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Archive for ocean carbon uptake and storage – Page 6

The causes of the 90-ppm glacial atmospheric CO2 drawdown still strongly debated

Posted by mmaheigan 
· Tuesday, July 9th, 2019 

Joint feature with GEOTRACES

Figure: Illustration of the two main mechanisms identified by this study to explain lower atmospheric CO2 during glacial periods. Left: present-day conditions; right: conditions around 19,000 years ago during the Last Glacial Maximum. The obvious explanation for lower CO2 during glacial periods – cooler ocean temperatures (darker blue shade) making CO2 more soluble, much as a glass of sparkling wine will remain fizzier for longer when it is colder – has long been dismissed as not being a significant factor. However, previous calculations assumed that the ocean cooled uniformly and was saturated in dissolved CO2. The model, consistent with reconstructions of sea surface temperature, predicts more cooling at mid latitudes compared with polar regions and also accounts for undersaturation. This nearly doubles the effect of temperature change and accounts for almost half the 90 ppm glacial-interglacial atmospheric CO2 difference. Another quarter is explained in this model by increased growth of marine algae (green blobs and inset) in the waters off Antarctica. Algae absorb CO2 from the atmosphere during photosynthesis and “pump” it into the deep ocean when they die and sink. But their growth in the present-day ocean, especially the waters off Antarctica, is limited by the availability of iron, an essential micronutrient primarily supplied by wind-borne dust. In our model an increased supply of iron to the Southern Ocean, likely originating from Patagonia, Australia and New Zealand, enhances their growth and sucks CO2 out of the atmosphere. This “fertilization” effect was greatly underestimated by previous studies. The study also finds that, contrary to the current consensus, a large expansion of sea ice off Antarctica and reconfiguration of ocean circulation may have played only a minor role in glacial-interglacial CO2 changes. Credit: Illustration by Andrew Orkney, University of Oxford.

Using an observationally constrained earth system model, S. Khatiwala and co-workers compare different processes that could lead to the 90-ppm glacial atmospheric CO2 drawdown, with an important improvement on the deep carbon storage quantification (i.e. Biological Carbon Pump efficiency). They demonstrate that circulation and sea ice changes had only a modest net effect on glacial ocean carbon storage and atmospheric CO2, whereas temperature and iron input effects were more important than previously thought due to their effects on disequilibrium carbon storage.

Authors:
Samar Khatiwala (University of Oxford, UK)
Andreas Schmittner and Juan Muglia (Oregon State University)

Zooplankton-fueled carbon export is changing in the North Atlantic Ocean

Posted by mmaheigan 
· Monday, June 10th, 2019 

Zooplankton-mediated carbon export is an important, but variable and relatively unconstrained part of the biological carbon pump—the processes that fix atmospheric carbon dioxide in organic material and transport it from the upper sunlit ocean to depth. Changes in the biological pump impact the climate system, but are challenging to quantify because such analyses require spatially and temporally explicit information about biological, chemical, and physical properties of the ocean, where empirical observations are in short supply.

A recent study in Nature, Ecology and Evolution focused on copepods in the northern half of the North Atlantic Ocean, where the Continuous Plankton Recorder (CPR) time series program has documented surface plankton abundance and taxonomic composition for nearly six decades. Copepods transport carbon passively by producing sinking fecal pellets while feeding near the sea surface, and actively via daily and seasonal migrations to deeper waters where carbon is released through respiration, defecation, and mortality. Using allometry, metabolic theory, and an optimal behavior model, the authors examined patterns of passive and active carbon transport from 1960 to 2014 and sensitivity of carbon export to different model inputs.

Figure caption: Spatial distribution and change, from 1960 to 2014, of modeled copepod-mediated carbon flux: top left – mean passive carbon flux (sinking fecal pellets), bottom left – change in passive carbon flux, top right – mean active carbon flux (respiration plus fecal pellets produced during diel vertical migration), bottom right – change in active carbon flux.

The authors observed that from southern Iceland to the Gulf of Maine, copepod-mediated carbon transport has increased over the last six decades, with the highest rates around 30 mgC m-2 y-1 each decade for passive flux, and 4 mgC m-2 y-1 each decade for active flux. Meanwhile, it has decreased across much of the more temperate central northern North Atlantic with highest rates around 69 mgC m-2 y-1 each decade for passive flux and 8 mgC m-2 y-1 each decade for active flux. This pattern is largely driven by changes in copepod population distributions and community structure, specifically the distributions of large and abundant species (e.g. Calanus spp.). These results suggest that shifts in species distributions driven by a changing global climate are already impacting ecosystem function across the northern North Atlantic Ocean. These shifts are not latitudinally uniform, thus highlighting the complexity of marine ecosystems. This study demonstrates the importance of these sustained plankton measurements and how plankton-mediated carbon fluxes can be mechanistically implemented in next-generation biogeochemical models.

Authors:
Philipp Brun (Technical University of Denmark and Swiss Federal Research Institute)
Karen Stamieszkin (University of Maine, Bigelow Lab and Virginia Institute of Marine Science)
Andre W. Visser (Technical University of Denmark)
Priscilla Licandro (Sir Alister Hardy Foundation for Ocean Science, Plymouth Marine Laboratory, and Stazione Zoologica Anton Dohrn, Italy)
Mark R. Payne (Technical University of Denmark)
Thomas Kiørboe (Technical University of Denmark)

 

Also see OCB2019 plenary session: The effect of size on ocean processes (allometry) and implications for export (Thursday, June 27, 2019)

South Pacific particulate organic carbon fate challenges Martin’s Law

Posted by mmaheigan 
· Tuesday, May 14th, 2019 

Joint science highlight with GEOTRACES

Carbon storage in the ocean is sensitive to the depths at which particulate organic carbon (POC) is respired back to CO2 within the twilight zone (100-1000m). For decades, it has been an oceanographic priority to determine the depth scale of this regeneration process. To investigate this, GEOTRACES scientists are deploying new isotopic tools that provide a high-resolution snapshot of POC flux and regeneration across steep biogeochemical gradients in the South Pacific Ocean.

A recent paper in PNAS reported on particulate organic carbon (POC) fluxes throughout the water column (focusing on the upper 1000 m) along the GP16 GEOTRACES section between Peru and Tahiti (Figure 1A).  POC fluxes (Figure 1B) were derived by normalizing concentrations of POC to 230Th following analysis of samples collected by in situ filtration. This work builds on a research theme initiated at the GEOTRACES-OCB synthesis workshop held at Lamont-Doherty Earth Observatory in 2016.

Figure caption: Site map and POC flux characteristics from GEOTRACES GP16 section. Plot A) shows the GP16 station locations as white circles, with nearby sediment trap deployments as black stars, with 2013 MODIS satellite-derived net primary productivity in the background. Plot B) shows POC fluxes from particulate 230Th-normalization from selected stations spanning the zonal extent of the GP16 section. Plot C) shows power law exponent b values for each GP16 station (blue), compared to estimates from bottom-moored sediment traps in the South Pacific (black and red dashed lines), a compilation of sediment traps in the North Pacific (green dashed line), and neutrally buoyant sediment traps in the subtropical North Pacific (yellow shaded band). GP16 regeneration length scales from 230Th-normalization agree most closely with the estimates from neutrally buoyant sediment traps.

The study results show that POC regeneration depth is shallower than anticipated, especially in warm stratified waters of the subtropical gyre. Regeneration depth—expressed in terms of the Martin-curve power-law exponent “b” (Figure 1C)—is shown to be greater than previous estimates (horizontal dashed lines), but similar to values obtained using neutrally buoyant sediment traps at the Hawaii Ocean Time-series Station Aloha. In contrast to the rapid regeneration of POC in warm stratified waters, POC regeneration within the ODZ is below our detection limits. Models have shown that shallower regeneration of POC leads to less efficient carbon storage in the ocean, making the authors speculate that global warming, yielding expanded and more stratified gyres, may induce a reduction of the ocean’s efficacy for carbon storage via the biological pump.

 

Authors:
Frank J. Pavia, Robert F. Anderson, Sebastian M. Vivancos, Martin Q. Fleisher (Columbia University)
Phoebe J. Lam (University of California Santa Cruz)
B.B. Cael (now at University of Hawai’i Manoa, formerly at MIT)
Yanbin Lu, Pu Zhang, R. Lawrence Edwards (University of Minnesota)
Hai Cheng (University of Minnesota and Xi’an Jiaotong University)

Nutrient and carbon limitation drive broad-scale patterns of mixotrophy in the ocean

Posted by mmaheigan 
· Tuesday, May 14th, 2019 

In the ocean, unicellular eukaryotes are often mixotrophic, which means they photosynthesize and also consume prey. In recent decades, it has become clear that mixotrophs are ubiquitous in sunlit ocean habitats. Additionally, models predict that mixotrophs have important impacts on productivity, nutrient cycling, carbon export, and food web structure. However, there is little understanding of the environmental conditions that select for a mixotrophic lifestyle, and it is unclear how mixotrophs succeed in competition with autotrophic and heterotrophic specialists. A recent study in PNAS that synthesized measurements of mixotrophic nanoflagellates showed that mixotrophs are more abundant in stratified, well-lit, low latitude environments (Figure 1A). They are also more abundant, relative to pure heterotrophs, in productive coastal environments (Figure 1B). A trait-based model analysis revealed that the success of mixotrophs depends on the fact that they are less nutrient-limited than autotrophs (due to prey-derived nutrients) and less carbon-limited than heterotrophs (due to photosynthesis). This synergy requires sufficient light, leading to success in low latitude environments. Similarly, a greater supply of dissolved nutrients relative to prey, as commonly observed in coastal environments, favors mixotrophs relative to heterotrophs. One implication of these results is that carbon fixation at lower latitudes may be enhanced by mixotrophy, while limiting nutrients may be more efficiently transferred to higher trophic levels.

Figure 1. Estimated abundance of autotrophic, mixotrophic, and heterotrophic nanoflagellates across environmental gradients in the ocean.

 

Author:
Kyle Edwards (Univ. Hawaii at Manoa)

A synthesis of North American coastal carbon fluxes

Posted by mmaheigan 
· Tuesday, April 30th, 2019 

Carbon fluxes in the coastal ocean and across its boundaries with the atmosphere, land, and the open ocean are an important but poorly constrained component of the global carbon budget. By synthesizing available observations and model simulations, a recent study aims to answer 1) whether the coastal ocean of North America takes up atmospheric CO2 and exports carbon to the open ocean; and 2) if so, how much? The authors estimate a net carbon sink of 160±80 Tg C yr−1 in the North American Exclusive Economic Zone (EEZ) with the Arctic, sub-Arctic and mid-latitude Atlantic EEZ regions as the major contributors.

Portion of EEZ Tg C yr−1 % of the total area
Arctic and sub-Arctic 104 51%
Mid-latitude Atlantic 62 25%
Mid-latitude Pacific -3.7 24%

Table 1: Regional breakdown of estimated carbon sink in the North Atlantic EEZ (negative values imply a carbon source).

 

Combining the net uptake with an estimate of carbon input from land of minus estimates of burial and accumulation of dissolved carbon in EEZ waters as follows implies a carbon export of 151±105 Tg C yr−1 to the open ocean.

160±80 

Tg C yr−1

+

106±30 

Tg C yr−1

–

65±55 

Tg C yr−1

–

50±25 

Tg C yr−1

=

151±105 

Tg C yr−1

Net uptake

 

Carbon input from land Estimated burial Estimated accumulation DOC in EEZ waters Carbon export to open ocean (estimated C export to open ocean)

 

The estimated uptake of atmospheric carbon in the North American EEZ amounts to 6.4% of the global ocean uptake of atmospheric CO2 (est. 2,500 Tg C yr−1). The North American EEZ only represents ~4% of the global ocean surface area, thus the CO2 uptake is about 50% more efficient in the North American EEZ than the global average. Given the importance of coastal margins, both in contributing to carbon budgets and in the societal benefits they provide, further efforts to improve assessments of the carbon cycle in these regions are paramount. It is critical to maintain and expand existing coastal observing programs, continue national and international coordination and integration of observations, modeling capabilities, and stakeholder needs.

 

Figure: Area-specific carbon fluxes for North American coastal regions (a, b and d) and total fluxes for a decomposition of the EEZ (c, e).

 

Authors:
Katja Fennel, Timothée Bourgeois (Dalhousie University, Canada)
Simone Alin, Richard A. Feely, Adrienne Sutton (NOAA Pacific Marine Environmental Laboratory)
Leticia Barbero (NOAA Atlantic Oceanographic and Meteorological Laboratory)
Wiley Evans (Hakai Institute, Canada)
Sarah Cooley (Ocean Conservancy)
John Dunne (NOAA Geophysical Fluid Dynamics Laboratory)
Jose Martin Hernandez-Ayon (Autonomous University of Baja California, Mexico)
Xinping Hu (Texas A&M University)
Steven Lohrenz (University of Massachusetts, Dartmouth)
Frank Muller-Karger, Lisa Robbins (University of South Florida)
Raymond Najjar (Pennsylvania State University)
Elizabeth Shadwick (CSIRO, Australia)
Samantha Siedlecki, Penny Vlahos (University of Connecticut)
Nadja Steiner (Department of Fisheries and Oceans Canada)
Daniela Turk (Lamont-Doherty Earth Observatory)
Zhaohui Aleck Wang (Woods Hole Oceanographic Institution)

Northeast Pacific time-series reveals episodic events as major player in carbon export

Posted by mmaheigan 
· Tuesday, April 16th, 2019 

Temporal fluctuations in the oceanic carbon budget play an important role in the cycling of organic matter from production in surface waters to consumption and sequestration in the deep ocean. A 29-year time-series (1989-2017) of particulate organic carbon (POC) fluxes and seafloor measurements of oxygen consumption in the abyssal northeast Pacific (Sta. M, 4,000 m depth) recently revealed an increasing proportional contribution from episodic events over the past seven years. From 2011 to 2017, 43% of POC flux arrived during high-magnitude (≥ mean + 2 σ) episodic events. Time lags between changes in satellite-estimated export flux (EF), POC flux to the seafloor, and seafloor oxygen consumption varied from 0 to 70 days among six flux events, which could be attributed to variable remineralization rates and/or particle sinking speeds. The Martin equation, a commonly used model to estimate carbon flux, predicted background fluxes well but missed episodic fluxes, subsequently underestimating the measured fluxes by almost 50% (Figure 1). This study reveals the potential importance of episodic POC pulses into the deep sea in the oceanic carbon budget, which has implications for observing infrastructure, model development, and field campaigns focused on quantifying carbon export.

Figure Caption: (A) Station M POC flux measured from sediment traps compared to Martin model estimates, from 1989 to 2017. (B) Model performance for years with >50% sampling coverage: (POC fluxMartin − POC fluxtrap)/POC fluxtrap 100.

 

Authors:
Kenneth Smith (MBARI)
Henry Ruhl (MBARI, NOC)
Christine Huffard (MBARI)
Monique Messié (MBARI, Aix Marseille Université)
Mati Kahru (Scripps)

 

See also https://www.mbari.org/carbon-pulses-climate-models/

Ocean color offers early warning signal of climate change’s impact on marine phytoplankton

Posted by mmaheigan 
· Monday, April 15th, 2019 

Marine phytoplankton form the foundation of the marine food web and play a crucial role in the earth’s carbon cycle. Typically, satellite-derived Chlorophyll a (Chl a) is used to evaluate trends in phytoplankton. However, it may be many decades (or longer) before we see a statistically significant signature of climate change in Chl a due to its inherently large natural variability. In a recent study in Nature Communications, authors explored how other metrics, in particular the color of the ocean, may show earlier and stronger signals of climate change at the base of the marine food web.

Figure 1. Computer model results indicating the year in which the signature of climate change impact is larger than the natural variability for (a) Chl a, and (b) remotely sensed reflectance in the blue-green waveband. White areas indicate where there is not a statistically significant change by 2100, or for regions that are currently ice-covered.

 

In this study, the authors use a unique marine physical-biogeochemical and ecosystem model that also captures how light penetrates the ocean and is reflected upward. The model shows that over the course of the 21st century, remote sensing reflectance (RRS, the ratio of upwelling radiance to the downwelling irradiance at the ocean’s surface) in the blue-green portions of the light spectrum is likely to have an earlier, more spatially extensive climate change-driven signal than Chl a (Figure 1). This is because RRS integrates not only changes to Chl a, but also alterations in other optically important water constituents. In particular, RRS also captures changes in phytoplankton community structure, which strongly affects ocean optics and is likely to be altered over the 21st century. Monitoring the response of marine phytoplankton to climate change is important for predicting changes at higher trophic levels, including commercial fisheries. Our study emphasizes the importance of 1) maintaining ocean color sensor compatibility and long-term stability, particularly in the blue-green wavebands; 2) maintaining long-term in situ time-series of plankton communities – e.g., the Continuous Plankton Recorder survey and repeat stations (e.g., HOT, BATS); and 3) reducing uncertainties in satellite-derived phytoplankton community structure estimates.

 

Authors:
Stephanie Dutkiewicz, Oliver Jahn (Massachusetts Institute of Technology)
Anna E. Hickman (University of Southampton)
Stephanie Henson (National Oceanography Centre Southampton)
Claudie Beaulieu (University of California, Santa Cruz)
Erwan Monier (University of California, Davis)

Antarctic Ocean CO2 helped end the ice age

Posted by mmaheigan 
· Tuesday, April 2nd, 2019 

Many scientists have long hypothesized that the ocean around Antarctica was responsible for changing CO2 levels during ice ages, but lacked definitive evidence. A new study in Nature provides the most direct evidence of this process to date and provides crucial evidence of the mechanisms—including changing sea ice cover and bipolar seesaw (warming in the Southern Hemisphere during cooling in the Northern Hemisphere) events—that controlled CO2 and climate during the ice ages.

Using samples of fossil deep-sea corals collected from 1000 m in the Drake Passage (Figure 1a), the authors were able to reconstruct the CO2 content of the deep ocean. They found that the deep ocean CO2 record was the “mirror image” of CO2 in the atmosphere (Figure 1b), with the ocean storing CO2 during an ice age and releasing it back to the atmosphere during deglaciation. CO2 rise during the last ice age occurred in a series of steps and jumps associated with intervals of rapid climate change.

a
a
b
b

As well as helping scientists better understand the ice ages, the new findings also provide context to current CO2 rise and climate change. Although the CO2 rise that helped end the last ice age was dramatic in geological terms, CO2 rise due to human activity over the last 100 years is even larger and about 100 times faster. CO2 rise at the end of the ice age helped drive major melting of ice sheets resulting in sea level rise of >100 meters. These results bolster the idea that if we want to prevent dangerous levels of global warming and sea level rise in the future, we need to reduce CO2 emissions as quickly as possible

Authors:
J. W. B. Rae (University of St Andrews, UK)
A. Burke (University of St Andrews, UK)
L. F. Robinson (University of Bristol, UK)
J. F. Adkins (California Institute of Technology)
T. Chen (University of Bristol, UK, Nanjing University, China)
C. Cole (University of St Andrews, UK)
R. Greenop (University of St Andrews, UK)
T. Li (University of Bristol, UK, Nanjing University, China)
E. F. M. Littley (University of St Andrews, UK)
D. C. Nita (University of St Andrews, UK, Babes-Bolyai University, Romania)
J. A. Stewart (University of St Andrews, UK, University of Bristol, UK)
B. J. Taylor (University of St Andrews, UK)

A half century perspective: Seasonal productivity and particulates in the Ross Sea

Posted by mmaheigan 
· Tuesday, April 2nd, 2019 

Studies of cruise observations in the Ross Sea are typically biased to a single or a few year(s), and long-term trends have predominantly come from satellites. Consequently, the in situ climatological patterns of nutrients and particulate matter have remained vague and unclear. What are the typical patterns of nutrients and particulate matter concentrations in the Ross Sea in spring and summer? How do these concentrations affect annual productivity estimates?

Patterns of nutrient and particulate matter in the Ross Sea can play a wide-ranging role in a productive region like the Ross Sea. Smith and Kaufman (2018) recently synthesized austral spring and summer (November to February) observations from 42 Ross Sea research cruises (1967-2016) to analyze broad biogeochemical patterns. The resulting climatologies revealed interesting seasonal patterns of nutrient uptake and particulate organic carbon (POC) to chlorophyll (chl) ratios (POC:chl). Temporal patterns in the nitrate and phosphate climatologies confirm the role of early spring haptophyte (Phaeocystis antarctica) growth, followed by limited nitrogen and phosphorus removal in summer. However, a notable increase in POC occurred later in summer that was largely independent of chlorophyll changes, resulting in a dramatic increase in POC:chl. A gradual decline in silicic acid concentrations throughout the summer, along with an increased occurrence of biogenic silica during this time suggest that diatoms may be responsible for this later POC spike. Revised estimates of primary productivity based on these observed climatological POC:chl ratios suggests that summer blooms may be a significant contributor to seasonal productivity, and that estimates of productivity based on satellite pigments underestimate annual production by at least 70% (Figure 1).

Figure 1. Bio-optical estimates of mean productivity using a constant POC:chl ratio (black dots and lines) and modified estimates of productivity using the monthly climatological POC:chl ratios (red dots and lines), in a) the Ross Sea polynya region and b) the western Ross Sea region.

 

By clarifying typical seasonal patterns of nutrient uptake and POC:chl, these climatologies underscore the biogeochemical importance of both spring haptophyte growth and previously underestimated summer diatom growth in the Ross Sea. Further investigation of the causes and consequences of elevated summer ratios is needed, as assessments of regional food webs and biogeochemical cycles depend on more accurate understanding of primary productivity patterns. Likewise, these results highlight the need for continued efforts to constrain satellite productivity estimates in the Ross Sea using in situ constituent ratios.

For other relevant work on seasonal biogeochemical patterns in the Ross Sea, please see https://doi.org/10.1016/j.dsr2.2003.07.010. And for intra-seasonal estimates of particulate organic carbon to chlorophyll using gliders, please see: https://doi.org/10.1016/j.dsr.2014.06.011.

 

Authors:
Walker O. Smith Jr. (VIMS, College of William and Mary)
Daniel E. Kaufman (VIMS, College of William and Mary; now at Chesapeake Research Consortium)

 

 

 

Pteropod populations stable or increasing according to long-term study along the Western Antarctic Peninsula

Posted by mmaheigan 
· Thursday, March 21st, 2019 

Shelled pteropods (pelagic snails) are abundant planktonic predators and prey, linking grazers and higher trophic levels and contributing to the carbon cycle via consumption and excretion. Pteropods have been heralded as bioindicators of ocean acidification, given their aragonitic shell’s susceptibility to dissolution, which could ultimately lead to declining abundance. However, pteropod population dynamics are understudied, particularly in the Southern Ocean, a region predicted to be highly impacted by both warming and ocean acidification. In a recent publication in Limnology and Oceanography, long-term data sets from the Western Antarctic Peninsula show that while there is considerable interannual variability in pteropod abundance, populations have remained stable over the past 25 years, with some pteropod species (gymnosomes (non-shelled pteropod) overall, L. antarctica and C. pyramidata (shelled pteropods) regionally) even increasing during this period (Figure 1).


Figure 1. Annual pteropod abundance anomalies for the entire Palmer Antarctica Long-Term Ecological Research (LTER) study region along the Western Antarctic Peninsula. (a) Limacina helicina antarctica (shelled pteropod), (b) Gymnosomes – nonshelled pteropods that prey on shelled pteropods (p = 0.007, r2 = 0.27), and (c) Clio pyramidata (shelled pteropod). Effect of environment on pteropod abundance. (d) SST vs. L. antarctica abundance, e) Sea ice advance vs. L. antarctica and Gymnosome abundance, (f) Sea ice retreat vs. C. pyramidata abundance. Data plotted are annual anomalies for each year of the time series (1993–2017). Sea ice advance is lagged 2-yr behind pteropod abundance (e.g., 2017 pteropod annual anomaly is plotted against 2015 sea ice advance annual anomaly) SST are lagged 1-yr behind L. antarctica abundance (e.g., 2017 L. antarctica annual anomaly is plotted against 2016 SST). Regression lines for significant linear relationships are shown, regression statistics are as follows: (d) SST vs. L. antarctica (circles): n = 25, p = 0.006, r2 = 0.25 (e) sea ice advance vs. L. antarctica (filled-circles) and Gymnosomes (empty-circles): n = 25, p = 0.003, r2 = 0.30 (dashed line); (f) sea ice retreat vs. C. pyramidata (squares): n = 14, p = 0.0003, r2 = 0.64.

There was no significant influence of carbonate chemistry parameters (e.g., aragonite saturation state) on pteropod abundance, since the Western Antarctic Peninsula has yet to experience prolonged conditions characteristic of ocean acidification. However, other environmental factors such as warming and associated sea ice retreat were more influential. For example, warmer, ice-free waters in one year typically led to higher pteropod abundances the following year, suggesting that pteropods may be better adapted than expected to warming conditions due to climate change. The authors propose that earlier sea ice retreat promotes recruitment and subsequent expansion of pteropods further South, which could explain their increased abundance in this subregion. These results increase our understanding of pteropod responses to environmental variability, which is important for predicting future effects of climate change on regional carbon cycling and plankton trophic interactions in the Southern Ocean.

 

Authors:
Patricia S. Thibodeau (VIMS)
Deborah K. Steinberg (VIMS)
Sharon E. Stammerjohn (University of Colorado at Boulder)
Claudine Hauri (University of Alaska Fairbanks)

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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 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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

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