A measurement of the 362 GHz absorption line of Mars atmospheric H2O2 |
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| Authors: | RT Clancy BJ Sandor |
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| Institution: | a Space Science Institute, 4750 Walnut Street, Suite 205, Boulder, CO 80301, USA
b National Research Council of Canada, Joint Astronomy Centre, 660 N. A'ohoku Place, Hilo, HI 96720, USA |
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| Abstract: | The 362.156 GHz absorption spectrum of H2O2 in the Mars atmosphere was observed on September 4 of 2003, employing the James Clerk Maxwell Telescope (JCMT) sub-millimeter facility on Mauna Kea, Hawaii. Radiative transfer analysis of this line absorption yields an average volume mixing ratio of 18±0.4 ppbv within the lower (0-30 km) Mars atmosphere, in general accordance with standard photochemical models (e.g., Nair et al., 1994, Icarus 111, 124-150). Our derived H2O2 abundance is roughly three times greater than the upper limit retrieved by Encrenaz et al. (2002, Astron. Astrophys. 396, 1037-1044) from infrared spectroscopy, although part of this discrepancy may result from the different solar longitudes (Ls) of observation. Aphelion-to-perihelion thermal forcing of the global Mars hygropause generates substantial (>200%) increases in HOx abundances above ∼10 km altitudes between the Ls=112° period of the Encrenaz et al. upper limit measurement and the current Ls=250° period of detection (Clancy and Nair, 1996, J. Geophys. Res. 101, 12785-12590). The observed H2O2 line absorption weakens arguments for non-standard homogeneous (Encrenaz et al., 2002, Astron. Astrophys. 396, 1037-1044) or heterogeneous (Krasnopolsky, 2003a, J. Geophys. Res. 108; 2003b, Icarus 165, 315-325) chemistry, which have been advocated partly on the basis of infrared (8 μm) non-detections for Mars H2O2. Observation of Mars H2O2 also represents the first measurement of a key catalytic specie in a planetary atmosphere other than our own. |
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