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We combine novel laboratory experiments and exospheric modeling to reveal that "dynamic" Ly-α photolysis of Plutonian methane generates a photolytic refractory distribution on Charon that increases with latitude, consistent with poleward darkening observed in the New Horizons images. The flux ratio of the condensing methane to the interplanetary medium Ly-α photons, φ, controls the distribution and composition of Charon's photoproducts. Mid-latitude regions are likely to host complex refractories emerging from low-φ photolysis, while high-φ photolysis at the polar zones primarily generate ethane. However, ethane being colorless does not contribute to the reddish polar hue. Solar wind radiolysis of Ly-α-cooked polar frost past spring sunrise may synthesize increasingly complex, redder refractories responsible for the unique albedo on this enigmatic moon.

Volatiles and refractories represent the two end-members in the volatility range of species in any surface-bounded exosphere. Volatiles include elements that do not interact strongly with the surface, such as neon (detected on the Moon) and helium (detected both on the Moon and at Mercury), but also argon, a noble gas (detected on the Moon) that surprisingly adsorbs at the cold lunar nighttime surface. Refractories include species such as calcium, magnesium, iron, and aluminum, all of which have very strong bonds with the lunar surface and thus need energetic processes to be ejected into the exosphere. Here we focus on the properties of species that have been detected in the exospheres of inner Solar System bodies, specifically the Moon and Mercury, and how they provide important information to understand source and loss processes of these exospheres, as well as their dependence on variations in external drivers., (© The Author(s) 2021.)

During three low-altitude (99, 66, 66 km) flybys through the Enceladus plume in 2010 and 2011, Cassini's ion neutral mass spectrometer (INMS) made its first high spatial resolution measurements of the plume's gas density and distribution, detecting in situ the individual gas jets within the broad plume. Since those flybys, more detailed Imaging Science Subsystem (ISS) imaging observations of the plume's icy component have been reported, which constrain the locations and orientations of the numerous gas/grain jets. In the present study, we used these ISS imaging results, together with ultraviolet imaging spectrograph stellar and solar occultation measurements and modeling of the three-dimensional structure of the vapor cloud, to constrain the magnitudes, velocities, and time variability of the plume gas sources from the INMS data. Our results confirm a mixture of both low and high Mach gas emission from Enceladus' surface tiger stripes, with gas accelerated as fast as Mach 10 before escaping the surface. The vapor source fluxes and jet intensities/densities vary dramatically and stochastically, up to a factor 10, both spatially along the tiger stripes and over time between flyby observations. This complex spatial variability and dynamics may result from time-variable tidal stress fields interacting with subsurface fissure geometry and tortuosity beyond detectability, including changing gas pathways to the surface, and fluid flow and boiling in response evolving lithostatic stress conditions. The total plume gas source has 30% uncertainty depending on the contributions assumed for adiabatic and nonadiabatic gas expansion/acceleration to the high Mach emission. The overall vapor plume source rate exhibits stochastic time variability up to a factor ∼5 between observations, reflecting that found in the individual gas sources/jets. Key Words: Cassini at Saturn-Geysers-Enceladus-Gas dynamics-Icy satellites. Astrobiology 17, 926-940.

Saturn's moon Enceladus has an ice-covered ocean; a plume of material erupts from cracks in the ice. The plume contains chemical signatures of water-rock interaction between the ocean and a rocky core. We used the Ion Neutral Mass Spectrometer onboard the Cassini spacecraft to detect molecular hydrogen in the plume. By using the instrument's open-source mode, background processes of hydrogen production in the instrument were minimized and quantified, enabling the identification of a statistically significant signal of hydrogen native to Enceladus. We find that the most plausible source of this hydrogen is ongoing hydrothermal reactions of rock containing reduced minerals and organic materials. The relatively high hydrogen abundance in the plume signals thermodynamic disequilibrium that favors the formation of methane from CO 2 in Enceladus' ocean., (Copyright © 2017, American Association for the Advancement of Science.)

Sharp magnetic perturbations found by the Cassini spacecraft at the edge of the Rhea flux tube are consistent with field-aligned flux tube currents. The current system results from the difference of ion and electron gyroradii and the requirement to balance currents on the sharp Rhea surface. Differential-type hybrid codes that solve for ion velocity and magnetic field have an intrinsic difficulty modeling the plasma absorber's sharp surface. We overcome this problem by instead using integral equations to solve for ion and electron currents and obtain agreement with the magnetic perturbations at Rhea's flux tube edge. An analysis of the plasma dispersion relations and Cassini data reveals that field-guided whistler waves initiated by (1) the electron velocity anisotropy in the flux tube and (2) interaction with surface sheath electrostatic waves on topographic scales may facilitate propagation of the current system to large distances from Rhea. Current systems like those at Rhea should occur generally, for plasma absorbers of any size such as spacecraft or planetary bodies, in a wide range of space plasma environments. Motion through the plasma is not essential since the current system is thermodynamic in origin, excited by heat flow into the object. The requirements are a difference of ion and electron gyroradii and a sharp surface, i.e., without a significant thick atmosphere., Key Points: Surface current balance condition yields a current system at astronomical bodiesCurrent system possible for sharp (airless) objects of any sizeCurrent system is thermoelectric and motion through the plasma nonessential.

The flyby measurements of the Cassini spacecraft at Saturn's moon Rhea reveal a tenuous oxygen (O(2))-carbon dioxide (CO(2)) atmosphere. The atmosphere appears to be sustained by chemical decomposition of the surface water ice under irradiation from Saturn's magnetospheric plasma. This in situ detection of an oxidizing atmosphere is consistent with remote observations of other icy bodies, such as Jupiter's moons Europa and Ganymede, and suggestive of a reservoir of radiolytic O(2) locked within Rhea's ice. The presence of CO(2) suggests radiolysis reactions between surface oxidants and organics or sputtering and/or outgassing of CO(2) endogenic to Rhea's ice. Observations of outflowing positive and negative ions give evidence for pickup ionization as a major atmospheric loss mechanism.

We report experimental studies of 100 keV Ar(+) ion irradiation of ice leading to the formation of molecular oxygen and its trapping and ejection from the surface, at temperatures between 80 and 150 K. The use of a mass spectrometer and a quartz-crystal microbalance and sputter depth profiling at 20 K with low energy Ar ions allowed us to obtain a consistent picture of the complex radiolytic mechanism. We show that the dependence of O(2) sputtering on ion fluence is mainly due to the buildup of trapped O(2) near the surface. A small proportion of the O(2) is ejected above 130 K immediately upon creation from a precursor such as OH or H(2)O(2). The distribution of trapped oxygen peaks at or near the surface and is shallower than the ion range. Measurements of sputtering of H(2) help to elucidate the role of this molecule in the process of O(2) formation: out-diffusion leading to oxygen enrichment near the surface. The competing phenomena of OH diffusion away from the ion track and hydrogen escape from the ice and their temperature dependence are used to explain the finding of opposite temperature dependencies of O(2) and H(2)O(2) synthesis. Based on the new data and understanding, we discuss the application of our findings to ices in the outer solar system and interstellar space.

We have characterized the porosity of vapor-deposited amorphous solid water (ice) films deposited at 30-40 K using several complementary techniques such as quartz crystal microgravimetry, UV-visible interferometry, and infrared reflectance spectrometry in tandem with methane adsorption. The results, inferred from the gas adsorption isotherms, reveal the existence of microporosity in all vapor-deposited films condensed from both diffuse and collimated water vapor sources. Films deposited from a diffuse source show a step in the isotherms and much less adsorption at low pressures than films deposited from a collimated source with the difference increasing with film thickness. Ice films deposited from a collimated vapor source at 77 degrees incidence are mesoporous, in addition to having micropores. Remarkably, mesoporosity is retained upon warming to temperatures as high as 140 K where the ice crystallized. The binding energy distribution for methane adsorption in the micropores of ice films deposited from a collimated source peaks at approximately 0.083 eV for deposition at normal incidence and at approximately 0.077 eV for deposition at >45 degrees incidence. For microporous ice, the intensity of the infrared bands due to methane molecules on dangling OH bonds on pore surfaces increases linearly with methane uptake, up to saturation adsorption. This shows that the multilayer condensation of methane does not occur inside the micropores. Rather, filling of the core volume results from coating the pore walls with the first layer of methane, indicating pore widths below a few molecular diameters. For ice deposited at 77 degrees incidence, the increase in intensity of the dangling bond absorptions modified by methane adsorption departs from linearity at large uptakes.

We report a very low density ( approximately 0.5 g/cm(3)) structure of solid ozone. It is produced by irradiation of solid oxygen with 100 keV protons at 20 K followed by heating to sublime unconverted oxygen. Upon heating to 47 K the porous ozone compacts to a density of approximately 1.6 g/cm(3) and crystallizes. We use a detailed analysis of the main infrared absorption band of the porous ozone to interpret previous research, where solid oxygen was irradiated by UV light and keV electrons.

We have studied the compaction of vapor-deposited amorphous solid water by energetic ions at 40 K. The porosity was characterized by ultraviolet-visible spectroscopy, infrared spectroscopy, and methane adsorption/desorption. These three techniques provide different and complementary views of the structural changes in ice resulting from irradiation. We find that the decrease in internal surface area of the pores, signaled by infrared absorption by dangling bonds, precedes the decrease in the pore volume during irradiation. Our results imply that impacts from cosmic rays can cause compaction in the icy mantles of the interstellar grains, which can explain the absence of dangling bond features in the infrared spectrum of molecular clouds.

We present results of the growth of thin films of crystalline H2O2 and H2O2*2H2O (dihydrate) in ultrahigh vacuum by distilling an aqueous solution of hydrogen peroxide. We traced the process using infrared reflectance spectroscopy, mass loss on a quartz crystal microbalance, and in a few cases ultraviolet-visible reflectance. We find that the different crystalline phases-water, dihydrate, and hydrogen peroxide-have very different sublimation rates, making distillation efficient to isolate the less volatile component, crystalline H2O2.

We present laboratory studies of the radiolysis of pure (97%) solid H2O2 films by 50 keV H+ at 17 K. Using UV-visible and infrared reflectance spectroscopies, a quartz-crystal microbalance, and a mass spectrometer, we measured the absolute concentrations of the H2O, O2, H2O2, and O3 products as a function of irradiation fluence. Ozone was identified by both UV and infrared spectroscopies and O2 from its forbidden transition in the infrared at 1550 cm(-1). From the measurements we derive radiation yields, which we find to be particularly high for the decomposition of hydrogen peroxide; this can be explained by the occurrence of a chemical chain reaction.