Ocean Carbon & Biogeochemistry
Studying marine ecosystems and biogeochemical cycles in the face of environmental change
  • Home
  • About OCB
    • About Us
    • Scientific Breadth
      • Biological Pump
      • Changing Marine Ecosystems
      • Changing Ocean Chemistry
      • Estuarine and Coastal Carbon Fluxes
      • Ocean Carbon Uptake and Storage
      • Ocean Observatories
    • Code of Conduct
    • Get Involved
    • Project Office
    • Scientific Steering Committee
    • OCB committees
      • Ocean Time-series
      • US Biogeochemical-Argo
      • Ocean-Atmosphere Interaction
  • Activities
    • Summer Workshop
    • OCB Webinars
      • GO-BGC Webinar Series
    • Guidelines for OCB Workshops & Activities
    • Topical Workshops
      • CMIP6 Models Workshop
      • Coastal BGS Obs with Fisheries
      • C-saw extreme events workshop
      • Ecological Forecasting – North American Coastlines
      • Expansion of BGC-Argo and Profiling Floats
      • Fish, fisheries and carbon
      • Future BioGeoSCAPES program
      • GO-BCG Scoping Workshop
      • Lateral Carbon Flux in Tidal Wetlands
      • Marine CDR Workshop
      • Ocean Nucleic Acids ‘Omics
      • Ocean-Atmosphere Interactions
      • Oceanic Methane & Nitrous Oxide
      • Pathways Connecting Climate Changes to the Deep Ocean
    • Small Group Activities
      • Aquatic Continuum OCB-NACP Focus Group
      • Arctic-COLORS Data Synthesis
      • BECS Benthic Ecosystem and Carbon Synthesis WG
      • Carbon Isotopes in the Ocean Workshop
      • CMIP6 WG
      • Filling the gaps air–sea carbon fluxes WG
      • Fish Carbon WG
        • Fish Carbon WG Workshop
        • Fish carbon workshop summary
      • mCDR
      • Metaproteomic Intercomparison
      • Mixotrophs & Mixotrophy WG
      • N-Fixation WG
      • Ocean Carbonate System Intercomparison Forum
      • Ocean Carbon Uptake WG
      • OOI BGC sensor WG
      • Operational Phytoplankton Observations WG
      • Phytoplankton Taxonomy WG
    • Other Workshops
    • Science Planning
      • Coastal CARbon Synthesis (CCARS)
      • North Atlantic-Arctic
    • Ocean Acidification PI Meetings
    • Training Activities
      • PACE Training Activity
  • Science Support
    • Data management and archival
    • Early Career
    • Funding Sources
    • Jobs & Postdocs
    • Meeting List
    • OCB Topical Websites
      • Ocean Fertilization
      • Trace gases
      • US IIOE-2
    • Outreach & Education
    • Promoting your science
    • Student Opportunities
    • OCB Activity Proposal Solicitations
      • Guidelines for OCB Workshops & Activities
    • Travel Support
  • Publications
    • Ocean Carbon Exchange
    • OCB Workshop Reports
    • Science Planning and Policy
    • Newsletter Archive
  • Science Highlights
  • News

Archive for human impact

Do rivers supply nutrients to the open ocean?

Posted by mmaheigan 
· Wednesday, May 24th, 2017 

Rivers carry large amounts of nutrients (e.g., nitrogen and phosphorus) to the sea, but we do not know how much of that riverine nutrient supply escapes biological and chemical processing in shallow coastal waters to reach the open ocean. Most global ocean biogeochemical models, which are typically unable to resolve coastal processes, assume that either all or none of the riverine nutrients entering coastal waters actually contribute to open ocean processes.

While we know a good deal about the dynamics of individual rivers entering the coastal ocean, studies to date have been limited to a few major river systems, mainly in in developed countries. Globally, there are over 6,000 rivers entering the coastal ocean. In a recent study, Sharples et al (2017) devised a simple approach to obtain a global-scale estimate of riverine nutrient inputs based on the knowledge that low-salinity waters entering the coastal ocean tend to form buoyant plumes that turn under the influence of Earth’s daily rotation to flow along the coastline. Using published data on such flows and incorporating the effect of Earth’s rotation, they obtained estimates of typical cross-shore plume width and compared them to the local width of the continental shelf. This was used to calculate the residence time of riverine nutrients on the shelf, which is the key to estimating how much of a given nutrient is consumed in shelf waters vs. how much is exported to the open ocean.

Global distribution of the amount of riverine dissolved inorganic nitrogen that escapes the continental shelf to reach the open ocean.

The results indicate that, on a global scale, 75% (80%) of the nitrogen (phosphorus) supplied by rivers reaches the open ocean, whereas 25% (20%) of the nitrogen (phosphorus) is consumed on the shelf (e.g., fueling coastal productivity). Limited knowledge of nutrient cycling and consumption in shelf waters represents the primary source of uncertainty in this study. However, well-defined global patterns related to human land use (e.g., agricultural fertilizer use in developed nations) emerged from this analysis, underscoring the need to understand how land-use changes and other human activities will alter nutrient delivery to the coastal ocean in the future.

 

Authors:
Jonathan Sharples (School of Environmental Sciences, University of Liverpool, UK)
Jack Middelburg (Department of Earth Sciences, Utrecht University, Netherlands)
Katja Fennel (Department of Oceanography, Dalhousie University, Canada)
Tim Jickells (School of Environmental Sciences, University of East Anglia, UK)

Filter by Keyword

abundance acidification africa air-sea interactions algae alkalinity allometry ammonium AMOC anoxic Antarctic anthro impacts anthropogenic carbon aquaculture aquatic continuum aragonite saturation arctic Argo argon arsenic artificial seawater Atlantic atmospheric CO2 atmospheric nitrogen deposition authigenic carbonates autonomous platforms 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 carbon budget carbon cycle carbon dioxide carbon export carbon sequestration carbon storage Caribbean CCA CCS changing marine ecosystems changing marine environments changing ocean chemistry chemical oceanographic data chemical speciation chemoautotroph chesapeake bay chl a chlorophyll circulation climate change climate variability CO2 coastal darkening coastal ocean cobalt Coccolithophores commercial community composition conservation cooling effect copepod coral reefs CTD currents cyclone daily cycles data data access data assimilation data management data product Data standards DCM dead zone decadal trends decomposers decomposition deep convection deep ocean deep sea coral deoxygenation depth diatoms DIC diel migration diffusion dimethylsulfide dinoflagellate discrete measurements DOC DOM domoic acid dust DVM ecology ecosystem management ecosystems eddy Education Ekman transport emissions ENSO enzyme equatorial regions ESM estuarine and coastal carbon fluxes estuary euphotic zone eutrophication evolution export export fluxes export production EXPORTS 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 geochemistry geoengineering geologic time GEOTRACES glaciers gliders global carbon budget global ocean global warming go-ship grazing greenhouse gas 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 isotopes jellies katabatic winds kelvin waves krill kuroshio lab vs field land-ocean continuum larvaceans lateral transport LGM lidar ligands light light attenuation lipids machine learning mangroves marine carbon cycle marine heatwave marine particles marine snowfall marshes Mediterranean meltwater mesopelagic mesoscale metagenome metals methane methods microbes microlayer microorganisms microscale microzooplankton midwater mixed layer mixed layers mixing mixotrophy model modeling model validation mode water molecular diffusion MPT multi-decade n2o NAAMES NASA 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 nuclear war nutricline nutrient budget nutrient cycling nutrient limitation nutrients OA ocean-atmosphere ocean acidification ocean acidification data ocean carbon uptake and storage ocean color ocean modeling ocean observatories ocean warming ODZ oligotrophic omics OMZ open ocean optics organic particles oscillation overturning circulation oxygen pacific paleoceanography parameter optimization particle flux partnerships pCO2 PDO peat pelagic PETM pH phenology phosphorus photosynthesis physical processes physiology phytoplankton PIC piezophilic piezotolerant plankton POC polar regions policy pollutants precipitation predation prediction pressure primary productivity Prochlorococcus 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 patterns seasonal trends sea spray seawater collection seaweed secchi sediments sensors shelf ocean shelf system shells ship-based observations shorelines silicate silicon cycle 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 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 volcano warming water clarity water mass water quality waves western boundary currents wetlands winter mixing zooplankton

Copyright © 2023 - 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.