Abstract

The Atmospheric Infrared Sounder (AIRS) on EOS/Aqua platform provides a measurement of global methane (CH4) in the mid-upper troposphere since September, 2002. As a thermal infrared sounder, the most sensitivity of AIRS to atmospheric CH4 is in the mid-upper troposphere with the degree of freedom of ~1.0. Validation of AIRS CH4 product versus thousands of aircraft profiles (convolved using the AIRS averaging kernels) demonstrates that its RMS error (RMSE) is mostly less than 1.5%, and its quality is pretty stable from 2003 to 2009. For scientific analysis of the spatial and temporal variation of mid-upper tropospheric CH4 (MUT-CH4) in the High Northern Hemisphere (HNH), it is more valuable to use the AIRS retrieved CH4 in a layer of about 100 hPa below tropopause (“Representative Layer”) than in a fixed pressure layer. Further analysis of deseasonalized time-series of AIRS CH4 in both a fixed pressure layer and the “Representative Layer” of AIRS (only for the HNH) from 2003 to 2009 indicates that, similar to the CH4 in the marine boundary layer (MBL) that was found to increase in 2007–2008, MUT-CH4 was also observed to have a recent increase but the most significant increase occurred in 2008. MUT-CH4 continued to increase in 2009, especially in the HNH. Moreover, the trend of MUT-CH4 from 2006 to 2008 is lower than the trend of CH4 in the MBL by 30–40% in both the southern hemisphere and HNH. This delay for the MUT-CH4 increase of about one year than CH4 in the MBL as well as the smaller increase trend for MUT-CH4 suggest that surface emission is likely a major driver for the recent CH4 increase. It is also found that the seasonal cycle of MUT-CH4 is different from CH4 in the MBL due to the impact of transport, in addition to the surface emission and the photochemical loss.

Highlights

  • As one of the most important greenhouse gases, atmospheric methane (CH4) is 25 times more effective on a per unit mass basis than carbon dioxide in absorbing long-wave radiation on a 100-year time horizon, and accounts for 18% of the total of 2.66 W m−2 of the anthropogenically produced greenhouse gas radiative forcing [1]

  • As a thermal infrared sounder, Atmospheric Infrared Sounder (AIRS) on Earth Observing System (EOS)/Aqua platform has provided a unique measurement of mid-upper tropospheric CH4 (MUT-CH4) since September 2002

  • Sensitivity, it is clear that AIRS is capable of detecting a less than 2% change of atmospheric CH4 total column in the tropics and mid-latitude regions, but its capability deteriorates to about 2% or more in the polar region

Read more

Summary

Introduction

As one of the most important greenhouse gases, atmospheric methane (CH4) is 25 times more effective on a per unit mass basis than carbon dioxide in absorbing long-wave radiation on a 100-year time horizon, and accounts for 18% of the total of 2.66 W m−2 of the anthropogenically produced greenhouse gas radiative forcing [1]. The TIR measurements in operation include the Tropospheric Emission Spectrometer (TES) on NASA Earth Observing System (EOS). As one of the space-borne thermal infrared sounders in operation, AIRS was launched in polar orbit (13:30, ascending node) on the EOS/Aqua satellite in May 2002. It is the first hyperspectral infrared sounder designed to support weather forecast [15] and CH4 is one of the research products.

Characteristics of CH4 Retrieval from AIRS
Sensitivities of AIRS
Validation Data Set
Validation Results
Global View of MUT-CH4 and Its Increase during 2007–2009
MUT-CH4 in Southern Hemisphere
MUT-CH4 in South Asia
MUT-CH4 in the HNH
Seasonal Cycle of MUT-CH4
Summary and Conclusions
30. GLOBALVIEW-CH4
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call