incomplete. While the enhancement of atmospheric INP concentrations with rainfall has been previously shown, a mechanistic understanding of the process is lacking. Here, we link detailed precipitation observations with near‐surface atmospheric INP concentrations at a semiarid grassland site in Colorado. Considering the during‐precipitation air samples, INP concentrations positively correlate with cumulative rainfall kinetic energy and amount, suggesting that INP aerosolization is induced by raindrop and hailstone impact. By additionally analyzing the INP content of precipitation water, terrestrial source samples, and heat‐treated samples, we demonstrate that local plants are the most plausible source of rain‐induced INPs during a precipitation event. Should INPs aerosolized by precipitation rise to cloud height, they could influence cloud ice fraction and initiate precipitation resulting in an aerosol‐cloud‐precipitation feedback. 

In the present work, four, well-studied, model peptides ( e.g. , substance P, bradykinin, angiotensin I and AT-Hook 3) were used to correlate structural information provided by ion mobility and ECD/CID fragmentation in a TIMS-q-EMS-ToF MS/MS platform, incorporporating an electromagnetostatic cell (EMS). The structural heterogeneity of the model peptides was observed by (i) multi-component ion mobility profiles (high ion mobility resolving power, R ∼115–145), and (ii) fast online characteristic ECD fragmentation patterns per ion mobility band (∼0.2 min). Particularly, it was demonstrated that all investigated species were probably conformers, involving cis / trans -isomerizations at X-Pro peptide bond, following the same protonation schemes, in good agreement with previous ion mobility and single point mutation experiments. The comparison between ion mobility selected ECD spectra and traditional FT-ICR ECD MS/MS spectra showed comparable ECD fragmentation efficiencies but differences in the ratio of radical (˙)/prime (′) fragment species (H˙ transfer), which were associated with the differences in detection time after the electron capture event. The analysis of model peptides using online TIMS-q-EMSToF MS/MS provided complementary structural information on the intramolecular interactions that stabilize the different gas-phase conformations to those obtained by ion mobility or ECD alone. 

We present a measurement of the branching fraction and fraction of longitudinal polarization of $B^0\to {\rho }^{+}{\rho }^{-}$decays, which have two ${\pi }^0$’s in the final state. We also measure time-dependent $CP$violation parameters for decays into longitudinally polarized ${\rho }^{+}{\rho }^{-}$pairs. This analysis is based on a data sample containing $(387\pm 6)\times {10}^6$ $\mathrm{\Upsilon }\left(4S\right)$mesons collected with the Belle II detector at the SuperKEKB asymmetric-energy $e^{+}{e}^{-}$collider in 2019–2022. We obtain $\mathcal{B}(B^0\to {\rho }^{+}{\rho }^{-})=\left(2.89_{-0.22}^{+0.23}{}_{-0.27}^{+0.29}\right)\times {10}^{-5}$, $f_L=0.921_{-0.025}^{+0.024}{}_{-0.015}^{+0.017}$, $S=-0.26\pm 0.19\pm 0.08$, and $C=-0.02\pm 0.12_{-0.05}^{+0.06}$, where the first uncertainties are statistical and the second are systematic. We use these results to perform an isospin analysis to constrain the Cabibbo-Kobayashi-Maskawa angle ${\varphi }_2$and obtain two solutions; the result consistent with other Standard Model constraints is ${\varphi }_2=\left({92.6}_{-4.7}^{+4.5}\right)°$. Published by the American Physical Society2025 

A<sc>bstract</sc> We perform the first search forCPviolation in$$ {D}_{(s)}^{+}\to {K}_S^0{K}^{-}{\pi}^{+}{\pi}^{+} $$ $D_{\left(s\right)}^{+}\to K_S^0{K}^{-}{\pi }^{+}{\pi }^{+}$decays. We use a combined data set from the Belle and Belle II experiments, which studye⁺e⁻collisions at center-of-mass energies at or near the Υ(4S) resonance. We use 980 fb⁻¹of data from Belle and 428 fb⁻¹of data from Belle II. We measure sixCP-violating asymmetries that are based on triple products and quadruple products of the momenta of final-state particles, and also the particles’ helicity angles. We obtain a precision at the level of 0.5% for$$ {D}^{+}\to {K}_S^0{K}^{-}{\pi}^{+}{\pi}^{+} $$ $D^{+}\to K_S^0{K}^{-}{\pi }^{+}{\pi }^{+}$decays, and better than 0.3% for$$ {D}_s^{+}\to {K}_S^0{K}^{-}{\pi}^{+}{\pi}^{+} $$ $D_s^{+}\to K_S^0{K}^{-}{\pi }^{+}{\pi }^{+}$decays. No evidence ofCPviolation is found. Our results for the triple-product asymmetries are the most precise to date for singly-Cabibbo-suppressedD⁺decays. Our results for the other asymmetries are the first such measurements performed for charm decays. 

Abstract The XLZD collaboration is developing a two-phase xenon time projection chamber with an active mass of 60–80 t capable of probing the remaining weakly interacting massive particle-nucleon interaction parameter space down to the so-called neutrino fog. In this work we show that, based on the performance of currently operating detectors using the same technology and a realistic reduction of radioactivity in detector materials, such an experiment will also be able to competitively search for neutrinoless double beta decay in¹³⁶Xe using a natural-abundance xenon target. XLZD can reach a 3σdiscovery potential half-life of 5.7 × 10²⁷years (and a 90% CL exclusion of 1.3 × 10²⁸years) with 10 years of data taking, corresponding to a Majorana mass range of 7.3–31.3 meV (4.8–20.5 meV). XLZD will thus exclude the inverted neutrino mass ordering parameter space and will start to probe the normal ordering region for most of the nuclear matrix elements commonly considered by the community. 

A<sc>bstract</sc> Using data samples of 983.0 fb⁻¹and 427.9 fb⁻¹accumulated with the Belle and Belle II detectors operating at the KEKB and SuperKEKB asymmetric-energye⁺e⁻colliders, singly Cabibbo-suppressed decays$$ {\Xi}_c^{+}\to p{K}_S^0 $$ ${\Xi }_c^{+}\to p{K}_S^0$,$$ {\Xi}_c^{+}\to \Lambda {\pi}^{+} $$ ${\Xi }_c^{+}\to \Lambda {\pi }^{+}$, and$$ {\Xi}_c^{+}\to {\Sigma}^0{\pi}^{+} $$ ${\Xi }_c^{+}\to {\Sigma }^0{\pi }^{+}$are observed for the first time. The ratios of branching fractions of$$ {\Xi}_c^{+}\to p{K}_S^0 $$ ${\Xi }_c^{+}\to p{K}_S^0$,$$ {\Xi}_c^{+}\to \Lambda {\pi}^{+} $$ ${\Xi }_c^{+}\to \Lambda {\pi }^{+}$, and$$ {\Xi}_c^{+}\to {\Sigma}^0{\pi}^{+} $$ ${\Xi }_c^{+}\to {\Sigma }^0{\pi }^{+}$relative to that of$$ {\Xi}_c^{+}\to {\Xi}^{-}{\pi}^{+}{\pi}^{+} $$ ${\Xi }_c^{+}\to {\Xi }^{-}{\pi }^{+}{\pi }^{+}$are measured to be$$ {\displaystyle \begin{array}{c}\frac{\mathcal{B}\left({\Xi}_c^{+}\to p{K}_S^0\right)}{\mathcal{B}\left({\Xi}_c^{+}\to {\Xi}^{-}{\pi}^{+}{\pi}^{+}\right)}=\left(2.47\pm 0.16\pm 0.07\right)\%,\\ {}\frac{\mathcal{B}\left({\Xi}_c^{+}\to \Lambda {\pi}^{+}\right)}{\mathcal{B}\left({\Xi}_c^{+}\to {\Xi}^{-}{\pi}^{+}{\pi}^{+}\right)}=\left(1.56\pm 0.14\pm 0.09\right)\%,\\ {}\frac{\mathcal{B}\left({\Xi}_c^{+}\to {\Sigma}^0{\pi}^{+}\right)}{\mathcal{B}\left({\Xi}_c^{+}\to {\Xi}^{-}{\pi}^{+}{\pi}^{+}\right)}=\left(4.13\pm 0.26\pm 0.22\right)\%.\end{array}} $$ $\begin{array}{c}\frac{B\left({\Xi }_c^{+}\to p{K}_S^0\right)}{B\left({\Xi }_c^{+}\to {\Xi }^{-}{\pi }^{+}{\pi }^{+}\right)}=\left(2.47\pm 0.16\pm 0.07\right)\%,\\ \frac{B\left({\Xi }_c^{+}\to \Lambda {\pi }^{+}\right)}{B\left({\Xi }_c^{+}\to {\Xi }^{-}{\pi }^{+}{\pi }^{+}\right)}=\left(1.56\pm 0.14\pm 0.09\right)\%,\\ \frac{B\left({\Xi }_c^{+}\to {\Sigma }^0{\pi }^{+}\right)}{B\left({\Xi }_c^{+}\to {\Xi }^{-}{\pi }^{+}{\pi }^{+}\right)}=\left(4.13\pm 0.26\pm 0.22\right)\%.\end{array}$ Multiplying these values by the branching fraction of the normalization channel,$$ \mathcal{B}\left({\Xi}_c^{+}\to {\Xi}^{-}{\pi}^{+}{\pi}^{+}\right)=\left(2.9\pm 1.3\right)\% $$ $B\left({\Xi }_c^{+}\to {\Xi }^{-}{\pi }^{+}{\pi }^{+}\right)=\left(2.9\pm 1.3\right)\%$, the absolute branching fractions are determined to be$$ {\displaystyle \begin{array}{c}\mathcal{B}\left({\Xi}_c^{+}\to p{K}_S^0\right)=\left(7.16\pm 0.46\pm 0.20\pm 3.21\right)\times {10}^{-4},\\ {}\mathcal{B}\left({\Xi}_c^{+}\to \Lambda {\pi}^{+}\right)=\left(4.52\pm 0.41\pm 0.26\pm 2.03\right)\times {10}^{-4},\\ {}\mathcal{B}\left({\Xi}_c^{+}\to {\Sigma}^0{\pi}^{+}\right)=\left(1.20\pm 0.08\pm 0.07\pm 0.54\right)\times {10}^{-3}.\end{array}} $$ $\begin{array}{c}B\left({\Xi }_c^{+}\to p{K}_S^0\right)=\left(7.16\pm 0.46\pm 0.20\pm 3.21\right)\times {10}^{-4},\\ B\left({\Xi }_c^{+}\to \Lambda {\pi }^{+}\right)=\left(4.52\pm 0.41\pm 0.26\pm 2.03\right)\times {10}^{-4},\\ B\left({\Xi }_c^{+}\to {\Sigma }^0{\pi }^{+}\right)=\left(1.20\pm 0.08\pm 0.07\pm 0.54\right)\times {10}^{-3}.\end{array}$ The first and second uncertainties above are statistical and systematic, respectively, while the third ones arise from the uncertainty in$$ \mathcal{B}\left({\Xi}_c^{+}\to {\Xi}^{-}{\pi}^{+}{\pi}^{+}\right) $$ $B\left({\Xi }_c^{+}\to {\Xi }^{-}{\pi }^{+}{\pi }^{+}\right)$. 

We measure the branching fraction and $CP$-violating flavor-dependent rate asymmetry of $B^0\to {\pi }^0{\pi }^0$decays reconstructed using the Belle II detector in an electron-positron collision sample containing $387\times {10}^6\mathrm{\Upsilon }\left(4S\right)$mesons. Using an optimized event selection, we find $125\pm 20$signal decays in a fit to background-discriminating and flavor-sensitive distributions. The resulting branching fraction is $(1.25\pm 0.23)\times {10}^{-6}$and the $CP$-violating asymmetry is $0.03\pm 0.30$. Published by the American Physical Society2025