Abstract
Photosynthesis in the surface ocean produces approximately 100 gigatonnes of organic carbon per year, of which 5 to 15 per cent is exported to the deep ocean. The rate at which the sinking carbon is converted into carbon dioxide by heterotrophic organisms at depth is important in controlling oceanic carbon storage. It remains uncertain, however, to what extent surface ocean carbon supply meets the demand of water-column biota; the discrepancy between known carbon sources and sinks is as much as two orders of magnitude. Here we present field measurements, respiration rate estimates and a steady-state model that allow us to balance carbon sources and sinks to within observational uncertainties at the Porcupine Abyssal Plain site in the eastern North Atlantic Ocean. We find that prokaryotes are responsible for 70 to 92 per cent of the estimated remineralization in the twilight zone (depths of 50 to 1,000 metres) despite the fact that much of the organic carbon is exported in the form of large, fast-sinking particles accessible to larger zooplankton. We suggest that this occurs because zooplankton fragment and ingest half of the fast-sinking particles, of which more than 30 per cent may be released as suspended and slowly sinking matter, stimulating the deep-ocean microbial loop. The synergy between microbes and zooplankton in the twilight zone is important to our understanding of the processes controlling the oceanic carbon sink.
Highlights
Photosynthesis in the surface ocean produces ~100 Gt of organic carbon per year, of which 5-15% is exported to the deep ocean[1,2]
Most of the exported organic carbon is processed by the water column biota, which converts it into CO2 via respiration
A key constraint in the analysis of carbon fluxes in the twilight zone is that, at steady state, the attenuation of particulate organic carbon (POC) flux with depth should be balanced by community metabolism
Summary
Input fluxes and respiration rates (mg C m-2 d-1) are based on measurements at the PAP site, North Atlantic. Community respiration (%) was estimated by combining highest and lowest estimates. Atlantic[47,48,49] (respective to publications: black circle, triangle and diamond) and North Pacific[50] (grey square). Error bars are s.e.m. c, Flow diagram of calculation of prokaryotic respiration using bootstrapping. The output gives 100,000 estimates of prokaryotic respiration, which are used to compute the uncertainty in the final estimate
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