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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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Gerald Moriarty Schieven
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