Space instrumentation

Abstract:

Hydrogen chloride gas was recently discovered in the atmosphere of Mars during southern summer seasons. Its connection with potential chlorine reservoirs and the related atmospheric chemistry is now of particular interest and actively studied. Measurements by the Atmospheric Chemistry Suite mid-infrared channel (ACS MIR) on the ExoMars Trace Gas Orbiter allow us to measure the ratio of hydrogen chloride two stable isotopologues, H35Cl and H37Cl. This work describes the observation, processing technique, and derived values for the chloride isotope ratio. Unlike other volatiles in the Martian atmosphere, because it is enriched with heavier isotopes, the δ37Cl is measured to be - 7 ± 20°, which is almost indistinguishable from the terrestrial ratio for chlorine. This value agrees with available measurements of the surface materials on Mars. We conclude that chlorine in observed HCl likely originates from dust and is not involved in any long-term, surface-atmosphere cycle.

Abstract:

Ultraviolet spectral imaging has been a powerful tool to investigate the cloud top of Venus, allowing for measurement of several minor gases (especially SO , SO, O ), of cloud top aerosol's microphysical properties and of atmospheric dynamics through tracking of the unevenly distributed UV absorber. After a brief review of recent UV instruments that orbited around Venus, we present the results of a state-of-the-art radiative transfer model from Marcq et al. (2020) to derive the spectral resolution and Signal-to-Noise ratio (SNR) required to derive abundances of these gases, retrieve optical properties of the aerosols beyond our current knowledge. This leads us to propose a two-channel UV hyperspectral push-broom imager called VeSUV (standing for Venusian Spectroscopy in UV) whose technical characteristics will improve on existing measurements by a factor of at least 2, and which is well suited to the integration into the payload of future low Venus orbit platforms such as the proposed EnVision mission to ESA M5 call. 2 3

Abstract:

The current Martian atmosphere is about five times more enriched in deuterium than Earth’s, providing direct testimony that Mars hosted vastly more water in its early youth than nowadays. Estimates of the total amount of water lost to space from the current mean D/H value depend on a rigorous appraisal of the relative escape between deuterated and non-deuterated water. Isotopic fractionation of D/H between the lower and the upper atmospheres of Mars has been assumed to be controlled by water condensation and photolysis, although their respective roles in influencing the proportions of atomic D and H populations have remained speculative. Here we report HDO and H2O profiles observed by the Atmospheric Chemistry Suite (ExoMars Trace Gas Orbiter) in orbit around Mars that, once combined with expected photolysis rates, reveal the prevalence of the perihelion season for the formation of atomic H and D at altitudes relevant for escape. In addition, while condensation-induced fractionation is the main driver of variations of D/H in water vapour, the differential photolysis of HDO and H2O is a more important factor in determining the isotopic composition of the dissociation products.

Abstract:

The current Martian atmosphere is about five times more enriched in deuterium than Earth’s, providing direct testimony that Mars hosted vastly more water in its early youth than nowadays. Estimates of the total amount of water lost to space from the current mean D/H value depend on a rigorous appraisal of the relative escape between deuterated and non-deuterated water. Isotopic fractionation of D/H between the lower and the upper atmospheres of Mars has been assumed to be controlled by water condensation and photolysis, although their respective roles in influencing the proportions of atomic D and H populations have remained speculative. Here we report HDO and H2O profiles observed by the Atmospheric Chemistry Suite (ExoMars Trace Gas Orbiter) in orbit around Mars that, once combined with expected photolysis rates, reveal the prevalence of the perihelion season for the formation of atomic H and D at altitudes relevant for escape. In addition, while condensation-induced fractionation is the main driver of variations of D/H in water vapour, the differential photolysis of HDO and H2O is a more important factor in determining the isotopic composition of the dissociation products.