scholarly journals Direct covariance measurement of CO2gas transfer velocity during the 2008 Southern Ocean Gas Exchange Experiment: Wind speed dependency

Author(s):  
J. B. Edson ◽  
C. W. Fairall ◽  
L. Bariteau ◽  
C. J. Zappa ◽  
A. Cifuentes-Lorenzen ◽  
...  
2014 ◽  
Vol 14 (21) ◽  
pp. 28453-28482
Author(s):  
T. G. Bell ◽  
W. De Bruyn ◽  
C. A. Marandino ◽  
S. D. Miller ◽  
C. S. Law ◽  
...  

Abstract. 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.


2009 ◽  
Vol 6 (6) ◽  
pp. 1105-1114 ◽  
Author(s):  
M. Ll. Calleja ◽  
C. M. Duarte ◽  
Y. T. Prairie ◽  
S. Agustí ◽  
G. J. Herndl

Abstract. Air-sea CO2 exchange depends on the air-sea CO2 gradient and the gas transfer velocity (k), computed as a function of wind speed. Large discrepancies among relationships predicting k from wind suggest that other processes also contribute significantly to modulate CO2 exchange. Here we report, on the basis of the relationship between the measured gas transfer velocity and the organic carbon concentration at the ocean surface, a significant role of surface organic matter in suppressing air-sea gas exchange, at low and intermediate winds, in the open ocean, confirming previous observations. The potential role of total surface organic matter concentration (TOC) on gas transfer velocity (k) was evaluated by direct measurements of air-sea CO2 fluxes at different wind speeds and locations in the open ocean. According to the results obtained, high surface organic matter contents may lead to lower air-sea CO2 fluxes, for a given air-sea CO2 partial pressure gradient and wind speed below 5 m s−1, compared to that observed at low organic matter contents. We found the bias in calculated gas fluxes resulting from neglecting TOC to co-vary geographically and seasonally with marine productivity. These results support previous evidences that consideration of the role of organic matter in modulating air-sea CO2 exchange may improve flux estimates and help avoid possible bias associated to variability in surface organic concentration across the ocean.


2004 ◽  
Vol 16 (4) ◽  
pp. 517-529 ◽  
Author(s):  
PETER S. LISS ◽  
ADELE L. CHUCK ◽  
SUZANNE M. TURNER ◽  
ANDREW J. WATSON

The flux of gases between the atmosphere and the oceans can be calculated from the product of the concentration difference across the sea surface and a kinetic term, often called a transfer velocity. The transfer velocity is frequently parameterized in terms of wind speed, although the actual exchange process is also affected by waves, bubbles, wind fetch, and less certainly by surfactants and chemical reactivity. There is currently an uncertainty of about a factor of two in using the wind speed parameterization. In view of the windiness of the Southern Ocean, transfer velocities will often be high, although there are few published in situ measurements of transfer rates made in the region. Data for gas concentration fields in the Southern Ocean are generally sparse compared to other better studied oceanic areas. In this paper we discuss what is known for the region for carbon dioxide, including the oceanic sink for man-made inputs to the atmosphere; dimethyl sulphide, where there appears to be a substantial source, which has the potential for a significant climatic effect due to the low particulate loading in the region; and organo-halogen and alkyl nitrate gases, where marine emissions may play an important role in controlling the oxidation capacity of the Antarctic atmosphere.


2021 ◽  
Author(s):  
Jacek Piskozub ◽  
Violetta Drozdowska ◽  
Iwona Wróbel-Niedźwiecka ◽  
Przemysław Makuch ◽  
Piotr Markuszewski ◽  
...  

<p>The air-sea gas flux is proportional to the difference of partial pressure between the sea-water and the overlying atmosphere multiplied by gas transfer velocity <em>k</em>, a measure of the effectiveness of the gas exchange. Because wind is the source of turbulence making the gas exchange more effective, <em>k</em> is usually parameterized by wind speed. Unfortunately, measured values of gas transfer velocity at a given wind speed have a large spread in values. Surfactants have been long suspected as the main reason of this variability but few measurements of gas exchange and surfactants have been performed at open sea simultaneously and therefore their results were inconclusive. Only recently, it has been shown that surfactants may decrease the CO<sub>2</sub> air-sea exchange by up to 50%. However the labour intensive methods used for surfactant study make it impossible to collect enough data to map the surfactant coverage or even create a gas transfer velocity parameterization involving a measure of surfactant activity. This is why we propose to use optical fluorescence as a proxy of surfactant activity.</p><p> </p><p>Previous research done by our group showed that fluorescence parameters allow estimation the surfactant enrichment of the surface microlayer, as well as types and origin of fluorescent organic matter involved. We plan to measure, from a research ship, all the variables needed for calculation of gas transfer velocity <em>k</em> (namely CO<sub>2</sub> partial pressure both in water and in air as well as vertical flux of this trace gas) and to use mathematical optimization methods to look for a parameterization involving wind speed and one of the fluorescence parameters which will minimize the residual <em>k</em> variability. Although our research will still involve water sampling and laboratory fluorescence measurements, the knowledge of which absorption and fluorescence emission bands are the best proxy for surfactant activity may allow to create remote sensing products (fluorescence lidars) allowing continuous measurements of surfactant activity at least from the ship board, if not from aircraft and satellites. The improved parameterization of the CO<sub>2</sub> gas transfer velocity will allow better constraining of basin-wide and global air-sea fluxes, an important component of global carbon budget.</p><p> </p><p>If an improved gas transfer velocity parametrization based on surfactant fluorescence spectrum in concert with a turbulence proxy (wind) were to be found, a tantalizing possibility arises of a remote sensing estimation of <em>k</em>. Namely a UV lidar can both excite and measure the fluorescence band identified as proxy of the surfactant effect on the gas transfer velocity. Depending on the wavelength bands needed to be utilized, the effect could be measured from a moving ship (already an improvements on methods needing sampling), an aircraft or possibly even a satellite. We intend to pursue this idea in cruises to both the Baltic and the North Atlantic, possibly in cooperation with other air-sea interaction groups (this presentation is in part an invitation to cooperation).</p>


2015 ◽  
Vol 15 (4) ◽  
pp. 1783-1794 ◽  
Author(s):  
T. G. Bell ◽  
W. De Bruyn ◽  
C. A. Marandino ◽  
S. D. Miller ◽  
C. S. Law ◽  
...  

Abstract. 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 show 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.


2020 ◽  
Author(s):  
Shuo Li ◽  
Alexander Babanin ◽  
Fangli Qiao ◽  
Dejun Dai ◽  
Shumin Jiang ◽  
...  

<p>Hydrodynamic processes at air-sea interface play a significant role on air-sea CO<sub>2</sub> gas exchange, which further affects global carbon cycle and climate change. CO<sub>2</sub> gas transfer velocity (K<sub>CO2</sub>) is generally parameterized with wind speed but ocean surface waves have direct impact on the gas exchange. Thus, the relationship between wave breaking and CO<sub>2</sub> gas exchange was studied through laboratory experiments and by utilizing field campaign data. The results from laboratory show that wave breaking plays a significant role in CO<sub>2</sub> gas exchange in all experiments while wind forcing can also influence K<sub>CO2</sub>. A non-dimensional empirical formula is established in which K<sub>CO2 </sub>is expressed as the product of wave breaking probability, transformed Reynolds number and an enhancement factor of wind speed. The parameterization is then improved by considering the bubble-mediated gas transfer based on both laboratory and ship campaign data sets. In the end, the formula is employed in the estimation of global CO<sub>2</sub> uptake by ocean and the result is found consistent with reported values.</p>


2008 ◽  
Vol 5 (6) ◽  
pp. 4209-4233
Author(s):  
M. Ll. Calleja ◽  
C. M. Duarte ◽  
Y. T. Prairie ◽  
S. Agustí ◽  
G. J. Herndl

Abstract. Air-sea CO2 exchange depends on the air-sea CO2 gradient and the gas transfer velocity (k), computed as a simple function of wind speed. Large discrepancies among relationships predicting k from wind suggest that other processes may also contribute significantly to modulate CO2 exchange. Here we report, on the basis of the relationship between the measured gas transfer velocity and the ocean surface organic carbon concentration at the ocean surface, a significant role of surface organic matter in suppressing air-sea gas exchange, at low and intermediate winds, in the open ocean. The potential role of total surface organic matter concentration (TOC) on gas transfer velocity (k) was evaluated by direct measurements of air-sea CO2 fluxes at different wind speeds and locations in the open ocean. According to the results obtained, high surface organic matter contents may lead to lower air-sea CO2 fluxes, for a given air-sea CO2 partial pressure gradient and wind speed below 5 m s−1, compared to that observed at low organic matter contents. We found the bias in calculated gas fluxes resulting from neglecting TOC to co-vary geographically and seasonally with marine productivity. These findings suggest that consideration of the role of organic matter in modulating air-sea CO2 exchange can improve flux estimates and help avoid possible bias associated to variability in surface organic concentration across the ocean.


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