Daily Papers

Giant planets form in protoplanetary discs, where the coupled dynamical and chemical evolution of gas and solids determines the composition of the material they accrete. We investigate how planet formation and migration shape the primordial elemental makeup of giant-planet atmospheres. Our aim is to link atmospheric compositions to planets' formation pathways and the time-dependent chemical properties of their natal discs. We couple 1D models of viscously evolving discs - incorporating radial dust drift and volatile chemistry - with N-body simulations of planetesimals interacting with a growing and migrating giant planet. Four chemical scenarios and three representative grain sizes (0.1, 20, and 100 micron) are explored. We track the accretion of carbon, oxygen, nitrogen, and sulphur to derive atmospheric elemental ratios normalised to stellar values (* denotes stellar normalisation). We identify three atmospheric classes corresponding to distinct accretion regimes: gas-dominated, characterised by N/O* > C/O* > C/N* and unconstrained or substellar S/N* (near-stellar C/S*); planetesimal-dominated, showing N/O* < C/O* < C/N*, S/N* >= C/N*, and C/S* <= C/O*; and drift-enhanced, exhibiting N/O* < C/O* < C/N* and markedly superstellar volatile-to-refractory ratios. N/O*, C/N*, and S/N* vary systematically with migration extent, although degeneracies arise for planets forming beyond the CO and N2 snowlines; C/O* remains largely insensitive. Metallicity alone does not uniquely trace the solid-to-gas accretion balance in drift-dominated regimes. Variations in the disc's chemical state and dust size imprint distinctive volatile-ratio patterns across these classes, providing complementary constraints on disc properties. This multi-element framework establishes predictive trends to guide the interpretation of atmospheric spectra from facilities like JWST and Ariel.

Context. Low-mass bodies, such as comets, asteroids, planetesimals, and free-floating planets, are continuously injected into the intra-cluster environment after expulsion from their host planetary systems. These can be modeled as massless particles (MLPs, hereafter). The dynamics of large populations of MLPs, however, has yet received little attention in literature. Aims. We investigate the dynamical evolution of MLP populations in star clusters, and characterize their kinematics and ejection rates. Methods. We present NBODY6++GPU-MASSLESS, a modified version of the N-body simulation code NBODY6++GPU, that allows fast integration of star clusters that contain large numbers of massless particles (MLPs). NBODY6++GPU-MASSLESS contains routines specifically directed at the dynamical evolution of low-mass bodies, such as planets. Results. Unlike stars, MLPs do not participate in the mass segregation process. Instead, MLPs mostly follow the gravitational potential of the star cluster, which gradually decreases over time due to stellar ejections and stellar evolution. The dynamical evolution of MLPs is primarily affected by the evolution of the core of the star cluster. This is most apparent in the outer regions for clusters with higher initial densities. High escape rates of MLPs are observed before the core-collapse, after which escape rates remain stable. Denser star clusters undergo a more intense core collapse, but this does not impact the dynamical evolution of MLPs. The speeds of escaping stars are similar to those of escaping MLPs, when disregarding the high-velocity ejections of neutron stars during the first 50 Myr.

Aromaticity is a common chemical functionalities in bioactive molecules. In interstellar and circumstellar environments benzene and other small aromatics are considered the precursor for more complex prebiotic molecules and they have shown to potentially have rich ice-phase photochemistry. The availability of small organic molecules in prebiotic networks depends on their photostability in astrophysical environments preceding planet formation, particularly during the protoplanetary disk stage, as the disk composition is linked to the chemical make-up of planets and planetesimals. We study the ultraviolet (UV) photodestruction (120-160 nm) of five aromatic molecules in undiluted ices and, for selected cases, in astrophysically relevant ice matrices (H2O, CO, CO2). For each ice, we measure the destruction cross sections as a function of photon exposure. In undiluted ices, aromatic molecules exhibit substantially lower photodestruction cross sections (sigma < 10-19 cm2) than aliphatic hydrocarbons, including cyclohexane, (sigma = 2.8-4x10-18 cm2). Furthermore, neither substituent nature nor size affects the aromatic stability in pure ices, suggesting that the strong intermolecular interactions among aromatic molecules provide protection against VUV exposure, even with small to mid-sized ring substituents. In mixed ices, the photodestruction and reactivity of aromatic molecules (sigma = 2.5-6.1x10-18 cm2) increases by more than an order of magnitude, but are still lower than in the gas-phase. We attribute this to a weaker cage effect and matrix-specific interactions. We use the experimental photodestruction cross sections to estimate the lifetime of aromatic molecules in protoplanetary disks, denileating the disks regions in which aromatic photochemistry is expected to be the most active.