The Mars Organic Molecule Analyzer (MOMA) instrument onboard the ESA/Roscosmos ExoMars rover (to launch in July, 2020) will analyze volatile and refractory organic compounds in martian surface and subsurface sediments. In this study, we describe the design, current status of development, and analytical capabilities of the instrument. Data acquired on preliminary MOMA flight-like hardware and experimental setups are also presented, illustrating their contribution to the overall science return of the mission. Key Words: Mars—Mass spectrometry—Life detection—Planetary instrumentation. Astrobiology 17, 655–685.
The concentration of tungsten (W) in basaltic melts provides a window into the behavior of this element during core-mantle separation, crust formation, silicate differentiation, and potentially core-mantle interaction. We have analyzed an extensive suite of modern basalts (n = 86) for their trace element chemistry via laser ablation ICP-MS, with barium (Ba), thorium (Th), uranium (U), and W concentrations typically determined to ≤ 5% (2σ) uncertainty. We find that the partitioning behavior of U mirrors that of W during basalt genesis, whereas Ba and Th both behave more incompatibly. The W/U ratio of our complete sample suite (0.65 ± 0.45, 2σ) is representative of the mean modern mantle, and is indistinguishable from that of mid-ocean ridge basalts (W/U MORB = 0.65 ± 0.41, n = 52), ocean island basalts (W/U OIB = 0.63 ± 0.07, n = 10), and back-arc basin basalts (W/U BABB = 0.62 ± 0.09, n = 12). This ratio is also consistent with the W/U ratio of the continental crust, and thus represents the W/U ratio of the entire silicate portion of the Earth. Assuming a concentration of 20 ± 8 (2σ) ng/g U in the bulk silicate Earth, the abundance of W in the silicate Earth is 13 ± 10 ng/g. Following mass balance, this implies a mean modern mantle and core composition of 8.3 ± 7.1 ng/g W and 500 ± 120 ng/g W, respectively. Additionally, the MORB source is modeled to contain approximately 3.0 ± 2.3 ng/g W, indicating a four-fold depletion of the highly incompatible elements in the MORB source relative to the silicate Earth. Although both the isotopic composition of W and the constancy of the silicate Earth W/U ratio allow for potential insight into core-mantle exchange, both of these proxies are extremely dependent on the chemical composition of the source. A case study of three Hawaiian picrites with enrichments in 186 Os-187 Os but terrestrial ε 182W can be explained by: i) a lack of a core component in the Hawaiian "plume," ii) crustal contamination, or iii) a source composition enriched in incompatible trace elements relative to the bulk silicate Earth.
The Sample Analysis at Mars (SAM) instrument on the Mars Science Laboratory (MSL) roverCuriosity detected evolved gases during thermal analysis of soil samples from the Rocknest aeolian deposit in Gale Crater. Major species detected (in order of decreasing molar abundance) were H 2 O, SO 2 , CO 2 , and O 2 , all at the μmol level, with HCl, H 2 S, NH 3 , NO, and HCN present at the tens to hundreds of nmol level. We compute weight % numbers for the major gases evolved by assuming a likely source and calculate abundances between 0.5 and 3 wt.%. The evolution of these gases implies the presence of both oxidized (perchlorates) and reduced (sulfides or H-bearing) species as well as minerals formed under alkaline (carbonates) and possibly acidic (sulfates) conditions. Possible source phases in the Rocknest material are hydrated amorphous material, minor clay minerals, and hydrated perchlorate salts (all potential H 2 O sources), carbonates (CO 2 ), perchlorates (O 2 and HCl), and potential N-bearing materials (e.g., Martian nitrates, terrestrial or Martian nitrogenated organics, ammonium salts) that evolve NH 3 , NO, and/or HCN. We conclude that Rocknest materials are a physical mixture in chemical disequilibrium, consistent with aeolian mixing, and that although weathering is not extensive, it may be ongoing even under current Martian surface conditions.
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