ALBERT

Description: In order to get a comprehensive picture of the distribution of nitrous oxide (N2O) in the North Atlantic Ocean, measurements of dissolved nitrous oxide were made during three cruises in the tropical, subtropical and cold-temperate North Atlantic Ocean in October/November 2002, March/April 2004, and May 2002, respectively. To account for the history of atmospheric N2O, we suggest a new depth-dependent calculation of excess N2O (ΔN2O). N2O depth profiles showed supersaturation throughout the water column with a distinct increasing trend from the cold-temperate to the tropical region. Lowest nitrous oxide concentrations, near equilibrium and with an average of 11.0±1.7 nmol L−1, were found in the cold-temperate North Atlantic where the profiles showed no clear maxima. Highest values up to 37.3 nmol L−1 occurred in the tropical North Atlantic with clear maxima at approximately 400 m. A positive correlation of nitrous oxide with nitrate, as well as excess nitrous oxide with the apparent oxygen utilization (AOU), was only observed in the subtropical and tropical regions. Therefore, we conclude that the formation of nitrous oxide via nitrification occurs in the tropical region rather than in the cold-temperate region of the North Atlantic Ocean

Description: In January 2003, a major inflow of cold and oxygen-rich North Sea Water terminated an ongoing stagnation period in parts of the central Baltic Sea. In order to investigate the role of North Sea Water inflow in the production of nitrous oxide (N2O), we measured dissolved and atmospheric N〈2O at 26 stations in the southern and central Baltic Sea in October 2003. At the time of our cruise, water renewal had proceeded to the eastern Gotland Basin, whereas the western Gotland Basin was still unaffected by the inflow. The deep water renewal was detectable in the distributions of temperature, salinity, and oxygen concentrations as well as in the distribution of the N2O concentrations: Shallow stations in the Kiel Bight and Pomeranian Bight were well-ventilated with uniform N2O concentrations near equilibrium throughout the water column. In contrast, stations in the deep basins, such as the Bornholm and the Gotland Deep, showed a clear stratification with deep water affected by North Sea Water. Inflowing North Sea Water led to changed environmental conditions, especially enhanced oxygen (O2) or declining hydrogen sulphide (H2S) concentrations, thus, affecting the conditions for the production of N2O. Pattern of N2O profiles and correlations with parameters like oxygen and nitrate differed between the basins. Because of the positive correlation between ΔN2O and AOU in oxic waters the dominant production pathway seems to be nitrification rather than denitrification. Advection of N2O by North Sea Water was found to be of minor importance. A rough budget revealed a significant surplus of in situ produced N2O after the inflow. However, due to the permanent halocline, it can be assumed that the N2O produced does not reach the atmosphere. Hydrographic aspects therefore are decisive factors determining the final release of N2O produced to the atmosphere.