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  • ASLO (Association for the Sciences of Limnology and Oceanography)  (1)
  • Copernicus  (1)
  • 2010-2014  (2)
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  • 1
    Publication Date: 2014-08-19
    Description: We present high-resolution autonomous measurements of carbon dioxide partial pressure p(CO2) taken in situ at the Porcupine Abyssal Plain sustained observatory (PAP-SO) in the Northeast Atlantic (49° N, 16.5° W; water depth of 4850 m) for the period 2010 to 2012. Measurements of p(CO2) made at 30 m depth on a sensor frame are compared with other autonomous biogeochemical measurements at that depth (including chlorophyll a-fluorescence and nitrate concentration data) to analyse weekly to seasonal controls on p(CO2) flux in the inter-gyre region of the North Atlantic. Comparisons are also made with in situ regional time-series data from a ship of opportunity and mixed layer depth (MLD) measurements from profiling Argo floats. There is a persistent under saturation of CO2 in surface waters throughout the year which gives rise to a perennial CO2 sink. Comparison with an earlier dataset collected at the site (2003 to 2005) confirms seasonal and inter-annual changes in surface seawater chemistry. There is year-to-year variability in the timing of stratification and deep winter mixing. The 2010 to 2012 period shows an overall increase in p(CO2) values when compared to the 2003–2005 period. This is despite similar surface temperature, wind speed and MLD measurements between the two periods of time. Future work should incorporate daily CO2 flux measurements made using CO2 sensors at 1 m depth and the in situ wind speed data now available from the UK Met Office Buoy.
    Print ISSN: 1810-6277
    Electronic ISSN: 1810-6285
    Topics: Biology , Geosciences
    Published by Copernicus on behalf of European Geosciences Union.
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  • 2
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    ASLO (Association for the Sciences of Limnology and Oceanography)
    In:  Limnology and Oceanography, 55 (5). pp. 2207-2218.
    Publication Date: 2017-10-24
    Description: To test the hypothesis that calcium carbonate (rather than opal) carries most organic carbon to the deep sea, total hydrolysable amino acid (THAA) analysis was applied to deep-sea (3000 m) sediment trap material from the northeast Atlantic (PAP Site), a variable but intrinsically carbonate-dominated system. THAAs were analyzed in conjunction with total organic carbon, biogenic silica, calcium carbonate, and inferred lithogenic fluxes. The THAA-based degradation state of organic carbon could not be systematically explained by changes in the flux of different mineral phases, which could account for only 16% of the observed variability. In addition amino acid parameters indicative of source organisms indicate that diatom cell walls are an important residual component of organic carbon reaching the deep ocean, a finding supported by comparison with data from previous studies of diverse oceanic environments. Finally, during 2001, very high organic carbon fluxes were associated with elevated lithogenic fluxes and low organic matter degradation relative to surrounding years. In accordance with other recent experimental and observational studies, the data indicate that under specific export scenarios, lithogenic fluxes can act as highly significant mediators of organic carbon transfer to the deep ocean.
    Type: Article , PeerReviewed
    Format: text
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