Nathan Briggs

Eddy-driven subduction exports particulate organic carbon from the spring bloom

Down with atmospheric carbon dioxide How does the ocean move carbon from surface waters to its deep interior? Current understanding is that carbon dioxide is removed from the atmosphere by phytoplankton that are eaten, and in turn their predators die and sink into deep water and seafloor sediments. In addition to this route, Omand et al. show that downwelling caused by ocean eddies 1 to 10 km across can deliver much of the carbon produced in spring to the deep sea. The eddies entrain small particles and dissolved organic carbon to augment the flux of large sinking particles. Science, this issue p. 222 Ocean eddies can transport appreciable quantities of organic carbon from the surface to depth. The export of particulate organic carbon (POC) from the surface ocean to depth is traditionally ascribed to sinking. Here, we show that a dynamic eddying flow field subducts surface water with high concentrations of nonsinking POC. Autonomous observations made by gliders during the North Atlantic spring bloom reveal anomalous features at depths of 100 to 350 meters with elevated POC, chlorophyll, oxygen, and temperature-salinity characteristics of surface water. High-resolution modeling reveals that during the spring transition, intrusions of POC-rich surface water descend as coherent, 1- to 10-kilometer–scale filamentous features, often along the perimeter of eddies. Such a submesoscale eddy-driven flux of POC is unresolved in global carbon cycle models but can contribute as much as half of the total springtime export of POC from the highly productive subpolar oceans.

Net community production and export from Seaglider measurements in the North Atlantic after the spring bloom

Mean rates of net community production (NCP) and particulate organic carbon (POC) export were estimated from sensor measurements of dissolved oxygen (O2), chlorophyll fluorescence (chl F), and particulate backscatter (bbp700) collected from three Seagliders that surveyed a 20 × 20 km area in the North Atlantic subsequent to a large diatom bloom. Since the Seagliders sampled geographically fixed patterns, care was taken in the calculation of all terms applicable to the Eulerian reference frame, including local rate of change, vertical mixing, air-sea exchange, and horizontal advection. Although similar studies of NCP in the open ocean have generally assumed advection to be insignificant, we have found that this term cannot be ignored when dealing with temporal scales of ≤1 month and/or spatial scales ≤20 km. The overlapping sampling pattern of the Seagliders was sufficiently rapid such that 4–5 day time scales observed in the O2 and POC data were adequately resolved and variations were not a consequence of aliasing spatial variability. During the study period, ratios of chlorophyll fluorescence-to-particulate backscatter (chl:bbp700) were lower than values encountered during the spring diatom bloom, suggesting the phytoplankton community was predominantly composed of smaller cells (picoplankton and nanoplankton) and/or coccolithophorids. Coupled budgets of oxygen and POC indicated a net community production of 1.0 mol C m−2 and carbon export of 0.6 mol C m−2, respectively, over a period of 23 days. Thus, the production and export of carbon that occurred over the month-long experiment period was comparable to that encountered during the spring bloom.

Plankton Assemblage Estimated with BGC‐Argo Floats in the Southern Ocean: Implications for Seasonal Successions and Particle Export

The Southern Ocean (SO) hosts plankton communities that impact the biogeochemical cycles of the global ocean. However, weather conditions in the SO restrict mainly in situ observations of plankton communities to spring and summer, preventing the description of biological successions at an annual scale. Here, we use shipboard observations collected in the Indian sector of the SO to develop a multivariate relationship between physical and bio-optical data, and, the composition and carbon content of the plankton community. Then we apply this multivariate relationship to five biogeochemical Argo (BGC-Argo) floats deployed within the same bio-geographical zone as the ship-board observations to describe spatial and seasonal changes in plankton assemblage. The floats reveal a high contribution of bacteria below the mixed layer, an overall low abundance of picoplankton and a seasonal succession from nano- to microplankton during the spring bloom. Both naturally iron-fertilized waters downstream of the Crozet and Kerguelen Plateaus show elevated phytoplankton biomass in spring and summer but they differ by a nano- or microplankton dominance at Crozet and Kerguelen, respectively. The estimated plankton group successions appear consistent with independent estimations of particle diameter based on the optical signals. Furthermore, the comparison of the plankton community composition in the surface layer with the presence of large mesopelagic particles diagnosed by spikes of optical signals provides insight into the nature and temporal changes of ecological vectors that drive particle export. This study emphasizes the power of BGC-Argo floats for investigating important biogeochemical processes at high temporal and spatial resolution.