Space instrumentation

Abstract:

Venus is home to thousands of volcanoes, with a wide range of volumes and sizes. Its surface is relatively young, with a temperature of approximately 735 K and an atmosphere of 92 bar. Past and possible ongoing volcanic outgassing is expected to provide a source to the sustenance of this massive atmosphere, dominated by CO2 and SO2. The lower atmosphere can be investigated in the near-infrared transparency windows on the nightside, such as the 2.3μm thermal emission window, which provides a chance of detection of species with volcanic origin, such as water vapor. The Planetary Spectrum Generator was used to simulate the nightside 2.3μm thermal emission window of Venus. We simulated the effect of a volcanic gas plume rising to a ceiling altitude, for species such as H2O, CO, OCS, HF and SO2. The sensitivity of the radiance spectrum at different wavelengths was explored as an attempt to qualitatively access detection for future measurements of both ground-based and space-instrumentation. We conclude from our qualitative analysis that for the H2O, CO and OCS plumes simulated there is potential to achieve a detection in the future, given a minimum required signal-to-noise ratio of 50. For SO2 and HF plumes, a higher signal-to-noise ratio would be needed.

Abstract:

Research into compositions of small bodies and planetary surfaces, such as asteroids, is key to understanding the origin of water and organics on Earth [1], as well as placing constraints on planetary dynamics and migration models [2] that can help understand how planetary systems around other stars may form and evolve. Compositional estimates can be found with thermal infrared (TIR; 5-25μm) spectroscopy, as the TIR region is rich in diagnostic information and can be used in remote sensing observations and laboratory measurements. However, TIR spectra of the same material may appear differently depending on several factors, such as particle size, surface roughness, porosity etc. This work quantifies the changes in spectral morphology (i.e., shapes and depths of spectral features) as particle size transitions from fine (90%), at several size fractions, aimed to be

Abstract:

Over four decades have elapsed since the last in situ spectrophotometric observations of the Venusian atmosphere, specifically from the Venera 11 (1978) and Venera 13 and 14 (1982) missions. These missions recorded spectral data during their descent from approximately 62 km to the surface. Unfortunately, the original data were lost; however, a portion has been reconstructed by digitising the graphical outputs that were generated during the initial data processing phase of each of the three missions [1]. This reconstructed data is crucial as it remains the sole set of in situ spectrophotometric observations of Venus’s atmosphere and is likely to be so for the foreseeable future.While re-analysing the reconstructed Venera datasets, we identified several artefacts, errors and sources of noise, necessitating the implementation of some corrections and validation checks to isolate the most unaffected part of the reconstructed data. Then, using NEMESIS, a radiative transfer and retrieval tool [2], we conducted a series of retrievals to simultaneously fit the downward-going spectra at all altitudes. During this process, several parameters were retrieved. The first set of retrievals focused on the structure of the main cloud deck (MCD), which includes the cloud base altitude and abundance profiles of all four cloud modes. Previous corrections that were used to account for the effect of the unknown UV absorber did not result in good fits with the spectra shortward of 0.6 µm. Hence, we derived a new correction by retrieving the imaginary refractive index spectra of the Mode 1 particles.In the next phase, the MCD retrievals were used to update the model atmospheres for each of the missions. Then, the H2O volume mixing ratio profiles were retrieved and compared with the previous retrievals using the same data by [1] along with other remote sensing observations. The final retrieval phase concentrated on characterising particulate matter in the deep atmosphere. In [3], we outlined a methodology for retrieving a near-surface particulate layer using the reconstructed Venera 13 dataset. In this new work, we apply this methodology to encompass the Venera 11 and 14 datasets and compare the retrievals from the three datasets.This research thus provides a comprehensive overview of three distinct retrievals: 1) main cloud deck, 2) H2O, and 3) near-surface particulates using the reconstructed spectrophotometric data of Venera 11, 13, and 14.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] 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).[3] Kulkarni, S. V., Irwin, P. G. J., Wilson, C. F., & Ignatiev, N. I. Journal of Geophysical Research: Planets, 130, e2024JE008728, (2025).

Abstract:

Introduction: The origins of Mars' moons, Phobos and Deimos, remain uncertain, with two main hypotheses under consideration: formation from debris following a high-energy impact between Mars and an asteroid [1], or capture of primitive asteroids [2]. To address this, JAXA's Martian Moons eXploration (MMX) mission aims to return samples from Phobos by 2031 [3]. The characterisation of these samples will determine the origin of Phobos.To ground-truth remote observations of Phobos, we have used X-ray diffraction (XRD), and Fourier transform infrared (FTIR) reflectance spectroscopy to characterise the bulk mineralogy and IR spectral properties of ureilites, carbonaceous and ordinary chondrites, the composition of which could be indicative of a captured asteroid [4], and Martian meteorites that could represent a collisional formation. By acquiring XRD and IR data from the same material, mineral abundances can be directly correlated with features in reflectance spectra [5]. When MMX reaches Phobos, meteorite data collected in the laboratory will play a crucial role towards interpreting the mineralogy and composition of materials on its surface.Methods: We have characterised the mineralogy and spectral properties of six CM (Mighei-like) carbonaceous chondrites, Tarda (C2-ung), the CO (Ornans-like) chondrite Kainsaz, a range of shock darkened ordinary chondrites (mostly falls) including L4-6, and H5-6, four CR2 chondrites, four ureilites, Martian meteorites Nakhla and Tissint, and a Tagish Lake (C2-ung) based simulant created by the University of Tokyo, known as UTPS-TB [6]. For the meteorites, chips of approximately 200 mg were ground to produce powders with grain sizes of less than 40 microns. The UTPS-TB sample came in a powdered form which was ground to the same grain size as the meteorites.Diffuse reflectance spectra (1.7 - 50 μm) were collected using a Bruker VERTEX 70V FTIR spectrometer at the University of Oxford Planetary Spectroscopy Facility. Spectra were calibrated at the start of each measurement day and between measurements of samples using a gold standard. The powdered sample was measured under a vacuum to reduce terrestrial atmospheric contributions.XRD patterns of the same powders were collected using an INEL X-ray diffractometer with a position-sensitive detector at the Natural History Museum, London. Around 50 mg of powdered sample was measured for 16 hours to achieve good signal-to-noise. Measurements of well-characterised standard minerals were collected for 30 minutes and compared with meteorite patterns to identify minerals and quantify their abundance in the sample [e.g. 7].Results & Discussion: The mineralogical and spectral characteristics of meteorites in this investigation are compared the reflectance spectra of Phobos’ surface. The CR chondrites are primitive, containing both anhydrous silicates (e.g. olivine and pyroxene) and aqueous alteration phases such as phyllosilicates, carbonates, magnetite, and sulfides. Their albedo is ~3-5% reflectance with a weak red slope in the visible to near-infrared (VNIR). The CRs have a 3 μm hydration band, due to partial aqueous alteration. Their low VNIR reflectance, red-sloped continuum, and weak 3 μm spectral absorption feature is like that of Phobos, supporting the captured asteroid origin theory. The CM chondrites share similar spectral features but have a lower albedo and a stronger μm hydration band, corresponding to a higher phyllosilicate composition.   The ureilites are achondritic ultramafic meteorites containing olivine, pyroxene and carbon phases. These samples have a low albedo (~6-15% in VNIR) due to their opaque carbonaceous composition. However, their VNIR spectra are blue-sloped, inconsistent with Phobos’ red-sloped spectra. Ureilites are also anhydrous and therefore lack the 3 μm hydration band seen in Phobos spectra. Their low reflectance and feature-poor spectra could resemble Phobos, however there is a significant difference in spectral slope and hydration features. Therefore, Phobos were composed of ureilitic material, its surface would need to be significantly modified by space weathering.Martian meteorites Nakhla (a nakhlite) and Tissint (a shergottite) have mineralogical and spectral features consistent with their basaltic origin. XRD measurements of these meteorites are dominated by pyroxene (augite, pigeonite), and olivine, consistent with their origin in the Martian crust. Their reflectance spectra have relatively high albedo, mafic absorption bands at ~1 and 2 μm, and a lack of hydration features. These features are inconsistent with the spectra of Phobos, which lack 1 or 2 μm bands and show significantly lower reflectance.CR and CM chondrites are the closest spectral match to Phobos from the samples studied. Their low albedo, red-sloped, hydrated spectra are consistent with surface measurements of Phobos. Ureilites share low reflectance but differ significantly in slope and hydration, while Martian meteorites differ in more spectral characteristics. These results support the interpretation that Phobos is composed of primitive, carbon-rich material, likely of outer solar system origin, and favour a capture scenario over a collisional formation from Martian ejecta. The similarities between the carbonaceous chondrites and Phobos indicates that the Martian moons may be captured asteroids and further demonstrates the importance of the MMX mission sample return for solving the mystery of their origin definitively.References: [1] R. Citron et al. (2015) Icarus 252:334-338. [2] M. Pajola et al. (2013) The Astrophysical Journal 777:127. [3] K. Kuramoto et al. (2022) Earth, Planets and Space 74:12. [4] K. D. Pang et al. (1978) Science 199(4324):64-66. [5] H. C. Bates et al. (2023) Meteoritics & Planetary Science 1-23. [6] H. Miyamoto et al. (2021) Earth, Planets and Space 73:1-17 [7] G. Cressey et al. (1996) Powder Diffraction 11:35-39.

Abstract:

Introduction: The Lunar Thermal Mapper (LTM) is a multispectral infrared radiometer, built by the Oxford Physics Instrumentation Group for the Lunar Trailblazer mission; a small satellite launched in February 2025 under NASA’s Small Innovative Missions for Planetary Exploration (SIMPLEx). Trailblazer aims to advance our understanding of the lunar water cycle by mapping surface temperature, water abundance, distribution and form (OH, H2O, ice) and silicate lithology (i.e., Si-O Christiansen spectral feature). LTM was developed to improve upon existing infrared instrumentation in lunar orbit (e.g., Diviner Lunar Radiometer Experiment, hereafter referred to as Diviner) to provide higher resolution temperature estimations and refine interpretations of thermophysical properties at the surface [2, 3]. Accurately determining surface temperatures on airless bodies is essential for deriving emissivity spectral features (such as the Christiansen Feature and Restrahlen bands, which are diagnostic of silicate lithologies) that are representative of the surface. Temperature errors can affect spectral shape, resulting in the misidentification of surface composition [5, 8].  Our team compared six methods for estimating LTM’s brightness temperature (BT), including the temperature retrieval approach used by Diviner, to (1) determine which method provides the most representative surface temperature and (2) assess how variations in BT estimation affect derived emissivity spectral shape. Despite challenges facing the Trailblazer mission, refining methods for BT estimation remains relevant to the planetary community, as future missions continue to depend on infrared instrumentation and accurate BT retrievals for remote compositional interpretation (e.g., LEAP, L-CIRiS, Europa Clipper).   Instrumentation: LTM is a 15-channel infrared imager that covers a range between 6 to 100 µm [2,3]. LTM advances infrared compositional analysis by incorporating eleven narrowband compositional filters across the 6.25 to 10 µm range. This expanded spectral coverage enables more precise characterization of key features, such as the Christiansen Feature, Reststrahlen bands, and transparency features, which are essential for identifying spectral endmembers (Table 1) [2,3].   LTM builds upon Diviner, a nine-channel instrument that has a broad spectral range from 0.3 to 400 µm (Table 1) [1]. Diviner’s three narrowband compositional channels, 7.55–8.05 µm (Channel 3), 8.10–8.40 µm (Channel 4), and 8.38–8.60 µm (Channel 5), are specifically tuned to capture the Christiansen Feature (CF), an emissivity peak that is diagnostic of broad silicate mineralogy and sensitive to variations in silica content [1,4].  Table 1: LTM and Diviner observational parameters.    Methodology: To assess BT and emissivity retrieval techniques for LTM, we measured four lunar analog samples under controlled laboratory conditions to retrieve high-resolution emission spectra. These laboratory spectra were down-sampled to match LTM’s narrowband spectral resolution. Six BT estimation methods were tested to determine how effectively each method preserved laboratory spectral shape and temperature. The following section describes the laboratory setup and the BT estimation methods examined in this study. Laboratory: Using the PASCALE (Planetary Analogue Surface Chamber for Asteroids and Lunar Environments) in conjunction with a Bruker 70V Fourier Transform Infrared (FTIR) spectrometer, we conducted thermal infrared measurements of four volcanic lunar analogue samples; dunite (Twin Sisters -1 and -2), basalt (BIR-1) and rhyolite (RGM-1) under controlled ambient conditions (350 K, 1000 mbar, N2 atmosphere) [4]. The integration of PASCALE with FTIR allows for the acquisition of thermal emission spectra (as opposed to typical laboratory reflectance), offering a more representative analog of data collected by orbiting infrared instrumentation. Spectra were measured across ~6000 to 350 cm⁻¹ at a resolution of 4 cm⁻¹. Quality assurance and calibration procedures followed established protocols outlined in [6,7,8].  BT Estimations: To evaluate BT performance at LTM’s spectral resolution, each sample’s measured radiance was convolved with LTM’s filter response to simulate instrument-resolution radiance. The resulting spectra were converted to BT using the Planck function. Seven distinct methods were applied to the LTM-resolution BT data to determine the maximum BT values for each sample (Table 2). Emissivity was subsequently derived as the ratio between the observed LTM-resolution radiance and an ideal blackbody at the retrieved maximum BT for each method across all samples. The accuracy of the BT estimation methods was assessed by comparing the resulting emissivity spectra and maximum BT values to the full laboratory reference data (350K and full resolution emissivity). Additionally, a focused comparison with Diviner’s BT retrieval method was conducted to identify method-specific discrepancies and evaluate cross-instrument consistency.Table 2: BT estimation methods Results & Discussion: Six BT estimation methods were applied to laboratory emissivity spectra of four lunar analogue samples (dunite, basalt, and rhyolite), as shown in Figure 2. The associated standard errors (SE) for each method are reported in Table 3. Among the tested approaches, four methods (3rd degree polynomial, quadratic, spline and narrowband maximum) showed close agreement with high-resolution laboratory spectra (Figure 2). Temperature variations across compositions were minor, with low SE values (Table 3).  Since the spline fit did not significantly outperform the simpler polynomial or narrowband methods, lower complexity approaches are preferred for LTM temperature retrievals, with a maximum SE of 3.42%.In contrast, due to limited spectral sampling, the Diviner method underestimates surface temperatures by up to 19 K (SE max: 5.55%) in the dunite (TS-2) sample. Expanding this analysis to include a broader range of lithologies or impacted processed samples would help assess whether the Diviner approach (and potential other methods with sparse spectral sampling) introduce systematic shifts in the Christiansen Feature (CF) position or affect the spectral shape relative to more spectrally resolved techniques.  Table 3: BT estimations and associated SE of temperature for dunite (TS-1, TS-2), basalt (BIR-1) and rhyolite (RGM-1). Fig 2: Six BT methods are fitted to laboratory emissivity spectra of four lunar analogues. Conclusion:Comparisons between BT estimation methods indicate the 3rd-degree polynomial, quadratic, and narrowband maximum methods offer the best agreement with laboratory data (SE max: 3.42%). Although Diviner’s method tends to underestimate surface temperatures (up to 19 K), it still preserves spectral shape and wavelength range, supporting the reliability of compositional interpretations. Expanding the dataset to include a broader range of compositions could confirm whether different approaches result in systematic shifts in the Christiansen Feature across different lithologies. This work enhances the accuracy of remote compositional interpretation and supports future exploration on airless bodies.