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JCMT Newsletter No.22 (Martian Prefer Blondes)

A Measurement of the 362 GHz Absorption Line of Mars Atmospheric H2O2


R. Todd Clancy, Brad Sandor
Space Science Institute
& Gerald Moriarty Schieven
Joint Astronomy Centre

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). Our derived H2O2 abundance is roughly three times greater than the upper limit retrieved by Encrenaz et al. (2002) 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). The observed H2O2 line absorption weakens arguments for non-standard homogeneous (Encrenaz et al., 2002) or heterogeneous (Krasnopolsky, 2003) chemistry, which have been advocated partly on the basis of infrared (8 µm) non-detections for Mars H2O2. Our observation of Mars H2O2 also represents the first measurement of a key catalytic specie in a planetary atmosphere other than our own.

Figure 1: A schematic of the Mars JCMT observing geometry for the September 4, 2003 spectral line H2O2 measurement. The solid outer circle represents the apparent Mars disk, as resolved by the FWHM primary diffraction beam (diagonally marked center circle) of the JCMT telescope at the observing frequency (362.156 GHz). The center local time and latitude, as well as the local times/latitudes of the beam FWHM limits, are indicated.

Photodissociation of water vapor is the fundamental source for Mars atmospheric H2O2, such that photochemical model H2O2 abundances scale roughly with input model water vapor densities. The vertical column of Mars water vapor varies by >100% versus latitude and Ls (Jakosky and Farmer, 1982; Smith, 2002), which requires that comparisons of model and observed H2O2 abundances be adjusted for equivalent water vapor conditions. Our measurement of 18±4 ppbv for the 0-30 km H2O2 mixing ratio corresponds to water vapor column densities of 15-20 pr-?m for the 50S-20N latitude range and southern summer season (Ls.= 254°) of observation (Smith, 2002).

Figure 2: The observed 362 GHz H2O2 absorption spectrum of Mars (solid line), which has been smoothed to an effective spectral resolution of 1 MHz. The line center offset of -2.45 MHz from zero is the Doppler shift associated with a Mars-Earth relative velocity at the (one week) post opposition period of observation. Synthetic spectra with equivalent 1 MHz spectral resolutions are calculated for Mars H2O2 abundances consistent with the Encrenaz et al. (2002) upper limit of 6 ppbv (square symbols) and a best-fit mixing ratio of 18 ppbv (asterisk symbols).


This discovery of H2O2 in the Martian atmosphere appeared in the March issue of Icarus (2004, Icarus, v168, pp116-121) and was issued as a press release on March 1 2004. The release was picked up by a significant number of newspapers, as well as CBS radio. See here for links to some of the press coverage.


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Click here for printable version.


Gerald Moriarty Schieven
Contact: Antonio Chrysostomou. Updated: Tue Aug 17 17:32:12 HST 2004

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