Optical proxy for particulate organic nitrogen from BGC-Argo floats.

Using biogeochemical-Argo float measurements, we propose, for the first time, an optical proxy for particulate organic nitrogen concentration (PON) in the Western Tropical South Pacific, an area influenced by dinitrogen (N2) fixation. Our results show a significant relationship between the backscattering coefficient at 700 nm (bbp) and PON, especially when the latter is measured using the wet oxidation method (R2=0.87). bbp may be used to estimate PON concentrations (PONopt) between 0.02 and 0.95 µM, allowing for unprecedented monitoring using autonomous profiling floats. The bbpvs PON relationship can be used to study phytoplanktonic biomass dynamics at relevant seasonal temporal scales, with clear evidence of PONopt as a proxy of phytoplanktonic biomass, at least for this specific area. Temporal analyses of PONopt show significant increases (from 0.16 to 0.80 µM) likely related to new production associated to N2 fixation events measured during stratification periods in the Melanesian Archipelago.

Biogeochemical controls of surface ocean phosphate.

Surface ocean phosphate is commonly below the standard analytical detection limits, leading to an incomplete picture of the global variation and biogeochemical role of phosphate. A global compilation of phosphate measured using high-sensitivity methods revealed several previously unrecognized low-phosphate areas and clear regional differences. Both observational climatologies and Earth system models (ESMs) systematically overestimated surface phosphate. Furthermore, ESMs misrepresented the relationships between phosphate, phytoplankton biomass, and primary productivity. Atmospheric iron input and nitrogen fixation are known important controls on surface phosphate, but model simulations showed that differences in the iron-to-macronutrient ratio in the vertical nutrient supply and surface lateral transport are additional drivers of phosphate concentrations. Our study demonstrates the importance of accurately quantifying nutrients for understanding the regulation of ocean ecosystems and biogeochemistry now and under future climate conditions.

Iron from a submarine source impacts the productive layer of the Western Tropical South Pacific (WTSP).

In the Western Tropical South Pacific, patches of high chlorophyll concentrations linked to the occurrence of N2-fixing organisms are found in the vicinity of volcanic islands. The survival of these organisms relies on a high bioavailable iron supply whose origin and fluxes remain unknown. Here, we measured high dissolved iron (DFe) concentrations (up to 66 nM) in the euphotic layer, extending zonally over 10 degrees longitude (174 E-175 W) at ∼20°S latitude. DFe atmospheric fluxes were at the lower end of reported values of the remote ocean and could not explain the high DFe concentrations measured in the water column in the vicinity of Tonga. We argue that the high DFe concentrations may be sustained by a submarine source, also characterized by freshwater input and recorded as salinity anomalies by Argo float in situ measurements and atlas data. The observed negative salinity anomalies are reproduced by simulations from a general ocean circulation model. Submarine iron sources reaching the euphotic layer may impact nitrogen fixation across the whole region.

Aphotic N2 fixation in the Eastern Tropical South Pacific Ocean.

We examined rates of N2 fixation from the surface to 2000 m depth in the Eastern Tropical South Pacific (ETSP) during El Niño (2010) and La Niña (2011). Replicated vertical profiles performed under oxygen-free conditions show that N2 fixation takes place both in euphotic and aphotic waters, with rates reaching 155 to 509 µmol N m(-2) d(-1) in 2010 and 24±14 to 118±87 µmol N m(-2) d(-1) in 2011. In the aphotic layers, volumetric N2 fixation rates were relatively low (<1.00 nmol N L(-1) d(-1)), but when integrated over the whole aphotic layer, they accounted for 87-90% of total rates (euphotic+aphotic) for the two cruises. Phylogenetic studies performed in microcosms experiments confirm the presence of diazotrophs in the deep waters of the Oxygen Minimum Zone (OMZ), which were comprised of non-cyanobacterial diazotrophs affiliated with nifH clusters 1K (predominantly comprised of α-proteobacteria), 1G (predominantly comprised of γ-proteobacteria), and 3 (sulfate reducing genera of the δ-proteobacteria and Clostridium spp., Vibrio spp.). Organic and inorganic nutrient addition bioassays revealed that amino acids significantly stimulated N2 fixation in the core of the OMZ at all stations tested and as did simple carbohydrates at stations located nearest the coast of Peru/Chile. The episodic supply of these substrates from upper layers are hypothesized to explain the observed variability of N2 fixation in the ETSP.

Coherence of particulate beam attenuation and backscattering coefficients in diverse open ocean environments.

We present an extensive data set of particle attenuation (c(p)), backscattering (b(bp)), and chlorophyll concentration (Chl) from a diverse set of open ocean environments. A consistent observation in the data set is the strong coherence between c(p) and b(bp) and the resulting constancy of the backscattering ratio (0.010 +/- 0.002). The strong covariability between c(p) and b(bp) must be rooted in one or both of two explanations, 1) the size distribution of particles in the ocean is remarkably conserved and particle types responsible for c(p) and b(bp) covary, 2) the same particle types exert influence on both quantities. Therefore, existing relationships between c(p) or Chl:c(p) and phytoplankton biomass and physiological indices can be conceptually extended to the use of b(bp). This finding lends support to use of satellite-derived Chl and b(bp) for investigation of phytoplankton biomass and physiology and broadens the applications of existing ocean color retrievals.

Phytoplankton in the ocean use non-phosphorus lipids in response to phosphorus scarcity.

Phosphorus is an obligate requirement for the growth of all organisms; major biochemical reservoirs of phosphorus in marine plankton include nucleic acids and phospholipids. However, eukaryotic phytoplankton and cyanobacteria (that is, 'phytoplankton' collectively) have the ability to decrease their cellular phosphorus content when phosphorus in their environment is scarce. The biochemical mechanisms that allow phytoplankton to limit their phosphorus demand and still maintain growth are largely unknown. Here we show that phytoplankton, in regions of oligotrophic ocean where phosphate is scarce, reduce their cellular phosphorus requirements by substituting non-phosphorus membrane lipids for phospholipids. In the Sargasso Sea, where phosphate concentrations were less than 10 nmol l-1, we found that only 1.3 +/- 0.6% of phosphate uptake was used for phospholipid synthesis; in contrast, in the South Pacific subtropical gyre, where phosphate was greater than 100 nmol l-1, plankton used 17 6% (ref. 6). Examination of the planktonic membrane lipids at these two locations showed that classes of sulphur- and nitrogen-containing membrane lipids, which are devoid of phosphorus, were more abundant in the Sargasso Sea than in the South Pacific. Furthermore, these non-phosphorus, 'substitute lipids' were dominant in phosphorus-limited cultures of all of the phytoplankton species we examined. In contrast, the marine heterotrophic bacteria we examined contained no substitute lipids and only phospholipids. Thus heterotrophic bacteria, which compete with phytoplankton for nutrients in oligotrophic regions like the Sargasso Sea, appear to have a biochemical phosphorus requirement that phytoplankton avoid by using substitute lipids. Our results suggest that phospholipid substitutions are fundamental biochemical mechanisms that allow phytoplankton to maintain growth in the face of phosphorus limitation.

A new method for nanomolar determination of silicic acid in seawater.

A novel method is proposed to determine concentrations of silicic acid in seawater in the nanomolar range of 3-500 nM. It preconcentrates silicic acid through a "Magnesium Induced Co-precipitation" (MAGIC) step before a classical spectrophotometric measurement. The detection limit (3+/-2 nM) is improved by a factor 10 in comparison to the conventional colorimetric methods. The best precision obtained to date is +/-2 nM for a natural sample of 69 nM Si. No interference of phosphate was observed by contrast to previous methods. This simple method offers a simple, sensitive and accurate tool for silicic acid determination in depleted seawater, where its availability remains unknown.