Archive for chl a

Industrial era climate forcing drives multi-century decline in North Atlantic productivity

Posted by mmaheigan 
· Wednesday, October 2nd, 2019 

Phytoplankton respond directly to climate forcing, and due to their central role in global oxygen production and atmospheric carbon sequestration, they are critical components of the Earth’s climate system. There are however few observations detailing past variability in marine primary productivity, particularly over multi-decadal to centennial timescales. This limits our understanding of the long-term impact of climatic forcing on both past and future marine productivity.

Multi-century decline of subarctic Atlantic productivity. From top: standardized (z-score units relative to ad 1958-2016) indices of Continuous Plankton Recorder (CPR)-based diatom, dinoflagellate and coccolithophore relative-abundances; North Atlantic [chlorophyll-α] reconstruction from Boyce et al. (2010, Nature); ice core-based [MSA] PC1 productivity index. The “Industrial Onset” range shows the estimated initiation of declining subarctic Atlantic productivity; reconstructed (Rahmstorf et al., 2015, Nat. Clim. Change) and observed sea-surface temperature-based Atlantic Meridional Overturning Circulation (i.e., AMOC) index, alongside 5-year averaged subarctic Atlantic freshwater storage anomalies (relative to A.D. 1955) from Curry and Mauritzen (2005; Science).

Authors of a new study published in Nature used a high-resolution signal of marine biogenic aerosol emissions (methanesulfonic acid, or “MSA”) preserved within twelve Greenland ice cores to reconstruct a ~250-year record of marine productivity variations across the subarctic Atlantic basin, one of the most biologically productive and climatically sensitive regions on Earth. These results provide the most continuous proxy-based reconstruction of basin-scale productivity to date in this region, illuminating the following major findings: (1) subarctic Atlantic marine productivity has declined over the industrial era by as much as 10 ± 7%; (2) the early 19th century onset of declining productivity coincides with the regional onset of industrial-era surface warming, and also strongly covaries with regional sea surface temperatures and basin-scale gyre circulation strength; (3) there is strong decadal- to centennial-scale coherence between northern Atlantic productivity variability and declining Atlantic Meridional Overturning Circulation (AMOC) strength, as predicted by prior model-based studies.

Future atmospheric warming is predicted to contribute to accelerating Greenland Ice Sheet runoff, ocean-surface freshening, and AMOC slowdown, suggesting the potential for continued declines in productivity across this dynamic and climatically important region. Such declines will, in turn, have important implications for future maritime economies, global food security, and drawdown of atmospheric carbon dioxide.

 

Authors:
Matthew Osman (Massachusetts Institute of Technology)
Sarah Das (Woods Hole Oceanographic Institution)
Luke Trusel (Rowan University)
Matthew Evans (Wheaton College)
Hubertus Fischer (University of Bern)
Mackenzie Griemann (University of California, Irvine)
Sepp Kipfstuhl (Alfred-Wegener-Institute)
Joseph McConnell (Desert Research Institute)
Eric Saltzman (University of California, Irvine)

 

Figure references:
Boyce, D. G., Lewis, M. R. & Worm, B. (2010) Global phytoplankton decline over the past century. Nature 466, 591–596.

Curry, R. & Mauritzen, C. (2005) Dilution of the northern North Atlantic Ocean in recent decades. Science 308, 1772–1774.

Rahmstorf, S. et al. (2015) Exceptional twentieth-century slowdown in Atlantic Ocean overturning circulation. Nat. Clim. Change 5, 475–480.

Can microzooplankton shape the depth distribution of phytoplankton?

Posted by mmaheigan 
· Tuesday, July 23rd, 2019 

Photosynthetic, single-celled phytoplankton form the base of many marine and lacustrine (lake) food webs. These microscopic algae typically occur in the sunlit surface layer, but in many ecosystems, there are also sub-surface peaks in phytoplankton and chlorophyll-a, their key photosynthetic pigment. Historically, scientists have explained deep chlorophyll maximum (DCM) formation by invoking “bottom-up” processes such as nutrient and light co-limitation, while less attention has been paid to “top-down” controls such as predation.

A recent study in Nature Communications challenges this conventional wisdom by arguing that microzooplankton (top-down control) can cause the formation of DCMs by preferentially consuming phytoplankton near the surface. This can occur when microzooplankton exhibit light-dependent grazing—a known but not well-understood phenomenon in which prey consumption rates increase with increasing light intensity. By incorporating this phenomenon into mathematical models, the authors showed that this can create a “spatial refuge” for phytoplankton in deeper, darker parts of the water column, where there is enough sunlight to photosynthesize, but too little for efficient microzooplankton predation. Furthermore, when light-dependent grazing is incorporated into a global ocean biogeochemistry model (COBALT: Carbon, Ocean Biogeochemistry and Lower Trophics – planktonic ecosystem model), DCMs that are already present due to bottom-up controls deepen, improving agreement between model predictions, satellite data, and in situ observations.

Figure legend: Global comparison of annual mean deep chlorophyll maxima (DCM) depths (A) predicted by the unmodified COBALT model, (B) predicted by the COBALT model modified to include light-dependent microzooplankton grazing, and (C) estimated based on satellite data. Incorporating light-dependent grazing deepens the DCM, especially in oligotrophic gyres, and improves agreement with observational data.

These findings highlight the importance of higher trophic levels in regulating aquatic primary productivity. The model predictions suggest that not only can microzooplankton suppress primary production near the surface, but by shifting phytoplankton abundances deeper, they may increase carbon export via the biological pump. Future field tests of this hypothesis—i.e. detailed grazing measurements in stratified water columns with DCMs—can elucidate the extent to which light-dependent grazing shapes phytoplankton distribution in real biological systems.

 

Authors:
Holly Moeller (University of California Santa Barbara)
Charlotte Laufkötter (University of Bern and Princeton University)
Edward Sweeney (Sea Education Association and Santa Barbara Museum of Natural History)
Matthew Johnson (Woods Hole Oceanographic Institution)

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 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 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 CO2 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 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.