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Studying marine ecosystems and biogeochemical cycles in the face of environmental change

Archive for New OCB Research – Page 22

Ocean’s heat cycle shows that atmospheric carbon may be headed elsewhere

Posted by hbenway

· Thursday, August 16th, 2018

Studies over the past 25 years have supported the existence of a large net land biosphere CO₂ sink of 0.5–2 PgC yr^-1. Significant uncertainties remain, however, regarding the long-term partitioning between northern, tropical, and southern land sinks, in part connected to the uncertain ocean carbon sink. These uncertainties limit our capacity to predict earth system response to anthropogenic changes and design effective mitigation strategies.

Land sinks from atmospheric inversion (1990-2010 average) with two different ocean/river fluxes: (top) previous ocean inversion-based carbon fluxes; and (bottom) updated pCO2-based air-sea flux with a scaled-up river flux of 0.78 PgC /yr.

In a recent study published in Nature Geoscience, Resplandy et al. (2018) used models and field observations to demonstrate that the world’s oceans transport heat between the northern and southern hemispheres in the same way that carbon is transported. The transport of heat, however, is easier to observe. By tracking this heat, they showed that the Southern Ocean — while still a substantial carbon sink —may not take up as much carbon as previously thought, and that ocean currents might transport 20 to 100% more carbon from the northern to the southern hemisphere. To maintain this additional transport of carbon, they showed that the amount of carbon entering the ocean from rivers may be as much as 70% higher than estimated in previous global carbon budget studies. These changes in the ocean and river carbon transport imply that up to 40% of the world’s atmospheric carbon absorbed by land ecosystems needs to be reallocated from existing estimates.

Authors
L. Resplandy, Princeton University
Ralph Keeling, Scripps Institution of Oceanography/ UCSD
Christian Rödenbeck, Max Planck Institute
Briton Stephens, NCAR
Matthew Long, NCAR
Samar Khatiwala, University of Oxford
Keith Rodgers, Princeton University
Laurent Bopp, ENS Paris
Pieter Tans, NOAA’s ESRL

Shelf-wide pCO2 increase across the South Atlantic Bight

Posted by mmaheigan

· Thursday, August 2nd, 2018

Relative to their surface area, coastal regions represent some of the largest carbon fluxes in the global ocean, driven by numerous physical, chemical and biological processes. Coastal systems also experience human impacts that affect carbon cycling, which has large socioeconomic implications. The highly dynamic nature of these systems necessitates observing approaches and numerical methods that can both capture high-frequency variability and delineate long-term trends.

Figure 1: The South Atlantic Bight (SAB) was divided into four sections using isobaths: the coastal zone (0 to 15 m), the inner shelf (15 to 30 m), the middle shelf (30 to 60 m), and the outer shelf (60 m and beyond). The X’s indicate the locations of the Gray’s Reef mooring (southern X) and the Edisto mooring (northern X).

In two recent studies using mooring- and ship-based ocean CO₂ system data, authors observed that pCO₂ is increasing from the coastal zone to the outer shelf of the South Atlantic Bight at rates greater than the global average oceanic and atmospheric increase (~1.8 µatm y^-1). In recent publications in Continental Shelf Research and JGR-Oceans, the authors analyzed pCO₂ data from 46 cruises (1991-2016) using a novel linear regression technique to remove the seasonal signal, revealing an increase in pCO₂ of 3.0-3.7 µatm y^-1on the outer and inner shelf, respectively. Using a Generalized Additive Mixed Model (GAMM) approach for trend analysis, authors observed that the rates of increase were slightly higher than the deseasonalization technique, yielding pCO₂ increases of 3.3 to 4.5 µatm y^-1 on the outer and inner shelf, respectively. The reported pCO₂ increases result in potential pH decreases of -0.003 to -0.004 units y^-1.

Figure 2: The time series of fCO2 in the four regions of the SAB (cruise observations) and from the Gray’s Reef mooring on the inner shelf indicate an increase across the shelf. These data are the observed values, however, the trend lines for each time series are calculated using deseasonalized values using the reference year method.

Analysis of the pCO₂ time-series from the Gray’s Reef mooring (using a NOAA Moored Autonomous pCO₂ system from July 2006 -July 2015) yielded a rate of increase (3.5 ± 0.9 µatm y^-1) that was comparable to the cruise data on the inner shelf (3.7 ± 2.2 and 4.5 ± 0.6 µatm y^-1, linear and GAMM methods, respectively). Validation data collected at the mooring suggest that underway data from cruises and the moored data are comparable. Neither thermal processes nor atmospheric dissolution (the primary driver of oceanic acidification) can explain the observed pCO₂ increase and concurrent pH decrease across the shelf. Unlike the middle and outer shelves, where an increase in SST could account for up to 1.1 µatm y^-1 of the observed pCO₂ trend, there is no thermal influence in the coastal zone and inner shelf. While 1.8 µatm y^-1 could be attributed to the global average atmospheric increase, the remainder is likely due to transport from coastal marshes and in situ biological processes. As the authors have shown, the increasing coastal and oceanic trend in pCO₂ can lead to a decrease in pH, especially if there is no increase in buffering capacity. More acidic waters can have a long term affect on coastal ecosystem services and biota.

Also see Eos Editor’s Vox on this research by Peter Brewer https://eos.org/editors-vox/coastal-ocean-warming-adds-to-co2-burden

Authors:

Multidecadal fCO2 Increase Along the United States Southeast Coastal Margin (JGR-Oceans)
Janet J. Reimer (University of Delaware)
Hongjie Wang (Texas A &M University – Corpus Christi)
Rodrigo Vargas (University of Delaware)
Wei-Jun Cai (University of Delaware)

And

Time series pCO2 at a coastal mooring: Internal consistency, seasonal cycles, and interannual variability (Continental Shelf Research)
Janet J. Reimer (University of Delaware)
Wei-Jun Cai (University of Delaware; University of Georgia)
Liang Xue (University of Delaware; First Institute of Oceanography, China)
Rodrigo Vargas (University of Delaware)
Scott Noakes (University of Georgia)
Xinping Hu (Texas A &M University – Corpus Christi)
Sergio R. Signorini (Science Applications International Corporation)
Jeremy T. Mathis (NOAA Arctic Research Program)
Richard A. Feely (NOAA Pacific Marine Environmental Laboratory)
Adrienne J. Sutton (NOAA Pacific Marine Environmental Laboratory; University of Washington)
Christopher Sabine (University of Hawaii Manoa)
Sylvia Musielewicz (NOAA Pacific Marine Environmental Laboratory; University of Washington)
Baoshan Chen (University of Delaware; University of Georgia)
Rik Wanninkhof (NOAA Atlantic Oceanographic and Meteorological Laboratory)

Marine Snowfall at the Equator

Posted by mmaheigan

· Thursday, July 19th, 2018

The continual flow of organic particles such as dead organisms and fecal material towards the deep sea is called “marine snow,” and it plays an important role in the ocean carbon cycle and climate-related processes. This snowfall is most intense where high primary production can be observed near the surface. This is the case along the equator in the Pacific and Atlantic Oceans. However, it is not well known how particles are distributed at depth and which processes influence this distribution. A recent study published in Nature Geoscience involved the use of high-resolution particle density data using the Underwater Vision Profiler (UVP) from the equatorial Atlantic and Pacific Oceans down to a depth of 5,000 meters, revealing that several previously accepted ideas on the downward flux of particles into the deep sea should be revisited.

Figure 1. The Underwater Vision Profiler (UVP) during a trial in the Kiel Fjord. The UVP provided crucial data for the new study. Photo: Rainer Kiko, GEOMAR

It is typically assumed that the largest particle density can be found close to the surface and that density attenuates continuously with depth. However, high-resolution particle data show that density increases again in the 300-600-meter depth range. The authors attribute this observation to the daily migratory behavior of organisms such as zooplankton that retreat to these depths during the day, contributing to the particle load via defecation and mortality.

Another surprising result is the observation of many small particles below 1,000 meters depth that contribute a large fraction of the bathypelagic particle flux. This observation counters the general assumption, especially in many biogeochemical models, that particle flux at depth comprises fast sinking particles such as fecal pellets. Diminished remineralization rates of small particles or increased disaggregation of larger particles may contribute to the elevated small particle fluxes at this depth.

Figure 2. Zonal current velocity and Particulate Organic Carbon (POC) content across the equatorial Atlantic at 23˚W as observed in November 2012. From left to right: Zonal current velocity, POC content in small particle fraction and POC content in large particle fraction (adapted from Kiko et al. 2017).

This study highlights the importance of coupled biological and physical processes in understanding and quantifying the biological carbon pump. Further work on this important topic can now also be submitted to the new Frontiers in Marine Science research topic “Zooplankton and Nekton: Gatekeepers of the Biological Pump” (https://www.frontiersin.org/research-topics/8114/zooplankton-and-nekton-gatekeepers-of-the-biological-pump; Co-editors R. Kiko, M. Iversen, A. Maas, H. Hauss and D. Bianchi). The research topic welcomes a broad range of contributions, from individual-based process studies, to local and global field observations, to modeling approaches to better characterize the role of zooplankton and nekton for the biological pump.

Authors:
R. Kiko (GEOMAR)
A. Biastoch (GEOMAR)
P. Brandt (GEOMAR, University of Kiel)
S. Cravatte (LEGOS, University of Toulouse)
H. Hauss (GEOMAR)
R. Hummels (GEOMAR)
I. Kriest (GEOMAR)
F. Marin (LEGOS, University of Toulouse)
A. M. P. McDonnell (University of Alaska Fairbanks)
A. Oschlies (GEOMAR)
M. Picheral (Laboratoire d’Océanographie de Villefranche-sur-Mer, Observatoire Océanologique)
F. U. Schwarzkopf (GEOMAR)
A. M. Thurnherr (Lamont-Doherty Earth Observatory,)
L. Stemmann (Sorbonne Universités, Observatoire Océanologique)

Long-term coastal data sets reveal unifying relationship between oxygen and pH fluctuations

Posted by mmaheigan

· Thursday, June 7th, 2018

Coastal habitats are critically important to humans, but without consistent and reliable observations we cannot understand the direction and magnitude of unfolding changes in these habitats. Environmental monitoring is therefore a prescient—yet still undervalued—societal service, and no effort better exemplifies this than the work conducted within the National Estuarine Research Reserve System (NERRS). NERRS is a network of 29 U.S. estuarine sites operated as a partnership between NOAA and the coastal states. NERRS has established a system-wide monitoring program with standardized instrumentation, protocols, and data reporting to guide consistent and comparable data collection across all NERRS sites. This has resulted in high-quality, comparable data on short- to long-term changes in water quality and biological systems to inform effective coastal zone management.

Figure 1: Using dissolved oxygen and salinity, monthly mean pH can be predicted within and across coastal systems due to the unifying metabolic coupling of oxygen and pH.

In a recent study published in Estuaries and Coasts, Baumann and Smith (2017) used a subset of this unique data set to analyze short- and long-term variability in pH and dissolved oxygen (DO) at 16 NERRS sites across the U.S. Atlantic, Caribbean, Gulf of Mexico, and Pacific coasts (> 5 million data points). They observed that large, metabolically driven fluctuations of pH and DO are indeed a unifying feature of nearshore habitats. Furthermore, mean pH or mean diel pH fluctuations can be predicted across habitats simply from salinity and oxygen levels/fluctuations (Fig.1). These results provide strong empirical evidence that common metabolic principles drive diel to seasonal pH and DO variations within and across a diversity of estuarine environments. As expected, the study did not yield interannual, monotonic trends in nearshore pH conditions; rather, interannual fluctuations were of similar magnitude to the pH decrease predicted for the average surface ocean over the next three centuries (Fig.2). Correlations of weekly anomalies of pH, oxygen, and temperature yielded strong empirical support for the hypothesis that coastal acidification—in addition to being driven by eutrophication and atmospheric CO₂ increases—is exacerbated by warming, likely via increased community respiration.

Figure 2: Interannual variations in temperature, pH, and dissolved oxygen (DO) anomalies in 16 NERRS sites across the US Atlantic, Gulf of Mexico, Caribbean, and Pacific coasts.

Analyses of these long-term data sets have provided important insights on biogeochemical variability and underlying drivers in nearshore environments, highlighting the value and utility of long-term monitoring efforts like NERRS. Sustained, high-quality data sets in these nearshore environments are essential for the study of environmental change and should be prioritized by funding agencies. The observed metabolically driven pH and DO fluctuations suggest that local measures to reduce nutrient pollution can be an effective management tool in support of healthy coastal environments, a boon for both the habitats and humans.

Authors:
Hannes Baumann (University of Connecticut)
Erik M. Smith (North Inlet-Winyah Bay National Estuarine Research Reserve, University of South Carolina)

Unexpected acidification of deep waters in the Sea of Japan due to global warming

Posted by mmaheigan

· Tuesday, May 22nd, 2018

Oceans worldwide are warming up, and thermohaline circulation is expected to slow down. At the same time, ocean acidity is increasing due to the influx of anthropogenic carbon dioxide (CO₂) from the atmosphere, a phenomenon called ocean acidification that has primarily been documented in shallow waters. In general, deeper waters contain less anthropogenic CO₂, but predicted reductions in ventilation of deep waters may impact deep ocean chemistry, as described in a recent study in Nature Climate Change.

Figure caption: Secular trend of total scale pH at in-situ temperature and pressure at various depths between 1965 and 2015 in the Sea of Japan.

The Sea of Japan is a marginal sea with its own deep- and bottom-water formation that maintains relatively elevated oxygen levels. However, time-series data from 1965-2015 (the longest time-series available) reveal that oxygen concentrations in these deep waters are declining, indicating a reduction in ventilation that increases their residence time. As organic matter decomposition in these waters continues to accumulate more CO₂, the pH decreases. As a result, the acidification rate near the bottom of the Sea of Japan is 27% higher than at the surface. As a miniature ocean with its own deep- and bottom-water formation, the Sea of Japan provides insight into how future warming might alter deep-ocean ventilation and chemistry.

Authors:
Chen-Tung Arthur Chen (National SunYat-sen University, Taiwan and Second Institute of Oceanography, China)
Hon-Kit Lui (National SunYat-sen University and Taiwan Research Institute)
Chia-Han Hsieh (National SunYat-sen University, Taiwan)
Tetsuo Yanagi (International Environmental Management of Enclosed Coastal Seas Center, Japan)
Naohiro Kosugi (Japan Meterological Agency)
Masao Ishii (Japan Meterological Agency)
Gwo-Ching Gong (National Taiwan Ocean University)

Sensitivity of future ocean acidification to carbon-climate feedbacks

Posted by mmaheigan

· Thursday, May 10th, 2018

There are vast unknowns about the future oceans, from what species or habitats may be most under threat to the continuity of earth system processes that maintain global climate. Modeling can be used to predict future states and explore the impacts of climate change, but several key uncertainties such as carbon-climate feedbacks hamper our predictive power.

Authors of a recent study in Biogeosciences (Matear and Lenton 2018) used a global earth system model to explore the effects of carbon-climate feedbacks on future ocean acidification. Ocean acidification can have wide-ranging impacts on keystone species from reef-building corals to pteropods, a major food web species in the Southern Ocean. The study included four representative scenarios (from IPCC) comparing concentration pathway simulations to emission pathway simulations (RCP2.6, RCP 4.5, RCP6, RCP8.5) to determine carbon-climate feedbacks. The high emission scenarios (RCP8.5 and RCP6) showed surface water undersaturation a decade or more earlier than expected. Surprisingly, the medium (RCP4.5) scenario carbon-climate feedbacks showed the greatest acidification response, doubling the extent of undersaturation and subsequently halving the area that could sustain coral reefs by 2100. The low emissions scenario also showed significant declines in saturation state.

Surface ocean aragonite saturation state for the 2090s for RCP2.6 and RCP 8.5 concentration and emission pathways. The contour line delineates a saturation state of 3 (coral reef threshold), the white line a saturation state of 1, when aragonite becomes unstable and corals dissolve.

The extra atmospheric CO₂ from the carbon-climate feedback resulted in accelerated ocean acidification in all emission scenarios. These feedbacks may also affect global warming and deoxygenation. This is particularly important, given that many policymakers are aiming for low emission commitments, but may still be severely underestimating the extent and timing of ocean acidification. There is a great need to improve our ability to predict carbon-climate feedbacks so we do not underestimate projected ocean acidification and its impacts on both sensitive ecosystems and the human communities that rely on them for food, coastal protection and other ecosystem services.

Authors:
Richard Matear (CSIRO Oceans and Atmosphere, Australia)
Andrew Lenton (Antarctic Climate and Ecosystems CRC, Australia)

Hotspots of biological production: Submesoscale changes in respiration and production

Posted by mmaheigan

· Thursday, April 26th, 2018

The biological pump is complex and variable. To better understand it, scientists have often focused on variations in biological parameters such as fluorescence and community structure, and have less often observed variations in rates of production. Production rates can be estimated using oxygen as a tracer, since photosynthesis produces oxygen and respiration consumes it. In a recent article in Deep Sea Research Part I, the authors presented high-resolution maps of oxygen in the upper 140 m of the ocean in the subtropical and tropical Atlantic, produced from a towed undulating instrument. This provides a synoptic, high-resolution view of oxygen anomalies in the surface ocean. These data reveal remarkable hotspots of biological production and respiration co-located with areas of elevated fluorescence. These hotspots are often several kilometers wide (horizontal) and ~10 m long (vertical). They are preferentially associated with edges of eddies, but not all edges sampled contained hotspots. Although this study captures only two-dimensional glimpses of these hotspots, precluding formal calculations of production rates, likely estimates of source water suggest that many of these hotspots may actually be areas of enhanced respiration rather than enhanced photosynthesis. The paper describes a conceptual model of nutrients, new production, respiration, fluorescence, and oxygen during the formation and decline of these hotspots. These data raise intriguing questions–if the hotspots do indeed have substantially different rates of production and respiration than surrounding waters, then they could lead to significant changes in estimates of production in the upper ocean. Additionally, understanding the mechanisms that produce these hotspots could be critical for predicting the effects of climate change on the magnitude of the biological pump.

(a) Oxygen concentrations and (b) fluorescence at ~1 km resolution over 300 km from 15.13°N, 57.47°W to 12.30°N, 56.42° W, as measured by sensors attached to the (c) Video Plankton Recorder II. Note that no contouring was used for this plot – every pixel represents an actual data point. Figure modified from Stanley et al., 2017. VPR image photograph by Phil Alatalo.

Authors:
Rachel H. R. Stanley (Wellesley College)
Dennis J. McGillicuddy Jr. (WHOI)
Zoe O. Sandwith (WHOI)
Haley Pleskow (Wellesley College)

Feedbacks mitigate the impacts of atmospheric nitrogen deposition in the western North Atlantic

Posted by mmaheigan

· Thursday, April 12th, 2018

How do phytoplankton respond to atmospheric nitrogen deposition in the western North Atlantic, an area downwind of large agricultural and industrial centers? The biogeochemical impacts of this ‘fertilization’ remain unclear, as direct oceanic observations of atmospheric deposition are limited and models often cannot resolve the important processes.

In a recent study, St-Laurent et al. (2017) simulated the biogeochemical impacts of nitrogen deposition on surface waters of the western North Atlantic by combining year-specific deposition rates from the Community Multiscale Air Quality (CMAQ) model and a realistic 3-D biogeochemical model of the waters off the US east coast. Westerly winds from the continent and large fluxes of heat and moisture over the Gulf Stream produce a ‘hotspot’ of wet nitrogen deposition along the path of the current. This nitrogen input increases the local surface primary productivity by up to 30% during the summer. However, the study also identified important processes that mitigate the impact of atmospheric nitrogen deposition in other seasons and regions. Deposition weakens vertical nitrogen gradients in the upper 20 m and thus decreases the upward transport of nitrogen to the surface layer (a negative feedback). Increases in surface phytoplankton concentrations also negatively impact light availability below the surface through shelf-shading.

Atmospheric nitrogen deposition along the US east coast. (Left) Wet deposition of oxidized nitrogen over the Gulf Stream as simulated by the Community Multiscale Air Quality model (average 2004-2008). (Right) Increase in summer surface primary productivity in response to the deposition (average 2004-2008).

These results indicate that atmospheric nitrogen deposition has important impacts on the surface biogeochemistry of the western North Atlantic but that the response is not simply proportional to the deposition. Additional research is necessary to clarify the role played by atmospheric deposition in this region in past and future centuries. While inputs of atmospheric nitrogen associated with power plants and industries have decreased since the passage of the Clean Air Act, recent studies have revealed increasing atmospheric concentrations of reduced nitrogen. Continued coordination between modeling and observing efforts (both on land and over the ocean) are needed to improve our understanding of the impacts of deposition on the biological pump in this region of the Atlantic ocean.

Authors:
Pierre St-Laurent (VIMS, College of William and Mary)
Marjorie A.M. Friedrichs (VIMS, College of William and Mary)
Raymond G. Najjar (Pennsylvania State University)
Doug Martins (FLIR Systems Inc.)
Maria Herrmann (Pennsylvania State University)
Sonya K. Miller (Pennsylvania State University)
John Wilkin (Rutgers University)

Volcanic carbon dioxide drove ancient global warming event

Posted by mmaheigan

· Thursday, March 29th, 2018

A study recently published in Nature suggests that an extreme global warming event 56 million years ago known as the Palaeocene-Eocene Thermal Maximum (PETM) was driven by massive CO₂ emissions from volcanoes during the formation of the North Atlantic Ocean. Using a combination of new geochemical measurements and novel global climate modelling, the study revealed that atmospheric CO₂ more than doubled in less than 25,000 years during the PETM.

The PETM lasted ~150,000 years and is the most rapid and extreme natural global warming event of the last 66 million years. During the PETM, global temperatures increased by at least 5^°C, comparable to temperatures projected in the next century and beyond. While it has long been suggested that the PETM event was caused by the injection of carbon into the ocean and atmosphere, the source and total amount of carbon, as well as the underlying mechanism have thus far remained elusive. The PETM roughly coincided with the formation of massive flood basalts resulting from of a series of eruptions that occurred as Greenland and North America started separating from Europe, thereby creating the North Atlantic Ocean. What was missing is evidence linking the volcanic activity to the carbon release and warming that marks the PETM.

To identify the source of carbon, the authors measured changes in the balance of isotopes of the element boron in ancient sediment-bound marine fossils called foraminifera to generate a new record of ocean pH throughout the PETM. Ocean pH tells us about the amount of carbon absorbed by ancient seawater, but we can get even more information by also considering changes in the isotopes of carbon, which provide information about the carbon source. When forced with these ocean pH and carbon isotope data, a numerical global climate model implicates large-scale volcanism associated with the opening of the North Atlantic as the primary driver of the PETM.

North Atlantic microfossil-derived isotope records from extinct planktonic foraminiferal species M. subbotinae relative to the onset of the PETM carbon isotope excursion (CIE). The negative trend in carbon isotope composition (A) during the carbon emission phase is accompanied by decreasing pH (decreasing δ¹¹B, panel B) and increasing temperature (decreasing δ¹⁸O, panel C). Panels D and E zoom in on the PETM CIE, showing microfossil δ¹³C (D) and δ¹¹B-based pH (E) reconstructions. Also included in E are data from Penman et al. (2014) on their original age model, with recalculated (lab-based) pH values.

These new results suggest that the PETM was associated with a total input of >12,000 petagrams of carbon from a predominantly volcanic source. This is a vast amount of carbon—30 times larger than all of the fossil fuels burned to date and equivalent to all current conventional and unconventional fossil fuel reserves. In the following Earth System Model simulations, it resulted in the concentration of atmospheric CO₂ increasing from ~850 parts per million to >2000 ppm. The Earth’s mantle contains more than enough carbon to explain this dramatic rise, and it would have been released as magma poured from volcanic rifts at the Earth’s surface.

How the ancient Earth system responded to this carbon injection at the PETM can tell us a great deal about how it might respond in the future to man-made climate change. Earth’s warming at the PETM was about what we would expect given the CO₂ emitted and what we know about the sensitivity of the climate system based on Intergovernmental Panel on Climate Change (IPCC) reports. However, the rate of carbon addition during the PETM was about twenty times slower than today’s human-made carbon emissions.

In the model outputs, carbon cycle feedbacks such as methane release from gas hydrates—once the favoured explanation of the PETM—did not play a major role in driving the event. Additionally, one unexpected result was that enhanced organic matter burial was important in ultimately drawing down the released carbon out of the atmosphere and ocean and thereby accelerating the recovery of the Earth system.

Authors:
Marcus Gutjahr (National Oceanography Centre Southamption, GEOMAR)
Andy Ridgwell (Bristol University, University of California Riverside)
Philip F. Sexton (The Open University, UK)
Eleni Anagnostou (National Oceanography Centre Southamption)
Paul N. Pearson (Cardiff University)
Heiko Pälike (University of Bremen)
Richard D. Norris (Scripps Institution of Oceanography)
Ellen Thomas (Yale University, Wesleyan University)
Gavin L. Foster (National Oceanography Centre Southamption)

Widespread nutrient co-limitation discovered in the South Atlantic

Posted by mmaheigan

· Thursday, March 15th, 2018

Unicellular photosynthetic microbes—phytoplankton—are responsible for virtually all oceanic primary production, which fuels marine food webs and plays a fundamental role in the global carbon cycle. Experiments to date have suggested that the growth of phytoplankton across much of the ocean is limited by either nitrogen or iron. But simultaneously low concentrations of these and other nutrients have been measured over large areas of the open ocean, raising the question: Are phytoplankton communities only limited by a single nutrient?

Authors of a study recently published in Nature tested this by conducting nutrient addition experiments on a GEOTRACES cruise in the nutrient-deficient South Atlantic gyre. Seawater samples were amended with nitrogen, iron, and cobalt both individually and in various combinations. Concurrent nitrogen and iron addition stimulated increased phytoplankton growth, yielding a ~40-fold increase in chlorophyll a. Supplementary addition of cobalt or cobalt-containing vitamin B₁₂ further enhanced phytoplankton growth in several experiments.

Experiments conducted throughout the southeast Atlantic GEOTRACES GA08 cruise transect (left panel) demonstrated that nitrogen and iron had to be added to significantly stimulate phytoplankton growth (right panel). Supplementary addition of cobalt (or cobalt-containing vitamin B12) stimulated significant additional growth.

In addition to co-limited sites, the study identified ‘singly’ and ‘serially’ limited sites. These limitation regimes could be predicted by the measured ambient seawater nutrient concentrations, demonstrating the potential for using nutrient datasets to make confident predictions about limitation at larger spatial scales, an approach that is being more widely used in programmes like GEOTRACES,.

Finally, a complex, state-of-the-art biogeochemical ocean model suggested a much smaller extent of nutrient co-limitation than the experiments indicated. Authors attributed this to relatively restricted microbial and nutrient diversity in the model. These findings have implications for how such models are constructed if they are to represent nutrient co-limitation in the ocean and accurately project changes in ocean productivity in the future.

Authors:
Thomas J. Browning (GEOMAR)
Eric P. Achterberg (GEOMAR)
Insa Rapp (GEOMAR)
Anja Engel (GEOMAR)
Erin M. Bertrand (Dalhousie University)
Alessandro Tagliabue (University of Liverpool)
Mark Moore (University of Southampton)

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.

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