Primary productivity à la mode

Posted by mmaheigan 
· Wednesday, October 10th, 2018 

The presence of large-scale Ekman downwelling is the textbook explanation for low nutrient concentrations, and hence low productivity, in subtropical gyres. However, recent research has suggested that mesoscale eddies oppose and substantially reduce this downwelling, a process known as eddy cancellation (Doddridge et al, 2016). Eddy cancellation represents a substantial alteration to the widely accepted notion of large-scale Ekman downwelling in subtropical gyres, and motivates our study of the processes that determine nutrient concentration within subtropical gyres.

Figure 1: Sensitivity experiments for mode water thickness (hmode) with two values of residual Ekman pumping. a) With no residual Ekman pumping, phosphate concentration responds strongly to mode water thickness. b) When Ekman pumping is strong, phosphate concentration does not depend on mode water thickness. The dashed lines represent transects of climatological phosphate concentration in the euphotic zone of the North Atlantic subtropical gyre (Garcia et al., 2013).

A recent paper published in the Journal of Geophysical Research: Oceans and featured in an MIT News article describes an idealized model for nutrient concentration in subtropical gyres that can account for this reduction in Ekman pumping. The model predicts that surface productivity is sensitive to the thickness of the underlying subtropical mode water layer, provided that the residual Ekman pumping is small (Figure 1). Comparison of this prediction with observations from the Bermuda Atlantic Time series Study (BATS) shows that surface productivity increases as the thickness of the underlying mode water increases (Figure 2), as predicted by the idealized model in the absence of substantial Ekman pumping.

Figure 2: Annually averaged primary productivity and mode water thickness from the BATS dataset. The linear fit between mode water thickness and primary productivity is statistically significant (p ≈ 0.027) and explains 19.5% of the variance in primary productivity.

The observed relationship between productivity and mode water thickness at BATS is consistent with a small residual Ekman pumping, indicating highly effective eddy cancellation in the subtropical North Atlantic. Previous research (Palter et al., 2005) has suggested that as the subtropical mode water layer thickens, it blocks nutrient entrainment from below, resulting in lower productivity in the euphotic zone. However, this study suggests that a thicker subtropical mode water layer actually increases the surface nutrient concentrations by promoting more effective recycling of nutrients within the gyre. With a thicker mode water layer, more of the nutrients in the particulate flux are remineralized before they pass through the thermocline and become isolated from the surface ocean. This means that a thicker mode water layer leads to higher nutrient concentrations and supports primary productivity in subtropical gyres. This represents a fundamental change in our understanding of how nutrients are supplied to the surface waters of subtropical gyres.

Authors:
Edward Doddridge (Department of Earth, Atmospheric and Planetary Sciences, MIT)
David Marshall (Atmospheric, Oceanic & Planetary Physics, University of Oxford)

See the Eos spotlight on this research

Filter by Keyword

abundance acidification additionality advection africa air-sea air-sea interactions algae alkalinity allometry ammonium AMO AMOC anoxic Antarctic Antarctica anthro impacts anthropogenic carbon anthropogenic impacts appendicularia aquaculture aquatic continuum aragonite saturation arctic Argo argon arsenic artificial seawater AT Atlantic atmospheric CO2 atmospheric nitrogen deposition authigenic carbonates autonomous platforms AUVs bacteria bathypelagic BATS BCG Argo benthic bgc argo bio-go-ship bio-optical bioavailability biogeochemical cycles biogeochemical models biogeochemistry Biological Essential Ocean Variables biological pump biophysics bloom blue carbon bottom water boundary layer buffer capacity C14 CaCO3 calcification calcite carbon carbon-climate feedback carbon-sulfur coupling carbonate carbonate system carbon budget carbon cycle carbon dioxide carbon export carbon fluxes carbon sequestration carbon storage Caribbean CCA CCS changing marine chemistry changing marine ecosystems changing marine environments changing ocean chemistry chemical oceanographic data chemical speciation chemoautotroph chesapeake bay chl a chlorophyll circulation clouds CO2 CO3 coastal and estuarine coastal darkening coastal ocean cobalt Coccolithophores commercial community composition competition conservation cooling effect copepod copepods coral reefs CTD currents cyclone daily cycles data data access data assimilation database data management data product Data standards DCM dead zone decadal trends decomposers decomposition deep convection deep ocean deep sea coral denitrification deoxygenation depth diatoms DIC diel migration diffusion dimethylsulfide dinoflagellate dinoflagellates discrete measurements distribution DOC DOM domoic acid DOP dust DVM ecology economics ecosystem management ecosystems eddy Education EEZ Ekman transport emissions ENSO enzyme equatorial current equatorial regions ESM estuarine and coastal carbon fluxes estuary euphotic zone eutrophication evolution export export fluxes export production extreme events faecal pellets fecal pellets filter feeders filtration rates fire fish Fish carbon fisheries fishing floats fluid dynamics fluorescence food webs forage fish forams freshening freshwater frontal zone functional role future oceans gelatinous zooplankton geochemistry geoengineering geologic time GEOTRACES glaciers gliders global carbon budget global ocean global warming go-ship grazing greenhouse gas greenhouse gases Greenland ground truthing groundwater Gulf of Maine Gulf of Mexico Gulf Stream gyre harmful algal bloom high latitude human food human impact human well-being hurricane hydrogen hydrothermal hypoxia ice age ice cores ice cover industrial onset inland waters in situ inverse circulation ions iron iron fertilization iron limitation isotopes jellies katabatic winds kelvin waves krill kuroshio lab vs field land-ocean continuum larvaceans lateral transport LGM lidar ligands light light attenuation lipids low nutrient machine learning mangroves marine carbon cycle marine heatwave marine particles marine snowfall marshes mCDR mechanisms Mediterranean meltwater mesopelagic mesoscale mesoscale processes metagenome metals methane methods microbes microlayer microorganisms microplankton microscale microzooplankton midwater mitigation mixed layer mixed layers mixing mixotrophs mixotrophy model modeling model validation mode water molecular diffusion MPT MRV multi-decade n2o NAAMES NCP nearshore net community production net primary productivity new ocean state new technology Niskin bottle nitrate nitrogen nitrogen cycle nitrogen fixation nitrous oxide north atlantic north pacific North Sea NPP nuclear war nutricline nutrient budget nutrient cycles nutrient cycling nutrient limitation nutrients OA observations ocean-atmosphere ocean acidification ocean acidification data ocean alkalinity enhancement ocean carbon storage and uptake ocean carbon uptake and storage ocean color ocean modeling ocean observatories ocean warming ODZ oligotrophic omics OMZ open ocean optics organic particles oscillation outwelling overturning circulation oxygen pacific paleoceanography PAR parameter optimization parasite particle flux particles partnerships pCO2 PDO peat pelagic PETM pH phenology phosphate phosphorus photosynthesis physical processes physiology phytoplankton PIC piezophilic piezotolerant plankton POC polar polar regions policy pollutants precipitation predation predator-prey prediction pressure primary productivity Prochlorococcus productivity prokaryotes proteins pteropods pycnocline radioisotopes remineralization remote sensing repeat hydrography residence time resource management respiration resuspension rivers rocky shore Rossby waves Ross Sea ROV salinity salt marsh satellite scale seafloor seagrass sea ice sea level rise seasonal seasonality seasonal patterns seasonal trends sea spray seawater collection seaweed secchi sediments sensors sequestration shelf ocean shelf system shells ship-based observations shorelines siderophore silica silicate silicon cycle sinking sinking particles size SOCCOM soil carbon southern ocean south pacific spatial covariations speciation SST state estimation stoichiometry subduction submesoscale subpolar subtropical sulfate surf surface surface ocean Synechococcus technology teleconnections temperate temperature temporal covariations thermocline thermodynamics thermohaline thorium tidal time-series time of emergence titration top predators total alkalinity trace elements trace metals trait-based transfer efficiency transient features trawling Tris trophic transfer tropical turbulence twilight zone upper ocean upper water column upwelling US CLIVAR validation velocity gradient ventilation vertical flux vertical migration vertical transport warming water clarity water mass water quality waves weathering western boundary currents wetlands winter mixing zooplankton

Copyright © 2025 - OCB Project Office, Woods Hole Oceanographic Institution, 266 Woods Hole Rd, MS #25, Woods Hole, MA 02543 USA Phone: 508-289-2838  •  Fax: 508-457-2193  •  Email: ocb_news@us-ocb.org

link to nsflink to noaalink to WHOI

Funding for the Ocean Carbon & Biogeochemistry Project Office is provided by the National Science Foundation (NSF) and the National Aeronautics and Space Administration (NASA). The OCB Project Office is housed at the Woods Hole Oceanographic Institution.