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4. Biogenic trace gas fluxes and the chemistry of the palaeoatmosphere

Personnel
Principal investigator:
Associated Personnel:


Professor D.J. Beerling

Professor P.J. Valdes (University of Reading)

Funding The Leverhulme Trust

Philip Leverhulme Prize in Earth Sciences to Professor Beerling

Project dates: October 2001 - September 2003

Summary
The chemistry of the ancient atmosphere is strongly regulated by emissions of extremely reactive volatile organic compounds (VOCs) and other trace gases (e.g. CH4 and NOx) from terrestrial ecosystems. Stratospheric ozone - needed to shield us from harmful UV radiation - is affected by atmospheric O2 concentration. Past changes in atmospheric O2, and the distribution and productivity of terrestrial ecosystems, will therefore have repercussions for the chemistry of the atmosphere which in turn will exert a direct feedback on climate.

This realization leads to an urgent need to answer some basic questions concerning the nature of plant-climate-atmosphere-chemistry feedbacks. Our multidisciplinary research addresses the problem with the development of a new interdisciplinary subject area in the Earth Sciences 'palaeoatmospheric chemistry'. The approach utilises modelling and experimental approaches, and geochemical analyses of fossil plants. We have begun our numerical simulations by focusing on recent atmospheric CH4 changes (1980-1990), and two intervals in the late Quaternary, the Holocene (past 10kyr) and last ice age (21kyr ago). The late Quaternary is an ideal time interval for study the behaviour of the atmosphere under conditions different from now because ice cores provide us with a wealth of critical information on its chemical state which can be used to examine the accuracy and validity of our simulations.

From the 'recent past' studies, we have begun to move further back in time, focusing in particular on the ancient 'greenhouse' world of the Eocene, 50 million years ago. Fossil sediments indicate wetlands and tropical forests were much more widespread than now. Since wetlands are a major source of CH4, and tropical forest emit VOCs, it follows that the atmospheric chemistry was probably rather different at that time. These differences could be the key to explaining the global warmth seen in marine oxygen isotope records, because atmospheric CH4 is a potent greenhouse gas. On-going work aims to quantify the feedback of these changes in atmospheric composition on climate and vegetation primary production.

Check out our latest research findings in the paper below:

Valdes, P.J., Beerling, D.J. & Johnson, C.E. (In revision) An Earth systems approach closes the ice-age global methane budget. Nature.

Climatic forcing of global climate in the Eocene (50 million years ago) by an equilibrium atmospheric CH4 level, computed using a three dimensional atmospheric chemistry model coupled to general circulation model of Eocene climate. The map shows the change in near surface winter (December, January and February) temperature due to the effects CH4.

Eocene Climate

 

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