Larry W. Thomason

Larry W. Thomason

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Larry W. Thomason

NASA Langley Research Center, Hampton, Virginia, USA

Research Focus & Metrics

Academic Career Length

45Years (1982-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 March 2016 in Reviews of Geophysics
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SKStefanie Kremser
Stefanie Kremser
LTLarry W. Thomason
Larry W. Thomason
MHMarc von Hobe
Marc von Hobe
MHMarkus Hermann
Markus Hermann
TDTerry Deshler
Terry Deshler
BMBrian Meland
Brian Meland
Interest in stratospheric aerosol and its role in climate have increased over the last decade due to the observed increase in stratospheric aerosol since 2000 and the potential for changes in the sulfur cycle induced by climate change. This review provides an overview about the advances in stratospheric aerosol research since the last comprehensive assessment of stratospheric aerosol was published in 2006. A crucial development since 2006 is the substantial improvement in the agreement between in situ and space‐based inferences of stratospheric aerosol properties during volcanically quiescent periods. Furthermore, new measurement systems and techniques, both in situ and space based, have been developed for measuring physical aerosol properties with greater accuracy and for characterizing aerosol composition. However, these changes induce challenges to constructing a long‐term stratospheric aerosol climatology. Currently, changes in stratospheric aerosol levels less than 20% cannot be confidently quantified. The volcanic signals tend to mask any nonvolcanically driven change, making them difficult to understand. While the role of carbonyl sulfide as a substantial and relatively constant source of stratospheric sulfur has been confirmed by new observations and model simulations, large uncertainties remain with respect to the contribution from anthropogenic sulfur dioxide emissions. New evidence has been provided that stratospheric aerosol can also contain small amounts of nonsulfate matter such as black carbon and organics. Chemistry‐climate models have substantially increased in quantity and sophistication. In many models the implementation of stratospheric aerosol processes is coupled to radiation and/or stratospheric chemistry modules to account for relevant feedback processes.

12 August 2011 in Science
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SSS. Solomon
S. Solomon
JDJ. S. Daniel
J. S. Daniel
RIRyan Ryenolds Neely III
Ryan Ryenolds Neely III
JVJ.-P. Vernier
J.-P. Vernier
EDE. G. Dutton
E. G. Dutton
LTL. W. Thomason
L. W. Thomason
An increase in the amount of aerosols in the stratosphere during the past decade has decreased the rate of global warming.

27 June 1998 in Journal of Geophysical Research: Atmospheres
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GSGeorgiy L. Stenchikov
Georgiy L. Stenchikov
IKIngo Kirchner
Ingo Kirchner
ARAlan Robock
Alan Robock
HGHans‐F. Graf
Hans‐F. Graf
JAJuan-Carlos Antuña-Marrero
Juan-Carlos Antuña-Marrero
LTLarry Thomason
Larry Thomason

30 June 2011 in Geophysical Research Letters
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Journal Article
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JVJ.-P. Vernier
J.-P. Vernier
LTL. W. Thomason
L. W. Thomason
JPJ.-P. Pommereau
J.-P. Pommereau
ABA. Bourassa
A. Bourassa
JPJ. Pelon
J. Pelon
Fabio VargasFabio Vargas
Fabio Vargas
[1] The variability of stratospheric aerosol loading between 1985 and 2010 is explored with measurements from SAGE II, CALIPSO, GOMOS/ENVISAT, and OSIRIS/Odin space‐based instruments. We find that, following the 1991 eruption of Mount Pinatubo, stratospheric aerosol levels increased by as much as two orders of magnitude and only reached “background levels” between 1998 and 2002. From 2002 onwards, a systematic increase has been reported by a number of investigators. Recently, the trend, based on ground‐based lidar measurements, has been tentatively attributed to an increase of SO2 entering the stratosphere associated with coal burning in Southeast Asia. However, we demonstrate with these satellite measurements that the observed trend is mainly driven by a series of moderate but increasingly intense volcanic eruptions primarily at tropical latitudes. These events injected sulfur directly to altitudes between 18 and 20 km. The resulting aerosol particles are slowly lofted into the middle stratosphere by the Brewer‐Dobson circulation and are eventually transported to higher latitudes.

12 March 2018 in Earth System Science Data
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LTLarry W. Thomason
Larry W. Thomason
NENicholas Ernest
Nicholas Ernest
LMLuis Millán
Luis Millán
LRLandon Rieger
Landon Rieger
ABAdam Bourassa
Adam Bourassa
TPThomas Peter
Thomas Peter
We describe the construction of a continuous 38-year record of stratospheric aerosol optical properties. The Global Space-based Stratospheric Aerosol Climatology, or GloSSAC, provided the input data to the construction of the Climate Model Intercomparison Project stratospheric aerosol forcing data set (1979–2014) and we have extended it through 2016 following an identical process. GloSSAC focuses on the Stratospheric Aerosol and Gas Experiment (SAGE) series of instruments through mid-2005, and on the Optical Spectrograph and InfraRed Imager System (OSIRIS) and the Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) data thereafter. We also use data from other space instruments and from ground-based, air, and balloon borne instruments to fill in key gaps in the data set. The end result is a global and gap-free data set focused on aerosol extinction coefficient at 525 and 1020 nm and other parameters on an “as available” basis. For the primary data sets, we developed a new method for filling the post-Pinatubo eruption data gap for 1991–1993 based on data from the Cryogenic Limb Array Etalon Spectrometer. In addition, we developed a new method for populating wintertime high latitudes during the SAGE period employing a latitude-equivalent latitude conversion process that greatly improves the depiction of aerosol at high latitudes compared to earlier similar efforts. We report data in the troposphere only when and where it is available. This is primarily during the SAGE II period except for the most enhanced part of the Pinatubo period. It is likely that the upper troposphere during Pinatubo was greatly enhanced over non-volcanic periods and that domain remains substantially under-characterized. We note that aerosol levels during the OSIRIS/CALIPSO period in the lower stratosphere at mid- and high latitudes is routinely higher than what we observed during the SAGE II period. While this period had nearly continuous low-level volcanic activity, it is possible that the enhancement in part reflects deficiencies in the data set. We also expended substantial effort to quality assess the data set and the product is by far the best we have produced. GloSSAC version 1.0 is available in netCDF format at the NASA Atmospheric Data Center at https://eosweb.larc.nasa.gov/. GloSSAC users should cite this paper and the data set DOI (https://doi.org/10.5067/GloSSAC-L3-V1.0).

20 April 1997 in Journal of Geophysical Research: Atmospheres
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LTL. W. Thomason
L. W. Thomason
LPL. R. Poole
L. R. Poole
TDT. Deshler
T. Deshler