Interpretation of Aura satellite observations of CO and aerosol index related to the December 2006 Australia fires
Author:
Luo M.,Boxe C.,Jiang J.,Nassar R.,Livesey N.
Abstract
Abstract. Enhanced Carbon Monoxide (CO) in the upper troposphere (UT) is shown by collocated Tropospheric Emission Spectrometer (TES) and Microwave Limb Sounder (MLS) measurements near and down-wind from the known wildfire region of SE Australia from 12–19 December 2006. Enhanced UV aerosol index (AI) derived from Ozone Monitoring Instrument (OMI) measurements correlate with these high CO concentrations. HYSPLIT model back trajectories trace selected air parcels to the SE Australia fire region as their initial location, where TES observes enhanced CO in the upper and lower troposphere. Simultaneously, they show a lack of vertical advection along their tracks. TES retrieved CO vertical profiles in the higher and lower southern latitudes are examined together with the averaging kernels and show that TES CO retrievals are most sensitive at approximately 300–400 hPa. The enhanced CO observed by TES at the upper (215 hPa) and lower (681 hPa) troposphere are, therefore, influenced by mid-tropospheric CO. GEOS-Chem model simulations with an 8-day emission inventory, as the wildfire source over Australia, are sampled to the TES/MLS observation times and locations. These simulations only show CO enhancements in the lower troposphere near and down-wind from the wildfire region of SE Australia with drastic underestimates of UT CO. Although CloudSat along-track ice-water content curtains are examined to see whether possible vertical convection events can explain the high UT CO values, sparse observations of collocated Aura CO and CloudSat along-track ice-water content measurements for the single event precludes any conclusive correlation. Vertical convection that uplift fire-induced CO (i.e. most notably referred to as pyro-cumulonimbus, pyroCb) may provide an explanation for the incongruence between these simulations and the TES/MLS observations of enhanced CO in the UT. Future GEOS-Chem simulations are needed to validate this conjecture as the the PyroCb mechanism is currently not incorporated in GEOS-Chem.
Publisher
Copernicus GmbH
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