Planetary atmosphere observation analysis

Abstract:

Selected in 2019 as a NASA SIMPLEx mission, Lunar Trailblazer is in implementation for flight system delivery at the end of 2022. The mission's goal is to understand the form, abundance, and distribution of water on the Moon and the lunar water cycle. Lunar Trailblazer also collects data of candidate landing sites to inform planning for future human and robotic exploration of the Moon and evaluate the potential for in situ resource utilization. Lunar Trailblazer's two science instruments, the High-resolution Volatiles and Minerals Moon Mapper (HVM3) and the Lunar Thermal Mapper (LTM) provide simultaneous high-resolution spectral imaging data to map OH/water, crustal composition, and thermophysical properties from a 100pm 30 km lunar polar orbit. The ∼210-kg flight system deploys from an ESPA Grande and utilizes a ∼1000 m/s Deltamathrm{V} hydrazine chemical propulsion system, similar to that employed by GRAIL. Trailblazing elements include the novel state-of-the-art dataset collected at substantially reduced price point, fully geographically co-registered data products delivered to the Planetary Data System, planetary mission team demographics, Caltech campus mission operations, and student staffing of select mission ops roles. Lunar Trailblazer's pioneering development is providing key lessons learned for future planetary small spacecraft.

Abstract:

In this study, we applied a sum to one constraint weighted least squares (STO WLS) model to thermal infrared (TIR) spectra of a suite of primitive asteroid analogs spectrally and volumetrically dominated by fine particulates (<38 μm). Since coarse particulate emissivity spectra combine linearly, deriving compositions from these are fairly straightforward. Across the TIR it is not as straightforward for fine particulate emissivity spectra due to the nonlinear behavior that arises from volumetric scattering between particles when the particle size becomes comparable to the wavelength of light. Using a WLS model, mixed spectra may be deconvolved into areal percentages of each end member which we assume corresponds to their volume percentages. We used a spectral library of pure mineral spectra to model TIR spectra of a suite of physical mixtures and meteorites obtained under ambient (Earth-like) and simulated asteroid environment (SAE) conditions collected for the OSIRIS-REx team (Donaldson Hanna et al., 2021, https://doi.org/10.1029/2020JE006624). The STO WLS model underestimated the modal abundances of the dominant mineral phases by ∼25.0 ± 0.1% on average over the full spectral range and ∼22.0 ± 0.4% over a limited spectral range in all of the ambient and SAE physical mixture and meteorite spectra. Minor phases present in the mixtures and meteorites (abundances ≤5%) were typically not modeled. Also, phases not present in the mixtures were commonly selected (∼2 phases on average with an average abundance of ∼25.2 ± 1.9%) to get the best mathematical fit.

Abstract:

Abstract Curiously, n-butane has yet to be detected at Titan, though it is predicted to be present in a wide range of abundances that span over 2.5 orders of magnitude. We have searched infrared spectroscopic observations of Titan for signals from n-butane (n-C4H10) in Titan’s stratosphere. Three sets of Cassini Composite Infrared Spectrometer Focal Plane 4 (1050–1500 cm−1) observations were selected for modeling, having been collected from different flybys and pointing latitudes. We modeled the observations with the Nonlinear Optimal Estimator for MultivariatE Spectral AnalySIS radiative transfer tool. Temperature profiles were retrieved for each of the data sets by modeling the ν 4 emission from methane near 1305 cm−1. Then, incorporating the temperature profiles, we retrieved abundances of all of Titan’s known trace gases that are active in this spectral region, reliably reproducing the observations. We then systematically tested a set of models with varying abundances of n-butane, investigating how the addition of this gas affected the fits. We did this for several different photochemically predicted abundance profiles from the literature, as well as for a constant-with-altitude profile. Ultimately, though we did not produce any firm detection of n-butane, we derived new upper limits on its abundance specific to the use of each profile and to multiple different ranges of stratospheric altitudes. These results will tightly constrain the C4 chemistry of future photochemical modeling of Titan’s atmosphere and also motivate the continued search for n-butane and its isomer, isobutane.

Abstract:

Context. The detection of sulphur species in the Martian atmosphere would be a strong indicator of volcanic outgassing from the surface of Mars.
Aims. We wish to establish the presence of SO2, H2S, or OCS in the Martian atmosphere or determine upper limits on their concentration in the absence of a detection.
Methods. We perform a comprehensive analysis of solar occultation data from the mid-infrared channel of the Atmospheric Chemistry Suite instrument, on board the ExoMars Trace Gas Orbiter, obtained during Martian years 34 and 35.
Results. For the most optimal sensitivity conditions, we determine 1σ upper limits of SO2 at 20 ppbv, H2S at 15 ppbv, and OCS at 0.4 ppbv; the last value is lower than any previous upper limits imposed on OCS in the literature. We find no evidence of any of these species above a 3σ confidence threshold. We therefore infer that passive volcanic outgassing of SO2 must be below 2 ktons day−1.