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Abstract:

The origin of the red colouration in Jupiter's Great Red Spot (GRS) is a long-standing question in planetary science. While several candidate chromophores have been proposed, no clear conclusions have been reached regarding its nature, evolution, or relationship to atmospheric dynamics. In this work, we perform microphysical simulations of the reddish haze over the GRS and quantify the production rates and timescales required to sustain it. Matching the previously reported chromophore column mass and effective radius in the GRS requires column-integrated injection fluxes in the range 1×10⁻¹²–7×10⁻¹² kg m⁻² s⁻¹, under low upwelling velocities in the upper troposphere (v<inf>trop</inf>≲1.5×10⁻⁴ m s⁻¹) and particle charges of at least 20 electrons/μm. Such rates exceed the mass flux that standard photochemical models of Jupiter currently supply via NH<inf>3</inf>–C<inf>2</inf>H<inf>2</inf> photochemistry at 0.1–0.2 bar, the most popular chromophore pathway in recent literature. We find a lower limit of 7 years on the haze formation time. We also assess commonly used size and vertical distribution parameterisations for the chromophore haze, finding that eddy diffusion prevents the long-term confinement of a thin layer and that the extinction is dominated by particles that can be represented by a single log-normal size distribution.

Abstract:

The extreme conditions in Venus’s lower atmosphere make robust calibration of in situ observations challenging. Consequently, measurements from past entry probes provided mixed evidence regarding the existence of a near-surface particulate layer (NSPL). Although the Venera 11 (1978) and Venera 13 and 14 (1982) landers performed in situ spectrophotometric observations during descent, the original datasets were later lost. However, a subset has been reconstructed by digitising graphical outputs produced during the missions’ initial data-processing phase [1]. Following careful analysis to identify and mitigate errors and other artefacts, the reconstructed dataset retains the reliable downward-looking spectra acquired by the three landers from ~62 km altitude to the surface.Previous retrievals from the reconstructed Venera 13 indicated an NSPL centred at ~3.5–5 km, with particulate optical properties consistent with a basaltic composition [2]. Following the methodology of [2], we use NEMESIS, a radiative transfer and retrieval code [3], to perform near-surface retrievals from the reconstructed Venera 11 and Venera 14 datasets. The results from Venera 11, 13, and 14 retrievals are compared with reported detections and non-detections from other instruments on earlier in situ missions, to explore potential formation pathways for the NSPL in light of the combined observational record.References:[1] Ignatiev, N. I., Moroz, V. I., Moshkin, B. E., Ekonomov, A. P., Gnedykh, V. I., Grigor’ev, A. V., and Khatuntsev, I. V. Cosmic Research 35(1), 1–14 (1997).[2] Kulkarni, S. V., Irwin, P. G. J., Wilson, C. F., & Ignatiev, N. I. Journal of Geophysical Research: Planets, 130, e2024JE008728, (2025).[3] Irwin, P. G., Teanby, N. A., de Kok, R., Fletcher, L. N., Howett, C. J., Tsang, C. C., Wilson, C. F., Calcutt, S. B., Nixon, C. A., and Parrish, P. D. Journal of Quantitative Spectroscopy and Radiative Transfer 109(6), 1136–1150 (2008). 

Abstract:

The ExoMars Trace Gas Orbiter (TGO) has characterised trace gases in the Martian atmosphere over several Mars years, improving the accuracy of species concentration measurements and observing temporal, vertical and spatial variations. Hydrogen chloride—detected for the first time with TGO [1,2]—has been investigated recently using the mid-infrared channel on the Atmospheric Chemistry Suite (ACS MIR). HCl observations show a strong seasonal variation, with almost all of the detections occurring during the latter half of the year (solar longitudes 180-360°) in the dusty season, when water vapour is present in the Martian atmosphere and ozone concentrations are low. Chlorine-bearing species such as HCl are important to understand in Mars’ atmosphere because on Earth they are involved in numerous processes throughout the planetary system, including volcanism, and they play a key role in atmospheric chemistry, e.g., by influencing concentrations of oxidative species such as oxygen (O2) and ozone (O3).Here, we use the Mars Planetary Climate Model—a 3-D global climate model that includes a photochemical network—to explore the atmospheric HCl observations. We build on existing chlorine photochemical networks [3,4] to investigate potential source and sink mechanisms, focusing in particular on heterogeneous chemistry involving ice aerosols, and exploring the possibility of its role in direct release of HCl to the atmosphere. We also explore how chlorine species are affected indirectly by changes in the abundances of oxidative species (e.g., OH and HO2,and by extension, O and O3),driven by heterogeneous chemistry. Understanding the role of oxidative chemistry on HCl and other trace gases is key to achieving a more complete picture of processes occurring in the present-day Mars atmosphere, as well as processes that have shaped its evolution and habitability.[1] Korablev O. I. et al. (2021). Sci. Adv., 7, eabe4386. [2] Olsen K. S. et al. (2021). Astron. Astrophys., 647, A161. [3] Rajendran, K. et al. (2025). JGR: Planets 130(3), p.e2024JE008537. [4] Streeter, P. M. et al. (2025). GRL 52(6), p.e2024GL111059.

Abstract:

Hydration on the Moon’s surface is widely detected in orbital datasets (e.g. M3 on Chandrayan-1), yet its abundance and physical form (-OH, H2O, frost, and/or ice) remain poorly constrained. The lunar surface is covered in regolith fines, which impacts local thermophysical conditions, obscures underlying volatiles and modifies detectable hydration bands. Our interpretation of hydration form and abundance on the lunar surface is further limited by existing experimental constraints of water-ice spectral behaviour at the regolith interface (photometric effects) and by the restriction of current orbital datasets to the near-infrared (< ~3 µm O–H stretching mode). We are developing a laboratory approach to quantify how dust layering, regolith maturity, grain size, composition, and ice abundance control the spectral expression of water-ice across the near- and mid-infrared (1.8–20 µm), with emphasis on the ~3 and 6 µm diagnostic regions. This poster presents a preliminary experimental set-up developed ahead of the full operation of a custom-built vacuum chamber, Polar Analogue of Dust Overlying Regolith–Ice (PANDOR-I), intended to simulate airless-body and cryogenic polar conditions. In this initial laboratory set-up, the sample compartment of a Bruker 70V Fourier Transform Infrared (FTIR) spectrometer is isolated using potassium bromide (KBr) windows to enable controlled, low-pressure (~0.2 mbar) reflectance measurements of anhydrous and hydrated analogue configurations to (i) characterise the spectral expression of hydration-related structure in the ~3 and 6 µm regions under regolith simulant fines, and (ii) provide benchmark spectra for direct comparison with a Mie–Hapke forward model (band shape,depth, and mixing trends) prior to cryogenic and airless body simulations with PANDOR-I. This preliminary work will establish an empirical reference for model validation and for designing the subsequent PANDOR-I cryogenic experiments, enabling a more robust interpretation of spectrally mixed hydration signatures in forthcoming lunar datasets.