François Fripiat

Significant mixed layer nitrification in a natural iron‐fertilized bloom of the Southern Ocean

Nitrification, the microbially mediated oxidation of ammonium into nitrate, is generally expected to be low in the Southern Ocean mixed layer. This paradigm assumes that nitrate is mainly provided through vertical mixing and assimilated during the vegetative season, supporting the concept that nitrate uptake is equivalent to the new primary production (i.e., primary production which is potentially available for export). Here we show that nitrification is significant (~40-80% of the seasonal nitrate uptake) in the naturally iron-fertilized bloom over the southeast Kerguelen Plateau. Hence, a large fraction of the nitrate-based primary production is regenerated, instead of being exported. It appears that nitrate assimilation (light dependent) and nitrification (partly light inhibited) are spatially separated between the upper and lower parts, respectively, of the deep surface mixed layers. These deep mixed layers, extending well below the euphotic layer, allow nitrifiers to compete with phytoplankton for the assimilation of ammonium. The high contributions of nitrification to nitrate uptake are in agreement with both low export efficiency (i.e., the percentage of primary production that is exported) and low seasonal nitrate drawdown despite high nitrate assimilation.

High turnover rates indicated by changes in the fixed N forms and their stable isotopes in Antarctic landfast sea ice

We report concentration and nitrogen and oxygen isotopic measurements of nitrate, total dissolved nitrogen, and particulate nitrogen from Antarctic landfast sea ice, covering almost the complete seasonal cycle of sea ice growth and decay (from April to November). When sea ice forms in autumn, ice algae growth depletes nitrate and accumulates organic N within the ice. Subsequent low biological activity in winter imposes minor variations in the partitioning of fixed N. In early spring, the coupling between nitrate assimilation and brine convection at the sea ice bottom traps a large amount of fixed N within sea ice, up to 20 times higher than in the underlying seawater. At this time, remineralization and nitrification also accelerate, yielding nitrate concentrations up to 5 times higher than in seawater. Nitrate δ15N and δ18O are both elevated, indicating a near-balance between nitrification and nitrate assimilation. These findings require high microbially mediated turnover rates for the large fixed N pools, including nitrate. When sea ice warms in the spring, ice algae grow through the full thickness of the ice. The warming stratifies the brine network, which limits the exchange with seawater, causing the once-elevated nitrate pool to be nearly completely depleted. The nitrate isotope data point to light limitation at the base of landfast ice as a central characteristic of the environment, affecting its N cycling (e.g., allowing for nitrification) and impacting algal physiology (e.g., as reflected in the N and O isotope effects of nitrate assimilation).

Biogenic silica recycling in sea ice inferred from Si-isotopes: constraints from Arctic winter first-year sea ice

We report silicon isotopic composition (δ30Si vs. NBS28) in Arctic sea ice, based on sampling of silicic acid from both brine and seawater in a small Greenlandic bay in March 2010. Our measurements show that just before the productive period, δ30Si of sea-ice brine similar to δ30Si of the underlying seawater. Hence, there is no Si isotopic fractionation during sea-ice growth by physical processes such as brine convection. This finding brings credit and support to the conclusions of previous work on the impact of biogenic processes on sea ice δ30Si: any δ30Si change results from a combination of biogenic silica production and dissolution. We use this insight to interpret data from an earlier study of sea-ice δ30Si in Antarctic pack ice that show a large accumulation of biogenic silica. Based on these data, we estimate a significant contribution of biogenic silica dissolution (D) to production (P), with a D:P ratio between 0.4 and 0.9. This finding has significant implications for the understanding and parameterization of the sea ice Si-biogeochemical cycle, i.e. previous studies assumed little or no biogenic silica dissolution in sea ice.

Nitrogen fixation in the eastern Atlantic reaches similar levels in the Southern and Northern Hemisphere

Euphotic layer dinitrogen (N-2) fixation and primary production (PP) were measured in the eastern Atlantic Ocean (38 degrees N-21 degrees S) using N-15(2) and C-13 bicarbonate tracer incubations. This region is influenced by Saharan dust deposition and waters with low nitrogen to phosphorus (N/P) ratios originating from the Subantarctic and the Benguela upwelling system. Depth-integrated rates of N-2 fixation in the north (0 degrees N-38 degrees N) ranged from 59 to 370 mu mol N m(-2) d(-1), with the maximal value at 19 degrees N under the influence of the northwest African upwelling. Diazotrophic activity in the south (0 degrees S-21 degrees S), though slightly lower, was surprisingly close to observations in the north, with values ranging from 47 to 119 mu mol N m(-2) d(-1). Our North Atlantic N-2 fixation rates correlate well with dust deposition, while those in the South Atlantic correlate strongly with excess phosphate relative to nitrate. There, the necessary iron is assumed to be supplied from the Benguela upwelling system. When converting N-2 fixation to carbon uptake using a Redfield ratio (6.6), we find that N-2 fixation may support up to 9% of PP in the subtropical North Atlantic (20 degrees N-38 degrees N), 5% in the tropical North Atlantic (0 degrees N-20 degrees N), and 1% of PP in the South Atlantic (0 degrees S-21 degrees S). Combining our data with published data sets, we estimate an annual N input of 27.610 Tg N yr(-1) over the open Atlantic Ocean, 11% of which enters the region between 20 degrees N and 50 degrees N, 71% between 20 degrees N and 10 degrees S, and 18% between 10 degrees N and 45 degrees S.

Physical and biological controls on DMS,P dynamics in ice shelf-influenced fast ice during a winter-spring and a spring-summer transitions

We report the seasonal and vertical variations of dimethylsulfide (DMS) and its precursor dimethylsulfoniopropionate (DMSP) in fast ice at Cape Evans, McMurdo Sound (Antarctica) during the spring-summer transition in 2011 and winter-spring transition in 2012. We compare the variations of DMS,P observed to the seasonal evolution of the ice algal biomass and of the physical properties of the ice cover, with emphasis on the ice texture and brine dynamics. Isolated DMS and DMSP maxima were found during both seasonal episodes in interior ice and corresponded to the occurrence of platelet crystals in the ice texture. We show that platelet crystals formation corresponded in time and depth to the incorporation of dinoflagellates (strong DMSP producers) in the ice cover. We also show that platelet crystals could modify the environmental stresses on algal cells and perturb the vertical redistribution of DMS,P concentrations. We show that during the winter-spring transition in 2012, the DMS,P profiles were strongly influenced by the development and decline of a diatom-dominated bloom in the bottom ice, with DMSP variations remarkably following chl a variations. During the spring-summer transition in 2011, the increase in brine volume fraction (influencing ice permeability) on warming was shown to trigger (1) an important release of DMS to the under-ice water through brine convection and (2) a vertical redistribution of DMSP across the ice.

Isotopic model of oceanic silicon cycling: The Kerguelen Plateau case study

A box model is presented describing the time evolution for the three stable Si isotopes (or total concentration and natural isotopic compositions), both in the dissolved and biogenic pools. Temporal variations are controlled by uptake, dissolution (both with isotopic fractionation), settling/export and mixing/advection (without isotopic fractionation). The basic building blocks of the model are combined to form a setup for the Kerguelen Plateau where distinct ‘‘plateau’’ and ‘‘out-plateau’’ areas exist and where measurements were made at the end of the growth season (early 2005, KEOPS cruise: Kerguelen Ocean and Plateau compared Study). In addition, we distinguished between surface (0–100 m) and subsurface (100–400 m) water. This resulted in a model composed of eight compartments, each containing three variables (the three Si isotopes) whose time evolution can be modelled. The model does not assume steady state, and can therefore be used to simulate transient events like blooms. We applied the model to simulate the 2004–2005 growth season. The model parameterisations were kept as simple as possible. Still, the KEOPS measurements were satisfactorily reproduced and estimates of instantaneous and seasonally integrated fluxes compared well with previous literature. & 2012 Elsevier Ltd. All rights reserved.

Using a new fluorescent probe of silicification to measure species-specific activities of diatoms under varying environmental conditions

A new method is presented that enables distinguishing between active and non-active cells with regard to biogenic silica deposition during frustule formation in natural communities of siliceous phytoplankton. The PDMPO method is based on the fluorescence of biogenic silica after incubation with the probe. Only those cells that have been depositing silica (by adjunction of intercalary plates during the cell cycle or by depositing a new frustule valve upon cell division) exhibit a typical fluorescence that is proportional to the amount of biogenic silica deposited. This new method has several advantages; it is easy to use at sea, very sensitive, and samples can be conserved for several months without major loss of fluorescence. This method offers new possibilities of investigation of ecophysiological controls within the natural diatom community and will also bring more information to the new generation of sophisticated multi-element multi-species biogeochemical models.