Properties of Water Ice and Dust Particles in the Atmosphere of Mars During the 2018 Global Dust Storm as Inferred From the Atmospheric Chemistry Suite

The properties of Martian aerosols are an integral part of the planetary climatology. Global dust storms (GDS) significantly alter spatial and vertical distributions of dust and water ice aerosols and their microphysical properties. We explored the 2018/Martian year 34 GDS with the Atmospheric Chemistry Suite instrument onboard the ESA-Roscosmos Trace Gas Orbiter mission. Solar occultation observations of thermal infrared and near infrared channels in the 0.7-6 μm spectral range with >103 signal-to-noise ratio are used to constrain the vertical dependence and the temporal evolution of the particle properties of water ice and dust (effective radius, effective variance, number density, and mass loading) before the 2018 GDS and during its onset and decay phases. In most of the observations, the particle size of dust and water ice decreases with altitude. The effective radius of dust and water ice particles ranges in 0.1−3.5 μm and 0.1−5.5 μm, respectively. The largest aerosol particles (>2.5 μm for dust and >3.5 μm for water ice) are present below 10 km before the onset and during the GDS decay phase. During the peak of the GDS, dust reached altitudes of 85 km; the most frequently observed effective radius is 1−2μm with 0.1−1 cm−3 number density and 0.1 effective variance. Detached layers of water ice composed of 0.1−1 μm particles are systematically observed at 50−100 km during this period. Below, at 0−50 km, we see the dust mixed with the main water ice layer comprising 1−4 μm particles.ExoMars is a space mission of ESA and Roscosmos. The ACS experiment is led by IKI, the Space Research Institute in Moscow, assisted by LATMOS in France. The science operations of ACS are funded by Roscosmos and ESA. We are grateful to Michael Wolff, an anonymous reviewer, and Journal of Geophysical Research: Planets editorial board whose comments helped to improve this paper. The early retrievals in 2019 were supported by Ministry of Science and Education of the Russian government. M. Luginin, A. Fedorova, N. Ignatiev, A. Trokhimovskiy, and O. Korablev acknowledge RSF funding of Sections 4 and 5 under grant number 20-42-09035. F. Montmessin acknowl-edges funding from CNES and ANR (PRCI, CE31 AAPG2019)

Martian Atmospheric Spectral End-Members Retrieval From ExoMars Thermal Infrared (TIRVIM) Data

Key knowledge about planetary composition can be recovered from the study of thermal infrared spectral range datasets. This range has a huge diagnostic potential because it contains diagnostic absorptions from a planetary surface and atmosphere. The main goal of this study is to process and interpret the dataset from the Thermal Infrared channel (TIRVIM) which is part of the Atmospheric Chemistry Suite of the ExoMars2016 Trace Gas Orbiter mission to find and characterize dust and water ice clouds in the atmosphere. The method employed here is based on the application of principal component analysis and target transformation techniques to extract the independent variable components present in the analyzed dataset. Spectral shapes of both atmospheric dust and water ice aerosols have been recovered from the analysis of TIRVIM data. The comparison between our results with those previously obtained on Thermal Emission Spectrometer (TES) data and with previous analysis on TIRVIM data, validates the methodology here applied, showing that it allows to correctly recover the atmospheric spectral endmembers present in the TIRVIM data. Moreover, comparison with atmospheric retrievals on PFS, TES and IRIS data, allowed us to assess the temporal stability and homogeneity of dust and water ice components in the Martian atmosphere over a time period of almost 50 years

The Atmospheric Chemistry Suite (ACS) of Three Spectrometers for the ExoMars 2016 Trace Gas Orbiter

The Atmospheric Chemistry Suite (ACS) package is an element of the Russian contribution to the ESA-Roscosmos ExoMars 2016 Trace Gas Orbiter (TGO) mission. ACS consists of three separate infrared spectrometers, sharing common mechanical, electrical, and thermal interfaces. This ensemble of spectrometers has been designed and developed in response to the Trace Gas Orbiter mission objectives that specifically address the requirement of high sensitivity instruments to enable the unambiguous detection of trace gases of potential geophysical or biological interest. For this reason, ACS embarks a set of instruments achieving simultaneously very high accuracy (ppt level), very high resolving power (>10,000) and large spectral coverage (0.7 to 17 μm—the visible to thermal infrared range). The near-infrared (NIR) channel is a versatile spectrometer covering the 0.7–1.6 μm spectral range with a resolving power of ∼20,000. NIR employs the combination of an echelle grating with an AOTF (Acousto-Optical Tunable Filter) as diffraction order selector. This channel will be mainly operated in solar occultation and nadir, and can also perform limb observations. The scientific goals of NIR are the measurements of water vapor, aerosols, and dayside or night side airglows. The mid-infrared (MIR) channel is a cross-dispersion echelle instrument dedicated to solar occultation measurements in the 2.2–4.4 μm range. MIR achieves a resolving power of >50,000. It has been designed to accomplish the most sensitive measurements ever of the trace gases present in the Martian atmosphere. The thermal-infrared channel (TIRVIM) is a 2-inch double pendulum Fourier-transform spectrometer encompassing the spectral range of 1.7–17 μm with apodized resolution varying from 0.2 to 1.3 cm−1. TIRVIM is primarily dedicated to profiling temperature from the surface up to ∼60 km and to monitor aerosol abundance in nadir. TIRVIM also has a limb and solar occultation capability. The technical concept of the instrument, its accommodation on the spacecraft, the optical designs as well as some of the calibrations, and the expected performances for its three channels are described

Reappraising the production and transfer of hydrogen atoms from the middle to the upper atmosphere of Mars at times of elevated water vapor

Water escape on Mars has recently undergone a paradigm shift with the discovery of unexpected seasonal variations in the population of hydrogen atoms in the exosphere where thermal escape occurs and results in water lost to space. This discovery led to the hypothesis that, contradicting the accepted pathway, atomic hydrogen in the exosphere was not only produced by molecular hydrogen but mostly by high altitude water vapor. Enhanced presence of water at high altitude during southern spring and summer, due to atmospheric warming and intensified transport, favors production of H through photon-induced ion chemistry of water molecules and thus appears to be the main cause of the observed seasonal variability in escaping hydrogen. This hypothesis is supported by the observation of large concentrations of water vapor between 50 km and 150 km during the southern summer solstice and global dust events. Using a simplified yet representative air parcel transport model, we show that in addition to the formation of atomic hydrogen from water photolysis above 80 km, a major fraction of the exospheric hydrogen is formed at altitudes as low as 60 km and is then directly advected to the upper atmosphere. Comparing the injection modes of a variety of events (global dust storm, perihelion periods, regional storm), we conclude that southern spring/summer controls H production and further ascent into the upper atmosphere on the long term with direct implication for water escape

Upper limits for phosphine (PH₃) in the atmosphere of Mars

Phosphine (PH3) is proposed to be a possible biomarker in planetary atmospheres and has been claimed to have been observed in the atmosphere of Venus, sparking interest in the habitability of Venus’s atmosphere. Observations of another biomarker, methane (CH4), have been reported several times in the atmosphere of Mars, hinting at the possibility of a past or present biosphere. The Atmospheric Chemistry Suite on the ExoMars Trace Gas Orbiter has a spectral range that includes several absorption lines of PH3 with line strengths comparable to previously observed CH4 lines. The signature of PH3 was not observed in the 192 observations made over a full Martian year of observations, and here we report upper limits of 0.1–0.6 ppbv

Seasonal changes in the vertical structure of ozone in the Martian lower atmosphere and its relationship to water vapour

The mid-infrared channel of the Atmospheric Chemistry Suite (ACS MIR) onboard the ExoMars Trace Gas Orbiter is capable of observing the infrared absorption of ozone (O3) in the atmosphere of Mars. During solar occulations, the 003←000 band (3000-3060 cm-1) is observed with spectral sampling of ∼0.045 cm-1. Around the equinoxes in both hemispheres and over the southern winters, we regularly observe around 200-500 ppbv of O3 below 30 km. The warm southern summers, near perihelion, produce enough atmospheric moisture that O3 is not detectable at all, and observations are rare even at high northern latitudes. During the northern summers, water vapour is restricted to below 10 km, and an O3 layer (100-300 ppbv) is visible between 20-30 km. At this same time, the aphelion cloud belt forms, condensing water vapour and allowing O3 to build up between 30-40 km. A comparison to vertical profiles of water vapour and temperature in each season reveals that water vapour abundance is controlled by atmospheric temperature, and H2O and O3 are anti-correlated as expected. When the atmosphere cools, over time or over altitude, water vapour condenses (observed as a reduction in its mixing ratio) and the production of odd hydrogen species is reduced, which allows O3 to build up. Conversely, warmer temperatures lead to water vapour enhancements and ozone loss. The LMD Mars Global Climate Model is able to reproduce vertical structure and seasonal changes of temperature, H2O, and O3 that we observe. However, the observed O3 abundance is larger by factors between 2 and 6, indicating important differences in the rate of odd-hydrogen photochemistry

Expected Performances of the NOMAD/ExoMars instrument

NOMAD (Nadir and Occultation for MArs Discovery) is one of the four instruments on board the ExoMars Trace Gas Orbiter, scheduled for launch in March 2016. It consists of a suite of three high-resolution spectrometers – SO (Solar Occultation), LNO (Limb, Nadir and Occultation) and UVIS (Ultraviolet and Visible Spectrometer). Based upon the characteristics of the channels and the values of Signal-to-Noise Ratio obtained from radiometric models discussed in [Vandaele et al., Optics Express, 2015] and [Thomas et al., Optics Express, 2015], the expected performances of the instrument in terms of sensitivity to detection have been investigated. The analysis led to the determination of detection limits for 18 molecules, namely CO, H2O, HDO, C2H2, C2H4, C2H6, H2CO, CH4, SO2, H2S, HCl, HCN, HO2, NH3, N2O, NO2, OCS, O3. NOMAD should have the ability to measure methane concentrations <25 parts per trillion (ppt) in solar occultation mode, and 11 parts per billion in nadir mode. Occultation detections as low as 10 ppt could be made if spectra are averaged [Drummond et al., Planetary Space and Science, 2011]. Results have been obtained for all three channels in nadir and in solar occultation

Annual Appearance of Hydrogen Chloride on Mars and a Striking Similarity With the Water Vapor Vertical Distribution Observed by TGO/NOMAD

Hydrogen chloride (HCl) was recently discovered in the atmosphere of Mars by two spectrometers onboard the ExoMars Trace Gas Orbiter. The reported detection made in Martian Year 34 was transient, present several months after the global dust storm during the southern summer season. Here, we present the full data set of vertically resolved HCl detections obtained by the NOMAD instrument, which covers also Martian year 35. We show that the particular increase of HCl abundances in the southern summer season is annually repeated, and that the formation of HCl is independent from a global dust storm event. We also find that the vertical distribution of HCl is strikingly similar to that of water vapor, which suggests that the uptake by water ice clouds plays an important role. The observed rapid decrease of HCl abundances at the end of the southern summer would require a strong sink independent of photochemical loss

Water Vapor Vertical Profiles on Mars in Dust Storms Observed by TGO/NOMAD

It has been suggested that dust storms efficiently transport water vapor from the near‐surface to the middle atmosphere on Mars. Knowledge of the water vapor vertical profile during dust storms is important to understand water escape. During Martian Year 34, two dust storms occurred on Mars: a global dust storm (June to mid‐September 2018) and a regional storm (January 2019). Here we present water vapor vertical profiles in the periods of the two dust storms (Ls = 162–260° and Ls = 298–345°) from the solar occultation measurements by Nadir and Occultation for Mars Discovery (NOMAD) onboard ExoMars Trace Gas Orbiter (TGO). We show a significant increase of water vapor abundance in the middle atmosphere (40–100 km) during the global dust storm. The water enhancement rapidly occurs following the onset of the storm (Ls~190°) and has a peak at the most active period (Ls~200°). Water vapor reaches very high altitudes (up to 100 km) with a volume mixing ratio of ~50 ppm. The water vapor abundance in the middle atmosphere shows high values consistently at 60°S‐60°N at the growth phase of the dust storm (Ls = 195°–220°), and peaks at latitudes greater than 60°S at the decay phase (Ls = 220°–260°). This is explained by the seasonal change of meridional circulation: from equinoctial Hadley circulation (two cells) to the solstitial one (a single pole‐to‐pole cell). We also find a conspicuous increase of water vapor density in the middle atmosphere at the period of the regional dust storm (Ls = 322–327°), in particular at latitudes greater than 60°S