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

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Abstract

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.

Figures

  • Figure 1. The ICE age Chemistry And Proxies (ICECAP) model framework consists of four global models, represented here by boxes with solid lines. The stratospheric and tropospheric chemistry schemes are coupled online in the GEOS-Chem chemical transport model (CTM). Arrows indicate the flow of model output. The ICECAP model framework was especially designed for simulating the oxidative capacity of past atmospheres. (Adapted from Murray et al., 2014, Fig. 1.)
  • Figure 2. Simulated sensitivity of the tropospheric mean mass-weighted oxidant burdens of OH, O3, H2O2, and NO3 to each combination of climate, chemistry, and plant isoprene emission scheme. Simulations are as described in Table 2. The climate scenarios are present day, preindustrial, warm LGM, and cold LGM, with decreasing sea surface temperatures within 15◦ of the Equator (SST15◦ S−◦N), going from left to right along the abscissa. The chemistry schemes are C1 (orange curves), C2 (green), and C3 (blue). Plant isoprene emissions are modeled without (light shaded) or with (dark shaded) sensitivity to atmospheric CO2 concentrations. The tropospheric burdens are calculated with the tropopause determined from the thermal lapse rate. The dotted light-orange line represents the results reported in Murray et al. (2014) for their “best estimate” lightning and fire emissions scenarios.
  • Table 1. Atmospheric CO2 concentrations and global annual terrestrial plant isoprene emissions for each climate scenario.
  • Figure 3. Percent changes (%) in the tropospheric mean massweighted OH burden for a range of scenarios relative to their respective preindustrial scenarios (e.g., C1-w present day relative to C1-w preindustrial). Simulations are as described in Table 2. The climate scenarios are present day, preindustrial, warm LGM, and cold LGM. The chemistry schemes are C1 (orange bars), C2 (green), and C3 (blue). Plant isoprene emissions are modeled without (light shaded) or with (dark shaded) sensitivity to atmospheric CO2 concentrations. For the present day, test simulations with and without CO2 sensitivity yield nearly identical isoprene emissions. We therefore perform all present-day simulations with CO2 sensitivity turned on and assume that these model results apply to the respective presentday “without” scenarios. (Note: The percent change at the warm LGM relative to the preindustrial is very small when the C1 chemistry scheme is used without consideration of the CO2 sensitivity (C1-wo), and so no light-orange bar is apparent in the middle panel.)
  • Table 2. Summary of the different climate, chemistry, and plant isoprene emission scenarios tested in this model study. For each climate scenario except for the present day, all possible combinations of chemistry and emission schemes are tested (for the present day, only the “with” CO2 sensitivity scheme is used). We perform 21 simulations in total.
  • Table 3. Calculated present-day methyl chloroform (MCF) and methane lifetimes against tropospheric oxidation by OH (τMCF, OH, τCH4,OH), with consideration of CO2 sensitivity of plant isoprene emissions.
  • Figure 4. Comparison of model results with observations of CO surface concentrations (ppbv) over Antarctica for the preindustrial (1770s) and present-day (1990s) simulations. The maroon crosses represent observations from different sources for each time slice. Wang et al. (2010) measured ice-core CO concentrations at the South Pole of 48± 4 ppbv for the year 1777 (±110 years); the associated errors represent analytical uncertainties. The mean CO surface concentration measured at the South Pole by the NOAA Global Monitoring Division for the 1990s is 49± 2 ppbv; the associated errors represent interannual variability. The squares represent values averaged over Antarctica from our model simulations tested with different chemistry and isoprene emission schemes for the preindustrial and present-day scenarios. Simulations are as described in Table 2; colors are as in Fig. 2. Error bars associated with the model results represent ±1 standard deviation of the spatially averaged mean value.
  • Table 4. Modeled percent changes in the surface [O3] / [OH] and [O3] / [RO2] ratios for the present day relative to the preindustrial and in the surface [OH] concentration for the warm and cold LGM relative to the preindustrial for different model sensitivity experiments. Surface [O3] / [OH] and [OH] values are averaged over the 46–66 ◦ S latitude band to compare with values inferred from ice-core measurements of 117O(SO2− 4 ) by Sofen et al. (2014) and Alexander et al. (2002). Surface [O3] / [RO2] are averaged over 34–54 ◦ S and 62.5–72.5◦W (extratropical South America) to compare with values inferred from ice-core measurements of 117O(NO− 3 ) by Sofen et al. (2014), as described in Sect. 3.2.

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Achakulwisut, P., Mickley, L. J., Murray, L. T., Tai, A. P. K., Kaplan, J. O., & Alexander, B. (2015). Uncertainties in isoprene photochemistry and emissions: Implications for the oxidative capacity of past and present atmospheres and for climate forcing agents. Atmospheric Chemistry and Physics, 15(14), 7977–7998. https://doi.org/10.5194/acp-15-7977-2015

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