Journal cover Journal topic
Biogeosciences An interactive open-access journal of the European Geosciences Union
Journal topic
Biogeosciences, 15, 3795–3810, 2018
https://doi.org/10.5194/bg-15-3795-2018
Biogeosciences, 15, 3795–3810, 2018
https://doi.org/10.5194/bg-15-3795-2018

Research article 21 Jun 2018

Research article | 21 Jun 2018

# Transfer of diazotroph-derived nitrogen to the planktonic food web across gradients of N2 fixation activity and diversity in the western tropical South Pacific Ocean

Transfer of diazotroph-derived nitrogen to the planktonic food web across gradients of N2 fixation activity and diversity in the western tropical South Pacific Ocean
Mathieu Caffin1, Hugo Berthelot1,2, Véronique Cornet-Barthaux1, Aude Barani1, and Sophie Bonnet1,3 Mathieu Caffin et al.
• 1Aix Marseille Univ., Université de Toulon, CNRS, IRD, MIO UM110, 13288, Marseille, France
• 2Laboratoire des sciences de l'environnement marin, IUEM, Université de Brest-UMR6539 CNRS/UBO/IRD/Ifremer, Plouzané, France
• 3Aix Marseille Univ., Université de Toulon, CNRS, IRD, MIO UM110, 98800, Nouméa, New Caledonia

Correspondence: Mathieu Caffin (mathieu.caffin@mio.osupytheas.fr)

Abstract

Biological dinitrogen (N2) fixation provides the major source of new nitrogen (N) to the open ocean, contributing more than atmospheric deposition and riverine inputs to the N supply. Yet the fate of the diazotroph-derived N (DDN) in the planktonic food web is poorly understood. The main goals of this study were (i) to quantify how much of DDN is released to the dissolved pool during N2 fixation and how much is transferred to bacteria, phytoplankton and zooplankton, and (ii) to compare the DDN release and transfer efficiencies under contrasting N2 fixation activity and diversity in the oligotrophic waters of the western tropical South Pacific (WTSP) Ocean. We used nanometre-scale secondary ion mass spectrometry (nanoSIMS) coupled with 15N2 isotopic labelling and flow cytometry cell sorting to track the DDN transfer to plankton, in regions where the diazotroph community was dominated by either Trichodesmium or by UCYN-B. After 48 h,  20–40 % of the N2 fixed during the experiment was released to the dissolved pool when Trichodesmium dominated, while the DDN release was not quantifiable when UCYN-B dominated;  7–15 % of the total fixed N (net N2 fixation + release) was transferred to non-diazotrophic plankton within 48 h, with higher transfer efficiencies (15 ± 3 %) when UCYN-B dominated as compared to when Trichodesmium dominated (9 ± 3 %). The pico-cyanobacteria Synechococcus and Prochlorococcus were the primary beneficiaries of the DDN transferred ( 65–70 %), followed by heterotrophic bacteria ( 23–34 %). The DDN transfer in bacteria was higher (34 ± 7 %) in the UCYN-B-dominating experiment compared to the Trichodesmium-dominating experiments (24 ± 5 %). Regarding higher trophic levels, the DDN transfer to the dominant zooplankton species was less efficient when the diazotroph community was dominated by Trichodesmium ( 5–9 % of the DDN transfer) than when it was dominated by UCYN-B ( 28 ± 13 % of the DDN transfer). To our knowledge, this study provides the first quantification of DDN release and transfer to phytoplankton, bacteria and zooplankton communities in open ocean waters. It reveals that despite UCYN-B fix N2 at lower rates compared to Trichodesmium in the WTSP, the DDN from UCYN-B is much more available and efficiently transferred to the planktonic food web than the DDN originating from Trichodesmium.

1 Introduction

Nitrogen (N) is one of the basic building blocks of life, though much of the global ocean surface ( 70 %) is oligotrophic and characterized by low N availability, which limits primary productivity and phytoplankton growth . In these N-depleted areas of the tropical and subtropical ocean, biological dinitrogen (N2) fixation (the reduction of atmospheric N2 into bioavailable ammonia) sustains the major part of new production and organic matter export . At the global scale, N2 fixation is the major source of new N to the ocean, before atmospheric deposition and riverine inputs (100–150 Tg N yr−1: ). N2 fixation is performed by prokaryotic organisms termed diazotrophs, which include the non-heterocystous filamentous cyanobacterium Trichodesmium , heterocystous cyanobacteria living in symbiosis with diatoms (or diatom–diazotroph associations, termed DDAs; ), unicellular cyanobacteria termed UCYN (subdivided into groups A, B and C based on the nifH gene sequence, , diverse non-cyanobacterial bacteria , and archaea . Although considerable efforts have been made over the past decades to quantify N2 fixation, identify the major players, and assess their biogeographical distribution in relation to environmental drivers, the fate of new N provided by N2 fixation in the ocean and its role in the planktonic food web structure and large-scale biogeochemical fluxes are still poorly understood.

Early studies have reported high dissolved organic N (DON) and ammonia (NH${}_{\mathrm{4}}^{+}$) concentrations during and following Trichodesmium blooms in the Indian Ocean , suggesting that Trichodesmium release part of the recently fixed N2 (hereafter referred to as diazotroph-derived N, DDN) to the dissolved pool, which could subsequently be consumed by the surrounding plankton communities. The first direct release measurements were performed in the early 1990s and showed that Trichodesmium colonies isolated from the tropical Atlantic Ocean release  50 % of the recently fixed N2 . Accumulations of DON and NH${}_{\mathrm{4}}^{+}$ have subsequently been confirmed near Trichodesmium blooms in the Pacific and Atlantic oceans, although not systematically , and in senescent Trichodesmium cultures , possibly related to the Trichodesmium programmed cell death (PCD, ). This DDN release has been attributed (i) to endogenous processes such as the dissipation of excess electrons linked to an excess of light or to a means for the filamentous diazotrophs to transfer fixed N from N2-fixing cells to vegetative cells and (ii) to exogenous processes such as viral lysis or “sloppy feeding” by copepods (O'Neil1999).

Numerous studies performed in culture and in the field focused on quantifying this release, and most of them were performed on Trichodesmium and were based on the difference between the measurement of gross N2 fixation (through the acetylene reduction method, ) and net N2 fixation rates (through the 15N2 isotope labelling method, ) . It was thus shown that the DDN released to the dissolved pool averages  50 % (10 to 80 %) of the total N2 fixation. The estimates based on this approach were then questioned since the discovery of the methodological underestimation of net 15N2 rates when the 15N2 tracer is injected as a bubble in the incubation bottles , leading to a potential overestimation of the DDN release. An alternative approach based on the direct measurement of the 15N enrichment of both the particulate and dissolved pools after incubation with 15N2 presents the advantage of providing a ratio of particulate N2 fixation vs. DDN release, without being affected by potential underestimation issues. The studies based on this approach reveal that the proportion of DDN released to the dissolved pool ranges from 10 to > 80 % of total N2 fixation measured in the field . The release appears to be higher when Trichodesmium dominates the diazotroph community than when UCYN dominate . The DDN release is generally much lower (< 5 %) in monospecific cultures than in field experiments, suggesting that external factors such as sloppy feeding and viral lysis have a strong influence on the DDN release by diazotrophs in the field.

The DDN released in the surface ocean is potentially available for surrounding planktonic communities, but its fate in the planktonic food web has been poorly quantified, mainly due to methodological locks. , who reported high DON and NH${}_{\mathrm{4}}^{+}$ concentrations near Trichodesmium blooms, were also the first to observe that during the decline of the Trichodesmium blooms, diatom abundances increased, followed by a succession of cladocerans, dinoflagellates, green algae and finally copepods. In the tropical Atlantic Ocean, high abundances of non-diazotrophic phytoplankton have also been observed following Trichodesmium blooms , and more recently, showed a positive correlation between abundances of Trichodesmium and diatoms in the Kuroshio. These studies suggest a link between diazotroph blooms and non-diazotrophic organisms. Studies based on size fractionation carried out during a Trichodesmium bloom incubated in the presence of 15N2 report that  10 % of the fixed N2 by Trichodesmium (recovered in the size fraction > 30 µm) was rapidly transferred to non-diazotrophic organisms (recovered in the < 30 µm fraction; ). Using similar methods, other studies suggested that during Trichodesmium blooms and Nodularia and Aphanizomenon blooms , 5 to 10 % of the DDN is transferred to the picoplankton compartment. However, the methods based on size fractionation do not discriminate the DDN transfer towards the non-diazotroph picoplankton to the potentially active N2 fixation within picoplankton, in particular the UCYN-A, one of the most abundant diazotrophs in our ocean . This method therefore potentially overestimates the DDN transfer and is not applicable to study the DDN transfer associated with UCYN. Moreover, it is not possible with size fractionation methods to determine which populations (e.g. autotrophic vs. heterotrophic plankton, small vs. large plankton) have benefited the most from this source of new N. The recent use of high-resolution nanometre-scale secondary ion mass spectrometry (nanoSIMS) coupled with 15N2 isotopic labelling and flow cytometry cell sorting has proven its efficiency in the quantification of the DDN transfer to specific groups of phytoplankton and bacteria. Applying this method during Trichodesmium blooms in the coastal western tropical South Pacific (WTSP), revealed that after 48 h 13 ± 2 to 48 ± 5 % of the fixed N2 was released to the dissolved pool and 6 ± 1 to 8 ± 2 % of this DDN was transferred to non-diazotrophic plankton, mainly diatoms (45 ± 4 to 61 ± 38 %) and bacteria (22 ± 27 to 38 ± 12 %). A mesocosm experiment performed in the New Caledonian lagoon during a UCYN-C bloom revealed that after 48 h 16 ± 6 % of the fixed N2 was released to the dissolved pool and 21 ± 4 % of this DDN was transferred to non-diazotrophic plankton, mainly picoplankton (18 ± 4 %) and diatoms (3 ± 2 %). Finally, a comparative study between Trichodesmium vs. UCYN blooms simulated thanks to culture isolates revealed that the DDN transfer to non-diazotrophic plankton is twice as high with Trichodesmium as with UCYN. The differences of DDN release and transfer rates observed between the different field experiments and the different diazotrophs suggest that these processes strongly depend on the physiological state of diazotrophs and the environment. However, the transfer of DDN to different groups of plankton from different diazotrophs (Trichodesmium vs. UCYN) in the open ocean, where most global marine N2 fixation takes place, has never been investigated.

Regarding higher trophic levels, the low 15N isotopic signature (δ15N) of zooplankton reveals that N2 fixation can significantly contribute to zooplankton N requirements in high N2 fixation areas . Few studies report active grazing of Trichodesmium by some specific copepods (Micro- and Macro-setella sp., ). However, Trichodesmium has been shown to be toxic for most of the grazers , and the low δ15N signature found in zooplankton (indicative of DDN consumption) where Trichodesmium thrive most likely originates from indirect transfer mediated by recycling processes rather than from direct grazing. A recent study based on 15N2 labelling in the coastal WTSP reveals that the DDN is less efficiently transferred to zooplankton when Trichodesmium and DDA dominate the diazotroph community than when UCYN-C dominate, suggesting that the DDN transfer efficiency to zooplankton strongly depends on the diazotroph involved in the N2 fixation. To our knowledge, this has never been investigated so far in the open ocean.

The WTSP Ocean has recently been identified as a hotspot of N2 fixation and is characterized by trophic and N2 fixation gradients , with oligotrophic waters characterized by high N2 fixation rates (631 ± 286 µmol N m−2 d−1) mainly associated with Trichodesmium in the western part, and ultra-oligotrophic waters characterized by low N2 fixation rates (85 ± 79 µmol N m−2 d−1) mainly associated with UCYN in the eastern part . We performed a series of experiments under contrasting situations (when either Trichodesmium or UCYN was dominating the diazotroph community) to study the fate of DDN in the planktonic food web, with the following specific goals: (1) quantify the proportion of DDN released to the dissolved pool relative to total N2 fixation, (2) quantify the DDN transfer to the non-diazotrophic phytoplankton and bacteria, and (3) quantify the DDN transfer to zooplankton.

2 Material and methods

## 2.1 Experimental set-up for DDN transfer experiments in phytoplankton and heterotrophic bacteria

This study was carried out during the OUTPACE (Oligotrophic to UlTra oligotrophic PACific Experiment) cruise (https://doi.org/10.17600/15000900), which took place in February–March 2015 (austral summer) onboard R/V L'Atalante. Samples were collected along a  4000 km west-to-east zonal transect along  19 S starting in New Caledonia and ending in French Polynesia, crossing Melanesian archipelago waters (hereafter referred to as MA waters) around New Caledonia, Vanuatu, and Fiji up to Tonga and South Pacific Gyre waters located at the western boundary of the South Pacific Gyre (hereafter referred to as GY waters) (see , for details). Three experiments are reported here (hereafter named E1, E2 and E3). Two were performed at stations located in MA waters: station LD A, 1912.8 S–16441.3 E, and station LD B, 1814.4 S–17051.5 W, where Trichodesmium accounted for 95 and 100 % of the total diazotroph community quantified by quantitative PCR . The third experiment was performed in GY waters: station LD C, 1825.2 S–16556.4 W, where UCYN accounted for 82 % of the total diazotroph community .

The experiments were designed according to and . For experiments E1 and E2, seawater was collected by the surface underway pumping system at 6 m in depth. For E3, seawater was collected at 55 m in depth using Niskin bottles mounted on a CTD rosette. For all experiments, seawater was collected into eight HCl-washed-sample rinsed (three times) 4.5 L polycarbonate bottles equipped with septum caps; 5 mL of 15N2 gas (98.9 at. % 15N2, Cambridge isotopes) were injected into all bottles using a gas-tight syringe. The purity of the 15N2 Cambridge isotope stocks was previously checked by and more recently by and , who concluded that the purity is satisfying (2 × 10−8 mol : mol N of 15N2) and therefore does not alter the results presented below. The bottles were shaken 30 times to facilitate the 15N2 dissolution and, except for the T0 set of bottles (see below), were incubated for 48 h in on-deck incubators covered with blue screening (50 % surface irradiance for E1 and E2 and 15 % surface irradiance for E3) and cooled with circulating surface seawater. At T0 and after incubation, a set of four bottles was collected and subsampled for the following measurements (see below for methods): N2 fixation rates, DDN release, quantification of diazotrophs, heterotrophic bacteria and pico-, nano- and micro-phytoplankton enumeration, organic and inorganic nutrient concentrations, and 15N enrichment on diazotrophic and non-diazotrophic plankton. Unless otherwise stated, each parameter reported below was measured in triplicate.

## 2.2 Net N2 fixation rates and DDN released to the dissolved pool

N2 fixation rates were measured using the 15N2 isotopic tracer technique (adapted from ), as described in .

The DDN released to the dissolved pool in the form of NH${}_{\mathrm{4}}^{+}$ and DON during the N2 fixation process was quantified using the three-step diffusion method extensively described in and derived from . As the NO${}_{\mathrm{3}}^{-}$ pool was negligible, the total dissolved N (TDN) pool was defined as the sum of DON and NH${}_{\mathrm{4}}^{+}$ pools (TDN = DON + NH${}_{\mathrm{4}}^{+}$). After incubation with the 15N2 tracer, 300 mL of the filtrate passed through pre-combusted Whatman GF/F filters was collected in 500 mL Duran Schott borosilicate flasks, poisoned with HgCl2 (300 µL, final concentration 20 mg L−1) and stored at 4 C in the dark until analysis. At the end of each step, NH${}_{\mathrm{4}}^{+}$ and DON fraction were recovered on acidified pre-combusted Whatman GF/F filters, dried 24 h at 60 C and stored in pre-combusted glass tubes until analysis on an elemental analyser coupled to an isotope ratio mass spectrometer (EA-IRMS, Integra2 Sercon Ltd) as described in .

## 2.3 Inorganic and organic nutrient analyses

NH${}_{\mathrm{4}}^{+}$ concentrations were measured fluorimetrically according to on a FP-2020 fluorimeter (Jasco, detection limit = 3 nM). NO${}_{\mathrm{3}}^{-}$ and nitrite (NO${}_{\mathrm{2}}^{-}$) concentrations were measured using standard colorimetric procedures on a AA3 AutoAnalyzer (Seal Analytical). DON concentrations were measured by the wet oxidation method according to .

## 2.4 Plankton abundance determination

The abundance of Trichodesmium and UCYN-B was determined microscopically: 2.2 L of each triplicate 15N2-amended 4.5 L bottle was gently filtered onto 2 µm pore size, 25 mm diameter Millipore polycarbonate filters and fixed with paraformaldehyde (2 % final concentration) for 1 h. Trichodesmium were enumerated on the entire surface of the filter at a ×100 magnification with a Zeiss Axio Observer epifluorescence microscope fitted with a green (510–560 nm) excitation filter. The number of cells per trichome was counted on 20 trichomes for each experiment; we counted an average of 85 and 115 cells trichome−1 for E1 and E2, respectively. UCYN-B were counted on 40 fields (1.3 mm2 fields; 0-2800 UCYN-B per field) scanned and analysed with the ImageJ1 software.

Samples for micro-phytoplankton identification and enumeration were collected in each of the triplicate 4.5 L incubated bottles (except for E1, where only one replicate was available) in five 50 mL sterile polypropylene tubes and preserved in an acidic Lugol solution (0.5 % final concentration). Diatoms were enumerated from a 250 mL subsample following the Utermöhl method (Hasle1978), using a Nikon TE2000 inverted microscope equipped with phase contrast and a long-distance condenser. Diatoms were identified to the lowest possible taxonomic level in one of the three replicates.

Pico-phytoplankton, nano-phytoplankton and heterotrophic bacteria abundances were determined by flow cytometry. After incubation, 1.8 mL was subsampled from triplicate 4.5 L bottles into cryotubes, fixed with paraformaldehyde (200 µL, 4 % final concentration) for 5 min at room temperature, flash-frozen in liquid N2, and stored at 80 C until analysis on a FACSCalibur (BD Biosciences, San Jose, CA) according to , at the PRECYM flow cytometry platform (https://precym.mio.univ-amu.fr/, last access: 31 December 2017). Phytoplankton communities were clustered as Prochlorococcus spp. cell like, Synechococcus spp. cell like, nano-eukaryotes cell like, pico-eukaryotes cell like, and UCYN-B cell like. Trucount TM (BD Biosciences) beads were used to determine the volume analysed.

## 2.5 Cell sorting and sampling for nanoSIMS analyses

For flow cytometry cell sorting and subsequent analysis using nanoSIMS, 1 L of one of the 4.5 L bottles was filtered onto 0.2 µm pore size 47 mm polycarbonate filters to preconcentrate the cells and facilitate cell sorting. Filters were placed in a 5 mL cryotube filled with 0.2 µm filtered seawater and PFA (2 % final concentration), and incubated for 1 h at room temperature in the dark. The cryovials were vortexed for  20 s to detach the cells from the filter and were stored at 80 C until analysis. Cell sorting was performed using a BD InfluxTM Mariner (BD Biosciences) high-speed cell sorter at the PRECYM platform, as described in Bonnet et al. (2016a, Supplement). Planktonic groups (pico-phytoplankton, nano-phytoplankton, bacteria and UCYN-B (for E3 only)) were separated using the same clusters as for the phytoplankton abundance determination. At the issue of the cell sorter, the cells were directly dropped onto a 0.2 µm pore size, 13 mm diameter polycarbonate filter (Millipore) connected to a low-pressure pump in order to concentrate them on a surface as tightly as possible. The filters were stored at 80 C until nanoSIMS analyses.

To recover large phytoplanktonic cells (Trichodesmium and diatoms), 1 L of the same 4.5 L bottle was filtered on 10 µm pore size 25 mm polycarbonate filters. The cells were fixed with PFA (2 % final concentration), incubated 1 h at ambient temperature and stored at 20 C until nanoSIMS analyses.

## 2.6 NanoSIMS analyses

Just before nanoSIMS analyses, filters were thawed at ambient temperature and sputtered with gold and palladium to ensure conductivity. Analyses were performed on a NanoSIMS N50 (Cameca, Gennevilliers, France) at the French National Ion MicroProbe Facility as previously described in and . Briefly, high-density cell areas were retrieved using the nanoSIMS optical camera (Fig. 1f). Samples were pre-sputtered prior to analyses for at least 2 min to remove surface contaminants and increase conductivity with a  22 pA caesium primary beam. For the analysis, a  1.2 pA caesium (16 KeV) primary beam focused onto a  100 nm spot diameter was scanned across a 256 × 256 or 512 × 512 pixel raster (depending on the image size, which ranged from 20 µm × 20 µm to 40 µm × 40 µm) with a counting time of 1 ms per pixel. Negative secondary ions (12C, 13C, 12C14N, 12C15N and 28Si) were collected by electron multiplier detectors, and secondary electrons were imaged simultaneously. A total of 20 serial quantitative secondary ion images were generated to create the final image. Individual cells were easily identified in nanoSIMS secondary electron, 12C, 12C14N and 28Si images that were used to define regions of interest (ROIs) around individual cells. A total of  1500 ROIs were analysed. For each ROI, the 15N enrichment was calculated;  80 cells on average were analysed for each plankton group and for each experiment (see Table S1 in the Supplement).

Figure 1NanoSIMS images showing the 15N enrichment (a, b, d, e) after 48 h of incubation in the presence of 15N2 for Trichodesmium (a), UCYN-B (b), nano-eukaryotes (d) and Synechococcus (e). The ROIs are represented with white lines. NanoSIMS images showing the secondary electron channel of UCYN (c) and optical camera image of Prochlorococcus spotted on the filter before NanoSIMS analyses (f).

## 2.7 Cell-specific N content and DDN transfer calculations

To determine cell-specific N contents, cell sizes of Trichodesmium and dominant diatoms were directly measured on each sample collected for microscopy (see Sect. 2.4). For Trichodesmium, cell length and width were measured on 25 to 50 cells per sample at ×400 magnification with a Zeiss Axio Observer epifluorescence microscope. For diatoms, the cell cross section and apical and transapical dimensions were measured on at least 20 cells using a Nikon TE2000 inverted microscope equipped with phase contrast and a long-distance condenser. For UCYN-B, cell diameters were directly measured on the nanoSIMS images and further confirmed on microscopic images. The biovolumes (BVs) of Trichodesmium, UCYN-B and diatoms were estimated following the geometric model of each cell type . The cellular carbon (C) contents were determined by using the relation between BV and C content according to for Trichodesmium and UCYN-B, and according to and for diatoms. The N content was calculated based on C : N ratios of 6 for Trichodesmium and 5 for UCYN-B , and a typical Redfield ratio of 6.6 for diatoms.

For Synechococcus and Prochlorococcus we used the C content reported in (255 and 36 fg C cell−1, respectively). For nano-eukaryotes we used the C content reported in , and converted it into N content according to the C : N Redfield ratio of 6.6 (leading to 3.2, 0.45 and 219 fmol N cell−1 for Synechococcus, Prochlorococcus and nano-eukaryotes). For bacteria, an average N content of 2.1 fg N cell−1 was used. For the pico-eukaryotes, the cellular N content of 9.2 ± 2.9 fmol N cell−1 was used as reported in .

The cell-specific N2 fixation rates and DDN transfer rates (in nmol N L−1 48 h−1) to non-diazotrophic phytoplankton were calculated for each plankton group analysed as follows:

${\mathrm{DD}}^{\mathrm{15}}\mathrm{N}=\frac{{}^{\mathrm{15}}{\mathrm{N}}_{\mathrm{ex}}}{{\mathrm{N}}_{\mathrm{sr}}}×{\mathrm{N}}_{\mathrm{con}}×A,$

where 15Nex (atom %) is the excess 15N enrichment of the individual cells measured by nanoSIMS after 48 h of incubation relative to the time zero value, Nsr (atom %) is the excess 15N enrichment of the source pool (N2) in the experimental bottles determined by MIMS, Ncon is the cellular N content (in nmol N cell−1) of each cell and A is the abundance of the specific plankton group (in cell L−1). Incertitude was estimated on each variable and the final incertitude was estimated using the propagation error rule.

## 2.8 Experimental set-up for DDN transfer experiments in zooplankton

The DDN transfer to zooplankton was measured in four experiments performed at the same stations where the E1, E2 and E3 experiments were performed (hereafter named Zoo-1, Zoo-3 and Zoo-4) plus an additional station (Zoo-2) located between LDA and LDB (SD9, 2057 S–17839 E). Trichodesmium dominated the diazotroph community in the Zoo-1, Zoo-2, and Zoo-3 experiments, and UCYN-B dominated the Zoo-4 experiment. The experiments consisted in incubations of freshly collected zooplankton in the presence of the natural planktonic assemblage pre-labelled with 15N2 as a food source. In parallel to the experiments described above, six additional HCl-washed-sample rinsed (three times) 1 L polycarbonate bottles equipped with septum caps were collected by the underway pumping system at 6 m in depth for Zoo-1, Zoo-2 and Zoo-3 and with Niskin bottles at 55 m in depth for Zoo-4. All bottles were amended with 1 mL of 15N2 (98.9 at. % 15N, Cambridge isotopes). The bottles were shaken 30 times to facilitate the 15N2 dissolution and incubated in on-deck incubators for 24–36 h as described above.

The incubation was stopped by filtering the bottles on 0.2 µm pore size 47 mm membrane filters in such a way that the 15N enrichment of the food source provided to zooplankton (hereafter referred to as 15N pre-labelled plankton) does not increase during the course of the experiment. For each experiment, the initial 15N enrichment of the 15N pre-labelled plankton was analysed in triplicate by EA-IRMS. Plankton was then re-suspended in six 1 L bottles filled with 0.2 µm filtered surface seawater collected at the same station. Meanwhile, zooplankton was collected using repeated net tows (120 mesh size) before dawn. Animals were recovered on a 120 µm sieve and placed into 4.5 L polycarbonate bottles filled with 0.2 µm filtered surface seawater in the dark for at least 6 h in order to allow them to empty their guts. Living animals were visually identified and the individuals belonging to the genus Clausocalanus, which largely dominated the zooplankton community at all stations , were handpicked and 12 animals were dispatched into each of the three 1 L bottles containing the 15N pre-labelled plankton before being incubated in on-deck incubators for 24 h as described above. The three other bottles were immediately filtered after the introduction of animals, firstly through a 120 µm mesh in order to recover the animals and secondly through precombusted (4 h, 450 C) GF/F filters, which were used to quantify the isotopic signature of the 15N pre-labelled plankton at the beginning of the experiment, together with the initial NH${}_{\mathrm{4}}^{+}$ concentrations in the incubation bottles. After 24 h, the triplicate bottles containing the mixture of 15N pre-labelled plankton and zooplankton were filtered in the same way. In addition, the filtrate was recovered as described in Sect. 2.2 in order the measure the NH${}_{\mathrm{4}}^{+}$ concentration and the 15N enrichment in the dissolved pool by using the two-step diffusion method. The recovered animals were placed on GF/F filters, which were analysed by EA-IRMS as described above in Sect. 2.2.

Table 1Environmental conditions at stations where experiments were performed. Station position, depth of sampling, concentrations of Chl a, NO${}_{\mathrm{3}}^{-}$, NH${}_{\mathrm{4}}^{+}$, DON, PO${}_{\mathrm{4}}^{-}$, DOP, dominant phytoplankton communities and dominant diazotrophs.

* Integrated in the upper photic layer.

3 Results

## 3.1 Description of the biogeochemical context at the studied stations

Regarding the chlorophyll a and nutrient concentrations, the four studied stations were divided into two main sub-regions (Table 1): (i) stations of E1/Zoo-1, Zoo-2 and E2/Zoo3 were located in the oligotrophic MA waters characterized by surface chlorophyll a concentrations of 0.159–0.377 µg L−1 and NO${}_{\mathrm{3}}^{-}$ and PO${}_{\mathrm{4}}^{-}$ concentrations below 50 nmol L−1, (ii) station E3/Zoo-4 located in the ultra-oligotrophic GY waters presenting lower chlorophyll a concentrations than in MA waters (0.053 µg L−1), NO${}_{\mathrm{3}}^{-}$ concentration below 50 nmol L−1, and PO${}_{\mathrm{4}}^{-}$ concentration  110 nmol L−1.

Trichodesmium dominated the diazotroph community (95–100 % of total nifH gene copies detected by qPCR, ) at 6 m in depth in the MA waters (E1/Zoo-1, Zoo-2 and E2/Zoo3), while UCYN-B dominated (82 % of nifH gene copies) at 55 m in depth in the GY waters (E3/Zoo-4 experiment). MA waters were characterized by a higher abundance of pico-phytoplankton (Synechococcus and Prochlorococcus) and bacteria abundances (125–200 and 271–424 × 1011 cells m−2, respectively) than GY waters ( 110 and  290 × 1011 cells m−2, respectively; ).

## 3.2 N2 fixation and DDN released to the dissolved pool

Net N2 fixation rates were 20.1 ± 13.4, 49.9 ± 2.4 and 3.2 ± 0.3 nmol N L−1 48 h−1 for the E1, E2 and E3 experiments, respectively (Fig. 2). The DDN released to the dissolved pool (the sum of DON and NH${}_{\mathrm{4}}^{+}$) was 14 ± 9 and 8 ± 2 nmol N L−1 48 h−1 in E1 and E2, and was below quantification limits in E3. Considering gross N2 fixation as the sum of net N2 fixation and DDN release rates , the DDN released to the dissolved pool accounted for 40 ± 27 and 14 ± 4 % of gross N2 fixation in E1 and E2, respectively (Fig. 4). DON accounted for the major part of the 15N released and accounted for  93 and  96 % of the total N release in E1 and E2, respectively.

Figure 2N2 fixation rates (black, nmol N L−1 48 h−1), DDN release nmol N L−1 (48 h−1) as NH${}_{\mathrm{4}}^{+}$ (light grey) and DON (white) for each experiment (E1, E2 and E3). Error bars represent the standard deviations of triplicate incubations.

## 3.3 Cell-specific 15N enrichment and DDN transfer to non-diazotrophic plankton

NanoSIMS analyses performed on individual trichomes (E1 and E2) and UCYN-B cells (E3) revealed significant (p< 0.05) 15N enrichment after 48 h of incubation (Fig. 1a, b) compared to T0 samples (0.371 ± 0.005 at. %, n=5), indicating active N2 fixation during the experiments: 1.946 ± 0.837 at. % (n=32) in E1, 1.523 ± 0.477 at. % (n=25) in E2 and 4.707 ± 0.210 at. % (n=192) in E3 (Fig. 3). Cell-specific N2 fixation rates of Trichodesmium were 252.7 ± 50.5 fmol N cell−1 48 h−1 in E1 and 341.5 ± 68.3 fmol N cell−1 48 h−1 in E2, and cell-specific rates of UCYN-B were 18.6 ± 3.8 fmol N cell-1 48 h−1 in E3.

NanoSIMS analyses performed on non-diazotrophic plankton (diatoms and cell-sorted Synechococcus (Fig. 1d), Prochlorococcus, bacteria, and pico- and nano-eukaryotes (Fig. 1e)) also revealed significant 15N enrichment as compared to T0 values (p< 0.05) (Fig. 3). The 15N enrichment of the non-diazotrophic plankton (all groups pooled together) was not statistically different (p> 0.05) between E1 and E2. However, it was significantly lower (p< 0.05) in E3 compared to E1 and E2.

Figure 3Left panels: boxplot of the 15N enrichment measured in diazotrophs (Trichodesmium for E1 and E2, and UCYN-B for E3). Right panels: 15N enrichment measured in non-diazotrophic plankton: Synechococcus, Prochlorococcus, bacteria, diatoms, pico-eukaryotes and nano-eukaryotes for each experiment. The black dotted line indicates the natural isotopic enrichment.

Over the 48 h of the experiment, 10 ± 2 % of the total DDN was transferred to non-diazotrophic plankton in E1, 7 ± 1 % in E2, and 15 ± 3 % in E3 (Fig. 4). DDN was mainly transferred to pico-cyanobacteria (Synechococcus and Prochlorococcus), accounting for 73 ± 15, 68 ± 14 and 65 ± 13 % of the total transfer into non-diazotrophs in E1, E2 and E3, respectively (Fig. 4). The transfer into heterotrophic bacteria accounted for 25 ± 5, 23 ± 5 and 34 ± 7 % of the total transfer, in E1, E2 and E3, respectively. Lastly, 50 ± 40, 79 ± 4 and 85 ± 9 % of the newly fixed 15N2 remained in the pool of diazotrophs, for E1, E2 and E3, respectively. This pool takes into account the major group of diazotrophs detected and analysed by nanoSIMS at each station (Trichodesmium or UCYN-B), other potential diazotrophs that have not been targeted by qPCR (such as non-cyanobacterial diazotrophs), and other groups of non-diazotrophic plankton to which 15N2 was transferred but that were not analysed by nanoSIMS (due to their very low abundance).

Figure 4DDN fate after 48 h for each experiment. Left pie charts: orange: DDN remained in diazotrophs (orange); yellow: DDN released to the dissolved pool; dark blue: DDN transferred to non-diazotrophic plankton. Right pie charts, from dark blue to light blue: relative DDN transferred to Synechococcus, Prochlorococcus, bacteria, diatoms, pico-eukaryotes and nano-eukaryotes in E1 (top), E2 (middle) and E3 (bottom pie chart).

## 3.4 DDN transfer to zooplankton

Before incubation with zooplankton, the isotopic enrichment of the 15N pre-labelled plankton was not significantly different in experiments Zoo-1, Zoo-2 and Zoo-3 (dominated by Trichodesmium) averaging 1.035 ± 0.091 at. % (n=9). The isotopic enrichment was lower in the Zoo-4 experiment (dominated by UCYN-B), averaging 0.385 ± 0.005 at. % (n=3). After 24 h of incubation with zooplankton, the 15N enrichment of the 15N pre-labelled plankton decreased to 0.431 ± 0.014 at. % on average in Zoo-1, Zoo-2 and Zoo-3, and to 0.372 ± 0.010 at. % in Zoo-4. Meanwhile, the 15N enrichment of zooplankton increased as compared to T0 values (0.383 at. % on average) and reached 0.482, 0.376, 0.513 and 0.368 at. % on average in Zoo-1, Zoo-2, Zoo-3 and Zoo-4, respectively. As the 15N enrichment of the initial source food (15N pre-labelled plankton) was different between the four stations/experiments, and in order to compare the results obtained among experiments, we normalized the values as the percentage of initial amount of 15N atoms in excess in the 15N pre-labelled plankton transferred to the different compartments (i.e. conserved in the 15N pre-labelled plankton pool, transferred to the zooplankton pool and to the NH${}_{\mathrm{4}}^{+}$ pool) at the end of the incubation. In the experiments where Trichodesmium dominated the diazotroph community (Zoo-1, Zoo-2, and Zoo-3), 19 ± 7 to 48 ± 21 % of the initial DD15N remained in the phytoplankton pool, 5 ± 5 to 9 ± 13 % was transferred to the zooplankton and 0.4 ± 0.3 to 7 ± 3 % was transferred to the NH${}_{\mathrm{4}}^{+}$ pool (Fig. 5). In Zoo-4 (where UCYN dominated the diazotroph community, Table 1), a greater proportion of DD15N was conserved in the phytoplankton (76 ± 34 %), but a greater transfer to the zooplankton was also observed (28 ± 8 %, Fig. 5). The recovery of the initial DD15N was comprised between 29 % and 100 %, suggesting that the remaining fraction was released to the DON pool. Interestingly, the recovery of the DD15N was in surplus in the Zoo-4 experiment (112.5 ± 8.5 %), suggesting that the DD15N transfer in the DON pool is close to zero.

Figure 5DD15N transferred (%) in the NH${}_{\mathrm{4}}^{+}$ pool (white), zooplankton (light grey), and what remained in the phytoplankton pool (black) after 24 h of incubation. Error bars represent the standard deviations of triplicate incubations and the propagated analytical errors.

4 Discussion

## 4.1 DDN release to the dissolved pool

The quantity and quality of N released by diazotrophs to the dissolved pool during N2 fixation potentially play a key role in shaping the planktonic and microbial food webs. In this study, Trichodesmium released 14 ± 4 to 40 ± 57 % of the newly fixed N into the dissolved pool, which is in agreement with values reported in the literature for field studies . DON accounted for  95 % of the DDN released by Trichodesmium (Fig. 2), according with contributions measured in culture (80–90 %; ) and in the field . The low contribution of NH${}_{\mathrm{4}}^{+}$ to the DDN release does not mean that it was not released, but is likely the result of immediate consumption by surrounding plankton, which shows a great affinity for NH${}_{\mathrm{4}}^{+}$. Similarly, part of the DON released by Trichodesmium was probably taken up by heterotrophic and mixotrophic plankton , but a significant fraction was likely refractory (not easily available for organisms), leading to the observed accumulation in the dissolved pool. If not refractory, the DON would likely have been immediately assimilated as the regions where these experiments were performed are strongly limited by N availability .

In the E1 experiment, we noticed a large variability of N2 fixation and DDN release rates among the three replicates, which explains the high standard deviations (Fig. 2): two replicates exhibited net N2 fixation rates  25–30 nmol N L−1 48 h−1 and DDN release rates  7–10 nmol N L−1 48 h−1, whereas in the third replicate, the DDN release ( 24 nmol N L−1 48 h−1) exceeded net N2 fixation rates (5 nmol N L−1 48 h−1). This can be attributed to the decline of Trichodesmium in this replicate as we counted much more degraded trichomes in the third replicate. This suggests that decaying Trichodesmium release DDN more efficiently than healthy Trichodesmium, which has already been observed by . This may also explain why the DDN transfer to non-diazotrophic plankton was slightly higher in E1 (10 ± 2 %) than in E2 (7 ± 1 %), despite both stations being dominated by Trichodesmium.

Conversely to E1 and E2, the DDN released by UCYN-B (E3) was not quantifiable in our study. However, significant DDN transfer into non-diazotrophic plankton was detected (15 ± 3 % of the total fixed N, Fig. 4), suggesting that the DDN released to the dissolved pool is likely immediately transferred to surrounding communities. To our knowledge, this is the first report of DDN release in the field in the presence of a diazotroph community dominated by UCYN-B. report low release from UCYN-C in coastal waters of the WTSP (16 ± 6 % of total N2 fixation) compared to Trichodesmium (13 ± 2 to 48 ± 5 %; ). This seems to indicate that the DDN from UCYN is generally lower than the DDN from Trichodesmium. Several hypotheses may explain the differences observed between Trichodesmium and UCYN. DDN compounds released by UCYN may be more bio-available than the DDN released by Trichodesmium, limiting its accumulation. The lack of accumulation in E3 could also be due to the more severe N limitation of planktonic communities in the ultra-oligotrophic waters as compared to MA waters , and to the nature of the resident community. Prochlorococcus was dominating the planktonic community at LD C (E3) and is known to have a high affinity with its small surface to volume ratio . PCD causing Trichodesmium bloom demise can also be involved in the relatively high DDN release and accumulation during Trichodesmium-dominated experiments . Exogenous factors, such as viral lyses (Fuhrman1999) and sloppy feeding , are also suspected to enhance the DDN release. These factors were found to exert a higher pressure in the MA waters where Trichodesmium dominated compared to ultra-oligotrophic waters , where UCYN-B dominated. Finally, part of the discrepancy might be due to a methodological artefact: different sampling procedures between E1 and E2 (pump) and E3 (Niskin bottles) as the pump is suspected to induce mechanical stress to the cells which may have potentially affected the DDN release.

The DDN release plays a key role in the transfer of N from diazotrophs to the surrounding non-diazotrophs, only it is not a good indicator of the DDN transfer efficiency as we observed that DDN transfer to non-diazotrophs was higher when the release was low (E3) than when it was high (E1 and E2). This has already been observed in coastal waters of the WTSP by .

## 4.2 DDN transfer efficiency and pathways in the WTSP

Here we report for the first time data on the transfer of DDN to the planktonic food web under contrasting diazotroph community composition in the open ocean. We reveal that 7 ± 1 to 15 ± 3 % of the DDN is transferred to the non-diazotrophic plankton (Fig. 4) at short timescales (48 h), which is of the same order of magnitude as the transfer ( 10 %) reported in coastal waters of the WTSP . In terms of efficiency, despite UCYN-B fix at lower rates compared to Trichodesmium, the DDN originating from UCYN-B is more efficiently transferred to non-diazotrophic plankton (15 ± 3 % of total fixed N in the E3 experiment, Fig. 4) compared to the DDN originating from Trichodesmium (10 ± 2 and 7 ± 1 % in the E1 and E2 experiments, respectively). This results is in accordance with the fact that we did not detect any accumulation of 15N-labelled N forms in the dissolved pool (see section above).

Several studies have proven that a fraction of the DDN release is transferred to surrounding non-diazotrophic plankton, and one of them concludes that diatoms are the major beneficiaries of the DDN originating from Trichodesmium and develop extensively during/after Trichodesmium blooms in the coastal WTSP ocean. Despite Trichodesmium being rarely recovered in sediment traps , these authors hypothesize a tight coupling between Trichodesmium blooms and export of organic matter as diatoms are efficient exporters of organic carbon to depth . In contrast, in the present study, > 90 % of the DDN was transferred to picoplankton (Synechococcus, Prochlorococcus and bacteria), whatever the station studied (Fig. 4). The cyanobacteria Synechococcus and Prochlorococcus were the primary beneficiaries (73 ± 15, 68 ± 14 and 65 ± 13 % of the DDN transfer, Fig. 4), which is consistent with , who observed a positive correlation between N2 fixation rates and the abundance of Synechococcus and Prochlorococcus in the WTSP. We attributed this difference between the present study and the study to the phytoplanktonic populations present in ambient waters at the time of the experiments. In the study, diatoms were accounting for  30 % of the non-diazotrophic phytoplankton biomass at T0, whereas diatoms were scarce (1 % of the non-diazotrophic phytoplankton biomass) in our offshore experiments, i.e. too low to show a significant increase in 48 h, even if they benefited from the DDN. However, in E2 (LD B), the diatom abundances were the highest of the three experiments and the bloom at this station was mainly composed of diatoms and Trichodesmium, suggesting that Trichodesmium contributed to sustain this bloom.

In the E1 and E2 experiments, where Trichodesmium was the dominant diazotroph , the DDN was preferentially transferred to Synechococcus, while it was preferentially transferred to Prochlorococcus in E3 where UCYN-B was the dominant diazotroph . This suggests a possible coupling between Synechococcus and Trichodesmium as ever mentioned by , who report higher Synechococcus abundances inside Trichodesmium blooms compared to surrounding waters, while it is not the case for other plankton groups. This difference may also be linked with the communities present at the time of the experiments: Prochlorococcus accounted for  65 % of pico-phytoplankton in E1 and E2, while it accounted for  80 % in GY in E3. While the transfer of DDN to Prochlorococcus and Synechococcus together was roughly equivalent for E1 and E2 ( 70 %, Fig. 4), Synechococcus abundances increased by 150 % in E1, and Prochlorococcus increased by 12 % during the time course of the experiment, while none of the populations increased in abundance in E2 (Fig. S1 in the Supplement). This result is in agreement with , who report an increase of the grazing pressure with the decrease of the oligotrophic degree as E1 was performed in more oligotrophic waters than E2.

Besides Prochlorococcus and Synechococcus, heterotrophic bacteria were the second beneficiaries of the DDN, especially when the diazotroph community was dominated by UCYN-B (34 ± 7 % of the DDN transfer, Fig. 4). In this experiment, bacteria abundances increased by 70 % on average (Fig. S1), which is in agreement with and , who reported similar bacterial increases in the coastal WTSP. When Trichodesmium was the dominant diazotroph, 23–25 % was transferred to bacteria, whose abundance increased by 135 and 15 % in E1 and E2, consistent with , who reported higher bacterial abundances in Trichodesmium blooms than in surrounding waters. The significant DDN transfer from Trichodesmium to bacteria concurs with Trichodesmium and bacteria association that has been largely highlighted in the last decades . That is in accordance with , who report that N2 fixation fuels 3–35 % of bacterial production in MA waters. Then, we could not discriminate the DDN transfer to pico- and nano-eukaryotes, but for diatoms, the DDN transfer represented a low contribution to the overall transfer into non-diazotrophs in this region of the open ocean.

## 4.3 Transfer of DDN to zooplankton

Regarding higher trophic levels, the experiments performed here show that the DDN transfer to the major group of zooplankton present in this ecosystem (the copepod Clausocalanus) was less efficient (Fig. 5) when the diazotroph community was dominated by Trichodesmium ( 5–9 %) than when it was dominated by UCYN-B ( 28 %). This result is consistent with a previous study based on analogous 15N2 labelling method in coastal waters of the WTSP , which also report a higher DDN transfer efficiency in the presence of UCYN. Regarding the DDN transfer from UCYN-B, although the transfer experiments to phytoplankton and bacteria (E3) and zooplankton (Zoo-4) were not performed in the same incubation bottles, they consistently report lower 15N enrichments in all the studied pools as compared to the experiments performed when Trichodesmium dominated, but in fine, the DDN transfer efficiency was more important in the presence of UCYN. We observed that a larger fraction of DDN was conserved in the UCYN-B pool than in the Trichodesmium pool, and a larger part of the DDN was missing (likely associated with the DON pool) with Trichodesmium than with UCYN-B (Fig. 5). These observations are consistent with the transfer experiments E1, E2, and E3 which show that Trichodesmium released more DDN in the dissolve pool (DON + NH${}_{\mathrm{4}}^{+}$) than UCYN-B. The DDN released in the NH${}_{\mathrm{4}}^{+}$ pool did not presented significant differences between Trichodesmium (Zoo-1, Zoo-2 and Zoo-3) and UCYN-B (Zoo-4), and in all experiments, the DDN contribution was low in the NH${}_{\mathrm{4}}^{+}$ pool, as it was immediately assimilated by surrounding organisms as explained in Sect. 4.1. We suggest that the DDN transfer was higher with UCYN than with Trichodesmium since the UCYN-B can be directly grazed due to their small size (2–3 µm) as mentioned in , who revealed high UCYN abundances in the copepod guts based on qPCR data, while less Trichodesmium was measured. This pleads for a direct transfer of DDN from UCYN-B to zooplankton and an indirect transfer from Trichodesmium through non-diazotrophs. At the ecosystem level, even if the DDN transfer efficiency ( 15 %) to zooplankton from UCYN-B is higher than the one of Trichodesmium, the ultimate quantity of DDN transferred to secondary producers is higher when Trichodesmium dominates, as cell-specific N2 fixation rates of Trichodesmium ( 250–340 fmol N cell−1 48 h−1) are far higher than those of UCYN-B ( 19 fmol N cell−1 48 h−1). This result is in agreement with results based on 15N isotopic data showing that  50–95 and  10–40 % of the zooplankton N content originates from N2 fixation in MA and GY waters, respectively. Finally, the DDN transferred to zooplankton, either directly or indirectly, may be released in the dissolved pool as NH${}_{\mathrm{4}}^{+}$, providing additional NH${}_{\mathrm{4}}^{+}$ from DDN in the environment that is likely assimilated by organisms in N-depleted waters. Thus, zooplankton N release appears as another DDN transfer pathway to the microbial communities in the WTSP. Zooplankton can contribute to organic matter export by production of sinking fecal pellets, active transport to depth and carcass export. These processes are increasingly recognized as important vectors of organic matter export, and the magnitudes of their contributions to organic matter export are highly dependent on regionally variable plankton community structure . In the WTSP, where N2 fixation sustains most of the new primary production and an important fraction of the DDN is transferred to zooplankton, it might play a key role in the export production and hence the CO2 sink which is the WTSP.

5 Conclusion and ecological impact of N2 fixation in the WTSP

N2 fixation acts as a natural N fertilizer in the ocean, releasing DDN in the dissolved pool, which is available for surrounding marine organisms. To our knowledge, this study provides the first quantification of DDN transfer to phytoplankton, bacteria and zooplankton communities in open ocean waters. The main interest of this study was to compare DDN transfer and release under contrasting N2 fixation activity and diversity.

Here, we reveal that Trichodesmium released more DDN than UCYN-B, but a significant part of the DDN released by Trichodesmium accumulated in the dissolved pool, while the DDN released by UCYN-B immediately assimilated by the surrounding plankton communities. The DDN transfer efficiency to non-diazotrophic plankton was higher when UCYN-B dominated the diazotroph community than when Trichodesmium dominated. In the open ocean, most N2 fixation is performed by Trichodesmium ; thus, on a global scale most of the DDN transfer can be attributed to Trichodesmium. The regions where UCYN are the dominant diazotrophs generally present lower N2 fixation rates than the ones where Trichodesmium dominates, but UCYN provide a continuous source of DDN to surrounding plankton communities. The DDN was transferred to pico-plankton, which dominated the WTSP, suggesting that N2 fixation fuelled the growth of biomass in the N-depleted environment. This is consistent with , who revealed that N2 fixation provides > 90 % of the new N to the photic layer of the WTSP. On a larger-scale view, the simulation performed by predicts that diazotrophs will support a large part of primary production ( 15 %) in low nutrient low chlorophyll regions of the Pacific Ocean, comprising the WTSP.

Overall, this study indicates that N2 fixation plays a key role in the marine biomass production, the structure of the planktonic food web, and finally the export of organic matter towards the deep ocean. The DDN can be exported to the deep ocean by different pathways: (i) the direct of export of diazotrophs, (ii) the export of non-diazotrophs which benefited from the DDN, and (iii) the export of zooplankton which benefited from the DDN. The direct export of diazotrophs accounted for  30 % of total C export at LD A (E1), 5 % at LD B (E2) and < 0.1 % at LD C (E3) . Using a δ15N budget, found that 50–80 % of exported material was sustained by N2 fixation (this includes both direct and indirect export of DDN). Thus, N2 fixation has ineluctably a key role in the biological carbon pump, as mentioned in , who reveal a significant biological “soft tissue” carbon pump in the MA waters almost exclusively sustained by N2 fixation, and acting as a net sink for of atmospheric CO2 in the WTSP.

Data availability
Data availability.

All data and metadata are available at the French INSU/CNRS LEFE CYBER database (scientific coordinator: Hervé Claustre; data manager and webmaster: Catherine Schmechtig) at the following web address: http://www.obs-vlfr.fr/proof/php/outpace/outpace.php (INSU/CNRS LEFE CYBER, 2017).

Supplement
Supplement.

Competing interests
Competing interests.

The authors declare that they have no conflict of interest.

Special issue statement
Special issue statement.

This article is part of the special issue “Interactions between planktonic organisms and biogeochemical cycles across trophic and N2 fixation gradients in the western tropical South Pacific Ocean: a multidisciplinary approach (OUTPACE experiment)”. It is not associated with a conference.

Acknowledgements
Acknowledgements.

This is a contribution of the OUTPACE (Oligotrophy from Ultra-oligoTrophy PACific Experiment) project (https://outpace.mio.univ-amu.fr/, last access: 31 December 2017) funded by the French research national agency (ANR-14-CE01-0007-01), the LEFE-CyBER program (CNRS-INSU), IRD, the GOPS program and the CNES (BC T23, ZBC 4500048836). The OUTPACE cruise (https://doi.org/10.17600/15000900) was managed by the MIO (OSU Institut Pytheas, AMU) from Marseille (France) and received funding from European FEDER Fund under project 1166-39417. The authors thank the crew of the R/V L'Atalante for outstanding shipboard operation. Gilles Rougier and Marc Picheral are warmly thanked for their efficient help in CTD rosette management and data processing, as is Catherine Schmechtig for the LEFE CYBER database management. The satellite-derived data of sea surface temperature, chl a concentration and current have been provided by CLS in the framework of the CNES funding; we warmly thank Marie Isabelle Pujol and Gillaume Taburet for their support in providing these data. We acknowledge NOAA, and in particular Rick Lumpkin, for providing the SVP drifter.

Edited by: Douglas G. Capone
Reviewed by: Carolin Löscher and one anonymous referee

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