Atmospheric Chemistry and Physics (Jul 2023)
Intra- and interannual changes in isoprene emission from central Amazonia
- E. Gomes Alves,
- E. Gomes Alves,
- R. Aquino Santana,
- C. Quaresma Dias-Júnior,
- C. Quaresma Dias-Júnior,
- S. Botía,
- T. Taylor,
- A. M. Yáñez-Serrano,
- A. M. Yáñez-Serrano,
- A. M. Yáñez-Serrano,
- J. Kesselmeier,
- E. Bourtsoukidis,
- J. Williams,
- P. I. Lembo Silveira de Assis,
- G. Martins,
- R. de Souza,
- S. Duvoisin Júnior,
- A. Guenther,
- D. Gu,
- A. Tsokankunku,
- M. Sörgel,
- B. Nelson,
- D. Pinto,
- S. Komiya,
- D. Martins Rosa,
- B. Weber,
- B. Weber,
- C. Barbosa,
- C. Barbosa,
- M. Robin,
- K. J. Feeley,
- A. Duque,
- V. Londoño Lemos,
- M. P. Contreras,
- A. Idarraga,
- N. López,
- C. Husby,
- B. Jestrow,
- I. M. Cely Toro
Affiliations
- E. Gomes Alves
- Department of Biogeochemical Processes, Max Planck Institute for Biogeochemistry, Jena, Germany
- E. Gomes Alves
- Climate and Environment Department, National Institute of Amazonian Research, Manaus, Brazil
- R. Aquino Santana
- Department of Atmospheric Sciences, Federal University of Western Para, Santarem, Brazil
- C. Quaresma Dias-Júnior
- Climate and Environment Department, National Institute of Amazonian Research, Manaus, Brazil
- C. Quaresma Dias-Júnior
- Federal Institute of Para, Belem, Brazil
- S. Botía
- Department of Biogeochemical Signals, Max Planck Institute for Biogeochemistry, Jena, Germany
- T. Taylor
- Department of Civil and Environmental Engineering, University of Michigan, Ann Arbor, MI, USA
- A. M. Yáñez-Serrano
- IDAEA-CSIC, 08034, Barcelona, Spain
- A. M. Yáñez-Serrano
- CREAF, E08193 Bellaterra, Cerdanyola del Vallès, Cerdanyola del Vallès, Catalonia, Spain
- A. M. Yáñez-Serrano
- Global Ecology Unit, CREAF-CSIC-UAB, E08193 Bellaterra, Cerdanyola del Vallès, Catalonia, Spain
- J. Kesselmeier
- Multiphase Chemistry Department, Max Planck Institute for Chemistry, Mainz, Germany
- E. Bourtsoukidis
- The Cyprus Institute, Nicosia, Cyprus
- J. Williams
- Atmospheric Chemistry Department, Max Planck Institute for Chemistry, Mainz, Germany
- P. I. Lembo Silveira de Assis
- Department of Tropical Forest Sciences, National Institute for Amazonian Research, Manaus, Brazil
- G. Martins
- Department of Tropical Forest Sciences, National Institute for Amazonian Research, Manaus, Brazil
- R. de Souza
- Meteorology Department, Amazonas State University, Manaus, Brazil
- S. Duvoisin Júnior
- Chemistry Department, Amazonas State University, Manaus, Brazil
- A. Guenther
- Department of Earth System Science, University of California, Irvine, CA, USA
- D. Gu
- Division of Environment and Sustainability, Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong, China
- A. Tsokankunku
- Atmospheric Chemistry Department, Max Planck Institute for Chemistry, Mainz, Germany
- M. Sörgel
- Atmospheric Chemistry Department, Max Planck Institute for Chemistry, Mainz, Germany
- B. Nelson
- Coordination of Environmental Dynamics, National Institute of Amazonian Research, Manaus, Brazil
- D. Pinto
- Department of Tropical Forest Sciences, National Institute for Amazonian Research, Manaus, Brazil
- S. Komiya
- Department of Biogeochemical Processes, Max Planck Institute for Biogeochemistry, Jena, Germany
- D. Martins Rosa
- Department of Tropical Forest Sciences, National Institute for Amazonian Research, Manaus, Brazil
- B. Weber
- Multiphase Chemistry Department, Max Planck Institute for Chemistry, Mainz, Germany
- B. Weber
- Division of Plant Sciences, Institute for Biology, University of Graz, Graz, Austria
- C. Barbosa
- Multiphase Chemistry Department, Max Planck Institute for Chemistry, Mainz, Germany
- C. Barbosa
- Division of Plant Sciences, Institute for Biology, University of Graz, Graz, Austria
- M. Robin
- Department of Biogeochemical Processes, Max Planck Institute for Biogeochemistry, Jena, Germany
- K. J. Feeley
- Department of Biological Sciences, University of Miami, Coral Gables, FL, USA
- A. Duque
- Departamento de Ciencias Forestales, Universidad Nacional de Colombia–Sede 19 Medellín, Medellín, Colombia
- V. Londoño Lemos
- Department of Plant and Microbial Biology, University of Minnesota, Minneapolis, MN, USA
- M. P. Contreras
- Jardín Botánico de Cartagena “Guillermo Piñeres”, Turbaco, Bolívar, Colombia
- A. Idarraga
- Fundación Jardín Botánico de Medellín, Antioquia, Colombia
- N. López
- Fundación Jardín Botánico de Medellín, Antioquia, Colombia
- C. Husby
- Fairchild Tropical Botanic Garden, Miami, FL, USA
- B. Jestrow
- Fairchild Tropical Botanic Garden, Miami, FL, USA
- I. M. Cely Toro
- Federal Institute of Para, Belem, Brazil
- DOI
- https://doi.org/10.5194/acp-23-8149-2023
- Journal volume & issue
-
Vol. 23
pp. 8149 – 8168
Abstract
Isoprene emissions are a key component in biosphere–atmosphere interactions, and the most significant global source is the Amazon rainforest. However, intra- and interannual variations in biological and environmental factors that regulate isoprene emission from Amazonia are not well understood and, thereby, are poorly represented in models. Here, with datasets covering several years of measurements at the Amazon Tall Tower Observatory (ATTO) in central Amazonia, Brazil, we (1) quantified canopy profiles of isoprene mixing ratios across seasons of normal and anomalous years and related them to the main drivers of isoprene emission – solar radiation, temperature, and leaf phenology; (2) evaluated the effect of leaf age on the magnitude of the isoprene emission factor (Es) from different tree species and scaled up to canopy with intra- and interannual leaf age distribution derived by a phenocam; and (3) adapted the leaf age algorithm from the Model of Emissions of Gases and Aerosols from Nature (MEGAN) with observed changes in Es across leaf ages. Our results showed that the variability in isoprene mixing ratios was higher between seasons (max during the dry-to-wet transition seasons) than between years, with values from the extreme 2015 El Niño year not significantly higher than in normal years. In addition, model runs considering in situ observations of canopy Es and the modification on the leaf age algorithm with leaf-level observations of Es presented considerable improvements in the simulated isoprene flux. This shows that MEGAN estimates of isoprene emission can be improved when biological processes are mechanistically incorporated into the model.