Abstract:
Concentrations of dissolved and atmospheric nitrous oxide, N2O, were measured in the austral spring of 1992 in the Drake Passage and Bellingshausen Sea as part of the United Kingdom Joint Global Ocean Flux Study expedition to the Southern Ocean. The measured atmospheric mixing ratio was 313 +/- 5 parts per billion by volume, in agreement with the hemispherically corrected global mean. In the Drake Passage, surface N2O saturations were generally very close to atmospheric equilibrium, 99.7 +/- 3%, although several anomalous points were associated with the presence of frontal and eddy-like features within the Antarctic Polar Frontal Zone and at the Continental Water Boundary. Further to the south, a series of oceanographic stations and two surface transects along the 85 degrees W meridian between 65.28 degrees S and 70.32 degrees S revealed a transition from undersaturated conditions in open water to oversaturated conditions in the marginal ice zone, in the upper mixed layer (75-100 m). These observations reflect upwelling of Circumpolar Deep Water at approximately 70 degrees S, resulting in the accumulation of N2O under the winter sea ice and its subsequent release to the atmosphere following the ice retreat. Sea-air N2O fluxes were estimated from the product of the surface N2O anomaly and the modelled gas transfer coefficients of Liss and Merlivat [1986] and Wanninkhof [1992] to find a maximum rate of +3.1 micromole N2O m-2 d -1. North of the upwelling region, Antarctic Surface Water formed from the mixing of surface waters and ice melt was moderately depleted in N2O with respect to the atmosphere, a minimum 90% of saturation. This sink area was estimated to extend between 65.28 degrees S and 69.57 degrees S with a mean sea-air flux of between -0.6 +/- 0.4 and -0.9 +/- 0.7 micromole N2O m-2 d-1. The region studied at 85 degrees W (65.28 degrees S to 70.32 degrees S) revealed source and sink areas which were largely determined by the changing physical hydrography, so that overall there was a small net negative flux of between -0.06 +/- 0.9 and -0.09 +/- 1.4 micromole N2O m-2 d-1.
Funding: The work was supported by NERC funding to the Plymouth Marine Laboratory, the British Antarctic Survey and from the U.K. Biogeochemical Flux Study (BOFS).
Keywords:
Antarctic, Bellingshausen Sea, Deception Island, Drakes Passage, Nitrous oxide
Rees, A.P., Owens, N.J.P., & Upstill-Goddard, R. (2024). Nitrous oxide in the Drakes Passage, Bellingshausen Sea and Deception Island during November-December 1992 (Version 1.0) [Data set]. NERC EDS UK Polar Data Centre. https://doi.org/10.5285/af64fb7a-6783-4951-b7e0-3ffc37b931e1
| Access Constraints: | None. |
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| Use Constraints: | This data is governed by the NERC data policy http://www.nerc.ac.uk/research/sites/data/policy/ and supplied under Open Government Licence v.3 http://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/. |
| Creation Date: | 2024-04-18 |
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| Dataset Progress: | Planned |
| Dataset Language: | English |
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| Parameters: |
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| Personnel: | |
| Name | UK PDC |
| Role(s) | Metadata Author |
| Organisation | British Antarctic Survey |
| Name | Andrew P Rees |
| Role(s) | Investigator, Technical Contact |
| Organisation | Plymouth Marine Laboratory |
| Name | Nicholas J P Owens |
| Role(s) | Investigator |
| Organisation | Scottish Association for Marine Science |
| Name | Robert Upstill-Goddard |
| Role(s) | Investigator |
| Organisation | University of Newcastle |
| Parent Dataset: | N/A |
| Reference: | Associated paper: Rees, A. P., Owens, N. P. J., and Upstill-Goddard, R. C. (1997), Nitrous oxide in the Bellingshausen Sea and Drake Passage, J. Geophys. Res., 102(C2), 3383-3391, doi:10.1029/96JC03350. Papers referenced in metadata: Elkins, J. W. (1980), Determination of dissolved nitrous oxide in aquatic systems by gas chromatography using electron-capture detection and multiple phase equilibration, Anal. Chem., 52, 263-267. doi:10.1021/ac50052a011. Liss, P. S., and Merlivat, L. (1986), Air-sea gas exchange rates: Introduction and synthesis, The Role of Air-Sea Exchange in Geochemical Cycling P. Buat-Menard, 113-127, D. Reidel, Norwell, Mass. Swanson, T. H., et al. (1992), Nitrous oxide and halocarbons division, Climate Monitoring and Diagnostics Laboratory No. 21: Summary Report 1992 J. T. Pearson, 59-75 Environ. Res. Lab., NOAA, Boulder, Colo. Upstill-Goddard, R. C., Watson, A. J., Liss, P. S., Liddicoat, M. I. (1990), Gas transfer velocities in lakes measured with SF6, Tellus, Ser. B, 42, 364-377. Upstill-Goddard, R. C., Rees, A. P., and Owens, N. J. P. (1996), Simultaneous high-precision measurements of methane and nitrous oxide in water and seawater by single phase equilibration gas chromatography. Deep-Sea Res. I: Oceanogr. Res. Pap., 43(10), 1669-1682. doi:10.1016/S0967-0637(96)00074-X. Wanninkhof, R. (1992), Relationship between wind speed and gas exchange over the ocean, J. Geophys. Res., 97, 7373-7382. doi:10.1029/92JC00188. Weiss, R. F., and Price, B. A. (1980), Nitrous oxide solubility in water and seawater, Mar. Chem., 8, 347-359. doi:10.1016/0304-4203(80)90024-9. |
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| Quality: | Primary method calibration was through a commercially prepared, certified N2O/CH4 mixture in an UHP N2 matrix (Air Products) with a certified accuracy of +/-1% or better. For routine analytical calibrations a series of four secondary standards (in the linear range of the detector) were used, prepared from the primary mixtures by pressure dilution [Upstill-Goddard et al., 1990]. Consequently, the best estimate for overall accuracy of the N2O secondary standards was +/-2%. The variability of the method during this study was generally better than 2-3% (mean = 0.97%, n=44), based on replicate analyses of standards, atmospheric air, and compressed air. In support of this calibration, the measured atmospheric mixing ratio of 313 +/- 5 parts per billion by volume (ppbv) shows less than 1% deviation from the interhemispheric corrected global mean and at worst provides an overestimate of 1.3% relative to 1992 data for the South Pole [Swanson et al., 1992]. | |
| Lineage: | Collection of Seawater Samples Seawaters were collected during the STERNA expedition of the RRS James Clark Ross between October and December 1992 - RRS James Clark Ross JR19921026 (JR02, JRXX7). For surface transects, samples were taken from the ship's nontoxic seawater supply (intake at 8 m). Samples for the vertical profiles were collected from a conductivity-temperature-depth (CTD) rosette sampler, using 10-L Go-Flo bottles. Sample collection was in 1-L volumetric flasks, overfilled at least three times to aid exclusion of air bubbles. Following the addition of 200-microlitre saturated HgCl2 solution to arrest microbial action, flasks were sealed with ground glass stoppers, inverted to disperse the HgCl2 and temperature equilibrated at 25.0 +/- 0.05 degrees C prior to N2O analysis. In preliminary work, water samples treated in this way showed no significant changes in N2O concentration during several days storage. Using a similar sampling protocol, Elkins [1980] reports dissolved N2O stabilities of at least 1.5 months. N2O Analysis Analyses of N2O in air and seawater were by gas chromatography with electron-capture detection (Shimadzu GC-8AIE, 10mCi 63Ni). For seawaters, analysis was always within 48 hours of collection using a single-phase equilibration technique. The analytical system is described in detail by Upstill-Goddard et al. (1996 - Simultaneous high-precision measurements of methane and nitrous oxide in water and seawater by single phase equilibration gas chromatography, Deep Sea Research, Part I.), where full details of method calibration are also presented. In brief, chromatographic separation of N2O was at 65 degrees C on Porapak-Q (80-100 mesh, 2 m x 2 mm stainless steel column), with prior removal of H2O vapor and CO2 on precolumns of magnesium perchlorate and carbosorb, respectively. The detector temperature was 320 degrees C. Carrier gas was ultrahigh purity (UHP) nitrogen at a flow rate of 15 mL min-1. The method returns gas partial pressures in the samples at the equilibrium temperature. Dissolved N2O concentrations in situ were calculated from the solubility tables of Weiss and Price [1980], for the equilibrium temperature (~25°C) and in situ salinity. Percent saturation of seawater with N2O was determined by ratioing the N2O partial pressures corrected to in situ temperature to the values determined in atmospheric air samples (mean 313 +/- 5 ppbv). |
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| Project: |
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| Temporal Coverage: | |
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| Start Date | 1992-11-01 |
| End Date | 1992-12-07 |
| Spatial Coverage: | |
| Latitude | |
| Southernmost | -70.27417 |
| Northernmost | -55.34717 |
| Longitude | |
| Westernmost | -85.52117 |
| Easternmost | -59.14983 |
| Altitude | |
| Min Altitude | N/A |
| Max Altitude | N/A |
| Depth | |
| Min Depth | 0 |
| Max Depth | 3775 |
| Location: | |
| Location | Southern Ocean |
| Detailed Location | Drakes Passage |
| Location | Bellingshausen Sea |
| Detailed Location | N/A |
| Location | South Shetland Islands |
| Detailed Location | Deception Island |
| Sensor(s): |
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| Data Collection: | Analyses of N2O in air and seawater were by gas chromatography with electron-capture detection (Shimadzu GC-8AIE, 10mCi 63Ni). |
| Distribution: | |
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| Distribution Media | Online Internet (HTTP) |
| Distribution Size | 9 KB |
| Distribution Format | ASCII |
| Fees | N/A |
| Data Storage: | 2x .csv files: Sterna1992_N2O_Profile.csv containing NO2 vertical profile Sterna1992_N2O_Transect.csv containing NO2 surface transect |