The marine iodine cycle has significant impacts on air quality and atmospheric chemistry. Specifically, the reaction of iodide with ozone in the top few micrometres of the surface ocean is an important sink for tropospheric ozone (a pollutant gas) and the dominant source of reactive iodine to the atmosphere. Sea surface iodide parameterisations are now being implemented in air quality models, but these are currently a major source of uncertainty. Relatively little observational data is available to estimate the global surface iodide concentrations, and this data has not hitherto been openly available in a collated, digital form. Here we present all available sea surface (<20 m depth) iodide observations. The dataset includes values digitised from published manuscripts, published and unpublished data supplied directly by the originators, and data obtained from repositories. It contains 1342 data points, and spans latitudes from 70°S to 68°N, representing all major basins. The data may be used to model sea surface iodide concentrations or as a reference for future observations.

Abstract. Volatile organic compounds (VOCs) are ubiquitous in the atmosphere and are important for atmospheric chemistry. Large uncertainties remain in the role of the ocean in the atmospheric VOC budget because of poorly constrained marine sources and sinks. There are very few direct measurements of air–sea VOC fluxes near the coast, where natural marine emissions could influence coastal air quality (i.e. ozone, aerosols) and terrestrial gaseous emissions could be taken up by the coastal seas. To address this, we present air–sea flux measurements of acetone, acetaldehyde and dimethylsulfide (DMS) at the coastal Penlee Point Atmospheric Observatory (PPAO) in the south-west UK during the spring (April–May 2018). Fluxes of these gases were measured simultaneously by eddy covariance (EC) using a proton-transfer-reaction quadrupole mass spectrometer. Comparisons are made between two wind sectors representative of different air–water exchange regimes: the open-water sector facing the North Atlantic Ocean and the terrestrially influenced Plymouth Sound fed by two estuaries. Mean EC (± 1 standard error) fluxes of acetone, acetaldehyde and DMS from the open-water wind sector were −8.0 ± 0.8, −1.6 ± 1.4 and 4.7 ± 0.6 µmol m−2 d−1 respectively (“−” sign indicates net air-to-sea deposition). These measurements are generally comparable (same order of magnitude) to previous measurements in the eastern North Atlantic Ocean at the same latitude. In comparison, the Plymouth Sound wind sector showed respective fluxes of −12.9 ± 1.4, −4.5 ± 1.7 and 1.8 ± 0.8 µmol m−2 d−1. The greater deposition fluxes of acetone and acetaldehyde within the Plymouth Sound were likely to a large degree driven by higher atmospheric concentrations from the terrestrial wind sector. The reduced DMS emission from the Plymouth Sound was caused by a combination of lower wind speed and likely lower dissolved concentrations as a result of the estuarine influence (i.e. dilution). In addition, we measured the near-surface seawater concentrations of acetone, acetaldehyde, DMS and isoprene from a marine station 6 km offshore. Comparisons are made between EC fluxes from the open-water and bulk air–sea VOC fluxes calculated using air and water concentrations with a two-layer (TL) model of gas transfer. The calculated TL fluxes agree with the EC measurements with respect to the directions and magnitudes of fluxes, implying that any recently proposed surface emissions of acetone and acetaldehyde would be within the propagated uncertainty of 2.6 µmol m−2 d−1. The computed transfer velocities of DMS, acetone and acetaldehyde from the EC fluxes and air and water concentrations are largely consistent with previous transfer velocity estimates from the open ocean. This suggests that wind, rather than bottom-driven turbulence and current velocity, is the main driver for gas exchange within the open-water sector at PPAO (depth of ∼ 20 m).

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Abstract. Volatile organic compounds (VOCs) are ubiquitous in the atmosphere and are important for atmospheric chemistry. Large uncertainties remain in the role of the ocean in the atmospheric VOC budget because of poorly constrained marine sources and sinks. There are very few direct measurements of air–sea VOC fluxes near the coast, where natural marine emissions could influence coastal air quality (i.e. ozone, aerosols) and terrestrial gaseous emissions could be taken up by the coastal seas. To address this, we present air–sea flux measurements of acetone, acetaldehyde and dimethylsulfide (DMS) at the coastal Penlee Point Atmospheric Observatory (PPAO) in the South-West UK during the spring (Apr–May 2018). Fluxes of these gases are quantified simultaneously by eddy covariance (EC) using a proton transfer reaction quadrupole mass spectrometer. Comparisons are made between two wind sectors representative of different air–water exchange regimes: the open water sector facing the North Atlantic Ocean and the fetch-limited Plymouth Sound fed by two estuaries. Mean EC (± 1 standard error) fluxes of acetone, acetaldehyde and DMS from the open-water wind sector were −8.0 ± 0.8, −1.6 ± 1.4 and 4.7 ± 0.6 μmol m−2 d−1 respectively (− sign indicates net air-to-sea deposition). These measurements are generally comparable (same order of magnitude) to previous measurements in the Eastern North Atlantic Ocean at the same latitude. In comparison, the terrestrially influenced Plymouth Sound wind sector showed respective fluxes of −12.9 ± 1.4, −4.5 ± 1.7 and 1.8 ± 0.8 μmol m−2 d−1. The greater deposition fluxes of acetone and acetaldehyde within the Plymouth Sound were likely to a large degree driven by higher atmospheric concentrations from the terrestrial wind sector. The reduced DMS emission from the Plymouth Sound was caused by a combination of lower wind speed and likely lower dissolved concentrations as a result of the freshwater estuarine influence (i.e. dilution). In addition, we measured the near surface seawater concentrations of acetone, acetaldehyde, DMS and isoprene from a marine station 6 km offshore. Comparisons are made between EC fluxes from the open water and bulk air–sea VOC fluxes calculated using air/water concentrations with a two-layer (TL) model of gas transfer. The calculated TL fluxes are largely consistent with the EC measurements with respect to the directions and magnitudes of fluxes. Accordingly, the computed transfer velocities of DMS and acetone from the EC fluxes and air/water concentrations are largely consistent with previous transfer velocity estimates from the open ocean.

&lt;p&gt;Volatile organic compounds (VOCs) are ubiquitous in the atmosphere and are important for atmospheric chemistry. Large uncertainties remain in the role of the ocean in the atmospheric VOC budget because of poorly constrained marine sources and sinks. There are very few direct measurements of air-sea VOC fluxes near the coast, where natural marine emissions could influence coastal air quality (i.e. ozone (O&lt;sub&gt;3&lt;/sub&gt;), aerosols) and terrestrial gaseous emissions could be taken up by the coastal seas.&lt;/p&gt;&lt;p&gt;To address this, we present air&amp;#8211;sea fluxes of acetone, acetaldehyde and dimethylsulfide (DMS) at the coastal Penlee Point Atmospheric Observatory (PPAO) in the South-West UK during the spring (Apr-May 2018). Fluxes are quantified simultaneously by eddy covariance (EC) using a proton transfer reaction quadrupole mass spectrometer. Comparisons are made between two wind sectors representative of different air-water exchange regimes: the open water sector facing the North Atlantic Ocean and the fetch-limited Plymouth Sound fed by two estuaries.&lt;/p&gt;&lt;p&gt;Mean EC (&amp;#177; 1 standard error) fluxes of acetone, acetaldehyde and DMS from the open-water wind sector were &amp;#8209;8.01&amp;#177;0.77, &amp;#8209;1.55&amp;#177;1.44 and 4.67&amp;#177;0.56 &amp;#956;mol m&lt;sup&gt;-2&lt;/sup&gt; d&lt;sup&gt;-1&lt;/sup&gt; respectively (- sign indicates air-to-sea deposition). These measurements are generally comparable (same order of magnitude) to previous measurements in the Eastern North Atlantic Ocean at the same latitude. In comparison, the terrestrially influenced Plymouth Sound wind sector showed respective fluxes of -12.93&amp;#177;1.37, -4.45&amp;#177;1.73 and 1.75&amp;#177;0.80 &amp;#956;mol m&lt;sup&gt;-2&lt;/sup&gt; d&lt;sup&gt;-1&lt;/sup&gt;. The greater deposition fluxes of acetaldehyde and acetone within the Plymouth Sound were largely driven by higher atmospheric concentrations from the terrestrial wind sector. The reduced DMS emission from the Plymouth Sound was caused by a combination of lower wind speed and likely lower dissolved concentrations as a result of the freshwater estuarine influence (i.e. dilution).&lt;/p&gt;&lt;p&gt;In addition, we measured the near surface seawater concentrations of acetone, acetaldehyde, DMS and isoprene from a marine station 6 km offshore. Comparisons are made between EC fluxes from the open water and diffusive VOC fluxes calculated with a two-layer (TL) model of gas transfer using air/water concentrations. The calculated TL fluxes are largely consistent with our direct measurements in the directions and magnitudes of fluxes. Generally, the TL model predicted acetone and acetaldehyde fluxes that were ~12&amp;#8211;33 % higher (greater deposition) than the EC measurements. This could be due to sea surface processes that produce these carbonyl compounds that were not accounted for by the TL technique.&lt;/p&gt;