ALBERT

Description: Shipboard measurements of eddy covariance dimethylsulfide (DMS) air–sea fluxes and seawater concentration were carried out in the North Atlantic bloom region in June/July 2011. Gas transfer coefficients (k660) show a linear dependence on mean horizontal wind speed at wind speeds up to 11 m s−1. At higher wind speeds the relationship between k660 and wind speed weakens. At high winds, measured DMS fluxes were lower than predicted based on the linear relationship between wind speed and interfacial stress extrapolated from low to intermediate wind speeds. In contrast, the transfer coefficient for sensible heat did not exhibit this effect. The apparent suppression of air–sea gas flux at higher wind speeds appears to be related to sea state, as determined from shipboard wave measurements. These observations are consistent with the idea that long waves suppress near-surface water-side turbulence, and decrease interfacial gas transfer. This effect may be more easily observed for DMS than for less soluble gases, such as CO2, because the air–sea exchange of DMS is controlled by interfacial rather than bubble-mediated gas transfer under high wind speed conditions.

Description: Very short-lived halocarbons are significant sources of reactive halogen in the marine boundary layer, and likely in the upper troposphere and lower stratosphere. Quantifying ambient concentrations in the surface ocean and atmosphere is essential for understanding the atmospheric impact of these trace gas fluxes. Despite the body of literature increasing substantially over recent years, calibration issues complicate the comparison of results and limit the utility of building larger-scale databases that would enable further development of the science (e.g. sea-air flux quantification, model validation, etc.). With this in mind, thirty-one scientists from both atmospheric and oceanic halocarbon communities in eight nations gathered in London in February 2008 to discuss the scientific issues and plan an international effort toward developing common calibration scales (http://tinyurl.com/c9cg58). Here, we discuss the outputs from this meeting, suggest the compounds that should be targeted initially, identify opportunities for beginning calibration and comparison efforts, and make recommendations for ways to improve the comparability of previous and future measurements.

Description: The proposed strong positive relationship between dimethylsulphide (DMS) concentration and the solar radiation dose (SRD) received into the surface ocean is tested using data from the Atlantic Meridional Transect (AMT) programme. In situ, daily data sampled concurrently with DMS concentrations is used for the component variables of the SRD (mixed layer depth, MLD, surface insolation, I0, and a light attenuation coefficient, k) to calculate SRDinsitu. This is the first time in situ data for all of the components, including k, has been used to test the SRD-DMS relationship over large spatial scales. We find a significant correlation (ρ=0.55 n=65 p

Description: We tested the recently proposed, strong positive relationship between dimethylsulphide (DMS) concentrations and the solar radiation dose (SRD) received into the surface ocean. We utilised in situ daily data sampled concurrently with DMS concentrations from the Atlantic Meridional Transect (AMT) programme for the component variables of the SRD; mixed layer depth (MLD), surface insolation (I0) and a light attenuation coefficient (k), to calculate SRDin situ. We find a significant correlation (ρ=0.53) but the slope of the relationship is approximately half that previously proposed. The correlation is improved (ρ=0.76) by replacing the in situ data with an estimated I0 (which assumes a constant 50% removal of the top of atmosphere value; 0.5×TOA), a MLD climatology and a fixed value for k following a previously described methodology. Equally significant, but non-linear relationships are also found between DMS and both in situ MLD (ρ=0.73) and the estimated I0 (ρ=0.76) alone. The DMS data shows an interesting relationship to an approximated UV attenuation depth profile. Using a cloud adjusted, satellite climatology of surface UVA irradiance to calculate a UV radiation dose (UVRD) provides an equivalent correlation (ρ=0.73) to DMS. With this data, MLD appears the dominant control upon DMS concentrations and remains a useful shorthand to prediction without fully resolving the biological processes involved. However, the implied relationship between incident solar/ultraviolet radiation dose and sea surface DMS concentrations (modulated by MLD) is critical for closing a climate feedback loop.

Description: Dimethylsulphide (DMS) is a globally important aerosol precurser. In 1987 Charlson and others proposed that an increase in DMS production by certain phytoplankton species in response to a warming climate could stimulate increased aerosol formation, increasing the lower-atmosphere's albedo, and promoting cooling. Despite two decades of research, the global significance of this negative climate feedback remains contentious. It is therefore imperative that schemes are developed and tested, which allow for the realistic incorporation of phytoplankton DMS production into Earth System models. Using these models we can investigate the DMS-climate feedback and reduce uncertainty surrounding projections of future climate. Here we examine two empirical DMS parameterisations within the context of an Earth System model and find them to perform marginally better than the standard DMS climatology at predicting observations from an independent global dataset. We then question whether parameterisations based on our present understanding of DMS production by phytoplankton, and simple enough to incorporate into global climate models, can be shown to enhance the future predictive capacity of those models. This is an important question to ask now, as results from increasingly complex Earth System models lead us into the 5th assessment of climate science by the Intergovernmental Panel on Climate Change. Comparing observed and predicted interannual variability, we suggest that future climate projections may underestimate the magnitude of surface ocean DMS change. Unfortunately this conclusion relies on a relatively small dataset, in which observed interannual variability may be exaggerated by biases in sample collection. We therefore encourage the observational community to make repeat measurements of sea-surface DMS concentrations an important focus, and highlight areas of apparent high interannual variability where sampling might be carried out. Finally, we assess future projections from two similarly valid empirical DMS schemes, and demonstrate contrasting results. We therefore conclude that the use of empirical DMS parameterisations within simulations of future climate should be undertaken only with careful appreciation of the caveats discussed.

Description: Shipboard measurements of eddy covariance DMS air/sea fluxes and seawater concentration were carried out in the North Atlantic bloom region in June/July 2011. Gas transfer coefficients (k660) show a linear dependence on mean horizontal wind speed at wind speeds up to 11 m s−1. At higher wind speeds the relationship between k660 and wind speed weakens. At high winds, measured DMS fluxes were lower than predicted based on the linear relationship between wind speed and interfacial stress extrapolated from low to intermediate wind speeds. In contrast, the transfer coefficient for sensible heat did not exhibit this effect. The apparent suppression of air/sea gas flux at higher wind speeds appears to be related to sea state, as determined from shipboard wave measurements. These observations are consistent with the idea that long waves suppress near surface water side turbulence, and decrease interfacial gas transfer. This effect may be more easily observed for DMS than for less soluble gases, such as CO2, because the air/sea exchange of DMS is controlled by interfacial rather than bubble-mediated gas transfer under high wind speed conditions.

Description: Air/sea dimethylsulfide (DMS) fluxes and bulk air/sea gradients were measured over the Southern Ocean in February/March 2012 during the Surface Ocean Aerosol Production (SOAP) study. The cruise encountered three distinct phytoplankton bloom regions, consisting of two blooms with moderate DMS levels, and a high biomass, dinoflagellate-dominated bloom with high seawater DMS levels (〉15 nM). Gas transfer coefficients were considerably scattered at wind speeds above 5 m s−1. Bin averaging the data resulted in a linear relationship between wind speed and mean gas transfer velocity consistent with that previously observed. However, the wind speed-binned gas transfer data distribution at all wind speeds is positively skewed. The flux and seawater DMS distributions were also positively skewed, which suggests that eddy covariance-derived gas transfer velocities are consistently influenced by additional, log-normal noise. A~flux footprint analysis was conducted during a transect into the prevailing wind and through elevated DMS levels in the dinoflagellate bloom. Accounting for the temporal/spatial separation between flux and seawater concentration significantly reduces the scatter in computed transfer velocity. The SOAP gas transfer velocity data shows no obvious modification of the gas transfer-wind speed relationship by biological activity or waves. This study highlights the challenges associated with eddy covariance gas transfer measurements in biologically active and heterogeneous bloom environments.

Description: We present air-sea fluxes of carbon dioxide (CO2), methane (CH4), momentum, and sensible heat measured by the eddy covariance method from the recently established Penlee Point Atmospheric Observatory (PPAO) on the South West coast of the United Kingdom. Measurements from the southwest direction (background marine air) at three different sampling heights (approximately 15, 18, 27 m above mean sea level, AMSL) in three different periods during 2014–2015 are shown. At sampling heights ≥ 18 m AMSL, measured fluxes of momentum and sensible heat demonstrate reasonable agreement with their expected transfer rates over the open ocean. This confirms the suitability of PPAO for air-sea exchange measurements. We observed reductions in the air-to-sea fluxes of CO2 from spring to summer in both years, which coincided with the breakdown of the spring phytoplankton bloom. At all sampling heights, mean CH4 fluxes were positive, suggesting marine emissions. Higher CH4 fluxes were observed during rising tides (20±3; 29±6; 38±3 μmole m−2 d−1 at 15, 27, 18 m AMSL) than during falling tides (14±2; 21±5; 22±2 μmole m−2 d−1, respectively), consistent with an elevated CH4 source from an estuarine outflow driven by local tidal circulation. Based on observations at PPAO, we also estimate the detection limit of the eddy covariance CH4 flux measurement to be ~20 μmole m−2 d−1 over hourly timescales (~4 μmole m−2 d−1 over 24 hours).

Description: Short-lived halocarbons are significant sources of reactive halogen in the troposphere and likely the lower stratosphere. Quantifying ambient concentrations in the surface ocean and atmosphere is essential for understanding the impact of fluxes of these gases on marine boundary layer oxidation and lower stratospheric ozone-depletion processes. Despite the body of literature increasing substantially over recent years, calibration issues complicate comparison of results and limit the utility of building larger-scale databases that would enable further development of the science (e.g. sea-air flux quantification, model validation, etc.). With this in mind, thirty-two scientists representing eight nations and from both atmospheric and oceanic halocarbon communities gathered in London in February 2008 to discuss the scientific issues and plan an international effort toward a common calibration scale. Here, we discuss the outputs from this meeting, suggest the compounds that should be targeted initially, identify opportunities for beginning calibration and comparison efforts, and make recommendations for ways to improve the comparability of previous and future measurements.

Description: Dimethylsulphide (DMS) is a globally important aerosol precurser. In 1987 Charlson and others proposed that an increase in DMS production by certain phytoplankton species in response to a warming climate could stimulate increased aerosol formation, increasing the lower-atmosphere's albedo, and promoting cooling. Despite two decades of research, the global significance of this negative climate feedback remains contentious. It is therefore imperative that schemes are developed and tested, which allow for the realistic incorporation of phytoplankton DMS production into Earth System models. Using these models we can investigate the DMS-climate feedback and reduce uncertainty surrounding projections of future climate. Here we examine two empirical DMS parameterisations within the context of an Earth System model and find them to perform marginally better than the standard DMS climatology at predicting observations from an independent global dataset. We then question whether parameterisations based on our present understanding of DMS production by phytoplankton, and simple enough to incorporate into global climate models, can be shown to enhance the future predictive capacity of those models. This is an important question to ask now, as results from increasingly complex Earth System models lead us into the 5th assessment of climate science by the Intergovernmental Panel on Climate Change. Comparing observed and predicted inter-annual variability, we suggest that future climate projections may underestimate the magnitude of surface ocean DMS change. Unfortunately this conclusion relies on a relatively small dataset, in which observed inter-annual variability may be exaggerated by biases in sample collection. We therefore encourage the observational community to make repeat measurements of sea-surface DMS concentrations an important focus, and highlight areas of apparent high inter-annual variability where sampling might be carried out. Finally, we assess future projections from two similarly valid empirical DMS schemes, and demonstrate contrasting results. We therefore conclude that the use of empirical DMS parameterisations within simulations of future climate should be undertaken only with careful appreciation of the caveats discussed.