ALBERT

Description: We present a global simulation of tropospheric iodine chemistry within the GEOS-Chem chemical transport model. This includes organic and inorganic iodine sources, standard gas-phase iodine chemistry and simplified higher iodine oxide (I2OX, X = 2, 3, 4) chemistry, photolysis, deposition and parametrised heterogeneous reactions. In comparisons with recent Iodine Oxide (IO) observations the iodine simulation shows an average bias of ~+66 % available surface observations in the marine boundary layer (outside of polar regions), and of ~+73 % within the free troposphere (350 〈 hPa 〈 900) over the eastern Pacific. Iodine emissions (3.8 Tg yr−1) are overwhelmingly dominated by the inorganic ocean source, with 76 % of this emission from Hypoiodous acid (HOI). HOI is also found to be the dominant iodine species in terms of global tropospheric IY burden (contributing up to 70 %). The iodine chemistry leads to a significant global tropospheric O3 burden decrease (9.0 %) compared to standard GEOS-Chem (v9-2). The iodine-driven OX loss rate (748 Tg OX yr−1) is by photolysis of HOI (78 %), photolysis of OIO (21 %), and reaction of IO and BrO (1 %). Increases in global mean OH concentrations (1.8 %) by increased conversion of hydroperoxy radicals exceeds the decrease in OH primary production from the reduced O3 concentration. We perform sensitivity studies on a range parameters and conclude that the simulation is sensitive to choices in parameterisation of heterogeneous uptake, ocean surface iodide, and I2OX (X = 2, 3, 4) photolysis. The new iodine chemistry combines with previously implemented bromine chemistry to yield a total bromine and iodine driven tropospheric O3 burden decrease of 14.4 % compared to a simulation without iodine and bromine chemistry in the model. This is a significant impact and so halogen chemistry needs to be considered in climate and air quality models.