Ocean Carbon & Biogeochemistry
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Archive for ocean carbon uptake and storage

New unified interface for existing ocean carbonate chemistry data products

Posted by mmaheigan 
· Tuesday, March 24th, 2026 

The paper provides a comprehensive synthesis of 68 existing ocean carbonate chemistry data products and data product sets, including cruise-based compilations, time-series datasets, gap-filled observational products, and model-based reconstructions. The authors highlight the diversity of available products, noting differences in spatial coverage, temporal resolution, methodologies, and intended scientific applications. By systematically cataloguing and comparing these datasets, the study helps researchers identify which products are most suitable for specific scientific questions related to ocean carbon cycling and ocean acidification.

ESSD Paper

Interface for the most updated list of products

Submission interface

 

Authors
Li-Qing Jiang (University of Maryland; NOAA National Centers for Environmental Information; Scripps Institution of Oceanography)
Amanda Fay (Columbia University / Lamont-Doherty Earth Observatory)
Jens Daniel Müller (ETH Zürich; Carbon to Sea Initiative)
Luke Gregor (ETH Zürich; Swiss Data Science Center)
Alizée Roobaert (Flanders Marine Institute, VLIZ)
Lydia Keppler (Vycarb Inc.)
Dustin Carroll (Moss Landing Marine Laboratories; NASA Jet Propulsion Laboratory)
Siv K. Lauvset (NORCE Research / Bjerknes Centre for Climate Research)
Tim DeVries (University of California, Santa Barbara)
Judith Hauck (Alfred Wegener Institute, Helmholtz Centre for Polar and Marine Research)
Christian Rödenbeck (Max Planck Institute for Biogeochemistry)
Nicolas Metzl (Sorbonne Université / LOCEAN)
Andrea J. Fassbender (NOAA Pacific Marine Environmental Laboratory)
Jean-Pierre Gattuso (Sorbonne Université / CNRS; Laboratoire d’Océanographie de Villefranche)
Peter Landschützer (Max Planck Institute for Meteorology)
Rik Wanninkhof (NOAA Atlantic Oceanographic and Meteorological Laboratory)
Christopher Sabine (University of Hawaii at Mānoa)
Simone R. Alin (NOAA Pacific Marine Environmental Laboratory)
Mario Hoppema (Alfred Wegener Institute)
Are Olsen (University of Bergen / Bjerknes Centre for Climate Research)
Matthew P. Humphreys (University of East Anglia)
Kunal Chakraborty (National Institute of Oceanography, India)
Ana C. Franco (University of Miami)
Kumiko Azetsu-Scott (Bedford Institute of Oceanography / Fisheries and Oceans Canada)
Dorothee C. E. Bakker (University of East Anglia)
Leticia Barbero (NOAA Atlantic Oceanographic and Meteorological Laboratory)
Nicholas R. Bates (Bermuda Institute of Ocean Sciences / Arizona State University)
Nicole Besemer (University of Natural Resources and Life Sciences Vienna)
Henry C. Bittig (GEOMAR Helmholtz Centre for Ocean Research Kiel)
Albert E. Boyd (University of Tasmania)
Daniel Broullón (Spanish Institute of Oceanography, IEO-CSIC)
Wei-Jun Cai (University of Delaware)
Brendan R. Carter (University of Washington)
Thi-Tuyet-Trang Chau (LSCE, CEA-CNRS-UVSQ)
Chen-Tung Arthur Chen (National Sun Yat-sen University)
Frédéric Cyr (Fisheries and Oceans Canada)
John E. Dore (University of Hawaii)
Ian Enochs (NOAA Atlantic Oceanographic and Meteorological Laboratory)
Richard A. Feely (NOAA Pacific Marine Environmental Laboratory)
Hernan E. Garcia (NOAA National Centers for Environmental Information)
Marion Gehlen (LSCE, CEA-CNRS-UVSQ)
Prasanna Kanti Ghoshal (CSIR-National Institute of Oceanography, India)
Lucas Gloege (Princeton University)
Melchor González-Dávila (University of Las Palmas de Gran Canaria)
Nicolas Gruber (ETH Zürich)
Debby Ianson (Fisheries and Oceans Canada / Institute of Ocean Sciences)
Yosuke Iida (Japan Meteorological Agency)
Masao Ishii (Meteorological Research Institute, Japan)
Apurva Padamnabh Joshi (CSIR-National Institute of Oceanography, India)
Esther Kennedy (NOAA Pacific Marine Environmental Laboratory)
Alex Kozyr (NOAA National Centers for Environmental Information)
Nico Lange (GEOMAR Helmholtz Centre for Ocean Research Kiel)
Claire Lo Monaco (Sorbonne Université / LOCEAN)
Derek P. Manzello (NOAA Atlantic Oceanographic and Meteorological Laboratory)
Galen A. McKinley (Columbia University / Lamont-Doherty Earth Observatory)
Natalie M. Monacci (NOAA Pacific Marine Environmental Laboratory)
Xosé A. Padin (Spanish Institute of Oceanography, IEO-CSIC)
Ana M. Palacio-Castro (Instituto de Investigaciones Marinas, CSIC)
Fiz F. Pérez (Spanish Institute of Oceanography, IEO-CSIC)
J. Magdalena Santana-Casiano (University of Las Palmas de Gran Canaria)
Jonathan Sharp (University of Delaware)
Adrienne Sutton (NOAA Pacific Marine Environmental Laboratory)
Jim Swift (Scripps Institution of Oceanography)
Toste Tanhua (GEOMAR Helmholtz Centre for Ocean Research Kiel)
Maciej Telszewski (International Ocean Carbon Coordination Project, IOCCP)
Jens Terhaar (University of Bern)
Ruben van Hooidonk (University of Miami / NOAA Coral Reef Watch)
Anton Velo (Spanish Institute of Oceanography, IEO-CSIC)
Andrew J. Watson (University of Exeter)
Angelicque E. White (Oregon State University)
Zelun Wu (University of Delaware)
Liang Xue (Xiamen University)
Hyelim Yoo (University of Maryland / NOAA NCEI)
Jiye Zeng (National Institute for Environmental Studies, Japan)
Guorong Zhong (Xiamen University)

How much carbon do fish move towards the seafloor as they feed and migrate in the water column?

Posted by mmaheigan 
· Tuesday, March 24th, 2026 

Ocean organisms transfer carbon via many natural processes from surface to seafloor. These include the passive sinking of carbon-rich particles and the active transport of carbon as animals swim downward. A recent study in GBC modeled how carbon stored in fish biomass moves from the sea surface to the seafloor in shelf–slope–abyssal systems through feeding interactions alone. This transport occurs as large fish eat smaller fish while occupying different vertical habitats in the water column. On average, this process delivers an amount equivalent to 5% of all carbon that reaches the seafloor—through sinking organic particles from phytoplankton and zooplankton. Yet, this can be as high as 20% in some shelf areas. On continental slopes, midwater fishes play a key role as a stepping-stone for carbon transfer (up to 50%) to the seafloor. Overall, the study reveals that the vertical movement of fish is an important pathway for delivering carbon to groundfish species, particularly on shelf areas where most commercially valuable fisheries operate.

Caption: Schematic of a shelf-slope-abyssal system with hypothesized fluxes of carbon among major functional groups (top panel); and model-estimated fluxes of carbon from functional groups to demersal fishes (bottom panel). Solid and dotted lines are mean fluxes for Eastern and Western North Atlantic systems, respectively, and shaded areas are standard deviations. Values are proportional.

 

 

Authors

Daniel Ottmann (Technical University of Denmark (DTU-Aqua); Institute of Marine Sciences of Andalusia)
Ken H. Andersen (Technical University of Denmark (DTU-Aqua))
Yixin Zhao (Technical University of Denmark (DTU-Aqua))
Colleen M. Petrik (Scripps Institution of Oceanography)
Charles A. Stock (Scripps Institution of Oceanography)
Clive Trueman (University of Southampton)
P. Daniël van Denderen (Technical University of Denmark (DTU-Aqua))

 

Follow the authors:
bluesky: @danielottmann.bsky.social; @kenandersen.bsky.social
LinkedIn accounts: Ottman; Andersen; Truman
X: @daniel_ottmann; @69kno; @OceanLifeCenter; @van_denderen; @clivetrue;

 

Active Transport of Carbon to Demersal Fish Communities in Shelf-Slope-Abyssal Systems of the North Atlantic Ocean
Global Biogeochemical Cycles, Vol 40:2, e2025GB008861. https://doi.org/10.1029/2025GB008861

The ocean is the largest natural carbon sink for atmospheric CO2

Posted by mmaheigan 
· Friday, January 23rd, 2026 

Only about half of human-made CO2 emissions remain in the atmosphere and drive global warming. The other half has so far been said to be taken up in roughly equal amounts by the biosphere on land and by physical-chemical processes in the ocean. In equal amounts?

In a new assessment, Friedlingstein et al. reassess the various components of the Global Carbon Budget. Major changes were suggested for the land and ocean sinks. For the land, the prior assumption of a preindustrial land-cover in the Dynamic Global Vegetation Models (DGVM) led to an overestimation of the natural land sink in previous studies. The land sink is further revised downwards by accounting for an anthropogenic perturbation of lateral carbon export to the ocean. For the ocean, adjustments were made for the known underestimation of the ocean sink from Global Ocean Biogeochemical Models and the cool and salty skin effect in surface fCO2-observation-based estimates. As a result, the ocean is now estimated to have taken up 29% of anthropogenic CO2 emissions in the last decade 2015-2024, while the land sink has taken up 21%. In this revised estimate with virtually no budget imbalance over the last decade and no significant trend in the budget imbalance since 1960, climate-driven impacts on the natural sinks are quantified: Land and ocean sinks would be 25% and 7% higher, respectively, without this carbon-climate feedback. Since 1960, the carbon-climate feedback has already contributed 8 ppm (8%) to the rise in atmospheric CO2 concentration.

The negative imprints of earth system changes (e.g., warming, droughts, changes in wind patterns and ocean circulation, etc.) on these important carbon sinks is worrisome and is expected to intensify as warming continues. The most effective way to protect these sinks is to drastically reduce CO2 emissions from fossil fuels and land-use changes, ultimately to net zero.

 

Authors
Judith Hauck (Alfred Wegener Institute Helmholtz Centre for Polar and Marine Research, University of Bremen)
Peter Landschützer (VLIZ)
Corinne Le Quéré (University of East Anglia)
Pierre Friedlingstein (University of Exeter)

Bluesky: @pfriedling @jhauck @clequere

A heat burp breaks the assumed relationship of cumulative CO2 emissions and warming

Posted by mmaheigan 
· Friday, January 23rd, 2026 

The ocean stores vast amounts of heat and carbon under anthropogenic CO₂ emissions, but its behavior under net-negative emission scenarios remains poorly understood. Here we use an Earth System Model of intermediate complexity and show results of an idealized future climate scenario that includes sustained net-negative emissions over centuries. After gradual global cooling, the model produces an abrupt “heat burp,” in which heat previously stored in the deep Southern Ocean resurfaces through deep convection, temporarily reversing the cooling and causing renewed warming. The release of heat is not accompanied by a comparable release of CO₂. The heat burp represents a breakdown of the assumed linear relationship between cumulative CO₂ emissions and warming, a metric that is used to calculate the remaining carbon budget. We call for assessing the robustness of how models forced with net-negative CO₂ emissions simulate durability of ocean storage of heat and CO₂, and pathways and time scales of loss to the atmosphere.

 

Fig caption: The temporal evolution of (a) global heat and carbon uptake and release; (b) surface air temperature (SAT) anomaly relative to preindustrial conditions; (c) Southern Ocean temperature anomaly relative to preindustrial conditions; gray shading/black bar indicate the period of comparatively abrupt ocean heat release that warms SAT, representing a climate feedback.

 

Authors
(all at GEOMAR)

Ivy Frenger
Svenja Frey (and Univ Copenhagen)
Andreas Oschlies
Julia Getzlaff
Torge Martin
Wolfgang Koeve

 

Frenger, I., Frey, S., Oschlies, A., Getzlaff, J., Martin, T., & Koeve, W. (2025). Southern Ocean heat burp in a cooling world. AGU Advances, 6, e2025AV001700. https://doi.org/10.1029/2025AV001700

A Microbial Conveyor Belt Beneath the South Pacific

Posted by mmaheigan 
· Friday, October 17th, 2025 

Global overturning circulation is a planetary conveyor belt: dense waters sink around Antarctica, spread through the deep ocean for centuries, and eventually rise elsewhere, redistributing heat, nutrients, and carbon. But how does this slow, pervasive movement of water impact marine microbes?

 

To find out, researchers collected over 300 water samples spanning the full depth of the ocean along the GO-SHIP P18 line in the South Pacific. They found that microbial genomes cluster into six spatial cohorts that are not only delineated by depth, but also circulatory features, like Antarctic Bottom Water formation, and ventilation age. Distinct functional signatures also emerged across these circulation-driven zones. For example, genes for light harvesting and iron uptake dominate in surface waters, while adaptations for cold, high pressure, or anaerobic metabolism characterize deep and ancient waters. Antarctic Bottom Water communities also carry hallmarks of rapid genetic exchange, suggesting horizontal gene transfer may help microbes adapt as they sink into the deep ocean. Even in waters isolated from the atmosphere for over a thousand years, many microbial genomes have coverage patterns that imply active replication, demonstrating that long-isolated water masses still support active microbial populations. In considering patterns of microbial diversity, researchers also identified a pervasive “prokaryotic phylocline” in which richness spikes just below the surface mixed layer and remains high to full ocean depth, only dipping slightly in very old water.

These results demonstrate that physical circulation, not just temperature or nutrients, partitions the ocean into microbial biomes. Understanding this linkage is critical because microbes determine the amount of carbon that is recycled or stored long-term in the deep ocean. As climate change alters overturning circulation, the functioning of these hidden microbial ecosystems and their role in regulating atmospheric CO₂ may shift in unexpected ways.

Authors
Bethany C. Kolody (University of California San Diego; UC Berkeley; J. Craig Venter Institute)
Rohan Sachdeva (UC Berkeley)
Hong Zheng (J. Craig Venter Institute)
Zoltán Füssy (UC San Diego; J. Craig Venter Institute)
Eunice Tsang (UC Berkeley)
Rolf E. Sonnerup (University of Washington)
Sarah G. Purkey (UC San Diego)
Eric E. Allen (UC San Diego)
Jillian F. Banfield (UC Berkeley; Lawrence Berkeley National Laboratory; Monash University)
Andrew E. Allen (UC San Diego; JCVI)

Social media
Twitter/X: @science_doodles, @Scripps_Ocean, @JCVenterInst
Bluesky: @banfieldlab.bsky.social, @bethanykolody.bsky.social, @scrippsocean.bsky.social, @jcvi.org

 

 

https://www.science.org/doi/10.1126/science.adv6903
Overturning circulation structures the microbial functional seascape of the South Pacific
Science

Marine plant metabolites give marine microbes gas

Posted by mmaheigan 
· Friday, October 17th, 2025 

A recent study in Nature Geosciences observed high concentrations of methane overlying permeable (sand) sand sediments in bays in Denmark and Australia. These environments are not one would expect to see methane because they are highly oxygenated and the high concentrations of sulfate in seawater typically inhibit methanogenesis. The authors showed that the methane was not being imported from local groundwater using geochemical methods. Using a combination of biogeochemical, microbial isolation, culturing and genomic approaches, revealed that methane was being produced by fast growing microbes resistant to oxygen exposure using plant produced substrates such as dimethylsulfide and amines. This work shows that where marine plants such as seaweed and seagrass grow and accumulate there may be high and sporadic production of methane. This has implications for how we account for the carbon sequestering capacity of coastal environments and the climate impact of increasing algal blooms such as coastal Ulva and the great sargassum bloom.

Authors
Perran Cook (Monash University)
Ning Hall (University of free spirit)

 

 

How does a persistent eddy impact the biological carbon pump?

Posted by mmaheigan 
· Friday, September 26th, 2025 

The Lofoten Basin Eddy (LBE) is a unique and persistent anticyclonic feature of the Norwegian Sea that stirs the water column year-round. However, its impact on biogeochemical processes that influence region carbon storage, including carbon fixation, particle aggregation and fragmentation, and remineralization, has remained largely unknown.

Figure caption: (a) Map of the Lofoten Basin Eddy study region including locations of 1886 profiles from 22 Biogeochemical-Argo floats (2010–2022) and a heatmap showing the relative extent of the LBE influence zone over the timeseries. (b–d) Mean monthly profiles and the difference (Δ) determined as inside minus outside the LBE influence zone of the mass concentration of particulate organic carbon in small particles (POCs). Arrows indicate key mechanisms regulating the regional biological carbon.

Using 12 years of data from Biogeochemical-Argo floats and satellite altimetry to track eddy movements, Koestner et al. (2025) examined how the LBE influences the seasonal transport of organic carbon from surface waters to the deep ocean. While the LBE can enhance carbon export during certain months, like during spring shoaling and late autumn subduction, it generally reduces the efficiency of the biological carbon pump. Inside the eddy, warmer subsurface waters and slower-sinking particles often lead to more respiration and remineralization, meaning less carbon reached the deep sea.

The LBE’s persistent influence on organic carbon cycling could affect regional climate feedbacks and marine ecosystems, including key fisheries in Norway. Understanding how features like the LBE modulate carbon sequestration is vital for improving climate models and managing ocean resources in a warming Arctic.

 

Authors
Daniel Koestner (University of Bergen)
Sophie Clayton (National Oceanography Centre)
Paul Lerner (Columbia University)
Alexandra E. Jones-Kellett (MIT & WHOI)
Stevie L. Walker (University of Washington)

Microbial Iron limitation in the ocean’s twilight zone

Posted by mmaheigan 
· Monday, March 31st, 2025 

How deep in the ocean do microbes feel the effects of nutrient limitation? Microbial production in one third of the surface ocean is limited by the essential micronutrient iron (Fe). This limitation extends to at least the bottom of the euphotic zone, but what happens below that?

In a study that recently published in Nature we investigated the abundance and distribution of siderophores, small metabolites synthesized by bacteria to promote Fe uptake. When environmental Fe concentrations become limiting and microbes become Fe deficient, some bacteria release siderophores into the environment to bind iron and facilitate its uptake. Siderophores are therefore a window into how microbes “see” environmental Fe. We found that siderophore concentrations were high in low Fe surface waters, but surprisingly we also found siderophores to be abundant in the twilight zone (200-500 m) underlying the North and South Pacific subtropical gyres, two key ecosystems for the marine carbon cycle. In shipboard experiments with siderophores labeled with the rare 57Fe isotope, we found rapid uptake of the label in twilight zone samples. After removing 57Fe from the 57Fe-siderophores complex, bacteria released the now unlabeled siderophores back into seawater to complex additional Fe (Figure. 1).

Figure 1: Iron-siderophore cycling in the twilight zone. When the seawater becomes Fe-deficient, some bacteria are able to synthesize siderophores and release them into the environment (middle left). These metabolites bind Fe (middle right) and the Fe-siderophore complex is taken up by bacteria using specialized TonB dependent transporters (TBDT; bottom right). Inside the cell, Fe is recovered from the Fe-siderophore complex (bottom left) and the siderophore excreted back into the environment to start the cycle anew.

Our results show that in large parts of the ocean microbes feel the effects of nutrient limitation deep in the water column, to at least 500 m. This greatly expands the region of the ocean where nutrients limit microbial metabolism. The effects of limitation this deep in the water column are unexplored, but twilight zone Fe deficiency could have unanticipated consequences for the efficiency of the ocean’s biological carbon pump.

 

Authors
Jingxuan Li, Lydia Babcock-Adams and Daniel Repeta
(all at Woods Hole Oceanographic Institution)

Persistent bottom trawling impairs seafloor carbon sequestration

Posted by mmaheigan 
· Friday, February 28th, 2025 

Bottom trawling, a fishing method that uses heavy nets to catch animals that live on and in the seafloor, could release a large amount of organic carbon from seafloor into the water, that metabolizes to CO2 then outgasses to the atmosphere. The magnitude of this indirect emission has been heavily debated, with estimates spanning from negligibly small to global climate relevant. Thus, a lack of reliable data and insufficient understanding of the process hinders management of bottom trawling for climate protection.

We set out to solve this problem in two steps. First, we analyzed a large field dataset containing more than 2000 sediment samples from one of the most intensely trawled regions globally, the North Sea. We identified a trawling-induced carbon reduction trend in the data, but only in samples taken in persistently intensively trawled areas with multi-year averaged swept area ratio larger than 1 yr-1. In less intensely trawled areas, there was no clear effect. In a second step, we applied numerical modelling to understand the processes behind the observed change (Fig. 1). Our model results suggest that bottom trawling annually releases one million tonnes of CO2 in the North Sea and 30 million tonnes globally. Along with sediment resuspension in the wake of the trawls, the main cause for altered sedimentary carbon storage is the depletion of macrofauna, whose locomotion and burrowing effectively buries freshly deposited carbon into deeper sediment layers. By contrast, macrofauna respiration is reduced owing to trawling-caused mortality, partly offsetting the organic carbon loss. Following a cessation of trawling, the simulated benthic biomass can recover in a few years, but the sediment carbon stock would take several decades to be restored to its natural state.

Figure 1. (a) Benthic–pelagic coupling in a natural system. (b) Processes involved in bottom trawling. (c) Model-estimated source and sink terms of organic carbon in surface sediments in the No-trawling (solid fill, n = 67 annual values for 1950–2016) and trawling (pattern fill, n = 67 ensemble-averaged values for 1950–2016) scenarios of the North Sea. © 2024, Zhang, W. et al., CC BY 4.0.

Marine conservation strategies traditionally favor hard bottoms, such as reefs, that are biologically diverse but accumulate limited amounts of organic carbon. Our results indicate that carbon in muddy sediments is more susceptible to trawling impacts than carbon in sand and point out a need to safeguard muddy habitats for climate protection. Our methods and results might be used in the context of marine spatial planning policies to gauge the potential benefits of limiting or ending bottom trawling within protected areas.

 

Zhang, W., Porz, L., Yilmaz, R. et al. Long-term carbon storage in shelf sea sediments reduced by intensive bottom trawling. Nat. Geosci. 17, 1268–1276 (2024). https://doi.org/10.1038/s41561-024-01581-4

Authors
Wenyan Zhang (Hereon)
Lucas Porz (Hereon)
Rümeysa Yilmaz (Hereon)
Klaus Wallmann (GEOMAR)
Timo Spiegel (GEOMAR)
Andreas Neumann (Hereon)
Moritz Holtappels (AWI)
Sabine Kasten (AWI)
Jannis Kuhlmann (BUND)
Nadja Ziebarth (BUND)
Bettina Taylor (BUND)
Ha Thi Minh Ho-Hagemann (Hereon)
Frank-Detlef Bockelmann (Hereon)
Ute Daewel (Hereon)
Lea Bernhardt (HWWI)
Corinna Schrum (Hereon)

OA could boost carbon export by appendicularia

Posted by mmaheigan 
· Wednesday, December 4th, 2024 

Gelatinous zooplankton comprise a widespread group of animals that are increasingly recognized as important components of pelagic ecosystems. Historically understudied, we have little knowledge of how much key taxa contribute to carbon fluxes. Likewise, there’s a critical knowledge gap of the impact of ocean change on these taxa.

Appendicularia are the most abundant gelatinous zooplankton in the world oceans. Their population dynamics display typical boom-and-bust characteristics, i.e. high grazing rates in combination with a short generation time and life cycle, results in intense blooms. The most prominent feature of appendicularians is their mucous feeding-structure (“house”), which is produced and discarded several times per day. These sinking houses can contribute substantially to carbon export.

Figure 1: Influence of ocean acidification on the Appendicularia Oikopleura dioica and carbon export. Appendicularian populations display typical boom-and-bust characteristics, resulting in intense blooms. The sinking of appendicularians’ discarded mucous feeding-structure several times per day can contribute substantially to carbon export. Low pH conditions (as expected for future ocean acidification extreme events) enhanced its population growth and contribution to carbon fluxes shown above (red lines/diamonds) vs ambient (blue lines/diamonds).
(Figure sources: Picture by Jean-Marie Bouquet, data plots from Taucher et al. (2024): The appendicularian Oikopleura dioica can enhance carbon export in a high CO2 ocean. Global Change Biology, doi:10.1111/gcb.17020)

A recent study in Global Change Biology quantified how much appendicularia can contribute to carbon export via the biological pump, and how this carbon flux could markedly increase under future ocean acidification and associated extreme pH events.

The findings are based on a large-volume in situ experimental approach that allowed observing natural plankton populations and carbon export under close-to-natural conditions for almost two months. Thereby, O. dioica population dynamics could be directly linked to sediment trap data to quantify the influence of this key species on carbon fluxes at unprecedented detail. During the appendicularia bloom up to 39% of total carbon export was attributed to them.

The most striking finding was that high CO2 conditions elevated carbon export by appendicularia increased by roughly 50%. Appendicularians physiologically benefit from low pH conditions, giving them a competitive advantage over other zooplankton, allowing them to contribute to a disproportionally large role in carbon export from the ecosystem.

Authors
Jan Taucher (GEOMAR)
Anna Katharina Lechtenbörger (GEOMAR)
Jean-Marie Bouquet (University of Bergen)
Carsten Spisla (GEOMAR)
Tim Boxhammer (GEOMAR)
Fabrizio Minutolo (GEOMAR)
Lennart Thomas Bach (University of Tasmania)
Kai T. Lohbeck (University of Konstanz)
Michael Sswat (GEOMAR)
Isabel Dörner (GEOMAR)
Stefanie M. H. Ismar-Rebitz (GEOMAR)
Eric M. Thompson (University of Bergen)
Ulf Riebesell (GEOMAR)

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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 gene transfer geochemistry geoengineering geologic time GEOTRACES glaciers gliders global carbon budget global ocean global ocean models global overturning circulation 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 iceberg 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 land-ocean continuum larvaceans lateral transport LGM lidar ligands light light attenuation lineage 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 migration minerals mitigation mixed layer mixed layers mixing mixotrophs mixotrophy model modeling model validation mode water molecular diffusion MPT MRV multi-decade N2 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 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 predators prediction pressure primary productivity Prochlorococcus productivity prokaryotes proteins pteropods pycnocline python 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 seasonal effects 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 solubility pump southern ocean south pacific spatial covariations speciation SST state estimation stoichiometry subduction submesoscale subpolar subtropical sulfate surf surface surface ocean surface waters Synechococcus technology teleconnections temperate temperature temporal covariations thermocline thermodynamics thermohaline thorium tidal time 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 column water mass water quality waves weathering western boundary currents wetlands winter mixing zooplankton

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