The solar magnetic field (SMF) has historically been considered as dipole in order to build models of the radially expanding corona, that is, the solar wind in the solar minimum. The simplified approach suggests the existence of only one quasi-stationary current sheet (QCS) of solar origin in the heliosphere, namely, the heliospheric current sheet (HCS). However, the SMF becomes more complicated over the solar cycle, comprising higher-order components. The overlapping of the dipole and multipole components of the SMF suggests a formation of more than one QCS in the corona, which may expand further to the heliosphere. We study the impact of the.,Qquadrupole and octupole harmonics of the SMF on the formation and spatial characteristics of QCSs, building a stationary axisymmetric MHD model of QCSs in the heliosphere. It is shown that if the dipole component dominates, a single QCS appears in the solar wind at low heliolatitudes as the classic HCS. In other.,Qcases, the number of QCSs varies from one to three, depending on the relative input of the quadrupole and octupole components. QCSs possess a conic form and may occur at a wide variety of heliolatitudes. The existence of QCSs opens wide opportunities for explanations of puzzling observations of cosmic rays and energetic particles in the heliosphere and, at the same time, raises a risk of misinterpretation of in situ crossings of QCSs because of mixing up the HCS and higherheliolatitude QCSs, which can be significantly disturbed in the dynamical solar wind.@en

Abstract: When exposed to a thermal beam of hydrogen atoms, gas-phase coronene cations C24H12+ can be sequentially hydrogenated. This process is accompanied by a gradual transition of the electronic structure from aromatic to aliphatic. The planar very stable coronene structure transforms into the significantly weaker corrugated structure, typical for aliphatic molecules. In this study, we have investigated the hydrogenation of 5 smaller polycyclic aromatic hydrocarbon cations using a combination of radiofrequency ion trapping with time-of-flight mass spectrometry. Anthracene (C14H10+), pyrene (C16H10+), triphenylene (C18H12+), tetracene (C18H12+) and 8-9-benzofluoranthene (C20H12+) only cover a small mass range, but differ in carbon/hydrogen ratio, number of outer-edge sites and overall structure. We have observed qualitatively similar initial hydrogenation patterns for all 5 molecular ions, with odd hydrogenation states being dominant. Strong quantitative differences in hydrogenation and in attachment-induced fragmentation were found. For the case of pyrene cations, we have also investigated exposure to atomic D. Clear lines of evidence for HD/D2 abstraction reactions of Eley–Rideal type were found, as previously observed for coronene cations. Graphical abstract: [Figure not available: see fulltext.].@en