Wolfgang Koeve

Basin‐wide particulate carbon flux in the Atlantic Ocean: Regional export patterns and potential for atmospheric CO2 sequestration

Particle flux data from 27 sites in the Atlantic Ocean have been compiled in order to determine regional variations in the strength and efficiency of the biological pump and to quantify carbon fluxes over the ocean basin, thus estimating the potential oceanic sequestration of atmospheric CO2. An algorithm is derived relating annual particulate organic carbon (POC) flux to primary production and depth that yields variations in the export ratio (ER = POC flux/primary production) at 125 m of between 0.08 and 0.38 over the range of production from 50 to 400 g C m−2 yr−1. Significant regional differences in changes of the export ratio with depth are related to the temporal stability of flux. Sites with more pulsed export have higher export ratios at 125 m but show more rapid decreases of POC flux with depth, resulting in little geographic variation in fluxes below ∼3000 m. The opposing effects of organic carbon production and calcification on ΔpCO2 of surface seawater are considered to calculate an “effective carbon flux” at the depth of the euphotic zone and at the base of the winter mixed layer. POC flux at the base of the euphotic zone integrated over the Atlantic Ocean between 65°N and 65°S amounts to 3.14 Gt C yr−1. Of this, 5.7% is remineralized above the winter mixed layer and thus does not contribute to CO2 sequestration on climatically relevant timescales. The effective carbon flux, termed Jeff, amounts to 2.47 Gt C yr−1 and is a measure of the potential sequestration of atmospheric CO2 for the area considered. A shift in the composition of sedimenting particles (seen in a decrease of the opal:carbonate ratio) is seen across the entire North Atlantic, indicating a basin-wide phenomenon that may be related to large-scale changes in climatic forcing.

C : N ratios in the mixed layer during the productive season in the northeast Atlantic Ocean

Redfield stoichiometry has proved a robust paradigm for the understanding of biological production and export in the ocean on a long-term and a large-scale basis. However, deviations of carbon and nitrogen uptake ratios from the Redfield ratio have been reported. A comprehensive data set including all carbon and nitrogen pools relevant to biological production in the surface ocean (DIC, DIN, DOC, DON, POC, PON) was used to calculate seasonal new production based on carbon and nitrogen uptake in summer along 20°W in the northeast Atlantic Ocean. The 20°W transect between 30 and 60°N covers different trophic states and seasonal stages of the productive surface layer, including early bloom, bloom, post-bloom and non-bloom situations. The spatial pattern has elements of a seasonal progression. We also calculated exported production, i.e., that part of seasonal new production not accumulated in particulate and dissolved pools, again separately for carbon and nitrogen. The pairs of estimates of `seasonal new production’ and `exported production’ allowed us to calculate the C : N ratios of these quantities. While suspended particulate matter in the mixed layer largely conforms to Redfield stoichiometry, marked deviations were observed in carbon and nitrogen uptake and export with progressing season or nutrient depletion. The spring system was characterized by nitrogen overconsumption and the oligotrophic summer system by a marked carbon overconsumption. The C : N ratios of seasonal new as well as exported production increase from early bloom values of 5–6 to values of 10–16 in the post-bloom/oligotrophic system. The summertime accumulation of nitrogen-poor dissolved organic matter can explain only part of this shift.

Marine dissolved organic matter: can its C:N ratio explain carbon overconsumption?

Carbon overconsumption, i.e. the consumption of inorganic carbon relative to inorganic nitrogen in excess of the Redfield ratio at the sea surface, was examined in relation to the dynamics of dissolved organic carbon and nitrogen (DOC and DON) in the northeast Atlantic. We observed the presence of N-poor dissolved organic matter (DOM) in surface water during summer, requiring the consumption of inorganic carbon and nitrogen in a ratio exceeding the Redfield ratio. The C : N ratio of bulk DOM is not only different from the Redfield ratio but also variable, i.e. no fixed conversion factor of C and N exists where DOM is important in C and N transformations. The existence of N-poor DOM is recognized as a feature typical of oligotrophic systems. At the same time, the C : N ratios of particles conform to Redfield stoichiometry as does deep-ocean chemistry. The implications of this finding are discussed, the conclusion being that, while DOM buildup contributes to CO2 drawdown seasonally, its impact on long-term carbon and nitrogen balance of the ocean is small.

Pelagic processes and vertical flux of particles: an overview of a long-term comparative study in the Norwegian Sea and Greenland Sea

Pelagic processes and their relation to vertical flux have been studied in the Norwegian and Greenland Seas since 1986. Results of long-term sediment trap deployments and adjoining process studies are presented, and the underlying methodological and conceptional background is discussed. Recent extension of these investigations at the Barents Sea continental slope are also presented. With similar conditions of input irradiation and nutrient conditions, the Norwegian and Greenland Seas exhibit comparable mean annual rates of new and total production. Major differences can be found between these regions, however, in the hydrographic conditions constraining primary production and in the composition and seasonal development of the plankton. This is reflected in differences in the temporal patterns of vertical particle flux in relation to new production in the euphotic zone, the composition of particles exported and in different processes leading to their modification in the mid-water layers.In the Norwegian Sea heavy grazing pressure during early spring retards the accumulation of phytoplankton stocks and thus a mass sedimentation of diatoms that is often associated with spring blooms. This, in conjunction with the further seasonal development of zooplankton populations, serves to delay the annual peak in sedimentation to summer or autumn. Carbonate sedimentation in the Norwegian Sea, however, is significantly higher than in the Greenland Sea, where physical factors exert a greater control on phytoplankton development and the sedimentation of opal is of greater importance. In addition to these comparative long-term studies a case study has been carried out at the continental slope of the Barents Sea, where an emphasis was laid on the influence of resuspension and across-slope lateral transport with an analysis of suspended and sedimented material.

An eddy‐permitting coupled physical‐biological model of the North Atlantic: 2. Ecosystem dynamics and comparison with satellite and JGOFS local studies data

A model of biological production in the euphotic zone of the North Atlantic has been developed by coupling a Nitrate, Phytoplankton, Zooplankton, Detritus (NPZD) nitrogen-based ecosystem model with an eddy-permitting circulation model. The upper ocean physical and biological results are presented for an experiment with monthly climatological forcing. A comparison with satellite ocean color data shows that the model is capable of a realistic description of the main seasonal and regional patterns of surface chlorophyll. Agreement is also good for primary production except in the subtropical gyre where the model produces values more than an order of magnitude smaller than derived from satellite observations. In situ data available at Joint Global Ocean Flux Study (JGOFS) time series and local study sites (Bermuda Atlantic Time-series Study (BATS), 32°N, 65°W; North Atlantic Bloom Experiment (NABE), 47°N, 2O°W; EUMELI oligotrophic, 21°N, 31°W) are used for a more detailed analysis of the models capability to simultaneously reproduce seasonal ecosystem dynamics in different biological provinces of the North Atlantic Ocean. The seasonal cycle of phytoplankton biomass and nitrate is simulated quite realistically at all sites. Main discrepancies between model and observations are a large zooplankton peak, required by the model to end the phytoplankton spring bloom at the 47°N, 20°W site, and the underestimation of primary production at EUMELI and under oligotrophic summer conditions at BATS. The former model deficiency can be related to the neglect of phytoplankton aggregation; the latter is caused by too inefficient recycling of nutrients within the euphotic zone. Model improvements are suggested for further steps toward a realistic basin-wide multiprovinces simulation with a single ecosystem model.

A new perspective on environmental controls of marine nitrogen fixation

Growing slowly, marine N2 fixers are generally expected to be competitive only where nitrogen (N) supply is low relative to that of phosphorus (P) with respect to the cellular N:P ratio (R) of non-fixing phytoplankton. This is at odds with observed high N2 fixation rates in the oligotrophic North Atlantic where the ratio of nutrients supplied to the surface is elevated in N relative to the average R (16:1). In this study, we investigate several mechanisms to solve this puzzle: iron limitation, phosphorus enhancement by preferential remineralization or stoichiometric diversity of phytoplankton, and dissolved organic phosphorus (DOP) utilization. Combining resource competition theory and a global coupled ecosystem-circulation model we find that the additional N and energy investments required for exo-enzymatic break-down of DOP gives N2 fixers a competitive advantage in oligotrophic P-starved regions. Accounting for this mechanism expands the ecological niche of N2-fixers also to regions where the nutrient supply is high in N relative to R, yielding, in our model, a pattern consistent with the observed high N2-fixation rates in the oligotrophic North Atlantic.

Upper ocean carbon fluxes in the Atlantic Ocean: The importance of the POC:PIC ratio

The mean depth distribution of the POC:PIC ratio of sinking particles, measured with particle interceptor traps deployed in the Atlantic Ocean, is fitted by an exponential function (POC:PIC = 64.3Z−0.56; r2 = 0.69) The function is successfully evaluated by comparison with (a) estimates of the POC:PIC ratio of export production, computed from seasonal changes of nitrate and alkalinity and (b) estimates of the POC:PIC ratio of remineralization on shallow isopycnals. The basin mean POC:PIC ratio of export production is 4.2–4.37. The POC:PIC-depth function is combined with empirical relationships between the flux of particulate organic matter, primary production and depth, satellite derived primary production data sets, and the regional distribution of ψ (the ratio of released CO2:precipitated carbonate during CaCO3 formation) in order to estimate the effective carbon flux (Jeff) in the Atlantic Ocean. Remineralization of organic carbon above the winter mixed layer (11–17%) and CaCO3 sequestration from the winter mixed layer (13–16%), which is the balance between CaCO3 production and shallow dissolution, are the two main processes which control the difference between export production (0.9 and 2.9 GT C yr−1) and Jeff (0.64 and 2.2 GT C yr−1) on the basin scale (65°N to 65°S). CaCO3 sequestration is the dominant process modulating effective carbon export in the tropics, while shallow POC remineralization dominates in temperate and polar waters. Observed regional patterns like polarward increases of the POC:PIC export ratio and of ψ counteract each other largely when Jeff is computed.

Storm-induced convective export of organic matter during spring in the northeast Atlantic Ocean

Observations during a spring phytoplankton bloom in the northeast Atlantic between March and May 1992 in the Biotrans region at 47°N, 20°W, are presented. During most of the observation period there was a positive heat flux into the ocean, winds were weak, and the mixed layer depth was shallow (<40 m). Phytoplankton growth conditions were favourable during this time. Phytoplankton biomass roughly doubled within the euphotic zone over the course of about 7 days during mid-April, and rapidly increased towards the end of the study until silicate was depleted. However, the stratification of the water column was transient, and the spring bloom development was repeatedly interrupted by gales. During two storms, in late March and late April, the mixed-layer depth increased to 250 and 175 m, respectively. After the storm events significant amounts of chlorophyll-a, particulate organic carbon and biogenic silica were found well below the euphotic zone. It is estimated that between 56% and 65% of the seasonal new production between winter and early May was exported from the euphotic zone by convective mixing, in particular, during the two storm events. Data from the NABE 47°N study during spring 1989 are re-evaluated. It is found that convective particle export was of importance during the early part of that bloom too, but negligible during the height of the bloom in May 1989. The overall impact of convective particle export during spring 1989 was equivalent to about 36% of new production. In view of these and previously published findings it is concluded that convective transport during spring is a significant process for the export of particulate matter from the euphotic zone in the temperate North Atlantic.

Limited impact of atmospheric nitrogen deposition on marine productivity due to biogeochemical feedbacks in a global ocean model

The impact of increasing anthropogenic atmospheric nitrogen deposition on marine biogeochemistry is uncertain. We performed simulations to quantify its effect on nitrogen cycling and marine productivity in a global 3-D ocean biogeochemistry model. Nitrogen fixation provides an efficient feedback by decreasing immediately to deposition, whereas water column denitrification increases more gradually in the slowly expanding oxygen deficient zones. Counterintuitively, nitrogen deposition near oxygen deficient zones causes a net loss of marine nitrogen due to the stoichiometry of denitrification. In our idealized atmospheric deposition simulations that only account for nitrogen cycle perturbations, these combined stabilizing feedbacks largely compensate deposition and suppress the increase in global marine productivity to 15%. Our study emphasizes including the dynamic response of nitrogen fixation and denitrification to atmospheric nitrogen deposition to predict future changes of the marine nitrogen cycle and productivity.

Patterns of deoxygenation: sensitivity to natural and anthropogenic drivers

Observational estimates and numerical models both indicate a significant overall decline in marine oxygen levels over the past few decades. Spatial patterns of oxygen change, however, differ considerably between observed and modelled estimates. Particularly in the tropical thermocline that hosts open-ocean oxygen minimum zones, observations indicate a general oxygen decline, whereas most of the state-of-the-art models simulate increasing oxygen levels. Possible reasons for the apparent model-data discrepancies are examined. In order to attribute observed historical variations in oxygen levels, we here study mechanisms of changes in oxygen supply and consumption with sensitivity model simulations. Specifically, the role of equatorial jets, of lateral and diapycnal mixing processes, of changes in the wind-driven circulation and atmospheric nutrient supply, and of some poorly constrained biogeochemical processes are investigated. Predominantly wind-driven changes in the low-latitude oceanic ventilation are identified as a possible factor contributing to observed oxygen changes in the low-latitude thermocline during the past decades, while the potential role of biogeochemical processes remains difficult to constrain. We discuss implications for the attribution of observed oxygen changes to anthropogenic impacts and research priorities that may help to improve our mechanistic understanding of oxygen changes and the quality of projections into a changing future. This article is part of the themed issue ‘Ocean ventilation and deoxygenation in a warming world’.