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Global emissions of terpenoid VOCs from terrestrial vegetation in the last millennium

We investigated the millennial variability (1000 A.D.–2000 A.D.) of global biogenic volatile organic compound (BVOC) emissions by using two independent numerical models: The Model of Emissions of Gases and Aerosols from Nature (MEGAN), for isoprene, monoterpene, and sesquiterpene, and Lund-Potsdam-J...

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Autores principales: Acosta Navarro, J C, Smolander, S, Struthers, H, Zorita, E, Ekman, A M L, Kaplan, J O, Guenther, A, Arneth, A, Riipinen, I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4370762/
https://www.ncbi.nlm.nih.gov/pubmed/25866703
http://dx.doi.org/10.1002/2013JD021238
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author Acosta Navarro, J C
Smolander, S
Struthers, H
Zorita, E
Ekman, A M L
Kaplan, J O
Guenther, A
Arneth, A
Riipinen, I
author_facet Acosta Navarro, J C
Smolander, S
Struthers, H
Zorita, E
Ekman, A M L
Kaplan, J O
Guenther, A
Arneth, A
Riipinen, I
author_sort Acosta Navarro, J C
collection PubMed
description We investigated the millennial variability (1000 A.D.–2000 A.D.) of global biogenic volatile organic compound (BVOC) emissions by using two independent numerical models: The Model of Emissions of Gases and Aerosols from Nature (MEGAN), for isoprene, monoterpene, and sesquiterpene, and Lund-Potsdam-Jena-General Ecosystem Simulator (LPJ-GUESS), for isoprene and monoterpenes. We found the millennial trends of global isoprene emissions to be mostly affected by land cover and atmospheric carbon dioxide changes, whereas monoterpene and sesquiterpene emission trends were dominated by temperature change. Isoprene emissions declined substantially in regions with large and rapid land cover change. In addition, isoprene emission sensitivity to drought proved to have significant short-term global effects. By the end of the past millennium MEGAN isoprene emissions were 634 TgC yr(−1) (13% and 19% less than during 1750–1850 and 1000–1200, respectively), and LPJ-GUESS emissions were 323 TgC yr(−1)(15% and 20% less than during 1750–1850 and 1000–1200, respectively). Monoterpene emissions were 89 TgC yr(−1)(10% and 6% higher than during 1750–1850 and 1000–1200, respectively) in MEGAN, and 24 TgC yr(−1) (2% higher and 5% less than during 1750–1850 and 1000–1200, respectively) in LPJ-GUESS. MEGAN sesquiterpene emissions were 36 TgC yr(−1)(10% and 4% higher than during 1750–1850 and 1000–1200, respectively). Although both models capture similar emission trends, the magnitude of the emissions are different. This highlights the importance of building better constraints on VOC emissions from terrestrial vegetation.
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spelling pubmed-43707622015-04-10 Global emissions of terpenoid VOCs from terrestrial vegetation in the last millennium Acosta Navarro, J C Smolander, S Struthers, H Zorita, E Ekman, A M L Kaplan, J O Guenther, A Arneth, A Riipinen, I J Geophys Res Atmos Research Articles We investigated the millennial variability (1000 A.D.–2000 A.D.) of global biogenic volatile organic compound (BVOC) emissions by using two independent numerical models: The Model of Emissions of Gases and Aerosols from Nature (MEGAN), for isoprene, monoterpene, and sesquiterpene, and Lund-Potsdam-Jena-General Ecosystem Simulator (LPJ-GUESS), for isoprene and monoterpenes. We found the millennial trends of global isoprene emissions to be mostly affected by land cover and atmospheric carbon dioxide changes, whereas monoterpene and sesquiterpene emission trends were dominated by temperature change. Isoprene emissions declined substantially in regions with large and rapid land cover change. In addition, isoprene emission sensitivity to drought proved to have significant short-term global effects. By the end of the past millennium MEGAN isoprene emissions were 634 TgC yr(−1) (13% and 19% less than during 1750–1850 and 1000–1200, respectively), and LPJ-GUESS emissions were 323 TgC yr(−1)(15% and 20% less than during 1750–1850 and 1000–1200, respectively). Monoterpene emissions were 89 TgC yr(−1)(10% and 6% higher than during 1750–1850 and 1000–1200, respectively) in MEGAN, and 24 TgC yr(−1) (2% higher and 5% less than during 1750–1850 and 1000–1200, respectively) in LPJ-GUESS. MEGAN sesquiterpene emissions were 36 TgC yr(−1)(10% and 4% higher than during 1750–1850 and 1000–1200, respectively). Although both models capture similar emission trends, the magnitude of the emissions are different. This highlights the importance of building better constraints on VOC emissions from terrestrial vegetation. Blackwell Publishing Ltd 2014-06-16 2014-06-09 /pmc/articles/PMC4370762/ /pubmed/25866703 http://dx.doi.org/10.1002/2013JD021238 Text en ©2014. The Authors. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Acosta Navarro, J C
Smolander, S
Struthers, H
Zorita, E
Ekman, A M L
Kaplan, J O
Guenther, A
Arneth, A
Riipinen, I
Global emissions of terpenoid VOCs from terrestrial vegetation in the last millennium
title Global emissions of terpenoid VOCs from terrestrial vegetation in the last millennium
title_full Global emissions of terpenoid VOCs from terrestrial vegetation in the last millennium
title_fullStr Global emissions of terpenoid VOCs from terrestrial vegetation in the last millennium
title_full_unstemmed Global emissions of terpenoid VOCs from terrestrial vegetation in the last millennium
title_short Global emissions of terpenoid VOCs from terrestrial vegetation in the last millennium
title_sort global emissions of terpenoid vocs from terrestrial vegetation in the last millennium
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4370762/
https://www.ncbi.nlm.nih.gov/pubmed/25866703
http://dx.doi.org/10.1002/2013JD021238
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