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Abstract Over the last ten years, satellite and geographically constrained in situ observations largely focused on the northern hemisphere have suggested that annual phytoplankton biomass cycles cannot be fully understood from environmental properties controlling phytoplankton division rates (e.g., nutrients and light), as they omit the role of ecological and environmental loss processes (e.g., grazing, viruses, sinking). Here, we use multi-year observations from a very large array of robotic drifting floats in the Southern Ocean to determine key factors governing phytoplankton biomass dynamics over the annual cycle. Our analysis reveals seasonal phytoplankton accumulation (‘blooming’) events occurring during periods of declining modeled division rates, an observation that highlights the importance of loss processes in dictating the evolution of the seasonal cycle in biomass. In the open Southern Ocean, the spring bloom magnitude is found to be greatest in areas with high dissolved iron concentrations, consistent with iron being a well-established primary limiting nutrient in this region. Under ice observations show that biomass starts increasing in early winter, well before sea ice begins to retreat. The average theoretical sensitivity of the Southern Ocean to potential changes in seasonal nutrient and light availability suggests that a 10% change in phytoplankton division rate may be associated with a 50% reduction in mean bloom magnitude and annual primary productivity, assuming simple changes in the seasonal magnitude of phytoplankton division rates. Overall, our results highlight the importance of quantifying and accounting for both division and loss processes when modeling future changes in phytoplankton biomass cycles. 

The deep ocean releases large amounts of old, pre‐industrial carbon dioxide (CO₂) to the atmosphere through upwelling in the Southern Ocean, which counters the marine carbon uptake occurring elsewhere. This Southern Ocean CO₂release is relevant to the global climate because its changes could alter atmospheric CO₂levels on long time scales, and also affects the present‐day potential of the Southern Ocean to take up anthropogenic CO₂. Here, year‐round profiling float measurements show that this CO₂release arises from a zonal band of upwelling waters between the Subantarctic Front and wintertime sea‐ice edge. This band of high CO₂subsurface water coincides with the outcropping of the 27.8 kg m⁻³isoneutral density surface that characterizes Indo‐Pacific Deep Water (IPDW). It has a potential partial pressure of CO₂exceeding current atmospheric CO₂levels (∆PCO₂) by 175 ± 32 μatm. Ship‐based measurements reveal that IPDW exhibits a distinct ∆PCO₂maximum in the ocean, which is set by remineralization of organic carbon and originates from the northern Pacific and Indian Ocean basins. Below this IPDW layer, the carbon content increases downwards, whereas ∆PCO₂decreases. Most of this vertical ∆PCO₂decline results from decreasing temperatures and increasing alkalinity due to an increased fraction of calcium carbonate dissolution. These two factors limit the CO₂outgassing from the high‐carbon content deep waters on more southerly surface outcrops. Our results imply that the response of Southern Ocean CO₂fluxes to possible future changes in upwelling are sensitive to the subsurface carbon chemistry set by the vertical remineralization and dissolution profiles.

 

We use observations from novel biogeochemical profiling floats deployed by the Southern Ocean Carbon and Climate Observations and Modeling program to estimate annual net community production (ANCP; associated with carbon export) from the seasonal drawdown of mesopelagic oxygen and surface nitrate in the Southern Ocean. Our estimates agree with previous observations in showing an increase in ANCP in the vicinity of the polar front (∼3 mol C m⁻² y⁻¹), compared to lower rates in the subtropical zone (≤ 1 mol C m⁻² y⁻¹) and the seasonal ice zone (<2 mol C m⁻² y⁻¹). Paradoxically, the increase in ANCP south of the subtropical front is associated with elevated surface nitrate and silicate concentrations, but decreasing surface iron. We hypothesize that iron limitation promotes silicification in diatoms, which is evidenced by the low silicate to nitrate ratio of surface waters around the Antarctic polar front. High diatom silicification increases the ballasting effect of particulate organic carbon and overall ANCP in this region. A model‐based assessment of our methods shows a good agreement between ANCP estimates based on oxygen and nitrate drawdown and the modeled downward organic carbon flux at 100 m. This agreement supports the presumption that net biological consumption is the dominant process affecting the drawdown of these chemical tracers and that, given sufficient data, ANCP can be inferred from observations of oxygen and/or nitrate drawdown in the Southern Ocean.

 

The storage of anomalous heat and carbon in the Southern Ocean in response to increasing greenhouse gases greatly mitigates atmospheric warming and exerts a large impact on the marine ecosystem. However, the mechanisms driving the ocean storage patterns are uncertain. Here using recent hydrographic observations, we compare for the first time the spatial patterns of heat and carbon storage, which show substantial differences in the Southern Ocean, in contrast with the conventional view of simple passive subduction into the thermocline. Using an eddy‐rich global climate model, we demonstrate that redistribution of the preindustrial temperature field is the dominant control on the heat storage pattern, whereas carbon storage largely results from passive transport of anthropogenic carbon uptake at the surface. Lastly, this study highlights the importance of realistic representation of wind and surface buoyancy flux in climate models to improve future projection of circulation change and thus heat and carbon storage.

 

The ocean is estimated to contribute up to ~20% of global fluxes of atmospheric nitrous oxide (N₂O), an important greenhouse gas and ozone depletion agent. Marine oxygen minimum zones contribute disproportionately to this flux. To further understand the partition of nitrification and denitrification and their environmental controls on marine N₂O fluxes, we report new relationships between oxygen concentration and rates of N₂O production from nitrification and denitrification directly measured with¹⁵N tracers in the Eastern Tropical Pacific. Highest N₂O production rates occurred near the oxic‐anoxic interface, where there is strong potential for N₂O efflux to the atmosphere. The dominant N₂O source in oxygen minimum zones was nitrate reduction, the rates of which were 1 to 2 orders of magnitude higher than those of ammonium oxidation. The presence of oxygen significantly inhibited the production of N₂O from both nitrification and denitrification. These experimental data provide new constraints to a multicomponent global ocean biogeochemical model, which yielded annual oceanic N₂O efflux of 1.7–4.4 Tg‐N (median 2.8 Tg‐N, 1 Tg = 10¹² g), with denitrification contributing 20% to the oceanic flux. Thus, denitrification should be viewed as a net N₂O production pathway in the marine environment.