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Understanding Iodine Chemistry Over the Northern and Equatorial Indian Ocean
Author(s) -
Mahajan Anoop S.,
Tinel Liselotte,
Sarkar Amit,
Chance Rosie,
Carpenter Lucy J.,
Hulswar Shrivardhan,
Mali Prithviraj,
Prakash Satya,
Vinayachandran P. N.
Publication year - 2019
Publication title -
journal of geophysical research: atmospheres
Language(s) - English
Resource type - Journals
eISSN - 2169-8996
pISSN - 2169-897X
DOI - 10.1029/2018jd029063
Subject(s) - iodide , iodine , seawater , dimethyl sulfide , ozone , biogeochemical cycle , oceanography , atmosphere (unit) , bromine , environmental science , mixed layer , atmospheric sciences , chemistry , environmental chemistry , geology , meteorology , geography , inorganic chemistry , sulfur , organic chemistry
Abstract Observations of halogen oxides, ozone, meteorological parameters, and physical and biogeochemical water column measurements were made in the Indian Ocean and its marine boundary layer as a part of the Second International Indian Ocean Expedition (IIOE‐2). The expedition took place on board the oceanographic research vessel Sagar Nidhi during 4–22 December 2015 from Goa, India, to Port Louis, Mauritius. Observations of mixed layer depth, averaged temperature, salinity, and nitrate concentrations were used to calculate predicted iodide concentrations in the seawater. The inorganic iodine ocean‐atmosphere flux (hypoiodous acid [HOI] and molecular iodine [I 2 ]) was computed using the predicted iodide concentrations, measured atmospheric ozone, and wind speed. Iodine oxide (IO) mixing ratios peaked at 0.47 ± 0.29 pptv (parts per trillion by volume) in the remote open ocean environment. The estimated iodide concentrations and HOI and I 2 fluxes peaked at 200/500 nM, 410/680 nmol·m −2 ·day −1 , and 20/80 nmol·m −2 ·day −1 , respectively, depending on the parameterization used. The calculated fluxes for HOI and I 2 were higher closer to the Indian subcontinent; however, atmospheric IO was only observed above the detection limit in the remote open ocean environment. We use NO 2 observations to show that titration of IO by NO 2 is the main reason for this result. These observations show that inorganic iodine fluxes and atmospheric IO show similar trends in the Indian Ocean marine boundary layer, but the impact of inorganic iodine emissions on iodine chemistry is buffered in elevated NO x environments, even though the estimated oceanic iodine fluxes are higher.