ALBERT

Description: We measured the vertical water column distribution of nitrous oxide (N2O) during the European Iron Fertilization Experiment (EIFEX) in the subpolar South Atlantic Ocean during February/March 2004 (R/V Polarstern cruise ANT XXI/3). Despite a huge build‐up and sedimentation of a phytoplankton bloom, a comparison of the N2O concentrations within the fertilized patch with concentrations measured outside the fertilized patch revealed no N2O accumulation within 33 days. This is in contrast to a previous study in the Southern Ocean, where enhanced N2O accumulation occurred in the pycnocline. Thus, we conclude that Fe fertilization does not necessarily trigger additional N2O formation and we caution that a predicted radiative offset due to a Fe‐induced additional release of oceanic N2O might be overestimated. Rapid sedimentation events during EIFEX might have hindered the build‐up of N2O and suggest, that not only the production of phytoplankton biomass but also its pathway in the water column needs to be considered if N2O radiative offset is modeled.

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.

Description: Nitrous oxide (N2O) was measured during the first German SOLAS (Surface Ocean – Lower Atmosphere Study) cruise in the tropical North Atlantic Ocean on board R/V Meteor during October/November 2002. About 900 atmospheric and dissolved N2O measurements were performed with a semi-continuous GC-ECD system equipped with a seawater-gas equilibrator. Surface waters along the main transect at 10°N showed no distinct longitudinal gradient. Instead, N2O saturations were highly variable ranging from 97% to 118% (in the Guinea Dome Area, 11°N, 24°W). When approaching the continental shelf of West Africa, N2O surface saturations went up to 113%. N2O saturations in the region of the equatorial upwelling (at 0–1.5°N, 23.5–26°W) were correlated with decreasing sea surface temperatures and showed saturations up to 109%. The overall mean N2O saturation was 104 ± 4% indicating that the tropical North Atlantic Ocean is a net source of atmospheric N2O.

Description: We use transit time distributions calculated from tracer data together with in situ measurements of N(2)O to estimate the concentration of biologically produced N(2)O ([N(2)O](xs)) and N(2)O production rates in the central North Atlantic Ocean. Our approach to estimation of N(2)O production rates integrates the effects of potentially varying production and decomposition mechanisms along the transport path of a water mass. We find that previously used approaches overestimate the oceanic equilibrium N(2)O concentrations by 8-13% and thus underestimate the strength of N(2)O sources in large parts of the water column. Thus the quantitative characteristics of the [N(2)O](xs)/AOU relationship used as an indicator of nitrification are distorted. We developed a new parameterization of N(2)O production during nitrification depending linearly on AOU and exponentially on temperature and depth, which can be applied to calculate N(2)O production due to nitrification in the entire ocean including oxygen minimum zones.

Description: Nitrous oxide (N2O) is a climate-relevant atmospheric trace gas. It is produced as an intermediate of the nitrogen cycle. The open and coastal oceans are major sources of atmospheric N2O. However, its oceanic distribution is still largely unknown. Here we present the first measurements of the water column distribution of N2O in the Gulf of Aqaba and the Red Sea. Samples for N2O depth profiles were collected at the time-series site Station A in the northern Gulf of Aqaba (June and September 2003, and February 2004) and at several stations in the central Red Sea (October 2014, January and August 2016). Additionally, we measured N2O concentrations in brine pool samples collected in the northern and central Red Sea (January 2005 and August 2016). In the Gulf of Aqaba, N2O surface concentrations ranged from 6 to 8 nmol L−1 (97–111% saturation) and were close to the equilibrium with the overlying atmosphere. A pronounced temporal variability of the N2O water column distribution was observed. We suggest that this variability is a reflection of the interplay between N2O production by nitrification and its consumption by N2 fixation in the layers below 150 m during summer. N2O surface concentrations and saturations in the central Red Sea basin ranged from 2 to 9 nmol L−1 (43–155% saturation). A pronounced temporal variability with significant supersaturation in October 2014 and undersaturation in January and August 2016 was observed in the surface layer. In October 2014, N2O in the water column seemed to result from production via nitrification. Low N2O water column concentrations in January and August 2016 indicated a significant removal of N2O. We speculate that either in-situ consumption or remote loss processes of N2O such as denitrification in coastal regions were responsible for this difference. Strong meso- and submesoscale processes might have transported the coastal signals into the central Red Sea. In addition, enhanced N2O concentrations of up to 39 nmol L−1 were found at the seawater-brine pool interfaces which point to an N2O production via nitrification and/or denitrification at low O2 concentrations. Our results indicate that the Red Sea and the Gulf of Aqaba are unique natural laboratories for the study of N2O production and consumption pathways under extreme conditions in one of the warmest and most saline regions of the global ocean.

Description: Aim of this study was the investigation of the vertical dis-tribution of N2O and the factors influencing this distribu-tion. Dissolved and atmospheric N2O was measured in the North Atlantic Ocean and the Baltic Sea. These data, in com-bination with physical and chemical parameters, were used to determine sources and sinks of N2O. Possible production pathways were investigated using the relationship between N2O and relevant production parameters, and their relation to physical processes in the oceans. The hypothesis whether N2O concentrations increased by oceanic iron fertilization via enhanced substrate supply for microbial respiration, was tested during the European Iron Fertilization Experi-ment (EIFEX) in the subpolar South Atlantic. The vertical structure of bacterial communities in the subtropical North Atlantic was investigated, with the intention to find corre-lations between the community structure of bacteria and the distribution of N2O. In summary, this study presents a de-tailed picture of the distribution of N2O in the North At-lantic Ocean and the Baltic Sea and adds 80 profiles of the Atlantic and 26 profiles of the Baltic Sea to the database.