Uncertainties in isoprene photochemistry and emissions: implications for the oxidative capacity of past and present atmospheres and for climate forcing agents

被引:12
作者
Achakulwisut, P. [1 ]
Mickley, L. J. [2 ]
Murray, L. T. [3 ,4 ]
Tai, A. P. K. [5 ]
Kaplan, J. O. [6 ]
Alexander, B. [7 ]
机构
[1] Harvard Univ, Dept Earth & Planetary Sci, Cambridge, MA 02138 USA
[2] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[3] NASA, Goddard Inst Space Studies, New York, NY 10025 USA
[4] Columbia Univ, Lamont Doherty Earth Observ, Palisades, NY USA
[5] Chinese Univ Hong Kong, Earth Syst Sci Programme, Hong Kong, Hong Kong, Peoples R China
[6] Ecole Polytech Fed Lausanne, ARVE Grp, Lausanne, Switzerland
[7] Univ Washington, Dept Atmospher Sci, Seattle, WA 98195 USA
基金
美国国家科学基金会;
关键词
BIOMASS-BURNING EMISSIONS; TROPOSPHERIC CHEMISTRY; HYDROXYL RADICALS; CARBON-MONOXIDE; AIR-QUALITY; ICE CORES; MODEL; PREINDUSTRIAL; OZONE; METHANE;
D O I
10.5194/acp-15-7977-2015
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Isoprene and its oxidation products are major players in the oxidative chemistry of the troposphere. Current understanding of the factors controlling biogenic isoprene emissions and of the fate of isoprene oxidation products in the atmosphere has been evolving rapidly. We use a climate-biosphere-chemistry modeling framework to evaluate the sensitivity of estimates of the tropospheric oxidative capacity to uncertainties in isoprene emissions and photochemistry. Our work focuses on two climate transitions: from the Last Glacial Maximum (LGM, 19 000-23 000 years BP) to the preindustrial (1770s) and from the preindustrial to the present day (1990s). We find that different oxidants have different sensitivities to the uncertainties tested in this study. Ozone is relatively insensitive, whereas OH is the most sensitive: changes in the global mean OH levels for the LGM-to-preindustrial transition range between 29 and +7% and those for the preindustrial-to-present-day transition range between -8 and +17% across our simulations. We find little variability in the implied relative LGM-preindustrial difference in methane emissions with respect to the uncertainties tested in this study. Conversely, estimates of the preindustrial-to-present-day and LGM-to-preindustrial changes in the global burden of secondary organic aerosol (SOA) are highly sensitive. We show that the linear relationship between tropospheric mean OH and tropospheric mean ozone photolysis rates, water vapor, and total emissions of NOx and reactive carbon - first reported in Murray et al. (2014) - does not hold across all periods with the new isoprene photochemistry mechanism. This study demonstrates how inadequacies in our current understanding of isoprene emissions and photochemistry impede our ability to constrain the oxidative capacities of the present and past atmospheres, its controlling factors, and the radiative forcing of some short-lived species such as SOA over time.
引用
收藏
页码:7977 / 7998
页数:22
相关论文
共 107 条
  • [1] Climate driven changes in the oxidation pathways of atmospheric sulfur
    Alexander, B
    Savarino, J
    Barkov, NI
    Delmas, RJ
    Thiemens, MH
    [J]. GEOPHYSICAL RESEARCH LETTERS, 2002, 29 (14) : 30 - 1
  • [2] Impact of preindustrial biomass-burning emissions on the oxidation pathways of tropospheric sulfur and nitrogen
    Alexander, B
    Savarino, J
    Kreutz, KJ
    Thiemens, MH
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2004, 109 (D8) : D083031 - 8
  • [3] Paleo-Perspectives on Potential Future Changes in the Oxidative Capacity of the Atmosphere Due to Climate Change and Anthropogenic Emissions
    Alexander, Becky
    Mickley, Loretta J.
    [J]. CURRENT POLLUTION REPORTS, 2015, 1 (02): : 57 - 69
  • [4] Pollen-based continental climate reconstructions at 6 and 21 ka: a global synthesis
    Bartlein, P. J.
    Harrison, S. P.
    Brewer, S.
    Connor, S.
    Davis, B. A. S.
    Gajewski, K.
    Guiot, J.
    Harrison-Prentice, T. I.
    Henderson, A.
    Peyron, O.
    Prentice, I. C.
    Scholze, M.
    Seppa, H.
    Shuman, B.
    Sugita, S.
    Thompson, R. S.
    Viau, A. E.
    Williams, J.
    Wu, H.
    [J]. CLIMATE DYNAMICS, 2011, 37 (3-4) : 775 - 802
  • [5] Critical issues in trace gas biogeochemistry and global change
    Beerling, David J.
    Hewitt, C. Nicholas
    Pyle, John A.
    Raven, John A.
    [J]. PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES, 2007, 365 (1856): : 1629 - 1642
  • [6] Global modeling of tropospheric chemistry with assimilated meteorology: Model description and evaluation
    Bey, I
    Jacob, DJ
    Yantosca, RM
    Logan, JA
    Field, BD
    Fiore, AM
    Li, QB
    Liu, HGY
    Mickley, LJ
    Schultz, MG
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2001, 106 (D19) : 23073 - 23095
  • [7] Two decades of OH variability as inferred by an inversion of atmospheric transport and chemistry of methyl chloroform
    Bousquet, P
    Hauglustaine, DA
    Peylin, P
    Carouge, C
    Ciais, P
    [J]. ATMOSPHERIC CHEMISTRY AND PHYSICS, 2005, 5 : 2635 - 2656
  • [8] Evaluation of climate models using palaeoclimatic data
    Braconnot, Pascale
    Harrison, Sandy P.
    Kageyama, Masa
    Bartlein, Patrick J.
    Masson-Delmotte, Valerie
    Abe-Ouchi, Ayako
    Otto-Bliesner, Bette
    Zhao, Yan
    [J]. NATURE CLIMATE CHANGE, 2012, 2 (06) : 417 - 424
  • [9] On the origin and timing of rapid changes in atmospheric methane during the last glacial period
    Brook, EJ
    Harder, S
    Severinghaus, J
    Steig, EJ
    Sucher, CM
    [J]. GLOBAL BIOGEOCHEMICAL CYCLES, 2000, 14 (02) : 559 - 572
  • [10] Large contribution of natural aerosols to uncertainty in indirect forcing
    Carslaw, K. S.
    Lee, L. A.
    Reddington, C. L.
    Pringle, K. J.
    Rap, A.
    Forster, P. M.
    Mann, G. W.
    Spracklen, D. V.
    Woodhouse, M. T.
    Regayre, L. A.
    Pierce, J. R.
    [J]. NATURE, 2013, 503 (7474) : 67 - +