@Article{SantosLGKGOFLHBF:2017:BiBuEm,
author = "Santos, Fernando Cavalcante dos and Longo, Karla Maria and
Guenther, Alex B. and Kim, Saewung and Gu, Dasa and Oram, Dave E.
and Forster, Grant L. and Lee, James and Hopkins, James R. and
Brito, Joel F. and Freitas, Saulo R.",
affiliation = "{Instituto Nacional de Pesquisas Espaciais (INPE)} and {Instituto
Nacional de Pesquisas Espaciais (INPE)} and {University of
California} and {University of California} and {University of
California} and {University of East Anglia} and {University of
East Anglia} and {University of York} and {University of York} and
{Universidade de S{\~a}o Paulo (USP)} and {NASA Goddard Space
Flight Center}",
title = "Biomass burning emissions disturbances on the isoprene oxidation
in a tropical forest",
journal = "Atmospheric Chemistry and Physics Discussion",
year = "2017",
volume = "1083",
pages = "1--35",
abstract = "We present a characterization of the chemical composition of the
atmosphere of the Brazilian Amazon rainforest based on trace gases
measurements carried out during the South American Biomass Burning
Analysis (SAMBBA) airborne experiment in September 2012. We
analyzed the observations of primary biomass burning emission
tracers, i.e., carbon monoxide (CO) and nitrogen oxides (NOx),
ozone (O3), isoprene, and its main oxidation products, methyl
vinyl ketone (MVK), methacrolein (MACR), and hydroxyhydroperoxides
(ISOPOOH). The focus of SAMBBA was primarily on biomass burning
emissions, but there were also several flights in areas of the
Amazon forest not directly affected by biomass burning, revealing
a background with a signature of biomass burning in the chemical
composition due to long-range transport of biomass burning tracers
from both Africa and the eastern part of Amazonia. We used the
[MVK+MACR+ ISOPOOH]/[Isoprene] ratio and the hydroxyl radical (OH)
indirect calculation to assess the oxidative capacity of the
Amazon forest atmosphere. We compared the background regions
(CO<150 ppbv), fresh and aged smoke plumes classified according to
their photochemical age ([O3]/[CO]), to evaluate the impact of
biomass burning emissions in the oxidative capacity of the Amazon
forest atmosphere. We observed that biomass burning emissions
disturb the isoprene oxidation reactions, especially for fresh
plumes ([MVK+MACR+ISOPOOH]/[isoprene] = 7). The oxidation of
isoprene is higher in fresh smoke plumes at lower altitudes (~ 500
m) than in aged smoke plumes, anticipating near the surface a
complex chain of oxidation reactions, which may be related to the
secondary organic aerosols (SOA) formation. We proposed a
refinement of the OH calculation based on the sequential reaction
model, which considers vertical and horizontal transport for both
biomass burning regimes and background environment. Our approach
for the [OH] estimation resulted in values of the same order of
magnitude of a recent observation in the Amazon rainforest [OH]
\≅ 106 (molecules cm-3 ). During the fresh plume regime,
the vertical profile of [OH] and the [MVK+MACR+ISOPOOH]/[isoprene]
ratio showed an evidence of an increase of the oxidizing power in
the transition from PBL to cloud layer (1,000 1,500 m). These high
values of [OH] (1.5 \ 106 molecules cm-3 ) and
[MVK+MACR+ISOPOOH]/[isoprene] (7.5) indicate a significant change
above and inside the cloud decks due to cloud edge effects on
photolysis rates, which have a major impact on OH production
rates.",
doi = "10.5194/acp-2017-1083",
url = "http://dx.doi.org/10.5194/acp-2017-1083",
issn = "1680-7367",
language = "en",
targetfile = "santos_biomass.pdf",
urlaccessdate = "26 abr. 2024"
}