Spatiotemporal Variability of Global Atmospheric Methane Observed from Two Decades of Satellite Hyperspectral Infrared Sounders

Author:

Zhou Lihang1ORCID,Warner Juying2,Nalli Nicholas R.34ORCID,Wei Zigang3,Oh Youmi5ORCID,Bruhwiler Lori5,Liu Xingpin3,Divakarla Murty34,Pryor Ken4ORCID,Kalluri Satya1,Goldberg Mitchell D.6

Affiliation:

1. NOAA JPSS Program Office, Silver Spring, MD 20706, USA

2. Department of Atmospheric & Oceanic Science, University of Maryland, College Park, MD 20742, USA

3. IM Systems Group, Inc., 3206 Tower Oaks, Blvd., Suite 300, Rockville, MD 20852, USA

4. NOAA/NESDIS Center for Satellite Applications and Research (STAR), 5830 University Research Court, College Park, MD 20740, USA

5. NOAA Global Monitoring Laboratory (GML), 325 Broadway R/GML, Boulder, CO 80305, USA

6. NOAA/NESDIS, 1335 East West Highway, Silver Spring, MD 20910, USA

Abstract

Methane (CH4) is the second most significant contributor to climate change after carbon dioxide (CO2), accounting for approximately 20% of the contributions from all well-mixed greenhouse gases. Understanding the spatiotemporal distributions and the relevant long-term trends is crucial to identifying the sources, sinks, and impacts on climate. Hyperspectral thermal infrared (TIR) sounders, including the Atmospheric Infrared Sounder (AIRS), the Cross-track Infrared Sounder (CrIS), and the Infrared Atmospheric Sounding Interferometer (IASI), have been used to measure global CH4 concentrations since 2002. This study analyzed nearly 20 years of data from AIRS and CrIS and confirmed a significant increase in CH4 concentrations in the mid-upper troposphere (around 400 hPa) from 2003 to 2020, with a total increase of approximately 85 ppb, representing a +4.8% increase in 18 years. The rate of increase was derived using global satellite TIR measurements, which are consistent with in situ measurements, indicating a steady increase starting in 2007 and becoming stronger in 2014. The study also compared CH4 concentrations derived from the AIRS and CrIS against ground-based measurements from NOAA Global Monitoring Laboratory (GML) and found phase shifts in the seasonal cycles in the middle to high latitudes of the northern hemisphere, which is attributed to the influence of stratospheric CH4 that varies at different latitudes. These findings provide insights into the global budget of atmospheric composition and the understanding of satellite measurement sensitivity to CH4.

Funder

NOAA JPSS Office

Global Monitoring Laboratory were supported by the NOAA OAR and NOAA JPSS

Publisher

MDPI AG

Subject

General Earth and Planetary Sciences

Reference82 articles.

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