Explore the vast range of titles available.

The loss of water from Mars to space is thought to result from the transport of water to the upper atmosphere, where it is dissociated to hydrogen and escapes the planet. Recent observations have suggested large, rapid seasonal intrusions of water into the upper atmosphere, boosting the hydrogen abundance. We use the Atmospheric Chemistry Suite on the ExoMars Trace Gas Orbiter to characterize the water distribution by altitude. Water profiles during the 2018–2019 southern spring and summer stormy seasons show that high-altitude water is preferentially supplied close to perihelion, and supersaturation occurs even when clouds are present. This implies that the potential for water to escape from Mars is higher than previously thought.

Recent observations from the ExoMars Trace Gas Orbiter (TGO) have revealed the presence of hydrogen chloride (HCl) in the martian atmosphere. HCl shows strong seasonality, primarily appearing during Mars' perihelion period before decreasing faster than projected from photolysis and gas‐phase chemistry. HCl profiles also display local anti‐correlation with water ice aerosol. One candidate explanation is heterogeneous chemistry. We present the first results from a heterogeneous chlorine chemistry scheme incorporated into a Mars global climate model (GCM), with atmospheric dust/water ice parameterized as an HCl source/sink respectively. Results were compared against a Mars GCM with gas‐phase only chlorine chemistry and observations from TGO's Atmospheric Chemistry Suite. We found that the heterogeneous scheme significantly improved the modeled HCl seasonal, latitudinal, and vertical distribution, supporting a crucial role for heterogeneous chemistry in Mars' chlorine cycle. Remaining discrepancies show that further work is needed to characterize the exact aerosol reactions involved. Plain Language Summary The ExoMars Trace Gas Orbiter (TGO) recently detected hydrogen chloride (HCl) for the first time in the martian atmosphere. Observations show that HCl appears around southern summer, when Mars is closest to the Sun, and abruptly decreases at the end of this season. This variation occurs on timescales far shorter than the expected photochemical lifespan of HCl, implying other processes are responsible. One possible explanation is heterogeneous chemistry: reactions between gaseous species and atmospheric dust and/or water ice. To investigate we implemented such a scheme into a Mars global climate model, whereby atmospheric dust and water ice aerosol act (respectively) as a source and sink for HCl. Comparing to TGO observations, we found that including heterogeneous chemistry significantly improved HCl representation. We were able to reproduce key observed features such as the HCl seasonal cycle, the greater HCl presence in the southern hemisphere, and to an extent the complex vertical structure. This strongly suggests that heterogeneous chemistry is a crucial component of the martian chlorine cycle. However, some questions remain, such as whether there is a causal relationship between dust storms and HCl presence. Further work is therefore needed to understand the relationships between aerosols and chlorine species. Key Points Latitudinal and seasonal behavior of observed Mars atmospheric hydrogen chloride (HCl) can be explained by heterogeneous chlorine chemistry Observed seasonal, hemispheric, and vertical HCl variation is qualitatively captured by heterogeneous dust emission and ice absorption We also predict enhanced north polar HCl during the aphelion season, not currently seen in Trace Gas Orbiter observations

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 H 2 O 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 H 2 O is a more important factor in determining the isotopic composition of the dissociation products. Three years of observations with the ExoMars TGO Atmospheric Chemistry Suite have clarified the mechanism of atmospheric water loss from Mars, and particularly the fraction of deuterium compared with hydrogen. Analysis of several isotopologues of water in the mid-atmosphere of Mars shows that atomic H and D are produced at perihelion in relative amounts controlled by photolysis. These atoms are able to escape from the atmosphere.

The atmosphere of Mars is enriched in heavy isotopes with respect to Earth as a result of the escape of the atmosphere to space over billions of years. Estimating this enrichment requires a rigorous understanding of all atmospheric processes that contribute to the evolution of isotopic ratios between the lower and upper atmosphere, where escape processes take place. We combine measurements of CO vertical profiles obtained by the Atmospheric Chemistry Suite on board the ExoMars Trace Gas Orbiter with the predictions of a photochemical model and find evidence of a process of photochemistry-induced fractionation that depletes the heavy isotopes of C and O in CO (δ13C = −160 ± 90‰ and δ18O = −20 ± 110‰). In the upper atmosphere, accounting for this process reduces the escape fractionation factor by ~25%, suggesting that less C has escaped from the atmosphere of Mars than previously thought. In the lower atmosphere, incorporation of this 13C-depleted CO fractionation into the surface could support the abiotic origin of recently found Martian organics.Measurements by the ExoMars Trace Gas Orbiter reveal a depletion of heavy CO isotopes in Mars’s atmosphere caused by photochemistry-induced fractionation. The observed depletion in heavy C has implications for our understanding of C escape to space and the formation of organic material on Mars’s surface.

Global dust storms on Mars are rare1,2 but can affect the Martian atmosphere for several months. They can cause changes in atmospheric dynamics and inflation of the atmosphere3, primarily owing to solar heating of the dust3. In turn, changes in atmospheric dynamics can affect the distribution of atmospheric water vapour, with potential implications for the atmospheric photochemistry and climate on Mars4. Recent observations of the water vapour abundance in the Martian atmosphere during dust storm conditions revealed a high-altitude increase in atmospheric water vapour that was more pronounced at high northern latitudes5,6, as well as a decrease in the water column at low latitudes7,8. Here we present concurrent, high-resolution measurements of dust, water and semiheavy water (HDO) at the onset of a global dust storm, obtained by the NOMAD and ACS instruments onboard the ExoMars Trace Gas Orbiter. We report the vertical distribution of the HDO/H2O ratio (D/H) from the planetary boundary layer up to an altitude of 80 kilometres. Our findings suggest that before the onset of the dust storm, HDO abundances were reduced to levels below detectability at altitudes above 40 kilometres. This decrease in HDO coincided with the presence of water-ice clouds. During the storm, an increase in the abundance of H2O and HDO was observed at altitudes between 40 and 80 kilometres. We propose that these increased abundances may be the result of warmer temperatures during the dust storm causing stronger atmospheric circulation and preventing ice cloud formation, which may confine water vapour to lower altitudes through gravitational fall and subsequent sublimation of ice crystals3. The observed changes in H2O and HDO abundance occurred within a few days during the development of the dust storm, suggesting a fast impact of dust storms on the Martian atmosphere.

The surname of author Cathy Quantin-Nataf was misspelled ‘Quantin-Nata’, authors Ehouarn Millour and Roland Young were missing from the ACS and NOMAD Science Teams list, and minor changes have been made to the author and affiliation lists; see accompanying Amendment. These errors have been corrected online.

ACS is a set of spectrometers for atmospheric studies (Atmospheric Chemistry Suite). It is one of the Russian instruments for the Trace Gas Orbiter (TGO) of the Russian-European “ExoMars” program. The purpose of the experiment is to study the Martian atmosphere by means of two observations regimes: sensitive trace gases measurements in solar occultations and by monitoring the atmospheric state during nadir observations. The experiment will allow us to approach global problems of Mars research such as current volcanism, and the modern climate status and its evolution. Also, the experiment is intended to solve the mystery of methane presence in the Martian atmosphere. Spectrometers of the ACS set cover the spectral range from the near IR-range (0.7 μm) to the thermal IR-range (17 μm) with spectral resolution λ/Δλ reaching 50000. The ACS instrument consists of three independent IR spectrometers and an electronics module, all integrated in a single unit with common mechanical, electrical and thermal interfaces. The article gives an overview of scientific tasks and presents the concept of the experiment.

Retrieving the optical depth of the Martian clouds (\\(_cld\\)) is a powerful way to monitor their spatial and temporal evolution. However, such retrievals from nadir imagery rely on several assumptions, including the vertical structure of the clouds in the atmosphere. Here we compare the results of cloud optical depth retrievals at 320 nm from the Emirates eXploration Imager (EXI) onboard the Emirates Mars Mission (EMM) \"Hope\" orbiter performed using a basic uniform cloud profile used in previous studies and using derived cloud profiles obtained from near-simultaneous Solar Occultation observations in the 3.1-3.4 \\(\\)m spectral range from the Middle-Infrared channel of the Atmospheric Chemistry Suite (ACS) instrument onboard the ESA Trace Gas Orbiter (TGO). We show that the latitudinal dependence of the cloud vertical profiles can have a strong impact on the nadir retrievals; neglecting it can lead to a significant underestimation of \\(_cld\\) in the polar regions (up to 25 % to 50 %, depending on the vertical distribution of the dust in the atmosphere) and to a lesser extent, to an overestimation of \\(_cld\\) around the equator. We also discuss the impact of a vertically-dependent particle size profile, as previous studies have shown the presence of very small water ice particles at the top of the clouds. From this analysis, we provide recommendations for the improvement of water ice cloud parameterization in radiative transfer algorithms in nadir atmospheric retrievals.

The surname of author Cathy Quantin-Nataf was misspelled 'Quantin-Nata' , authors Ehouarn Millour and Roland Young were missing from the ACS Science Team list, and minor changes have been made to the author and affiliation lists; see accompanying Amendment. These errors have been corrected online.

In 2020, hydrogen chloride (HCl) in the gas phase was discovered in the atmosphere of Mars with the Atmospheric Chemistry Suite (ACS) onboard the Trace Gas Orbiter (TGO) mission (Korablev et al., 2021). Its volume mixing ratio (VMR) shows a seasonal increase of up to 5 ppbv during the perihelion season, followed by a sudden drop to undetectable levels, contradicting previous estimations of the HCl lifetime of several months. In the Earth's stratosphere, heterogeneous uptake of HCl onto water ice is known to be a major sink for this species. Modelling of associated chemistry involving heterogeneous reactions indicates that H2O ice becomes the most effective sink for HCl above 20 km with the characteristic time shorter than 12 hours. In this work, we use simultaneous measurements of water ice particles and HCl abundance obtained by the ACS instrument and show particular structures in the vertical profiles, forming detached layers of gas at the ice free altitudes ('ice-holes'). We demonstrate that the heterogeneous uptake of HCl onto water ice operates on Mars and is potentially a major mechanism regulating the HCl abundance in the atmosphere of Mars.