Prof. Patrick Irwin

Abstract:

The Ultraviolet Spectrograph (UVS) instrument on the Juno mission records far-ultraviolet reflected sunlight from Jupiter. These spectra are sensitive to the abundances of chemical species in the upper atmosphere and to the distribution of the stratospheric haze layer. We combine observations from the first 30 perijoves of the mission in order to study the meridional distribution of acetylene (C2H2) in Jupiter's stratosphere. We find that the abundance of C2H2 decreases toward the poles by a factor of 2–4, in agreement with previous analyses of mid-infrared spectra. This result is expected from insolation rates: near the equator, the UV solar flux is higher, allowing more C2H2 to be generated from the UV photolysis of CH4. The decrease in abundance toward the poles suggests that horizontal mixing rates are not rapid enough to homogenize the latitudinal distribution.

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.

Abstract:

NASA's Spitzer Infrared Spectrometer (IRS) acquired mid-infrared (5–37 μm) disc-averaged spectra of Uranus very near to its equinox in December 2007. A mean spectrum was constructed from observations of multiple central meridian longitudes, spaced equally around the planet, which has provided the opportunity for the most comprehensive globally-averaged characterisation of Uranus' temperature and composition ever obtained (Orton et al., 2014a,b). In this work we analyse the disc-averaged spectra at four separate central meridian longitudes to reveal significant longitudinal variability in thermal emission occurring in Uranus' stratosphere during the 2007 equinox. We detect a variability of up to 15% at wavelengths sensitive to stratospheric methane, ethane and acetylene at the ~0.1-mbar level. The tropospheric hydrogen‑helium continuum and deuterated methane absorption exhibit a negligible variation (less than 2%), constraining the phenomenon to the stratosphere. Building on the forward-modelling analysis of the global average study, we present full optimal estimation inversions (using the NEMESIS retrieval algorithm, Irwin et al., 2008) of the Uranus-2007 spectra at each longitude to distinguish between thermal and compositional variability. We found that the variations can be explained by a temperature change of less than 3 K in the stratosphere. Near-infrared observations from Keck II NIRC2 in December 2007 (Sromovsky et al., 2009; de Pater et al., 2011), and mid-infrared observations from VLT/VISIR in 2009 (Roman et al., 2020), help to localise the potential sources to either large scale uplift or stratospheric wave phenomena.